Variant #0001009506 (NC_000001.10:g.94493000C>T, NC_000001.10(NM_000350.2):c.4539+2001G>A (ABCA4))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.94493000C>T
DNA change (hg38) g.94027444C>T
Published as -
ISCN -
DB-ID ABCA4_000015 See all 97 reported entries
Variant remarks ACMG PS4, PM3_V, BP4_m; severity category severe
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCA4 NM_000350.2 +/. 30i c.4539+2001G>A r.[=,4539_4540ins4539+1891_4540-2162] p.[=,Arg1514LeufsTer36]


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