MSH2 c.651dup ;(p.Q218Sfs*14)

Variant ID: 2-47639556-A-AT

NM_000251.2(MSH2):c.651dup;(p.Q218Sfs*14)

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:

Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instability.

British Journal Of Cancer
Kets, C M CM; van Krieken, J H J M JH; Hebeda, K M KM; Wezenberg, S J SJ; Goossens, M M; Brunner, H G HG; Ligtenberg, M J L MJ; Hoogerbrugge, N N
Publication Date: 2006-12-18

Variant appearance in text: MSH2: 651dup
PubMed Link: 17117178
Variant Present in the following documents:
  • Main text
  • 95-6603478a.pdf
View BVdb publication page