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MSH6 c.2533T>C ;(p.Y845H)
Variant ID: 2-48027655-T-C
NM_000179.2(
MSH6
):c.2533T>C;(p.Y845H)
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:
Novel Implications in Molecular Diagnosis of Lynch Syndrome.
Gastroenterology Research And Practice
Liccardo, Raffaella R; De Rosa, Marina M; Izzo, Paola P; Duraturo, Francesca F
Publication Date: 2017
Variant appearance in text: MSH6: 2533T>C
PubMed Link:
28250766
Variant Present in the following documents:
Main text
GRP2017-2595098.pdf
View BVdb publication page