Variant #0000933711 (NC_000001.10:g.94577530C>T, NC_000001.10(NM_000350.2):c.161-395G>A (ABCA4))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.94577530C>T
DNA change (hg38) g.94111974C>T
Published as -
ISCN -
DB-ID ABCA4_002453 See all 4 reported entries
Variant remarks expression cloning midi-gene splicing assay, 0.36 normally spliced mRNA; predicted severity moderate
Reference PubMed: Corradi 2023, Journal: Corradi 2023
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2023-09-29 13:37:48 +02:00 (CEST)
Date last edited 2023-09-29 16:24:36 +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 +?/. 2i c.161-395G>A r.[161_302del,=,160_161ins161-484_161–394] p.[Cys54Serfs*14,=,Cys54Cysfs*75]


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