Variant #0000934315 (NC_000001.10:g.94496602G>T, NM_000350.2:c.4203C>A (ABCA4))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.94496602G>T
DNA change (hg38) g.94031046G>T
Published as -
ISCN -
DB-ID ABCA4_000913 See all 61 reported entries
Variant remarks functional analysis using an in vitro midi-gene splicing assay; predicted clinical effect benign
Reference PubMed: Kaltak 2023
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.02345 View details
Owner Melita Kaltak
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2023-10-12 19:27:24 +02:00 (CEST)
Date last edited 2023-10-12 19:52:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCA4 NM_000350.2 -?/. - c.4203C>A r.4203c>a p.Pro1401=


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