MGMT c.253C>T ;(p.H85Y)

Variant ID: 10-131506286-C-T

NM_002412.3(MGMT):c.253C>T;(p.H85Y)

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:

Dominantly Inherited Hereditary Nonpolyposis Colorectal Cancer Not Caused by MMR Genes.

Journal Of Clinical Medicine
Terradas, Mariona M; Capellá, Gabriel G; Valle, Laura L
Publication Date: 2020-06-23

Variant appearance in text: MGMT: 346C>T; His116Tyr
PubMed Link: 32585810
Variant Present in the following documents:
  • Main text
  • jcm-09-01954.pdf
View BVdb publication page