ATM c.5089A>C ;(p.T1697P)

Variant ID: 11-108170524-A-C

NM_000051.3(ATM):c.5089A>C;(p.T1697P)

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:

Whole exome sequencing of pediatric leukemia reveals a novel InDel within FLT-3 gene in AML patient from Mizo tribal population, Northeast India.

Bmc Genomic Data
Vanlallawma, Andrew A; Lallawmzuali, Doris D; Pautu, Jeremy L JL; Scaria, Vinod V; Sivasubbu, Sridhar S; Kumar, Nachimuthu Senthil NS
Publication Date: 2022-03-28

Variant appearance in text: ATM: T1697P
PubMed Link: 35350997
Variant Present in the following documents:
  • 12863_2022_Article_1037.pdf
View BVdb publication page