Variant #0000167042 (NC_000001.10:g.171086481C>T, NM_001002294.2:c.1498C>T (FMO3))

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.171086481C>T
DNA change (hg38) g.171117341C>T
Published as -
ISCN -
DB-ID FMO3_000016 See all 9 reported entries
Variant remarks abolishes activity for TMA and 5-DPT
Reference PubMed: Yamazaki 2007
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Ornicha Prapapan
Database submission license No license selected
Created by Ornicha Prapapan
Date created 2013-05-15 15:35:52 +02:00 (CEST)
Date last edited 2020-06-05 15:15:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMO3 NM_001002294.2 +/+ 9 c.1498C>T - r.(?) p.Arg500*


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.