Variant #0000000602 (NC_000011.9:g.17464335C>T, NM_000352.3:c.1562G>A (ABCC8))

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.17464335C>T
Reference -
DB-ID ABCC8_000002
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00011 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Admin
Date created 2024-07-29 06:09:09 +00:00 (UTC)
Date last edited 2025-10-09 09:29:42 +00:00 (UTC)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Class     
ABCC8 NM_000352.3 +?/+? 10 c.1562G>A r.(?) p.(Arg521Gln) likely pathogenic