Variant #0000933821 (NC_000001.10:g.94463701T>C, NC_000001.10(NM_000350.2):c.6480-35A>G (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.94463701T>C
DNA change (hg38) g.93998145T>C
Published as -
ISCN -
DB-ID ABCA4_002548 See all 5 reported entries
Variant remarks in vitro expression analysis midigene splice assay
Reference PubMed: Rodríguez-Hidalgo 2023, Journal: Rodríguez-Hidalgo 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 2023-10-05 17:15:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCA4 NM_000350.2 +/. 47i c.6480-35A>G r.[6479_6480ins[6480-47_6480-36;g;6480-34_6480-1]|0.67,=|0.3,6387_6479del] p.[Phe2161Profs*4,=,Ser2129_Lys2160delinsArg]


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