CDC14B[gene] and "single gene"[properties] - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2376013	NM_033331.4(CDC14B):c.1493G>A (p.Arg498His)	CDC14B (R459H +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2468372	NM_033331.4(CDC14B):c.1480A>G (p.Lys494Glu)	CDC14B (K455E +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2570378	NM_033331.4(CDC14B):c.1449C>G (p.Ser483Arg)	CDC14B (S446R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2530421	NM_033331.4(CDC14B):c.1379C>T (p.Thr460Ile)	CDC14B (T423I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3140775	NM_033331.4(CDC14B):c.985A>G (p.Ile329Val)	CDC14B (I292V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2204497	NM_033331.4(CDC14B):c.869C>T (p.Thr290Ile)	CDC14B (T253I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2495411	NM_033331.4(CDC14B):c.857C>T (p.Ala286Val)	CDC14B (A286V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2270143	NM_033331.4(CDC14B):c.842A>G (p.His281Arg)	CDC14B (H244R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392305	NM_033331.4(CDC14B):c.835G>A (p.Asp279Asn)	CDC14B (D279N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2518859	NM_033331.4(CDC14B):c.815G>A (p.Arg272His)	CDC14B (R235H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239064	NM_033331.4(CDC14B):c.812A>G (p.Lys271Arg)	CDC14B (K271R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2561483	NM_033331.4(CDC14B):c.724C>A (p.Gln242Lys)	CDC14B (Q205K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2520261	NM_033331.4(CDC14B):c.660A>G (p.Ile220Met)	CDC14B (I197M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2558505	NM_033331.4(CDC14B):c.637A>C (p.Asn213His)	CDC14B (N213H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2290217	NM_033331.4(CDC14B):c.620A>G (p.His207Arg)	CDC14B (H207R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2486917	NM_033331.4(CDC14B):c.593A>G (p.Asn198Ser)	CDC14B (N175S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619501	NM_033331.4(CDC14B):c.545G>A (p.Cys182Tyr)	CDC14B (C159Y +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2362768	NM_033331.4(CDC14B):c.514A>G (p.Ser172Gly)	CDC14B (S172G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2334086	NM_033331.4(CDC14B):c.371C>G (p.Ser124Cys)	CDC14B (S101C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2610339	NM_033331.4(CDC14B):c.323T>C (p.Leu108Ser)	CDC14B (L85S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2380384	NM_033331.4(CDC14B):c.286A>G (p.Met96Val)	CDC14B (M59V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2464820	NM_033331.4(CDC14B):c.259G>A (p.Ala87Thr)	CDC14B (A64T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140773	NM_033331.4(CDC14B):c.154A>G (p.Ile52Val)	CDC14B (I52V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140768	NM_033331.4(CDC14B):c.108G>C (p.Gln36His)	CDC14B (Q36H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140774	NM_033331.4(CDC14B):c.80G>C (p.Gly27Ala)	CDC14B (G27A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2376717	NM_033331.4(CDC14B):c.76C>G (p.Pro26Ala)	CDC14B (P26A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335890	NM_033331.4(CDC14B):c.68C>G (p.Ser23Trp)	CDC14B (S23W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2273128	NM_033331.4(CDC14B):c.38C>T (p.Ala13Val)	CDC14B (A13V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359568	NM_033331.4(CDC14B):c.14G>C (p.Ser5Thr)	CDC14B (S5T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 29