ATM c.2863C>A ;(p.P955T)

Variant ID: 11-108141815-C-A

NM_000051.3(ATM):c.2863C>A;(p.P955T)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Next-generation sequencing in thyroid cancers: do targetable alterations lead to a therapeutic advantage?: A multicenter experience.

Medicine
Moore, Assaf A; Bar, Yael Y; Maurice-Dror, Corinne C; Finkel, Inbar I; Goldvaser, Hadar H; Dudnik, Elizabeth E; Goldstein, Daniel A DA; Gordon, Noa N; Billan, Salem S; Gutfeld, Orit O; Wolf, Ido I; Popovtzer, Aron A
Publication Date: 2021-06-25

Variant appearance in text: ATM: P955T
PubMed Link: 34160418
Variant Present in the following documents:
  • Main text
  • medi-100-e26388.pdf
View BVdb publication page