Variant #0000000097 (NC_000011.9:g.17434263G>A, NM_000352.3:c.2506C>T (ABCC8))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.17434263G>A
Reference -
DB-ID ABCC8_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 6.0E-5 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2020-03-03 14:36:29 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCC8 NM_000352.3 +/+ 21 c.2506C>T r.(?) p.(Arg836*)