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MSH2 c.1127dup ;(p.L376Ffs*13)
Variant ID: 2-47656928-C-CT
NM_000251.2(
MSH2
):c.1127dup;(p.L376Ffs*13)
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:
Clinical Features and Therapeutic Outcomes in Men with Advanced Prostate Cancer and DNA Mismatch Repair Gene Mutations.
European Urology
Antonarakis, Emmanuel S ES; Shaukat, Farah F; Isaacsson Velho, Pedro P; Kaur, Harsimar H; Shenderov, Eugene E; Pardoll, Drew M DM; Lotan, Tamara L TL
Publication Date: 2019-03
Variant appearance in text: MSH2: L376Ffs*13
PubMed Link:
30337059
Variant Present in the following documents:
Main text
View BVdb publication page