ATM c.2879C>T ;(p.P960L)

Variant ID: 11-108141831-C-T

NM_000051.3(ATM):c.2879C>T;(p.P960L)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


A computational and structural analysis of germline and somatic variants affecting the DDR mechanism, and their impact on human diseases.

Scientific Reports
Magraner-Pardo, Lorena L; Laskowski, Roman A RA; Pons, Tirso T; Thornton, Janet M JM
Publication Date: 2021-07-12

Variant appearance in text: ATM: 2879C>T; P960L; rs587779828
PubMed Link: 34253785
Variant Present in the following documents:
  • 41598_2021_93715_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



Pancreatic endocrine tumours: mutational and immunohistochemical survey of protein kinases reveals alterations in targetable kinases in cancer cell lines and rare primaries.

Annals Of Oncology : Official Journal Of The European Society For Medical Oncology
Corbo, V V; Beghelli, S S; Bersani, S S; Antonello, D D; Talamini, G G; Brunelli, M M; Capelli, P P; Falconi, M M; Scarpa, A A
Publication Date: 2012-01

Variant appearance in text: ATM: 2879C>T
PubMed Link: 21447618
Variant Present in the following documents:
  • Main text
View BVdb publication page



Mutational profiling of kinases in human tumours of pancreatic origin identifies candidate cancer genes in ductal and ampulla of vater carcinomas.

Plos One
Corbo, Vincenzo V; Ritelli, Rossana R; Barbi, Stefano S; Funel, Niccola N; Campani, Daniela D; Bardelli, Alberto A; Scarpa, Aldo A
Publication Date: 2010-09-08

Variant appearance in text: ATM: 2879C>T
PubMed Link: 20838624
Variant Present in the following documents:
  • Main text
View BVdb publication page