All variants in the FMO3 gene

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

6 entries on 1 page. Showing entries 1 - 6.
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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     
-/- 7 c.855C>T - r.(=) p.(=) - benign g.171083174C>T g.171114034C>T 21375C>T (Asn285Asn) - FMO3_000093 - PubMed: Koukouritaki et al. 2005 - rs909530 Germline no HapMap 0.279 (Eur), 0.407 (Jpn), 0.540 (Afr) - 0 - Ian Phillips
-/. - c.855C>T - r.(?) p.(Asn285=) - benign g.171083174C>T g.171114034C>T FMO3(NM_001002294.3):c.855C>T (p.N285=) - FMO3_000093 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Nijmegen
?/- 7 c.855C>T - r.(?) p.(Asn285=) - VUS g.171083174C>T g.171114034C>T Asn285Asn - FMO3_000093 - PubMed: Ferreira 2013 - rs909530 Germline - - - 0 - Johan den Dunnen
+?/- 7 c.855C>T - r.(?) p.(Asn285=) - likely pathogenic g.171083174C>T g.171114034C>T Asn285Asn - FMO3_000093 - PubMed: Ferreira 2013 - rs909530 Germline - - - 0 - Johan den Dunnen
+?/- 7 c.855C>T - r.(?) p.(Asn285=) - likely pathogenic g.171083174C>T g.171114034C>T Asn285Asn - FMO3_000093 - PubMed: Ferreira 2013 - rs909530 Germline - - - 0 - Johan den Dunnen
-/. - c.855C>T - r.(?) p.(Asn285=) - benign g.171083174C>T g.171114034C>T FMO3(NM_001002294.3):c.855C>T (p.N285=) - FMO3_000093 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Groningen
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