ATM c.5229A>G ;(p.T1743=)

Variant ID: 11-108172426-A-G

NM_000051.3(ATM):c.5229A>G;(p.T1743=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identifying sequence variants contributing to hereditary breast and ovarian cancer in BRCA1 and BRCA2 negative breast and ovarian cancer patients.

Scientific Reports
Jarhelle, Elisabeth E; Riise Stensland, Hilde Monica Frostad HMF; Hansen, Geir Åsmund Myge GÅM; Skarsfjord, Siri S; Jonsrud, Christoffer C; Ingebrigtsen, Monica M; Strømsvik, Nina N; Van Ghelue, Marijke M
Publication Date: 2019-12-27

Variant appearance in text: ATM: 5229A>G
PubMed Link: 31882575
Variant Present in the following documents:
  • Main text
  • 41598_2019_Article_55515.pdf
View BVdb publication page