FBXO17[gene] and "single gene"[properties] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2403804	NM_024907.7(FBXO17):c.790G>A (p.Ala264Thr)	FBXO17 (A273T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2460283	NM_024907.7(FBXO17):c.754G>A (p.Gly252Arg)	FBXO17 (G252R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2233856	NM_024907.7(FBXO17):c.706T>C (p.Phe236Leu)	FBXO17 (F236L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093605	NM_024907.7(FBXO17):c.689G>A (p.Arg230Gln)	FBXO17 (R239Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2525231	NM_024907.7(FBXO17):c.659C>T (p.Pro220Leu)	FBXO17 (P220L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278097	NM_024907.7(FBXO17):c.655G>A (p.Asp219Asn)	FBXO17 (D228N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 218800	NM_024907.7(FBXO17):c.644C>A (p.Ser215Ter)	FBXO17 (S215* +1 more)	Single nucleotide variant (nonsense +1 more)	not specified	GUncertain significance
Select item 2296984	NM_024907.7(FBXO17):c.610C>A (p.Leu204Met)	FBXO17 (L204M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093604	NM_024907.7(FBXO17):c.544T>C (p.Cys182Arg)	FBXO17 (C182R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093603	NM_024907.7(FBXO17):c.529G>A (p.Ala177Thr)	FBXO17 (A177T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278096	NM_024907.7(FBXO17):c.502G>A (p.Gly168Arg)	FBXO17 (G168R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2205436	NM_024907.7(FBXO17):c.455C>G (p.Ser152Cys)	FBXO17 (S152C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2274652	NM_024907.7(FBXO17):c.382G>A (p.Gly128Arg)	FBXO17 (G128R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2271349	NM_024907.7(FBXO17):c.346G>A (p.Glu116Lys)	FBXO17 (E116K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093602	NM_024907.7(FBXO17):c.338C>A (p.Ser113Tyr)	FBXO17 (S122Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278098	NM_024907.7(FBXO17):c.320G>T (p.Arg107Leu)	FBXO17 (R107L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278095	NM_024907.7(FBXO17):c.319C>G (p.Arg107Gly)	FBXO17 (R107G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2385717	NM_024907.7(FBXO17):c.307G>T (p.Ala103Ser)	FBXO17 (A103S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2510561	NM_024907.7(FBXO17):c.250A>C (p.Ser84Arg)	FBXO17 (S84R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2263799	NM_024907.7(FBXO17):c.215G>C (p.Arg72Pro)	FBXO17 (R72P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2371446	NM_024907.7(FBXO17):c.158T>G (p.Val53Gly)	FBXO17 (V62G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2405662	NM_024907.7(FBXO17):c.154A>G (p.Ile52Val)	FBXO17 (I61V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2325447	NM_024907.7(FBXO17):c.114G>T (p.Leu38Phe)	FBXO17 (L38F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374256	NM_024907.7(FBXO17):c.56A>G (p.Asp19Gly)	FBXO17 (D28G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2460754	NM_024907.7(FBXO17):c.29T>C (p.Leu10Pro)	FBXO17 (L10P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 25