Variant #0001009396 (NC_000001.10:g.94497447_94497470dup, NM_000350.2:c.3995_4018dup (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.94497447_94497470dup
DNA change (hg38) g.94031891_94031914dup
Published as -
ISCN -
DB-ID ABCA4_001857 See all 5 reported entries
Variant remarks ACMG PS4, 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 ?/. 27 c.3995_4018dup r.(?) p.(Gln1332_Cys1339dup)


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