Variant #0000714442 (NC_000001.10:g.68903896A>G, NM_000329.2:c.1102T>C (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.68903896A>G
DNA change (hg38) g.68438213A>G
Published as Y368H
ISCN -
DB-ID RPE65_000001 See all 101 reported entries
Variant remarks expression cloning abolished isomerohydrolase activity, reduced protein level, descreased protein stability, probably disrupted membrane association
Reference PubMed: Takahashi 2006
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 7.0E-5 View details
Owner LOVD
Database submission license No license selected
Created by Martin Zenker, Prof. Dr. med.
Date created 2021-01-30 18:40:18 +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 +/. - c.1102T>C - p.Tyr368His


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