Variant #0000413317 (NC_000007.13:g.99364063G>A, NM_017460.5:c.802C>T (CYP3A4))
| Chromosome |
7 |
| 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.99364063G>A |
| DNA change (hg38) |
g.99766440G>A |
| Published as |
17633C>T (R268Stop) |
| ISCN |
- |
| DB-ID |
CYP3A4_000027 See all 2 reported entries |
| Variant remarks |
Enzime activity in_vitro: None |
| Reference |
PubMed: Werk 2014 |
| ClinVar ID |
- |
| dbSNP ID |
rs138105638 |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
7.0E-5 View details |
| Owner |
Julia Lopez |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2018-11-01 17:41:38 +01:00 (CET) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
|