Variant #0010679271 (NC_000017.10:g.48712329G>A, NM_003786.3:c.32G>A (ABCC3))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48712329G>A
DB-ID -
dbSNP ID rs11568609
gnomAD frequency 16/19076
gnomAD homozygote count 0/9522
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     
ABCC3 NM_001144070.1 ./. c.32G>A r.(?) p.(Gly11Asp)
ABCC3 NM_003786.3 ./. c.32G>A r.(?) p.(Gly11Asp)