MSH6 c.1265A>C ;(p.D422A)

Variant ID: 2-48026387-A-C

NM_000179.2(MSH6):c.1265A>C;(p.D422A)

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:

Transcriptional mutagenesis induced by 8-oxoguanine in mammalian cells.

Plos Genetics
Brégeon, Damien D; Peignon, Paul-Antoine PA; Sarasin, Alain A
Publication Date: 2009-07

Variant appearance in text: MSH6: D422A
PubMed Link: 19629170
Variant Present in the following documents:
  • Main text
  • pgen.1000577.pdf
View BVdb publication page