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MSH6 c.3261C>A ;(p.P1087=)
Variant ID: 2-48030647-C-A
NM_000179.2(
MSH6
):c.3261C>A;(p.P1087=)
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:
Germline MSH6 mutations are more prevalent in endometrial cancer patient cohorts than hereditary non polyposis colorectal cancer cohorts.
The Ulster Medical Journal
Devlin, Lisa A LA; Graham, Colin A CA; Price, John H JH; Morrison, Patrick J PJ
Publication Date: 2008-01
Variant appearance in text: MSH6: Pro1087Pro
PubMed Link:
18269114
Variant Present in the following documents:
Main text
umj7701-025.pdf
View BVdb publication page