Variant #0000792233 (NC_000001.10:g.150316692C>T, NM_004698.2:c.1481C>T (PRPF3))
| Chromosome |
1 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.150316692C>T |
| DNA change (hg38) |
- |
| Published as |
p.T494M |
| ISCN |
- |
| DB-ID |
PRPF3_000019 See all 22 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Tanackovic 2011 |
| 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 |
Creative Commons Attribution 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2021-08-02 20:37:33 +02:00 (CEST) |
| Date last edited |
2024-02-09 15:16:32 +01:00 (CET) |

Variant on transcripts
|