Variant #0000974169 (NC_000001.10:g.94496039C>T, NM_000350.2:c.4297G>A (ABCA4))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.94496039C>T
DNA change (hg38) -
Published as ABCA4(NM_000350.2):c.4297G>A (p.V1433I), ABCA4(NM_000350.3):c.4297G>A (p.V1433I, p.(Val1433Ile))
ISCN -
DB-ID ABCA4_000552 See all 63 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00158 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:20:39 +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 -?/. - c.4297G>A r.(?) p.(Val1433Ile)


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