Variant #0000604204 (NC_000001.10:g.94577135C>T, NM_000350.2:c.161G>A (ABCA4))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.94577135C>T
DNA change (hg38) g.94111579C>T
Published as -
ISCN -
DB-ID ABCA4_000240 See all 155 reported entries
Variant remarks Midigene splicing assay shows 56% expression of deletion and 44% expression of missense variant.
Reference PubMed: Fadaie et al 2019; Journal: Fadaie et al 2019
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Zeinab Fadaie
Database submission license Creative Commons Attribution-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2019-11-18 12:54:55 +01:00 (CET)
Date last edited 2020-07-14 21:57:48 +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.161G>A r.[161_302del,161g>a] p.[Cys54Serfs*14,Cys54Tyr]


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