ATM c.1562G>C ;(p.R521T)

Variant ID: 11-108121754-G-C

NM_000051.3(ATM):c.1562G>C;(p.R521T)

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:

Targeted sequencing identifies the mutational signature of double primary and metastatic malignancies: a case report.

Diagnostic Pathology
Rao, Chuangzhou C; Nie, Liangqin L; Miao, Xiaobo X; Lizaso, Analyn A; Zhao, Guofang G
Publication Date: 2019-09-04

Variant appearance in text: ATM: 1562G>C; R521T
PubMed Link: 31484545
Variant Present in the following documents:
  • 13000_2019_Article_874.pdf
View BVdb publication page