Variant #0001008626 (NC_000001.10:g.(?_94458792)_(94461752_94463416)del, NM_000350.2:c.(6729+1_6730-1)_(*1_?)del (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.(?_94458792)_(94461752_94463416)del
DNA change (hg38) g.(?_93993236)_(93996196_93997860)del
Published as -
ISCN -
DB-ID NPHS2_000000 See all 244 reported entries
Variant remarks ACMG PVS1_S, PM2_sup, PM3_sup; 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 +?/. 48i_50_ c.(6729+1_6730-1)_(*1_?)del r.? p.?


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