Variant #0000441193 (NC_000007.13:g.99277593G>A, NM_000777.3:c.-74C>T (CYP3A5))
| Chromosome |
7 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Does not affect function |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.99277593G>A |
| DNA change (hg38) |
g.99679970G>A |
| Published as |
+30C>T |
| ISCN |
- |
| DB-ID |
CYP3A5_000006 See all 2 reported entries |
| Variant remarks |
normal activity in vitro for total midazolam hydroxylase or basal or rifampin-inducible testosterone 6-beta hydroxylase activity |
| Reference |
PubMed: Kuehl 2001 |
| ClinVar ID |
- |
| dbSNP ID |
rs28371764 |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2018-12-20 18:38:46 +01:00 (CET) |
| Date last edited |
2020-07-14 22:00:36 +02:00 (CEST) |

Variant on transcripts
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