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) |

Variant on transcripts
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