Variant #0000092800 (NC_000001.10:g.94549028_94549029insAC, NC_000001.10(NM_000350.2):c.769-32_769-31insGT (ABCA4))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.94549028_94549029insAC
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA4_000515
Frequency 6/12504
Freq. EA 0/8250
Freq. AA 6/4254
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:20:35 +02:00 (CEST)
Date last edited 2018-08-23 09:42:54 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA4 NM_000350.2 ?/? c.769-32_769-31insGT r.(=) p.(=)