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MSH6 c.917G>C ;(p.G306A)
Variant ID: 2-48026039-G-C
NM_000179.2(
MSH6
):c.917G>C;(p.G306A)
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:
Multilocus Inherited Neoplasia Allele Syndrome (MINAS): an update.
European Journal Of Human Genetics : Ejhg
McGuigan, Anthony A; Whitworth, James J; Andreou, Avgi A; Hearn, Timothy T; , ; Tischkowitz, Marc M; Maher, Eamonn R ER
Publication Date: 2022-03
Variant appearance in text: MSH6: 917G>C; G306A
PubMed Link:
34983940
Variant Present in the following documents:
41431_2021_1013_MOESM1_ESM.pdf
View BVdb publication page