MSH2 c.966C>T ;(p.G322=)

Variant ID: 2-47643458-C-T

NM_000251.2(MSH2):c.966C>T;(p.G322=)

This variant was identified in 1 publication

View GRCh38 version.




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: Gly322Gly
PubMed Link: 25134804
Variant Present in the following documents:
  • Main text
  • 10689_2014_Article_9746.pdf
View BVdb publication page