MSH6 c.2641_2643delinsAAG ;(p.G881K)

Variant ID: 2-48027763-GGT-AAG

NM_000179.2(MSH6):c.2641_2643delinsAAG;(p.G881K)

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:

MSH6 missense mutations are often associated with no or low cancer susceptibility.

British Journal Of Cancer
Kariola, R R; Hampel, H H; Frankel, W L WL; Raevaara, T E TE; de la Chapelle, A A; Nyström-Lahti, M M
Publication Date: 2004-10-04

Variant appearance in text: MSH6: G881K
PubMed Link: 15354210
Variant Present in the following documents:
  • Main text
  • 91-6602129a.pdf
View BVdb publication page