C0342739[trait identifier] AND "Illumina Laboratory Services, Illumina - ClinVar

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Items: 55

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 293685	NM_001002294.3(FMO3):c.-25G>A	FMO3	Single nucleotide variant (5 prime UTR variant)	Trimethylaminuria	GUncertain significance
Select item 874915	NM_001002294.3(FMO3):c.132+13T>C	FMO3	Single nucleotide variant (intron variant)	Trimethylaminuria	GUncertain significance
Select item 293686	NM_001002294.3(FMO3):c.225C>T (p.Pro75=)	FMO3	Single nucleotide variant (synonymous variant +1 more)	Trimethylaminuria +1 more	GConflicting classifications of pathogenicity
Select item 293687	NM_001002294.3(FMO3):c.245T>C (p.Met82Thr)	FMO3 (M82T +1 more)	Single nucleotide variant (missense variant +1 more)	Trimethylaminuria	GUncertain significance
Select item 293688	NM_001002294.3(FMO3):c.260T>A (p.Ile87Asn)	FMO3 (I87N +1 more)	Single nucleotide variant (missense variant +1 more)	Trimethylaminuria	GUncertain significance
Select item 875848	NM_001002294.3(FMO3):c.329T>C (p.Val110Ala)	FMO3 (V110A +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 875849	NM_001002294.3(FMO3):c.341A>G (p.Asn114Ser)	FMO3 (N114S +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria +3 more	GConflicting classifications of pathogenicity
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
Select item 293690	NM_001002294.3(FMO3):c.628-6T>C	FMO3	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 876847	NM_001002294.3(FMO3):c.660G>A (p.Val220=)	FMO3	Single nucleotide variant (synonymous variant)	Trimethylaminuria +1 more	GConflicting classifications of pathogenicity
Select item 876848	NM_001002294.3(FMO3):c.684T>C (p.Gly228=)	FMO3	Single nucleotide variant (synonymous variant)	Trimethylaminuria	GUncertain significance
Select item 293691	NM_001002294.3(FMO3):c.706G>A (p.Val236Ile)	FMO3 (V236I +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria +2 more	GBenign/Likely benign
Select item 874042	NM_001002294.3(FMO3):c.713G>A (p.Arg238Gln)	FMO3 (R218Q +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria +1 more	GConflicting classifications of pathogenicity
Select item 874043	NM_001002294.3(FMO3):c.729C>G (p.Leu243=)	FMO3	Single nucleotide variant (synonymous variant)	Trimethylaminuria	GUncertain significance
Select item 874044	NM_001002294.3(FMO3):c.743C>T (p.Pro248Leu)	FMO3 (P185L +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria	GUncertain significance
Select item 16305	NM_001002294.3(FMO3):c.769G>A (p.Val257Met)	FMO3 (V257M +2 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 260077	NM_001002294.3(FMO3):c.830T>C (p.Val277Ala)	FMO3 (V277A +2 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 260078	NM_001002294.3(FMO3):c.855C>T (p.Asn285=)	FMO3	Single nucleotide variant (synonymous variant)	Trimethylaminuria +2 more	GBenign
Select item 293692	NM_001002294.3(FMO3):c.889G>T (p.Val297Leu)	FMO3 (V297L +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria	GUncertain significance
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 38395	NM_001002294.3(FMO3):c.923A>G (p.Glu308Gly)	FMO3 (E308G +2 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 631576	NM_001002294.3(FMO3):c.929C>T (p.Ser310Leu)	FMO3 (S310L +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria +2 more	GLikely pathogenic
Select item 260079	NM_001002294.3(FMO3):c.969C>T (p.Asp323=)	FMO3	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 293693	NM_001002294.3(FMO3):c.979T>G (p.Phe327Val)	FMO3 (F327V +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria	GUncertain significance
Select item 293694	NM_001002294.3(FMO3):c.994A>G (p.Ser332Gly)	FMO3 (S332G +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria	GUncertain significance
Select item 874972	NM_001002294.3(FMO3):c.1084G>C (p.Glu362Gln)	FMO3 (E299Q +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria +1 more	GConflicting classifications of pathogenicity
Select item 631577	NM_001002294.3(FMO3):c.1123dup (p.Leu375fs)	FMO3 (L375fs +2 more)	Duplication (frameshift variant)	Trimethylaminuria	GUncertain significance
Select item 293695	NM_001002294.3(FMO3):c.1204A>G (p.Met402Val)	FMO3 (M402V +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 260066	NM_001002294.3(FMO3):c.1221T>C (p.Asn407=)	FMO3	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 874973	NM_001002294.3(FMO3):c.1222G>T (p.Asp408Tyr)	FMO3 (D345Y +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria	GUncertain significance
Select item 875898	NM_001002294.3(FMO3):c.1250G>A (p.Arg417His)	FMO3 (R354H +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria	GUncertain significance
Select item 293696	NM_001002294.3(FMO3):c.1288T>C (p.Tyr430His)	FMO3 (Y430H +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria	GUncertain significance
Select item 16314	NM_001002294.3(FMO3):c.1302G>A (p.Met434Ile)	FMO3 (M434I +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 875899	NM_001002294.3(FMO3):c.1322T>C (p.Ile441Thr)	FMO3 (I421T +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria +1 more	GConflicting classifications of pathogenicity
Select item 875900	NM_001002294.3(FMO3):c.1462A>G (p.Thr488Ala)	FMO3 (T425A +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria	GUncertain significance
Select item 16309	NM_001002294.3(FMO3):c.1474C>T (p.Arg492Trp)	FMO3 (R492W +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely pathogenic
Select item 293697	NM_001002294.3(FMO3):c.1505T>G (p.Val502Gly)	FMO3 (V502G +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria +2 more	GLikely benign
Select item 875901	NM_001002294.3(FMO3):c.1507G>A (p.Gly503Arg)	FMO3 (G440R +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria	GUncertain significance
Select item 713884	NM_001002294.3(FMO3):c.1530C>T (p.Phe510=)	FMO3	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 293698	NM_001002294.3(FMO3):c.1539T>C (p.His513=)	FMO3	Single nucleotide variant (synonymous variant)	Trimethylaminuria +1 more	GConflicting classifications of pathogenicity
Select item 876895	NM_001002294.3(FMO3):c.*4T>C	FMO3	Single nucleotide variant (3 prime UTR variant)	Trimethylaminuria	GUncertain significance
Select item 293699	NM_001002294.3(FMO3):c.*52G>A	FMO3	Single nucleotide variant (3 prime UTR variant)	Trimethylaminuria	GUncertain significance
Select item 876896	NM_001002294.3(FMO3):c.*261A>G	FMO3	Single nucleotide variant (3 prime UTR variant)	Trimethylaminuria	GUncertain significance
Select item 293700	NM_001002294.3(FMO3):c.*364C>T	FMO3	Single nucleotide variant (3 prime UTR variant)	Trimethylaminuria	GUncertain significance
Select item 293701	NM_001002294.3(FMO3):c.*374A>G	FMO3	Single nucleotide variant (3 prime UTR variant)	Trimethylaminuria	GUncertain significance

ClinVar

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Items: 55