ATM c.4315C>T ;(p.L1439F)

Variant ID: 11-108160407-C-T

NM_000051.3(ATM):c.4315C>T;(p.L1439F)

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:

Case Report: Triple Primary Malignant Tumors of the Esophagus, Stomach, and Colon in a Patient With Genetic Analysis.

Frontiers In Genetics
Zhan, Xiaoli X; He, Lingzhe L; Song, Kai K; Cao, Shuliang S; Meng, Erhong E; Wang, Yuedong Y
Publication Date: 2021

Variant appearance in text: ATM: 4315C>T; L1439F
PubMed Link: 34306021
Variant Present in the following documents:
  • Main text
  • fgene-12-676497.pdf
View BVdb publication page