Variant #0007092432 (NC_000011.9:g.17498331C>A, NM_000352.3:c.-8G>T (ABCC8))

Chromosome 11
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.17498331C>A
DB-ID -
dbSNP ID rs200091822
gnomAD frequency 365/142556
gnomAD homozygote count 2/70914
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC8 NM_000352.3 ./. c.-8G>T r.(=) p.(=)