MLH1 c.1772A>G ;(p.D591G)

Variant ID: 3-37089050-A-G

NM_000249.3(MLH1):c.1772A>G;(p.D591G)

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:

Microsatellite instability in the peripheral blood leukocytes of HNPCC patients.

Human Mutation
Coolbaugh-Murphy, Mary I MI; Xu, Jing-Ping JP; Ramagli, Louis S LS; Ramagli, Brian C BC; Brown, Barry W BW; Lynch, Patrick M PM; Hamilton, Stanley R SR; Frazier, Marsha L ML; Siciliano, Michael J MJ
Publication Date: 2010-03

Variant appearance in text: MLH1: Asp591Gly
PubMed Link: 20052760
Variant Present in the following documents:
  • Main text
View BVdb publication page