MSH2 c.1064G>A ;(p.R355K)

Variant ID: 2-47643556-G-A

NM_000251.2(MSH2):c.1064G>A;(p.R355K)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Quantifying prediction of pathogenicity for within-codon concordance (PM5) using 7541 functional classifications of BRCA1 and MSH2 missense variants.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Loong, Lucy L; Cubuk, Cankut C; Choi, Subin S; Allen, Sophie S; Torr, Beth B; Garrett, Alice A; Loveday, Chey C; Durkie, Miranda M; Callaway, Alison A; Burghel, George J GJ; Drummond, James J; Robinson, Rachel R; Berry, Ian R IR; Wallace, Andrew A; Eccles, Diana M DM; Tischkowitz, Marc M; Ellard, Sian S; Ware, James S JS; Hanson, Helen H; Turnbull, Clare C; ,
Publication Date: 2022-03

Variant appearance in text: MSH2: 1064G>A; Arg355Lys
PubMed Link: 34906453
Variant Present in the following documents:
  • mmc1.xlsx, sheet 3
View BVdb publication page



Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.

Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09

Variant appearance in text: MSH2: R355K
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



Integrated analysis of mismatch repair system in malignant astrocytomas.

Plos One
Rodríguez-Hernández, Irene I; Garcia, Juan Luis JL; Santos-Briz, Angel A; Hernández-Laín, Aurelio A; González-Valero, Jose María JM; Gómez-Moreta, Juan Antonio JA; Toldos-González, Oscar O; Cruz, Juan Jesús JJ; Martin-Vallejo, Javier J; González-Sarmiento, Rogelio R
Publication Date: 2013

Variant appearance in text: MSH2: Arg355Lys
PubMed Link: 24073290
Variant Present in the following documents:
  • Main text
  • pone.0076401.pdf
View BVdb publication page