<opt>
  <data id="7_100318423_duplication" allele_string="duplication" assembly_name="GRCh38" end="100321323" input="7 100318423 100321323 DUP 1" most_severe_consequence="splice_polypyrimidine_tract_variant" seq_region_name="7" start="100318423" strand="1">
    <transcript_consequences biotype="protein_coding" bp_overlap="2901" cdna_end="2312" gene_id="ENSG00000214300" gene_symbol="SPDYE3" gene_symbol_source="HGNC" hgnc_id="HGNC:35462" impact="LOW" percentage_overlap="20.01" strand="1" transcript_id="ENST00000332397" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>coding_sequence_variant</consequence_terms>
      <consequence_terms>3_prime_UTR_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>feature_elongation</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="retained_intron" bp_overlap="2712" gene_id="ENSG00000214300" gene_symbol="SPDYE3" gene_symbol_source="HGNC" hgnc_id="HGNC:35462" impact="LOW" percentage_overlap="40.51" strand="1" transcript_id="ENST00000380765" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000674842" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4334" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000674972" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="885" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="7.31" strand="-1" transcript_id="ENST00000674981" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="2436" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="13.98" strand="-1" transcript_id="ENST00000675162" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="415" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000675610" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4337" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000675620" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000675639" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4337" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000675640" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000676155" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="828" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="5.37" strand="-1" transcript_id="ENST00000676198" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="2102" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="12.54" strand="-1" transcript_id="ENST00000676200" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000676204" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="885" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="5.71" strand="-1" transcript_id="ENST00000676241" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="retained_intron" bp_overlap="409" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="4.63" strand="-1" transcript_id="ENST00000676256" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000676274" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4334" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000685342" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000685473" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000685499" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="2901" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" percentage_overlap="8.08" strand="-1" transcript_id="ENST00000685541" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
      <consequence_terms>feature_elongation</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4337" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000685607" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000685670" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000685700" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="2901" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" percentage_overlap="8.07" strand="-1" transcript_id="ENST00000685724" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
      <consequence_terms>feature_elongation</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000685805" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000685852" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="415" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.76" strand="-1" transcript_id="ENST00000685901" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="981" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="6.28" strand="-1" transcript_id="ENST00000686203" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4336" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000686569" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4337" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000686594" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="414" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000686797" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4337" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000686825" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="988" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="6.32" strand="-1" transcript_id="ENST00000686838" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000686890" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4334" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000687026" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4337" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000687053" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="825" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="5.33" strand="-1" transcript_id="ENST00000687177" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="2429" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="14.22" strand="-1" transcript_id="ENST00000687616" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="408" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000687713" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000687801" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000688104" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000688544" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="412" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000689000" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="410" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000689019" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000689267" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000689447" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4336" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000689538" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000689609" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000689719" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="416" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.76" strand="-1" transcript_id="ENST00000689817" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000689907" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="415" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000690446" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4337" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000690914" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="409" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000690988" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000691046" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4334" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000691107" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000691110" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000691247" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000691275" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="659" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="4.3" strand="-1" transcript_id="ENST00000691424" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000691428" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4337" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000691660" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000691707" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000691816" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4341" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000691842" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000691905" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000691910" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4337" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000692231" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="422" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.8" strand="-1" transcript_id="ENST00000692261" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="2901" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" percentage_overlap="8.07" strand="-1" transcript_id="ENST00000692351" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
      <consequence_terms>feature_elongation</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4337" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000692675" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000692687" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4337" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000692752" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000692947" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000693010" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000693042" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000693192" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000693215" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000693302" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000693490" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000700850" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4320" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000700905" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="410" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000701011" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000701138" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="2901" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" percentage_overlap="8.1" strand="-1" transcript_id="ENST00000701204" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
      <consequence_terms>feature_elongation</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000701582" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="401" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.67" strand="-1" transcript_id="ENST00000701649" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000701653" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000701849" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="413" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000701970" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4337" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000702039" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="2901" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" percentage_overlap="8.08" strand="-1" transcript_id="ENST00000702062" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
      <consequence_terms>feature_elongation</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000702164" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000702228" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4337" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000702250" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000702364" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000702448" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4337" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000702527" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000702566" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000702596" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000702608" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="411" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000702615" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="407" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="LOW" percentage_overlap="2.71" strand="-1" transcript_id="ENST00000702718" variant_allele="duplication">
      <consequence_terms>splice_polypyrimidine_tract_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" bp_overlap="2901" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" percentage_overlap="9.66" strand="-1" transcript_id="ENST00000702720" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
      <consequence_terms>feature_elongation</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4337" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000702773" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4337" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000702822" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="processed_transcript" distance="4341" gene_id="ENSG00000078319" gene_symbol="PMS2P1" gene_symbol_source="HGNC" hgnc_id="HGNC:9123" impact="MODIFIER" strand="-1" transcript_id="ENST00000702891" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
  </data>
</opt>
