Variant #0000588887 (NC_000001.10:g.94586594A>G, NM_000350.2:c.8T>C (ABCA4))

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.94586594A>G
DB-ID -
dbSNP ID -
gnomAD frequency 1/246258
gnomAD homozygote count 0/123128
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.8T>C r.(?) p.(Phe3Ser)