ATM c.5723C>T ;(p.T1908I)

Variant ID: 11-108178672-C-T

NM_000051.3(ATM):c.5723C>T;(p.T1908I)

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:

The Importance of Targeted Next-Generation Sequencing Usage in Cytogenetically Normal Myeloid Malignancies.

Mediterranean Journal Of Hematology And Infectious Diseases
Atli, Emine Ikbal EI; Gurkan, Hakan H; Atli, Engin E; Kirkizlar, Hakki Onur HO; Yalcintepe, Sinem S; Demir, Selma S; Demirci, Ufuk U; Eker, Damla D; Mail, Cisem C; Kalkan, Rasime R; Demir, Ahmet Muzaffer AM
Publication Date: 2021

Variant appearance in text: ATM: 5723C>T
PubMed Link: 33489052
Variant Present in the following documents:
  • mjhid-13-1-e2021013.pdf
View BVdb publication page