Variant #0007859664 (NC_000012.11:g.22089619A>G, NM_005691.2:c.-11T>C (ABCC9))

Chromosome 12
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.22089619A>G
DB-ID -
dbSNP ID rs72559432
gnomAD frequency 321/245188
gnomAD homozygote count 4/122276
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     
ABCC9 NM_005691.2 ./. c.-11T>C r.(=) p.(=)
ABCC9 NM_020297.2 ./. c.-11T>C r.(=) p.(=)