MSH6 c.95_96delinsAG ;(p.G32E)

Variant ID: 2-48010467-GC-AG

NM_000179.2(MSH6):c.95_96delinsAG;(p.G32E)

This variant was identified in 1 publication

View GRCh38 version.



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

Publications:

DNA mismatch repair network gene polymorphism as a susceptibility factor for pancreatic cancer.

Molecular Carcinogenesis
Dong, Xiaoqun X; Li, Yanan Y; Chang, Ping P; Hess, Kenneth R KR; Abbruzzese, James L JL; Li, Donghui D
Publication Date: 2012-06

Variant appearance in text: MSH6: G32E
PubMed Link: 21681824
Variant Present in the following documents:
  • Main text
View BVdb publication page