MED23 c.479T>C ;(p.L160P)

Variant ID: 6-131943037-A-G

NM_004830.3(MED23):c.479T>C;(p.L160P)

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:

Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases.

Genome Biology
,
Publication Date: 2015-06-26

Variant appearance in text: MED23: L160P
PubMed Link: 26112015
Variant Present in the following documents:
  • 13059_2015_693_MOESM2_ESM.xls, sheet 1
  • 13059_2015_693_MOESM1_ESM.xls, sheet 1
View BVdb publication page