ATM c.4486G>T ;(p.D1496Y)

Variant ID: 11-108163395-G-T

NM_000051.3(ATM):c.4486G>T;(p.D1496Y)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Sequencing of Lynch syndrome tumors reveals the importance of epigenetic alterations.

Oncotarget
Porkka, Noora N; Valo, Satu S; Nieminen, Taina T TT; Olkinuora, Alisa A; Mäki-Nevala, Satu S; Eldfors, Samuli S; Peltomäki, Päivi P
Publication Date: 2017-12-08

Variant appearance in text: ATM: D1496Y
PubMed Link: 29296220
Variant Present in the following documents:
  • oncotarget-08-108020-s006.xlsx, sheet 1
View BVdb publication page