MSH2 c.14_15delinsAT ;(p.P5H)

Variant ID: 2-47630344-CG-AT

NM_000251.2(MSH2):c.14_15delinsAT;(p.P5H)

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:

Missense mutations of MLH1 and MSH2 genes detected in patients with gastrointestinal cancer are associated with exonic splicing enhancers and silencers.

Oncology Letters
Zhu, Ming M; Chen, Hui-Mei HM; Wang, Ya-Ping YP
Publication Date: 2013-05

Variant appearance in text: MSH2: Pro5His
PubMed Link: 23760103
Variant Present in the following documents:
  • Main text
View BVdb publication page