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

Variant ID: 2-47643458-C-A

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

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Need for high-resolution Genetic Analysis in iPSC: Results and Lessons from the ForIPS Consortium.

Scientific Reports
Popp, Bernt B; Krumbiegel, Mandy M; Grosch, Janina J; Sommer, Annika A; Uebe, Steffen S; Kohl, Zacharias Z; Plötz, Sonja S; Farrell, Michaela M; Trautmann, Udo U; Kraus, Cornelia C; Ekici, Arif B AB; Asadollahi, Reza R; Regensburger, Martin M; Günther, Katharina K; Rauch, Anita A; Edenhofer, Frank F; Winkler, Jürgen J; Winner, Beate B; Reis, André A
Publication Date: 2018-11-21

Variant appearance in text: MSH2: 966C>A; Gly322Gly
PubMed Link: 30464253
Variant Present in the following documents:
  • 41598_2018_35506_MOESM5_ESM.xlsx, sheet 4
View BVdb publication page



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