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MSH6 c.3114T>A ;(p.Y1038*)
Variant ID: 2-48028236-T-A
NM_000179.2(
MSH6
):c.3114T>A;(p.Y1038*)
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:
The spectrum of genetic variants in hereditary pancreatic cancer includes Fanconi anemia genes.
Familial Cancer
Slavin, Thomas P TP; Neuhausen, Susan L SL; Nehoray, Bita B; Niell-Swiller, Mariana M; Solomon, Ilana I; Rybak, Christina C; Blazer, Kathleen K; Adamson, Aaron A; Yang, Kai K; Sand, Sharon S; Guerrero-Llamas, Nancy N; Castillo, Danielle D; Herzog, Josef J; Wu, Xiwei X; Tao, Shu S; Raja, Shivali S; Chung, Vincent V; Singh, Gagandeep G; Nadesan, Sue S; Brown, Sandra S; Cruz-Correa, Marcia M; Petersen, Gloria M GM; Weitzel, Jeffrey J; ,
Publication Date: 2018-04
Variant appearance in text: MSH6: Y1038*
PubMed Link:
28687971
Variant Present in the following documents:
Main text
View BVdb publication page