Variant #0000413189 (NC_000001.10:g.60377930T>C, NM_000775.2:c.427A>G (CYP2J2))
Chromosome |
1 |
Allele |
Parent #1 |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Probably does not affect function |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.60377930T>C |
DNA change (hg38) |
g.59912258T>C |
Published as |
14489A>G (T143A) |
ISCN |
- |
DB-ID |
CYP2J2_000007 See all 2 reported entries |
Variant remarks |
Enzime activity in_vitro: Reduced AA and LA metabolism |
Reference |
PubMed: King 2002 |
ClinVar ID |
- |
dbSNP ID |
rs55753213 |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Julia Lopez |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Julia Lopez |
Date created |
2018-11-01 17:40:32 +01:00 (CET) |
Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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