Variant #0000167066 (NC_000001.10:g.171061871G>T, FMO3(NM_001002294.2):c.72G>T)

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.171061871G>T
DNA change (hg38) g.171092730G>T
Published as -
ISCN -
DB-ID FMO3_000034 See all 2 reported entries
Variant remarks small increase in kcat/Km for TMA and methimazole; no effect for sulindac or ethylenethiourea
Reference PubMed: Koukouritaki 2005, PubMed: Koukouritaki 2007
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Ornicha Prapapan
Database submission license No license selected
Created by Ornicha Prapapan
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMO3 NM_001002294.2 ?/? 2 c.72G>T - r.(?) p.Glu24Asp