Variant #0000167009 (NC_000001.10:g.171254890C>T, NM_002021.1:c.*207C>T (FMO1))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.171254890C>T
DNA change (hg38) g.171285751C>T
Published as -
ISCN -
DB-ID FMO1_000010 See all 3 reported entries
Variant remarks in smokers variant enhances FMO1*6 association with increased dose-adjusted serum olanzapine concentrations
Reference PubMed: Soderberg 2012
ClinVar ID -
dbSNP ID rs7877
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Elizabeth A. Shephard
Database submission license No license selected
Created by Elizabeth A. Shephard
Date created 2013-08-07 10:16:37 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     

Enzyme activity     
FMO1 NM_002021.1 ?/? 9 c.*207C>T FMO1*1O r.(?) p.(=) -


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