Variant #0007092398 (NC_000011.9:g.17498201G>A, NM_000352.3:c.123C>T (ABCC8))

Chromosome 11
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.17498201G>A
DB-ID -
dbSNP ID rs778891891
gnomAD frequency 2/240806
gnomAD homozygote count 0/120401
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.123C>T r.(?) p.(Phe41=)