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MSH2 c.1021_1022delinsGC ;(p.L341A)
Variant ID: 2-47643513-CT-GC
NM_000251.2(
MSH2
):c.1021_1022delinsGC;(p.L341A)
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: L341A
PubMed Link:
31819097
Variant Present in the following documents:
41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page
Evolutionary Covariance Combined with Molecular Dynamics Predicts a Framework for Allostery in the MutS DNA Mismatch Repair Protein.
The Journal Of Physical Chemistry. B
Lakhani, Bharat B; Thayer, Kelly M KM; Hingorani, Manju M MM; Beveridge, David L DL
Publication Date: 2017-03-09
Variant appearance in text: MSH2: L341A
PubMed Link:
28135092
Variant Present in the following documents:
Main text
jp6b11976_si_001.pdf
View BVdb publication page