FBXO10[gene] and "single gene"[properties] - ClinVar

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Items: 42

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3093584	NM_012166.3(FBXO10):c.2804C>T (p.Thr935Met)	FBXO10 (T935M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278083	NM_012166.3(FBXO10):c.2800G>A (p.Ala934Thr)	FBXO10 (A934T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278078	NM_012166.3(FBXO10):c.2758C>T (p.Arg920Cys)	FBXO10 (R920C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093583	NM_012166.3(FBXO10):c.2703T>A (p.Asp901Glu)	FBXO10 (D901E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093582	NM_012166.3(FBXO10):c.2557G>A (p.Ala853Thr)	FBXO10 (A853T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219388	NM_012166.3(FBXO10):c.2527C>T (p.Arg843Trp)	FBXO10 (R843W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093581	NM_012166.3(FBXO10):c.2506G>A (p.Asp836Asn)	FBXO10 (D836N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 786908	NM_012166.3(FBXO10):c.2382C>G (p.Leu794=)	FBXO10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2256374	NM_012166.3(FBXO10):c.2339G>A (p.Arg780Gln)	FBXO10 (R780Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482414	NM_012166.3(FBXO10):c.2254A>T (p.Ile752Phe)	FBXO10 (I752F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093580	NM_012166.3(FBXO10):c.2140C>T (p.Pro714Ser)	FBXO10 (P714S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245173	NM_012166.3(FBXO10):c.2093A>T (p.Asp698Val)	FBXO10 (D698V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333989	NM_012166.3(FBXO10):c.2074C>G (p.Gln692Glu)	FBXO10 (Q692E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223144	NM_012166.3(FBXO10):c.2002A>G (p.Asn668Asp)	FBXO10 (N668D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483291	NM_012166.3(FBXO10):c.1984A>G (p.Ser662Gly)	FBXO10 (S662G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093577	NM_012166.3(FBXO10):c.1975C>G (p.His659Asp)	FBXO10 (H659D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411131	NM_012166.3(FBXO10):c.1970T>G (p.Leu657Arg)	FBXO10 (L657R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278080	NM_012166.3(FBXO10):c.1873G>A (p.Asp625Asn)	FBXO10 (D625N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278081	NM_012166.3(FBXO10):c.1751A>G (p.Asn584Ser)	FBXO10 (N584S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216661	NM_012166.3(FBXO10):c.1730G>A (p.Arg577His)	FBXO10 (R577H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 785286	NM_012166.3(FBXO10):c.1485C>T (p.Gly495=)	FBXO10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2314556	NM_012166.3(FBXO10):c.1424T>G (p.Ile475Ser)	FBXO10 (I475S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517054	NM_012166.3(FBXO10):c.1372A>G (p.Ile458Val)	FBXO10 (I458V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093576	NM_012166.3(FBXO10):c.1333T>G (p.Phe445Val)	FBXO10 (F445V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278079	NM_012166.3(FBXO10):c.1329C>T (p.Gly443=)	FBXO10	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3093575	NM_012166.3(FBXO10):c.1300A>G (p.Lys434Glu)	FBXO10 (K434E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 725121	NM_012166.3(FBXO10):c.1293C>T (p.Leu431=)	FBXO10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2354797	NM_012166.3(FBXO10):c.1279G>A (p.Val427Met)	FBXO10 (V427M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093573	NM_012166.3(FBXO10):c.1187G>A (p.Gly396Glu)	FBXO10 (G396E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327728	NM_012166.3(FBXO10):c.1157G>A (p.Gly386Glu)	FBXO10 (G386E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362423	NM_012166.3(FBXO10):c.1150G>A (p.Val384Ile)	FBXO10 (V384I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462663	NM_012166.3(FBXO10):c.1148C>T (p.Pro383Leu)	FBXO10 (P383L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522371	NM_012166.3(FBXO10):c.1118G>A (p.Arg373Lys)	FBXO10 (R373K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 716196	NM_012166.3(FBXO10):c.1050C>T (p.Thr350=)	FBXO10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3093585	NM_012166.3(FBXO10):c.712G>A (p.Val238Met)	FBXO10 (V238M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263504	NM_012166.3(FBXO10):c.710A>G (p.Asn237Ser)	FBXO10 (N237S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 786571	NM_012166.3(FBXO10):c.634C>A (p.His212Asn)	FBXO10 (H212N)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2377083	NM_012166.3(FBXO10):c.620A>G (p.Asn207Ser)	FBXO10 (N207S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278077	NM_012166.3(FBXO10):c.506G>A (p.Ser169Asn)	FBXO10 (S169N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278076	NM_012166.3(FBXO10):c.434G>A (p.Gly145Asp)	FBXO10 (G145D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093579	NM_012166.3(FBXO10):c.205G>A (p.Glu69Lys)	FBXO10 (E69K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311470	NM_012166.3(FBXO10):c.202C>G (p.Pro68Ala)	FBXO10 (P68A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 42