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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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