VRK2[gene] and "single gene"[properties] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3189073	NM_006296.7(VRK2):c.16A>G (p.Asn6Asp)	VRK2 (N6D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3189072	NM_006296.7(VRK2):c.160A>G (p.Lys54Glu)	VRK2 (K54E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2334741	NM_006296.7(VRK2):c.187G>A (p.Glu63Lys)	VRK2 (E40K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2257311	NM_006296.7(VRK2):c.358G>C (p.Val120Leu)	VRK2 (V120L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512136	NM_006296.7(VRK2):c.367A>G (p.Arg123Gly)	VRK2 (R123G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605989	NM_006296.7(VRK2):c.419A>G (p.Lys140Arg)	VRK2 (K140R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211809	NM_006296.7(VRK2):c.446G>A (p.Arg149Gln)	VRK2 (R126Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3189074	NM_006296.7(VRK2):c.560A>G (p.Tyr187Cys)	VRK2 (Y164C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472022	NM_006296.7(VRK2):c.587A>G (p.Asn196Ser)	VRK2 (N78S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3189075	NM_006296.7(VRK2):c.635G>A (p.Gly212Glu)	VRK2 (G212E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3189076	NM_006296.7(VRK2):c.641T>C (p.Ile214Thr)	VRK2 (I191T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321632	NM_006296.7(VRK2):c.649A>G (p.Thr217Ala)	VRK2 (T194A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531462	NM_006296.7(VRK2):c.689G>A (p.Arg230Gln)	VRK2 (R112Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356164	NM_006296.7(VRK2):c.696C>G (p.Asp232Glu)	VRK2 (D232E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3189077	NM_006296.7(VRK2):c.724C>T (p.Arg242Trp)	VRK2 (R124W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3189078	NM_006296.7(VRK2):c.725G>A (p.Arg242Gln)	VRK2 (R242Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3189080	NM_006296.7(VRK2):c.857G>A (p.Cys286Tyr)	VRK2 (C263Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3189081	NM_006296.7(VRK2):c.917A>G (p.Tyr306Cys)	VRK2 (Y283C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3189082	NM_006296.7(VRK2):c.946C>T (p.His316Tyr)	VRK2 (H198Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3189083	NM_006296.7(VRK2):c.983A>G (p.Lys328Arg)	VRK2 (K328R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289032	NM_006296.7(VRK2):c.1025T>C (p.Val342Ala)	VRK2 (V342A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240542	NM_006296.7(VRK2):c.1073G>A (p.Arg358Lys)	VRK2 (R335K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3189068	NM_006296.7(VRK2):c.1089A>T (p.Lys363Asn)	VRK2 (K245N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3189069	NM_006296.7(VRK2):c.1105A>G (p.Ser369Gly)	VRK2 (S251G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261211	NM_006296.7(VRK2):c.1115C>A (p.Ser372Tyr)	VRK2 (S254Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 978180	NC_000002.11:g.58271895_58333429dup	VRK2	Duplication	Seizure	GUncertain significance

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Items: 26