MSH6 c.421G>T ;(p.G141C)

Variant ID: 2-48018226-G-T

NM_000179.2(MSH6):c.421G>T;(p.G141C)

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:

Germline mutational spectrum in Armenian breast cancer patients suspected of hereditary breast and ovarian cancer.

Human Genome Variation
Moradian, Mike M MM; Babikyan, Davit T DT; Markarian, Sione S; Petrosyan, Jonny G JG; Avanesian, Nare N; Arutunyan, Tereza T; Sarkisian, Tamara F TF
Publication Date: 2021-02-09

Variant appearance in text: MSH6: 421G>T; Gly141Trp
PubMed Link: 33558524
Variant Present in the following documents:
  • Main text
  • 41439_2021_Article_140.pdf
View BVdb publication page