Variant #0001008615 (NC_000001.10:g.94402743_94505682del, NM_000350.2:c.3525_*400{0} (ABCA4))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.94402743_94505682del
DNA change (hg38) g.93937187_94040126del
Published as c.3524_*56050del
ISCN -
DB-ID ABCA4_002888
Variant remarks ACMG PVS1, PM2_sup; severity category not assesed
Reference Journal: Cornelis 2023
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Stéphanie Cornelis
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-09-25 16:00:58 +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 +?/. 24_50 c.3525_*400{0} r.? p.?


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