Variant #0000955421 (NC_000001.10:g.68915573C>T, NC_000001.10(NM_000329.2):c.11+5G>A (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.68915573C>T |
| DNA change (hg38) |
g.68449890C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
RPE65_000058 See all 92 reported entries |
| Variant remarks |
midigene in vitro splicing assay; cell line analysis show overall decreased expression levels |
| Reference |
PubMed: Vazquez-DomÃnguez 2022 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
8.0E-5 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2024-01-14 20:57:45 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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