Variant #0007091512 (NC_000011.9:g.17449521G>C, NM_000352.3:c.2041-32delCinsG (ABCC8))

Chromosome 11
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.17449521G>C
DB-ID -
dbSNP ID -
gnomAD frequency 0/234020
gnomAD homozygote count 0/117009
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC8 NM_000352.3 ./. c.2041-32delCinsG r.(=) p.(=)