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 |

Variant on transcripts
|