MSH6 c.1714C>A ;(p.Q572K)

Variant ID: 2-48026836-C-A

NM_000179.2(MSH6):c.1714C>A;(p.Q572K)

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: 1714C>A
PubMed Link: 28250766
Variant Present in the following documents:
  • Main text
  • GRP2017-2595098.pdf
View BVdb publication page