MSH2 c.2388T>G ;(p.T796=)

Variant ID: 2-47705588-T-G

NM_000251.2(MSH2):c.2388T>G;(p.T796=)

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:

Novel germline MSH2 mutation in lynch syndrome patient surviving multiple cancers.

Hereditary Cancer In Clinical Practice
Janavicius, Ramunas R; Elsakov, Pavel P
Publication Date: 2012-01-10

Variant appearance in text: MSH2: Thr796Thr
PubMed Link: 22234272
Variant Present in the following documents:
  • Main text
  • 1897-4287-10-1.pdf
View BVdb publication page