Variant #0000000600 (NC_000011.9:g.17436147G>A, NM_000352.3:c.2302C>T (ABCC8))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.17436147G>A
Reference -
DB-ID ABCC8_000005
Frequency -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Admin
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Admin
Date created 2024-07-29 06:05:55 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCC8 NM_000352.3 ?/? 19 c.2302C>T r.(?) p.(Pro768Ser)