Variant #0000000677 (NC_000011.9:g.17408771C>T, NM_000525.3:c.868G>A (KCNJ11))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.17408771C>T
Reference -
DB-ID KCNJ11_000002
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2025-10-06 07:26:17 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Class     
KCNJ11 NM_000525.3 +?/+? - c.868G>A r.(?) p.(Val290Met) likely pathogenic