Variant #0000588886 (NC_000001.10:g.94586593G>A, NM_000350.2:c.9C>T (ABCA4))

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.94586593G>A
DB-ID -
dbSNP ID -
gnomAD frequency 1/246252
gnomAD homozygote count 0/123125
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA4 NM_000350.2 ./. c.9C>T r.(?) p.(Phe3=)