Variant #0000441194 (NC_000007.13:g.99277605C>T, NM_000777.3:c.-86G>A (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.99277605C>T |
DNA change (hg38) |
g.99679982C>T |
Published as |
+18G>A |
ISCN |
- |
DB-ID |
CYP3A5_000007 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 |
rs28365095 |
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 18:42:43 +01:00 (CET) |
Date last edited |
2020-07-14 22:00:36 +02:00 (CEST) |

Variant on transcripts
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