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MSH2 c.763_766delinsTT ;(p.S255Ffs*28)
Variant ID: 2-47639670-AGTG-TT
NM_000251.2(
MSH2
):c.763_766delinsTT;(p.S255Ffs*28)
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:
HNPCC: six new pathogenic mutations.
Bmc Medical Genetics
Kunstmann, Erdmute E; Vieland, Judith J; Brasch, Frank E FE; Hahn, Stephan A SA; Epplen, Joerg T JT; Schulmann, Karsten K; Schmiegel, Wolff W
Publication Date: 2004-06-24
Variant appearance in text: MSH2: 763_766delAGTGinsTT
PubMed Link:
15217520
Variant Present in the following documents:
Main text
1471-2350-5-16.pdf
View BVdb publication page