Variant #0010679596 (NC_000017.10:g.48735837G>A, NM_003786.3:c.654delGinsA (ABCC3))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48735837G>A
DB-ID -
dbSNP ID rs35669870
gnomAD frequency 216/246266
gnomAD homozygote count 2/122918
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.654delGinsA r.(?) p.(LeuPhe218=)
ABCC3 NM_003786.3 ./. c.654delGinsA r.(?) p.(LeuPhe218=)