CDC14B[gene] - ClinVar

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Items: 76

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 160862	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC124210612, LOC124210613 +3786 more	Copy number gain	See cases	GPathogenic
Select item 150340	GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3	LOC121331326, LOC121331327 +3785 more	Copy number gain	See cases	GPathogenic
Select item 150050	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3	LOC126860737, LOC126860738 +3786 more	Copy number gain	See cases	GPathogenic
Select item 149828	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3	ABCA1, ABCA2 +3786 more	Copy number gain	See cases	GPathogenic
Select item 59875	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3	LOC110121197, LOC110121234 +3786 more	Copy number gain	See cases	GPathogenic
Select item 33205	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC121331342, LOC121331343 +3786 more	Copy number gain	See cases	GPathogenic
Select item 153518	GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3	LOC113839542, LOC113839543 +3786 more	Copy number gain	See cases	GPathogenic
Select item 155409	GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3	ABCA1, ABCA2 +3786 more	Copy number gain	See cases	GPathogenic
Select item 144309	GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445)	LOC130002189, LOC130002190 +3786 more	Copy number gain	See cases	GPathogenic
Select item 147624	GRCh38/hg38 9q21.11-31.2(chr9:68420430-106579493)x3	ABCA1, ABHD17B +1072 more	Copy number gain	See cases	GPathogenic
Select item 151006	GRCh38/hg38 9q21.12-31.3(chr9:69627642-111454304)x3	ABCA1, ABHD17B +1188 more	Copy number gain	See cases	GPathogenic
Select item 59881	GRCh38/hg38 9q22.1-32(chr9:88522292-113687796)x3	LOC130002218, LOC130002219 +994 more	Copy number gain	See cases	GPathogenic
Select item 59118	GRCh38/hg38 9q22.31-22.33(chr9:91596533-97018746)x1	AOPEP, ASPN +268 more	Copy number loss	See cases	GPathogenic
Select item 59902	GRCh38/hg38 9q22.31-22.33(chr9:92561720-98122580)x3	LOC132089736, LOC132089737 +313 more	Copy number gain	See cases	GPathogenic
Select item 145977	GRCh38/hg38 9q22.32-22.33(chr9:94713892-98121186)x1	ANP32B, AOPEP +197 more	Copy number loss	See cases	GPathogenic
Select item 217298	GRCh37/hg19 9q22.32(97579146-99280739)x1	LOC124310599, LOC124310600 +94 more	Copy number loss	Gorlin syndrome	GPathogenic
Select item 144971	GRCh38/hg38 9q22.32-31.3(chr9:95061030-108695569)x1	LOC130002205, LOC130002206 +417 more	Copy number loss	See cases	GPathogenic
Select item 59904	GRCh38/hg38 9q22.32-22.33(chr9:96094968-96620662)x3	CDC14B, HABP4 +32 more	Copy number gain	See cases	GPathogenic
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 2460602	NM_033331.4(CDC14B):c.1268A>G (p.Asn423Ser)	CDC14B, LOC126860691 (N400S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140772	NM_033331.4(CDC14B):c.1241A>C (p.Glu414Ala)	CDC14B, LOC126860691 (E414A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140771	NM_033331.4(CDC14B):c.1240G>A (p.Glu414Lys)	CDC14B, LOC126860691 (E391K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2207210	NM_033331.4(CDC14B):c.1177C>T (p.Leu393Phe)	CDC14B, LOC126860691 (L393F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3264927	NM_033331.4(CDC14B):c.1163C>T (p.Ala388Val)	CDC14B, LOC126860691 (A351V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140770	NM_033331.4(CDC14B):c.1136A>G (p.Lys379Arg)	CDC14B, LOC126860691 (K342R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3140769	NM_033331.4(CDC14B):c.1124G>A (p.Arg375His)	CDC14B, LOC126860691 (R352H +2 more)	Single nucleotide variant (missense variant +1 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
Select item 3063071	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3	DMAC1, DMRT1 +769 more	Copy number gain	not specified	GPathogenic
Select item 2671591	Single allele	CARD19, MIR24-1 +106 more	Deletion	not provided	GPathogenic
Select item 1711101	GRCh37/hg19 9p24.3-q34.11(chr9:203861-131603223)x3	ADAMTSL1, CEP78 +596 more	Copy number gain	See cases	GPathogenic
Select item 1703688	GRCh37/hg19 9p22.1-q33.1(chr9:19356861-119513311)	ATOSB, ATP6V1G1 +417 more	Copy number loss	Distal tetrasomy 15q	GUncertain significance
Select item 1527521	GRCh37/hg19 9q21.11-33.2(chr9:71349994-122603410)	ABCA1, ABHD17B +261 more	Copy number gain	not specified	GLikely pathogenic
Select item 1527491	GRCh37/hg19 9p24.3-q34.3(chr9:353349-141020389)	ANKRD18A, ANKRD18B +768 more	Copy number gain	not specified	GPathogenic
Select item 1341973	GRCh37/hg19 9q22.2-31.1(chr9:93864974-106661581)x1	ALDOB, ALG2 +87 more	Copy number loss	Gorlin syndrome	GPathogenic
Select item 997816	Single allele	PRXL2C, TBC1D2 +55 more	Deletion	Intellectual disability	GPathogenic
Select item 929316	GRCh37/hg19 9q22.31-31.2(chr9:96126075-108535272)x1	TSTD2, XPA +84 more	Copy number loss	See cases	GPathogenic
Select item 694460	NC_000009.11:g.12246100_101559378inv	ANKS6, ANP32B +326 more	Inversion	Abnormal chromosome morphology +1 more	GLikely pathogenic
Select item 688872	GRCh37/hg19 9q22.32-22.33(chr9:98849008-99405481)x1	CDC14B, HABP4 +4 more	Copy number loss	not provided	GUncertain significance
Select item 688061	GRCh37/hg19 9q22.32-22.33(chr9:98156960-99345624)x1	CDC14B, ERCC6L2 +5 more	Copy number loss	not provided	GPathogenic
Select item 687100	GRCh37/hg19 9q21.11-34.3(chr9:71416475-141020389)x3	AMBP, ANAPC2 +552 more	Copy number gain	not provided	GPathogenic
Select item 685192	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3	MSMP, OR13D1 +769 more	Copy number gain	not provided	GPathogenic
Select item 523294	GRCh37/hg19 9q21.11-34.3(chr9:71069743-140999928)	ANGPTL2, ANKS6 +555 more	Copy number gain	Seizure +2 more	GLikely pathogenic
Select item 443986	GRCh37/hg19 9p24.3-q34.3(chr9:203862-141020389)	ODF2, OGN +769 more	Copy number gain	See cases	GPathogenic
Select item 443721	GRCh37/hg19 9q22.33(chr9:99302837-99576623)x1	CDC14B, PRXL2C +1 more	Copy number loss	See cases	GLikely benign
Select item 443720	GRCh37/hg19 9q22.32-22.33(chr9:96732332-100175689)x1	AOPEP, CCDC180 +26 more	Copy number loss	See cases	GPathogenic
Select item 442793	GRCh37/hg19 9q22.32-31.1(chr9:97553176-102919383)x3	ALG2, ANKS6 +40 more	Copy number gain	See cases	GLikely pathogenic
Select item 395707	GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407)	ABCA1, ABCA2 +771 more	Copy number gain	See cases	GPathogenic
Select item 394717	GRCh37/hg19 9q22.32-22.33(chr9:97355862-99805480)x1	AOPEP, CDC14B +17 more	Copy number loss	See cases	GPathogenic
Select item 253402	GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3	ABCA1, ABCA2 +771 more	Copy number gain	See cases	GPathogenic

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Items: 76