MSH2 c.1276+1394A>T

Variant ID: 2-47658474-A-T

NM_000251.2(MSH2):c.1276+1394A>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic Polymorphisms of DNA Repair Pathways in Sporadic Colorectal Carcinogenesis.

Journal Of Cancer
Liu, Jingwei J; Zheng, Bowen B; Li, Ying Y; Yuan, Yuan Y; Xing, Chengzhong C
Publication Date: 2019

Variant appearance in text: rs3771273
PubMed Link: 31031852
Variant Present in the following documents:
  • Main text
  • jcav10p1417.pdf
View BVdb publication page



Partial loss of heterozygosity events at the mutated gene in tumors from MLH1/MSH2 large genomic rearrangement carriers.

Bmc Cancer
Zavodna, Katarina K; Krivulcik, Tomas T; Bujalkova, Maria Gerykova MG; Slamka, Tomas T; Martinicky, David D; Ilencikova, Denisa D; Bartosova, Zdena Z
Publication Date: 2009-11-20

Variant appearance in text: MSH2: 1276+1394A>T; rs3771273
PubMed Link: 19930554
Variant Present in the following documents:
  • Main text
  • 1471-2407-9-405.pdf
View BVdb publication page