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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