ATM c.357A>C ;(p.E119D)

Variant ID: 11-108106422-A-C

NM_000051.3(ATM):c.357A>C;(p.E119D)

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:

Deep phylogeny of cancer drivers and compensatory mutations.

Communications Biology
Rochman, Nash D ND; Wolf, Yuri I YI; Koonin, Eugene V EV
Publication Date: 2020-10-02

Variant appearance in text: ATM: E119D
PubMed Link: 33009502
Variant Present in the following documents:
  • Main text
  • 42003_2020_Article_1276.pdf
View BVdb publication page