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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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