MSH2 c.381T>C ;(p.N127=)

Variant ID: 2-47637247-T-C

NM_000251.2(MSH2):c.381T>C;(p.N127=)

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:

Gly322Asp and Asn127Ser single nucleotide polymorphisms (SNPs) of hMSH2 mismatch repair gene and the risk of triple-negative breast cancer in Polish women.

Familial Cancer
Smolarz, Beata B; Makowska, Marianna M; Samulak, Dariusz D; Michalska, Magdalena M MM; Romanowicz, Hanna H
Publication Date: 2015-03

Variant appearance in text: MSH2: Asn127Asn
PubMed Link: 25134804
Variant Present in the following documents:
  • Main text
  • 10689_2014_Article_9746.pdf
View BVdb publication page