"Illumina Laboratory Services, Illumina"[submitter] AND "LOC126805916" - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 260072	NM_001002294.3(FMO3):c.394G>C (p.Asp132His)	FMO3, LOC126805916 (D132H +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 875850	NM_001002294.3(FMO3):c.428T>A (p.Val143Glu)	FMO3, LOC126805916 (V123E +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria	GUncertain significance
Select item 293689	NM_001002294.3(FMO3):c.430A>G (p.Met144Val)	FMO3, LOC126805916 (M144V +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria	GUncertain significance
Select item 260073	NM_001002294.3(FMO3):c.441C>T (p.Ser147=)	FMO3, LOC126805916	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 16308	NM_001002294.3(FMO3):c.458C>T (p.Pro153Leu)	FMO3, LOC126805916 (P153L +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 38394	NM_001002294.3(FMO3):c.472G>A (p.Glu158Lys)	FMO3, LOC126805916	Single nucleotide variant (missense variant)	not provided +3 more	GBenign
Select item 876843	NM_001002294.3(FMO3):c.484+13T>C	FMO3, LOC126805916	Single nucleotide variant (intron variant)	Trimethylaminuria	GUncertain significance
Select item 876844	NM_001002294.3(FMO3):c.539G>T (p.Gly180Val)	FMO3, LOC126805916 (G160V +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria +1 more	GBenign
Select item 876845	NM_001002294.3(FMO3):c.613C>T (p.Arg205Cys)	FMO3, LOC126805916 (R142C +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria +2 more	GConflicting classifications of pathogenicity
Select item 260076	NM_001002294.3(FMO3):c.627+10C>G	FMO3, LOC126805916	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 876846	NM_001002294.3(FMO3):c.627+13G>A	FMO3, LOC126805916	Single nucleotide variant (intron variant)	Trimethylaminuria	GUncertain significance