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