Variant #0000150698 (NC_000007.13:g.75609714A>G, NM_000941.2:c.424A>G (POR))
Chromosome |
7 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.75609714A>G |
DNA change (hg38) |
g.75980396A>G |
Published as |
T142A |
ISCN |
- |
DB-ID |
POR_000059 See all 4 reported entries |
Variant remarks |
cDNA expression cloning in bacteria showed cytochrome C reduction 0.49, NADPH oxidation 0.52 |
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) |
0 View details |
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 |
2022-10-13 03:02:03 +02:00 (CEST) |

Variant on transcripts
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