Variant #0000000602 (NC_000011.9:g.17464335C>T, NM_000352.3:c.1562G>A (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.17464335C>T
Reference -
DB-ID ABCC8_000002 See all 2 reported entries
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00011 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 06:09:09 +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 ?/? 10 c.1562G>A r.(?) p.(Arg521Gln)