Variant #0000714435 (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 activity <0.03
Reference PubMed: Redmond 2005
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner LOVD
Database submission license No license selected
Created by Martin Zenker, Prof. Dr. med.
Date created 2021-01-30 18:25:36 +01:00 (CET)
Date last edited 2021-01-30 18:28:10 +01:00 (CET)
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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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