MSH2 c.1276+1349T>A

Variant ID: 2-47658429-T-A

NM_000251.2(MSH2):c.1276+1349T>A

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

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+1349T>A; rs3771272
PubMed Link: 19930554
Variant Present in the following documents:
  • Main text
  • 1471-2407-9-405.pdf
View BVdb publication page