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MSH6 c.715A>T ;(p.R239W)
Variant ID: 2-48025837-A-T
NM_000179.2(
MSH6
):c.715A>T;(p.R239W)
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:
Collaborative Group of the Americas on Inherited Gastrointestinal Cancers (CGA-IGC) Annual Virtual Meeting, November 13-15, 2021.
Familial Cancer
Publication Date: 2022-10
Variant appearance in text: MSH6: Arg239Trp
PubMed Link:
35366121
Variant Present in the following documents:
Main text
10689_2021_Article_284.pdf
View BVdb publication page