Variant #0000150732 (NC_000007.13:g.75615113G>A, NM_000941.2:c.1615G>A (POR))
Chromosome |
7 |
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.75615113G>A |
DNA change (hg38) |
g.75985795G>A |
Published as |
G539R |
ISCN |
- |
DB-ID |
POR_000017 See all 5 reported entries |
Variant remarks |
in vitro assay showed 17a-hydroxylase activity support 0.46, 17,20-lyase (P450c17) support 0.08 |
Reference |
PubMed: Huang 2005 |
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 |
2016-12-17 13:43:34 +01:00 (CET) |
Date last edited |
2024-03-06 21:29:09 +01:00 (CET) |

Variant on transcripts
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