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BRCA2 c.2746_2747delinsAC ;(p.C916T)
Variant ID: 13-32911238-TG-AC
NM_000059.3(
BRCA2
):c.2746_2747delinsAC;(p.C916T)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Neurofibromin 1 (NF1) defects are common in human ovarian serous carcinomas and co-occur with TP53 mutations.
Neoplasia (New York, N.Y.)
Sangha, Navneet N; Wu, Rong R; Kuick, Rork R; Powers, Scott S; Mu, David D; Fiander, Diane D; Yuen, Kit K; Katabuchi, Hidetaka H; Tashiro, Hironori H; Fearon, Eric R ER; Cho, Kathleen R KR
Publication Date: 2008-12
Variant appearance in text: BRCA2: C916T
PubMed Link:
19048115
Variant Present in the following documents:
Main text
View BVdb publication page