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 InternationalCreative Commons License
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP3A5 NM_000777.3 -/- 1 c.-86G>A r.= p.= -


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