Variant #0000167040 (NC_000001.10:g.171072991G>T, FMO3(NM_001002294.2):c.198G>T)

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.171072991G>T
DNA change (hg38) g.171103850G>T
Published as -
ISCN -
DB-ID FMO3_000012 See all 3 reported entries
Variant remarks abolishes activity for TMA
Reference PubMed: Treacy 1998,PubMed: Akerman 1999
ClinVar ID -
dbSNP ID rs72549323
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 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 +/+ 3 c.198G>T - r.(?) p.Met66Ile