Variant #0000792234 (NC_000001.10:g.150316688C>T, NM_004698.2:c.1477C>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.150316688C>T |
DNA change (hg38) |
- |
Published as |
p.P493S |
ISCN |
- |
DB-ID |
PRPF3_000034 See all 9 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
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