Variant #0000443223 (NC_000023.10:g.24521596G>A, PDK3(NM_005391.4):c.473G>A)
Chromosome |
X |
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.24521596G>A |
DNA change (hg38) |
g.24503479G>A |
Published as |
- |
ISCN |
- |
DB-ID |
PDK3_000003 See all 4 reported entries |
Variant remarks |
expression cloning, PKD3 hyperactivity (5x increased) |
Reference |
PubMed: Kennerson 2013 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2013-03-15 18:53:20 +01:00 (CET) |
Date last edited |
2020-07-17 21:21:13 +02:00 (CEST) |

Variant on transcripts
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