MSH6 c.766_767delinsGC ;(p.S256A)

Variant ID: 2-48025888-AG-GC

NM_000179.2(MSH6):c.766_767delinsGC;(p.S256A)

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:

Phosphorylated hMSH6: DNA mismatch versus DNA damage recognition.

Mutation Research
Kaliyaperumal, Saravanan S; Patrick, Steve M SM; Williams, Kandace J KJ
Publication Date: 2011-01-10

Variant appearance in text: MSH6: S256A
PubMed Link: 21035467
Variant Present in the following documents:
  • Main text
View BVdb publication page