MED23 c.2166C>G ;(p.F722L)

Variant ID: 6-131921232-G-C

NM_004830.3(MED23):c.2166C>G;(p.F722L)

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:

Identification and ranking of recurrent neo-epitopes in cancer.

Bmc Medical Genomics
Blanc, Eric E; Holtgrewe, Manuel M; Dhamodaran, Arunraj A; Messerschmidt, Clemens C; Willimsky, Gerald G; Blankenstein, Thomas T; Beule, Dieter D
Publication Date: 2019-11-27

Variant appearance in text: MED23: F722L
PubMed Link: 31775766
Variant Present in the following documents:
  • 12920_2019_611_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page