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VARIANT - TERM ANNOTATION REPORT

RGD ID: 8599005
Species: Homo sapiens
RGD Object: Variant
Symbol: CV27408
Name: NM_000546.6(TP53):c.451C>A (p.Pro151Thr)
Acc ID: DOID:0111503
Term: Li-Fraumeni syndrome 1
Definition: A Li-Fraumeni syndrome that has_material_basis_in heterozygous mutation in the TP53 gene on chromosome 17p13.1. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/1978757 "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)
CV27408 IAGP 8554872ClinVarClinVar Annotator: match by term: Li-Fraumeni syndrome 1PMID:10713666 PMID:11479205 PMID:12826609 PMID:16861262 PMID:20128691 PMID:20522432 PMID:21343334 PMID:23625637 PMID:25503501 PMID:25741868 PMID:26619011 PMID:28492532 PMID:29979965 PMID:30224644 PMID:7881428 PMID:8364550
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