Variant #0000586384 (NC_000001.10:g.94476989C>A, NM_000350.2:c.5461-48delGinsT (ABCA4))

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.94476989C>A
DB-ID -
dbSNP ID rs762648096
gnomAD frequency 6/231446
gnomAD homozygote count 0/115710
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
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.5461-48delGinsT r.(=) p.(=)