Variant #0000955421 (NC_000001.10:g.68915573C>T, NC_000001.10(NM_000329.2):c.11+5G>A (RPE65))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.68915573C>T
DNA change (hg38) g.68449890C>T
Published as -
ISCN -
DB-ID RPE65_000058 See all 92 reported entries
Variant remarks midigene in vitro splicing assay; cell line analysis show overall decreased expression levels
Reference PubMed: Vazquez-Domínguez 2022
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 8.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-01-14 20:57:45 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPE65 NM_000329.2 +/. 1i c.11+5G>A r.[=|red,11_12ins[guaaa;11+6_11+124]] p.?


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