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MSH6 c.3678A>G ;(p.A1226=)
Variant ID: 2-48033374-A-G
NM_000179.2(
MSH6
):c.3678A>G;(p.A1226=)
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:
Screening of the DNA mismatch repair genes MLH1, MSH2 and MSH6 in a Greek cohort of Lynch syndrome suspected families.
Bmc Cancer
Thodi, Georgia G; Fostira, Florentia F; Sandaltzopoulos, Raphael R; Nasioulas, George G; Grivas, Anastasios A; Boukovinas, Ioannis I; Mylonaki, Maria M; Panopoulos, Christos C; Magic, Mirjana Brankovic MB; Fountzilas, George G; Yannoukakos, Drakoulis D
Publication Date: 2010-10-11
Variant appearance in text: MSH6: 3678A>G; Ala1226Ala
PubMed Link:
20937110
Variant Present in the following documents:
Main text
1471-2407-10-544.pdf
View BVdb publication page