Variant #0000413194 (NC_000001.10:g.60392494C>A, NM_000775.2:c.-76G>T (CYP2J2))
| Chromosome |
1 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.60392494C>A |
| DNA change (hg38) |
g.59926822C>A |
| Published as |
-76G>T |
| ISCN |
- |
| DB-ID |
CYP2J2_000009 See all 2 reported entries |
| Variant remarks |
Enzime activity in_vitro: Reduced transcription due to loss of Sp1 binding site |
| Reference |
PubMed: King 2002, PubMed: Spiecker 2004 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| 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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