Variant #0000167023 (NC_000001.10:g.171077252A>C, FMO3(NM_001002294.2):c.517A>C)

Chromosome 1
Allele Unknown
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.171077252A>C
DNA change (hg38) g.171108111A>C
Published as -
ISCN -
DB-ID FMO3_000102 See all 2 reported entries
Variant remarks impaired benzydamine N-oxygenation in compound het with P153L
Reference PubMed: Mayatepek 2004
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Elizabeth A. Shephard
Database submission license No license selected
Created by Elizabeth A. Shephard
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMO3 NM_001002294.2 +/+ 5 c.517A>C - r.(?) p.Ser173Arg