Variant #0000017090 (NC_000001.10:g.171076835A>G, FMO3(NM_001002294.2):c.341A>G)

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.171076835A>G
DNA change (hg38) g.171107694A>G
Published as g.15036A>G
ISCN -
DB-ID FMO3_000005 See all 3 reported entries
Variant remarks not causative of TMAU, no effect in vitro
Reference PubMed: Shimizu et al. 2007
ClinVar ID -
dbSNP ID rs186763441
Origin Germline
Segregation no
Frequency 0/100 chromosomes
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00074 View details
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 -/- 4 c.341A>G - r.(?) p.(Asn114Ser)