MLH1 c.545+2T>A

Variant ID: 3-37050398-T-A

NM_000249.3(MLH1):c.545+2T>A

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:

A novel MLH1 intronic variant in a young Japanese patient with Lynch syndrome.

Human Genome Variation
Kiyozumi, Yoshimi Y; Matsubayashi, Hiroyuki H; Horiuchi, Yasue Y; Oishi, Takuma T; Abe, Masato M; Ohnami, Sumiko S; Naruoka, Akane A; Kusuhara, Masatoshi M; Yamaguchi, Ken K
Publication Date: 2018

Variant appearance in text: MLH1: 545+2T>A
PubMed Link: 29760937
Variant Present in the following documents:
  • Main text
  • 41439_2018_Article_2.pdf
View BVdb publication page