Variant #0000167041 (NC_000001.10:g.171083483G>A, NM_001002294.2:c.1164G>A (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.171083483G>A
DNA change (hg38) g.171114343G>A
Published as -
ISCN -
DB-ID FMO3_000026 See all 2 reported entries
Variant remarks abolishes activity for TMA
Reference PubMed: Shimizu 2007
ClinVar ID -
dbSNP ID rs72549325
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Ornicha Prapapan
Database submission license No license selected
Created by Ornicha Prapapan
Date created 2013-02-19 22:47:06 +01:00 (CET)
Date last edited 2020-06-05 15:15:29 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMO3 NM_001002294.2 +/+ 7 c.1164G>A - r.(?) p.Trp388*


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