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MSH2 c.115_117delinsAGC ;(p.R39S)
Variant ID: 2-47630445-CGG-AGC
NM_000251.2(
MSH2
):c.115_117delinsAGC;(p.R39S)
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:
Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.
Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09
Variant appearance in text: MSH2: R39S
PubMed Link:
31819097
Variant Present in the following documents:
41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page
Molecular epidemiology of DNA repair gene polymorphisms and head and neck cancer.
Journal Of Biomedical Research
Wang, Meilin M; Chu, Haiyan H; Zhang, Zhengdong Z; Wei, Qingyi Q
Publication Date: 2013-05
Variant appearance in text: MSH2: Arg39Ser
PubMed Link:
23720673
Variant Present in the following documents:
Main text
View BVdb publication page