FBXO34[gene] and "single gene"[properties] - ClinVar

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Items: 40

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2527998	NM_017943.4(FBXO34):c.25C>T (p.Leu9Phe)	FBXO34 (L9F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206253	NM_017943.4(FBXO34):c.47C>T (p.Pro16Leu)	FBXO34 (P16L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3093694	NM_017943.4(FBXO34):c.65C>T (p.Thr22Met)	FBXO34 (T22M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248057	NM_017943.4(FBXO34):c.91A>G (p.Lys31Glu)	FBXO34 (K31E)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3093688	NM_017943.4(FBXO34):c.137G>C (p.Ser46Thr)	FBXO34 (S46T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550709	NM_017943.4(FBXO34):c.137G>T (p.Ser46Ile)	FBXO34 (S46I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278154	NM_017943.4(FBXO34):c.139G>A (p.Val47Ile)	FBXO34 (V47I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332767	NM_017943.4(FBXO34):c.267G>T (p.Lys89Asn)	FBXO34 (K89N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528479	NM_017943.4(FBXO34):c.284C>T (p.Thr95Met)	FBXO34 (T95M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296411	NM_017943.4(FBXO34):c.535C>A (p.Pro179Thr)	FBXO34 (P179T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093693	NM_017943.4(FBXO34):c.578G>T (p.Ser193Ile)	FBXO34 (S193I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265416	NM_017943.4(FBXO34):c.586G>A (p.Gly196Arg)	FBXO34 (G196R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278156	NM_017943.4(FBXO34):c.590A>G (p.Asp197Gly)	FBXO34 (D197G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278157	NM_017943.4(FBXO34):c.593G>C (p.Gly198Ala)	FBXO34 (G198A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538210	NM_017943.4(FBXO34):c.622A>T (p.Ile208Leu)	FBXO34 (I208L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093695	NM_017943.4(FBXO34):c.697C>T (p.Pro233Ser)	FBXO34 (P233S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311304	NM_017943.4(FBXO34):c.821G>A (p.Ser274Asn)	FBXO34 (S274N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510249	NM_017943.4(FBXO34):c.833G>A (p.Arg278His)	FBXO34 (R278H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526060	NM_017943.4(FBXO34):c.838C>T (p.Leu280Phe)	FBXO34 (L280F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306850	NM_017943.4(FBXO34):c.846G>C (p.Met282Ile)	FBXO34 (M282I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339548	NM_017943.4(FBXO34):c.869G>A (p.Cys290Tyr)	FBXO34 (C290Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351786	NM_017943.4(FBXO34):c.890G>A (p.Arg297His)	FBXO34 (R297H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093698	NM_017943.4(FBXO34):c.956A>G (p.Asn319Ser)	FBXO34 (N319S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374976	NM_017943.4(FBXO34):c.1009G>C (p.Asp337His)	FBXO34 (D337H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539558	NM_017943.4(FBXO34):c.1138G>T (p.Val380Leu)	FBXO34 (V380L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544284	NM_017943.4(FBXO34):c.1175G>A (p.Gly392Asp)	FBXO34 (G392D)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2524398	NM_017943.4(FBXO34):c.1225G>A (p.Asp409Asn)	FBXO34 (D409N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475682	NM_017943.4(FBXO34):c.1252T>C (p.Ser418Pro)	FBXO34 (S418P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3093689	NM_017943.4(FBXO34):c.1394A>G (p.Lys465Arg)	FBXO34 (K465R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093690	NM_017943.4(FBXO34):c.1417T>C (p.Ser473Pro)	FBXO34 (S473P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337948	NM_017943.4(FBXO34):c.1546G>C (p.Gly516Arg)	FBXO34 (G516R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355325	NM_017943.4(FBXO34):c.1589C>T (p.Pro530Leu)	FBXO34 (P530L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545034	NM_017943.4(FBXO34):c.1723A>G (p.Met575Val)	FBXO34 (M575V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093691	NM_017943.4(FBXO34):c.1727C>A (p.Ala576Asp)	FBXO34 (A576D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242197	NM_017943.4(FBXO34):c.1762A>G (p.Arg588Gly)	FBXO34 (R588G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454608	NM_017943.4(FBXO34):c.1808G>A (p.Cys603Tyr)	FBXO34 (C603Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093692	NM_017943.4(FBXO34):c.1965C>G (p.Cys655Trp)	FBXO34 (C655W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510926	NM_017943.4(FBXO34):c.1998G>A (p.Met666Ile)	FBXO34 (M666I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613735	NM_017943.4(FBXO34):c.2086C>G (p.Arg696Gly)	FBXO34 (R696G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 564093	GRCh37/hg19 14q22.3(chr14:55697853-55803026)x3	FBXO34	Copy number gain	not provided	GLikely benign

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Items: 40