Variant #0000714438 (NC_000001.10:g.(68904742T>G), NM_000329.2:c.(881A>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.(68904742T>G) |
| DNA change (hg38) |
g.(68439059T>G) |
| Published as |
K294T |
| ISCN |
- |
| DB-ID |
RPE65_000014 See all 6 reported entries |
| Variant remarks |
expression cloning activity 0.16 |
| 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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