ATM c.3853G>T ;(p.D1285Y)

Variant ID: 11-108155060-G-T

NM_000051.3(ATM):c.3853G>T;(p.D1285Y)

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:

Higher Mutation Burden in High Proliferation Compartments of Heterogeneous Melanoma Tumors.

International Journal Of Molecular Sciences
Grzywa, Tomasz M TM; Koppolu, Agnieszka A AA; Paskal, Wiktor W; Klicka, Klaudia K; Rydzanicz, Małgorzata M; Wejman, Jarosław J; Płoski, Rafał R; Włodarski, Paweł K PK
Publication Date: 2021-04-09

Variant appearance in text: ATM: 3853G>T; Asp1285Tyr
PubMed Link: 33918692
Variant Present in the following documents:
  • Main text
View BVdb publication page