ATM c.2606C>G ;(p.A869G)

Variant ID: 11-108138037-C-G

NM_000051.3(ATM):c.2606C>G;(p.A869G)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A computational and structural analysis of germline and somatic variants affecting the DDR mechanism, and their impact on human diseases.

Scientific Reports
Magraner-Pardo, Lorena L; Laskowski, Roman A RA; Pons, Tirso T; Thornton, Janet M JM
Publication Date: 2021-07-12

Variant appearance in text: N/A
PubMed Link: 34253785
Variant Present in the following documents:
View BVdb publication page