Variant #0001008796 (NC_000001.10:g.94549781G>A, NC_000001.10(NM_000350.2):c.769-784C>T (ABCA4))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.94549781G>A
DNA change (hg38) g.94084225G>A
Published as -
ISCN -
DB-ID ABCA4_001046 See all 61 reported entries
Variant remarks reduced penetrance reported (21-40%) Runhart 2020 (PMID:32815999); variant likely underreported due to reduced penetrance and intronic location, Runhart 2019 (PMID:31618761); ACMG BP4_m; severity category benign
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 -?/. 6i c.769-784C>T r.[=,768_769ins769-617_769-778] p.[=,Leu257AspfsTer3]


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.