MSH6 c.2294G>A ;(p.C765Y)

Variant ID: 2-48027416-G-A

NM_000179.2(MSH6):c.2294G>A;(p.C765Y)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Distinctive DNA mismatch repair and APC rare variants in African Americans with colorectal neoplasia.

Oncotarget
Ashktorab, Hassan H; Azimi, Hamed H; Varma, Sudhir S; Tavakoli, Payaam P; Nickerson, Michael L ML; Brim, Hassan H
Publication Date: 2017-11-21

Variant appearance in text: MSH6: C765Y
PubMed Link: 29245953
Variant Present in the following documents:
  • oncotarget-08-99966-s003.xlsx, sheet 2
View BVdb publication page



MSH6 mutations arise in glioblastomas during temozolomide therapy and mediate temozolomide resistance.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Yip, Stephen S; Miao, Jiangyong J; Cahill, Daniel P DP; Iafrate, A John AJ; Aldape, Ken K; Nutt, Catherine L CL; Louis, David N DN
Publication Date: 2009-07-15

Variant appearance in text: MSH6: 2294G>A; Cys765Tyr
PubMed Link: 19584161
Variant Present in the following documents:
  • Main text
View BVdb publication page