Variant #0010681348 (NC_000017.10:g.48768486A>G, NM_003786.3:c.4509delAinsG (ABCC3))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48768486A>G
DB-ID -
dbSNP ID rs1051640
gnomAD frequency 35424/246224
gnomAD homozygote count 2914/90602
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_003786.3 ./. c.4509delAinsG r.(?) p.(GluPhe1503=)
ANKRD40 NM_052855.3 ./. c.*4872T>C r.(=) p.(=)