MED23 c.3494A>G ;(p.H1165R)

Variant ID: 6-131912645-T-C

NM_004830.3(MED23):c.3494A>G;(p.H1165R)

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:

Exome sequencing in 51 early onset non-familial CRC cases.

Molecular Genetics & Genomic Medicine
Thutkawkorapin, Jessada J; Lindblom, Annika A; Tham, Emma E
Publication Date: 2019-05

Variant appearance in text: MED23: H1165R; rs755548604
PubMed Link: 30809968
Variant Present in the following documents:
  • MGG3-7-e605-s002.xlsx, sheet 1
View BVdb publication page