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ATM c.2645T>C ;(p.I882T)
Variant ID: 11-108139143-T-C
NM_000051.3(
ATM
):c.2645T>C;(p.I882T)
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:
Integrating somatic variant data and biomarkers for germline variant classification in cancer predisposition genes.
Human Mutation
Walsh, Michael F MF; Ritter, Deborah I DI; Kesserwan, Chimene C; Sonkin, Dmitriy D; Chakravarty, Debyani D; Chao, Elizabeth E; Ghosh, Rajarshi R; Kemel, Yelena Y; Wu, Gang G; Lee, Kristy K; Kulkarni, Shashikant S; Hedges, Dale D; Mandelker, Diana D; Ceyhan-Birsoy, Ozge O; Luo, Minjie M; Drazer, Michael M; Zhang, Liying L; Offit, Kenneth K; Plon, Sharon E SE
Publication Date: 2018-11
Variant appearance in text: ATM: Ile882Thr
PubMed Link:
30311369
Variant Present in the following documents:
Main text
View BVdb publication page