Variant #0001009602 (NC_000001.10:g.94486965C>T, NM_000350.2:c.4849G>A (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.94486965C>T
DNA change (hg38) g.94021409C>T
Published as -
ISCN -
DB-ID ABCA4_001063 See all 8 reported entries
Variant remarks ACMG PS3_M, PM2_sup, PM3, PP3_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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCA4 NM_000350.2 +?/. 35 c.4849G>A r.[4849_5018del,4849_5109del,=] p.[Val1617AlafsTer113,Val1617Met,=]


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