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.




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