Variant #0000586518 (NC_000001.10:g.94485131C>T, NM_000350.2:c.5196+7delGinsA (ABCA4))

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.94485131C>T
DB-ID -
dbSNP ID rs61753023
gnomAD frequency 0/221756
gnomAD homozygote count 0/110877
Average frequency (gnomAD v.2.1.1) Retrieve
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.5196+7delGinsA r.(=) p.(=)