Variant #0001009772 (NC_000001.10:g.94476388C>G, NM_000350.2:c.5682G>C (ABCA4))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.94476388C>G
DNA change (hg38) g.94010832C>G
Published as -
ISCN -
DB-ID ABCA4_000890 See all 14 reported entries
Variant remarks ACMG BS1, BP4_m, BP7
Reference Journal: Cornelis 2023
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.2154 View details
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 -/. 40 c.5682G>C r.(?) p.(Leu1894=)


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