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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