Variant #0000588860 (NC_000001.10:g.94586503C>A, NC_000001.10(NM_000350.2):c.66+33G>T (ABCA4))

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.94586503C>A
DB-ID -
dbSNP ID rs750207786
gnomAD frequency 1/244594
gnomAD homozygote count 0/122293
Average frequency (gnomAD v.2.1.1) 0 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.66+33G>T r.(=) p.(=)