Variant #0000588448 (NC_000001.10:g.94546247A>G, NM_000350.2:c.886delTinsC (ABCA4))

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.94546247A>G
DB-ID -
dbSNP ID rs747346334
gnomAD frequency 2/245500
gnomAD homozygote count 0/122743
Average frequency (gnomAD v.2.1.1) 1.0E-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.886delTinsC r.(?) p.(AspLeu295=)