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VARIANT - TERM ANNOTATION REPORT

RGD ID: 8559000
Species: Homo sapiens
RGD Object: Variant
Symbol: CV20929
Name: NM_006502.3(POLH):c.1117C>T (p.Gln373Ter)
Acc ID: DOID:0110847
Term: xeroderma pigmentosum variant type
Definition: A xeroderma pigmentosum characterized by normal DNA excision repair, but defective postreplication repair that has_material_basis_in mutations in the POLH gene on chromosome 6p21.1. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/10385124 "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/1054497 "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
CV20929 IAGP 8554872ClinVarClinVar Annotator: match by term: Xeroderma pigmentosum variant typePMID:10398605 PMID:11773631 PMID:24130121 PMID:25256075 PMID:28492532
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