Variant #0000167058 (NC_000001.10:g.171077274G>T, FMO3(NM_001002294.2):c.539G>T)

Chromosome 1
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.171077274G>T
DNA change (hg38) g.171108133G>T
Published as -
ISCN -
DB-ID FMO3_000042 See all 4 reported entries
Variant remarks no effect on N-oxygenation of TMA or S-oxygenation of methimazole
Reference PubMed: Dolphin 2000
ClinVar ID -
dbSNP ID rs75904274
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01258 View details
Owner Ornicha Prapapan
Database submission license No license selected
Created by Ornicha Prapapan
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMO3 NM_001002294.2 -/- 5 c.539G>T - r.(?) p.Gly180Val