Variant #0000588682 (NC_000001.10:g.94568746C>A, NM_000350.2:c.443-48delGinsT (ABCA4))

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.94568746C>A
DB-ID -
dbSNP ID rs769736897
gnomAD frequency 0/241300
gnomAD homozygote count 0/120648
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     
ABCA4 NM_000350.2 ./. c.443-48delGinsT r.(=) p.(=)