MLH1 c.688G>T ;(p.E230*)

Variant ID: 3-37055933-G-T

NM_000249.3(MLH1):c.688G>T;(p.E230*)

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:

Molecular and Pathological Features of Gastric Cancer in Lynch Syndrome and Familial Adenomatous Polyposis.

International Journal Of Molecular Sciences
Fornasarig, Mara M; Magris, Raffaella R; De Re, Valli V; Bidoli, Ettore E; Canzonieri, Vincenzo V; Maiero, Stefania S; Viel, Alessandra A; Cannizzaro, Renato R
Publication Date: 2018-06-06

Variant appearance in text: MLH1: 688G>T
PubMed Link: 29882764
Variant Present in the following documents:
  • Main text
  • ijms-19-01682.pdf
View BVdb publication page