Variant #0001008848 (NC_000001.10:g.94546029C>T, NC_000001.10(NM_000350.2):c.1099+5G>A (ABCA4))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.94546029C>T
DNA change (hg38) g.94080473C>T
Published as -
ISCN -
DB-ID ABCA4_001318 See all 4 reported entries
Variant remarks ACMG PS3_M, PM2_sup, PM3_sup, PP3; severity category uncertain
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 ?/. 8i c.1099+5G>A r.spl? p.?


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