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.




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