MSH2 c.2639G>A ;(p.G880D)

Variant ID: 2-47709922-G-A

NM_000251.2(MSH2):c.2639G>A;(p.G880D)

This variant was identified in 2 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: 2639G>A; G880D
PubMed Link: 34906453
Variant Present in the following documents:
  • mmc1.xlsx, sheet 3
View BVdb publication page



Treatment-associated TP53 DNA-binding domain missense mutations in the pathogenesis of secondary gliosarcoma.

Oncotarget
Pain, Margaret M; Wang, Huaien H; Lee, Eunjee E; Strahl, Maya M; Hamou, Wissam W; Sebra, Robert R; Zhu, Jun J; Yong, Raymund L RL
Publication Date: 2018-01-05

Variant appearance in text: MSH2: G880D
PubMed Link: 29416795
Variant Present in the following documents:
  • Main text
  • oncotarget-09-2603.pdf
View BVdb publication page