NBK1103 AND genereviews[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 16313	NM_001002294.3(FMO3):c.182A>G (p.Asn61Ser)	FMO3 (N61S +1 more)	Single nucleotide variant (missense variant +1 more)	Trimethylaminuria	GLikely pathogenic
Select item 16308	NM_001002294.3(FMO3):c.458C>T (p.Pro153Leu)	FMO3, LOC126805916 (P153L +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria +1 more	GConflicting classifications of pathogenicity
Select item 217371	NM_006894.4(FMO3):c.[472G>A;560T>C]	LOC126805916, FMO3 (V187A +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria	GPathogenic
Select item 16318	NM_006894.4(FMO3):c.[472G>A;923A>G]	LOC126805916, FMO3 (E308G +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria +1 more	GPathogenic/Likely pathogenic
Select item 16304	NM_001002294.3(FMO3):c.913G>T (p.Glu305Ter)	FMO3 (E305* +2 more)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic
Select item 21464	NM_001002294.3(FMO3):c.1079T>C (p.Leu360Pro)	FMO3 (L360P +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign

ClinVar