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MSH2 c.186_187insTA ;(p.V63*)
Variant ID: 2-47630516-G-GTA
NM_000251.2(
MSH2
):c.186_187insTA;(p.V63*)
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:
Mutation spectrum in South American Lynch syndrome families.
Hereditary Cancer In Clinical Practice
Dominguez-Valentin, Mev M; Nilbert, Mef M; Wernhoff, Patrik P; López-Köstner, Francisco F; Vaccaro, Carlos C; Sarroca, Carlos C; Palmero, Edenir Ines EI; Giraldo, Alejandro A; Ashton-Prolla, Patricia P; Alvarez, Karin K; Ferro, Alejandra A; Neffa, Florencia F; Caris, Junea J; Carraro, Dirce M DM; Rossi, Benedito M BM
Publication Date: 2013-12-18
Variant appearance in text: MSH2: V63fsX1
PubMed Link:
24344984
Variant Present in the following documents:
Main text
1897-4287-11-18.pdf
View BVdb publication page