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MSH6 c.3267A>T ;(p.L1089F)
Variant ID: 2-48030653-A-T
NM_000179.2(
MSH6
):c.3267A>T;(p.L1089F)
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:
Validation and clinical application of a targeted next-generation sequencing gene panel for solid and hematologic malignancies.
Peerj
Prieto-Potin, Iván I; Carvajal, Nerea N; Plaza-Sánchez, Jenifer J; Manso, Rebeca R; Aúz-Alexandre, Carmen Laura CL; Chamizo, Cristina C; Zazo, Sandra S; López-Sánchez, Almudena A; Rodríguez-Pinilla, Socorro María SM; Camacho, Laura L; Longarón, Raquel R; Bellosillo, Beatriz B; Somoza, Rosa R; Hernández-Losa, Javier J; Fernández-Soria, Víctor Manuel VM; Ramos-Ruiz, Ricardo R; Cristóbal, Ion I; García-Foncillas, Jesús J; Rojo, Federico F
Publication Date: 2020
Variant appearance in text: MSH6: 3267A>T; Leu1089Phe
PubMed Link:
33083132
Variant Present in the following documents:
peerj-08-10069-s013.xlsx, sheet 1
peerj-08-10069-s012.xlsx, sheet 1
peerj-08-10069-s010.xlsx, sheet 1
peerj-08-10069-s009.xlsx, sheet 1
View BVdb publication page