Variant #0000000603 (NC_000011.9:g.17417479T>C, NC_000011.9(NM_000352.3):c.4120-2A>G (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.17417479T>C
Reference -
DB-ID ABCC8_000007
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Admin
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Admin
Date created 2024-07-29 06:10:58 +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 +?/+? 33 c.4120-2A>G r.spl? p.?