MSH2 c.2802G>A ;(p.T934=)

Variant ID: 2-47710085-G-A

NM_000251.2(MSH2):c.2802G>A;(p.T934=)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Comprehensive Constitutional Genetic and Epigenetic Characterization of Lynch-Like Individuals.

Cancers
Dámaso, Estela E; González-Acosta, Maribel M; Vargas-Parra, Gardenia G; Navarro, Matilde M; Balmaña, Judith J; Ramon Y Cajal, Teresa T; Tuset, Noemí N; Thompson, Bryony A BA; Marín, Fátima F; Fernández, Anna A; Gómez, Carolina C; Velasco, Àngela À; Solanes, Ares A; Iglesias, Sílvia S; Urgel, Gisela G; López, Consol C; Del Valle, Jesús J; Campos, Olga O; Santacana, Maria M; Matias-Guiu, Xavier X; Lázaro, Conxi C; Valle, Laura L; Brunet, Joan J; Pineda, Marta M; Capellá, Gabriel G
Publication Date: 2020-07-05

Variant appearance in text: MSH2: 2802G>A; rs150259097
PubMed Link: 32635641
Variant Present in the following documents:
  • Main text
  • cancers-12-01799.pdf
View BVdb publication page



Sources of discordance among germ-line variant classifications in ClinVar.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Yang, Shan S; Lincoln, Stephen E SE; Kobayashi, Yuya Y; Nykamp, Keith K; Nussbaum, Robert L RL; Topper, Scott S
Publication Date: 2017-10

Variant appearance in text: MSH2: 2802G>A
PubMed Link: 28569743
Variant Present in the following documents:
  • gim201760x7.xlsx, sheet 2
View BVdb publication page