Variant #0000150701 (NC_000007.13:g.75610876C>T, NM_000941.2:c.683C>T (POR))
Chromosome |
7 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.75610876C>T |
DNA change (hg38) |
g.75981558C>T |
Published as |
P228L |
ISCN |
- |
DB-ID |
POR_000040 See all 6 reported entries |
Variant remarks |
cDNA expression cloning in bacteria showed cytochrome C reduction 0.75, NADPH oxidation 0.72 |
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) |
0.00246 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 |
2024-10-10 01:58:14 +02:00 (CEST) |

Variant on transcripts
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