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ATM c.4912A>T ;(p.N1638Y)
Variant ID: 11-108168016-A-T
NM_000051.3(
ATM
):c.4912A>T;(p.N1638Y)
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 Genome Interpretation for a Family of Five.
Frontiers In Genetics
Corpas, Manuel M; Megy, Karyn K; Mistry, Vanisha V; Metastasio, Antonio A; Lehmann, Edmund E
Publication Date: 2021
Variant appearance in text: ATM: 4912A>T
PubMed Link:
33763108
Variant Present in the following documents:
Main text
View BVdb publication page