All variants in the FMO3 gene

Information The variants shown are described using the NM_001002294.2 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

Haplotype     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-/- 4 c.341A>G - r.(?) p.(Asn114Ser) - benign g.171076835A>G g.171107694A>G g.15036A>G - FMO3_000005 not causative of TMAU, no effect in vitro PubMed: Shimizu et al. 2007 - rs186763441 Germline no 0/100 chromosomes - 0 - Ornicha Prapapan
-/- 4 c.341A>G - r.(?) p.(Asn114Ser) - benign g.171076835A>G g.171107694A>G - - FMO3_000005 - PubMed: Shimizu 2012 - rs186763441 Germline no 1/1280 chromosomes - 0 - Ornicha Prapapan
-?/. - c.341A>G - r.(?) p.(Asn114Ser) - likely benign g.171076835A>G g.171107694A>G - - FMO3_000005 classification based on frequency in 305 unrelated individuals PubMed: Le 2019 - - Germline - frequency 0.014 - 0 - Global Variome, with Curator vacancy
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