MLH1 c.1896G>T ;(p.E632D)

Variant ID: 3-37089174-G-T

NM_000249.3(MLH1):c.1896G>T;(p.E632D)

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:

Thyroid cancer in a patient with a germline MSH2 mutation. Case report and review of the Lynch syndrome expanding tumour spectrum.

Hereditary Cancer In Clinical Practice
Stulp, Rein P RP; Herkert, Johanna C JC; Karrenbeld, Arend A; Mol, Bart B; Vos, Yvonne J YJ; Sijmons, Rolf H RH
Publication Date: 2008-02-15

Variant appearance in text: MLH1: E632D
PubMed Link: 19706203
Variant Present in the following documents:
  • Main text
  • 1897-4287-6-1-15.pdf
View BVdb publication page