ClinVar for Gene (Select 64866) - ClinVar

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Links from Gene

Items: 66

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3265105	NM_022842.5(CDCP1):c.1852A>C (p.Ile618Leu)	CDCP1 (I618L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265104	NM_022842.5(CDCP1):c.2171A>G (p.Lys724Arg)	CDCP1 (K724R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265103	NM_022842.5(CDCP1):c.2008C>G (p.Leu670Val)	CDCP1 (L670V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265102	NM_022842.5(CDCP1):c.460A>G (p.Ser154Gly)	CDCP1 (S154G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265100	NM_022842.5(CDCP1):c.1834C>T (p.Arg612Trp)	CDCP1 (R612W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265099	NM_022842.5(CDCP1):c.406G>A (p.Gly136Ser)	CDCP1 (G136S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265098	NM_022842.5(CDCP1):c.622G>A (p.Gly208Ser)	CDCP1 (G208S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265097	NM_022842.5(CDCP1):c.130A>G (p.Ile44Val)	CDCP1 (I44V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141053	NM_022842.5(CDCP1):c.877G>A (p.Glu293Lys)	CDCP1 (E293K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141051	NM_022842.5(CDCP1):c.511G>A (p.Val171Met)	CDCP1 (V171M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141050	NM_022842.5(CDCP1):c.330G>C (p.Gln110His)	CDCP1 (Q110H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141048	NM_022842.5(CDCP1):c.2491C>G (p.Pro831Ala)	CDCP1 (P831A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141047	NM_022842.5(CDCP1):c.2450G>A (p.Ser817Asn)	CDCP1 (S817N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3141046	NM_022842.5(CDCP1):c.2344A>G (p.Arg782Gly)	CDCP1 (R782G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141044	NM_022842.5(CDCP1):c.2005A>G (p.Ile669Val)	CDCP1 (I669V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3141043	NM_022842.5(CDCP1):c.182C>T (p.Ser61Phe)	CDCP1 (S61F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141041	NM_022842.5(CDCP1):c.1562C>G (p.Ala521Gly)	CDCP1 (A521G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141040	NM_022842.5(CDCP1):c.1560T>A (p.Phe520Leu)	CDCP1 (F520L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141039	NM_022842.5(CDCP1):c.1556C>A (p.Thr519Asn)	CDCP1 (T519N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141038	NM_022842.5(CDCP1):c.1391C>G (p.Ala464Gly)	CDCP1 (A464G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141037	NM_022842.5(CDCP1):c.1078G>A (p.Glu360Lys)	CDCP1 (E360K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2685915	GRCh37/hg19 3p21.31(chr3:44563378-45177006)x3	CDCP1, CLEC3B +12 more	Copy number gain	not provided	GUncertain significance
Select item 2613522	NM_022842.5(CDCP1):c.2174G>A (p.Gly725Glu)	CDCP1 (G725E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611353	NM_022842.5(CDCP1):c.1416C>A (p.His472Gln)	CDCP1 (H472Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608814	NM_022842.5(CDCP1):c.692G>C (p.Gly231Ala)	CDCP1 (G231A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597270	NM_022842.5(CDCP1):c.493G>A (p.Gly165Ser)	CDCP1 (G165S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540724	NM_022842.5(CDCP1):c.497G>A (p.Arg166Gln)	CDCP1 (R166Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537576	NM_022842.5(CDCP1):c.1034A>T (p.Tyr345Phe)	CDCP1 (Y345F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531400	NM_022842.5(CDCP1):c.635C>T (p.Ala212Val)	CDCP1 (A212V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525041	NM_022842.5(CDCP1):c.1789G>A (p.Val597Met)	CDCP1 (V597M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513608	NM_022842.5(CDCP1):c.196A>G (p.Thr66Ala)	CDCP1 (T66A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511501	NM_022842.5(CDCP1):c.907G>A (p.Gly303Arg)	CDCP1 (G303R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492417	NM_022842.5(CDCP1):c.2114G>A (p.Gly705Asp)	CDCP1 (G705D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489865	NM_022842.5(CDCP1):c.970G>T (p.Gly324Trp)	CDCP1 (G324W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472058	NM_022842.5(CDCP1):c.554G>A (p.Arg185Gln)	CDCP1 (R185Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409517	NM_022842.5(CDCP1):c.1781G>A (p.Arg594Gln)	CDCP1 (R594Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381747	NM_022842.5(CDCP1):c.1623C>A (p.Phe541Leu)	CDCP1 (F541L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377128	NM_022842.5(CDCP1):c.1033T>C (p.Tyr345His)	CDCP1 (Y345H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375631	NM_022842.5(CDCP1):c.2254G>A (p.Gly752Ser)	CDCP1 (G752S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360604	NM_022842.5(CDCP1):c.766G>A (p.Val256Ile)	CDCP1 (V256I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2336622	NM_022842.5(CDCP1):c.2177G>A (p.Arg726Gln)	CDCP1 (R726Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334275	NM_022842.5(CDCP1):c.2347G>T (p.Ala783Ser)	CDCP1 (A783S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319520	NM_022842.5(CDCP1):c.1058G>A (p.Arg353Gln)	CDCP1 (R353Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317770	NM_022842.5(CDCP1):c.149C>T (p.Thr50Ile)	CDCP1 (T50I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315251	NM_022842.5(CDCP1):c.1903A>G (p.Ser635Gly)	CDCP1 (S635G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298920	NM_022842.5(CDCP1):c.2012T>C (p.Ile671Thr)	CDCP1 (I671T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280341	NM_022842.5(CDCP1):c.434G>A (p.Arg145His)	CDCP1 (R145H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245489	NM_022842.5(CDCP1):c.1867G>A (p.Glu623Lys)	CDCP1 (E623K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234307	NM_022842.5(CDCP1):c.1087C>A (p.Pro363Thr)	CDCP1 (P363T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231743	NM_022842.5(CDCP1):c.68T>G (p.Leu23Arg)	CDCP1 (L23R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231193	NM_022842.5(CDCP1):c.1752G>C (p.Gln584His)	CDCP1 (Q584H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223390	NM_022842.5(CDCP1):c.809A>G (p.Asn270Ser)	CDCP1 (N270S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211441	NM_022842.5(CDCP1):c.1747G>A (p.Asp583Asn)	CDCP1 (D583N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2208225	NM_022842.5(CDCP1):c.23T>C (p.Val8Ala)	CDCP1 (V8A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205662	NM_022842.5(CDCP1):c.2160A>C (p.Lys720Asn)	CDCP1 (K720N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1801811	NM_022842.5(CDCP1):c.2170A>T (p.Lys724Ter)	CDCP1 (K724*)	Single nucleotide variant (nonsense)	Myoepithelial tumor	GUncertain significance
Select item 1341974	GRCh37/hg19 3p21.31(chr3:44948482-49115809)x1	NCKIPSD, NDUFAF3 +71 more	Copy number loss	not provided	GPathogenic
Select item 814439	GRCh37/hg19 3p21.31(chr3:44444902-45413927)x1	CDCP1, CLEC3B +16 more	Copy number loss	not provided	GUncertain significance
Select item 791240	NM_022842.5(CDCP1):c.2288G>A (p.Arg763Gln)	CDCP1 (R763Q)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 773572	NM_022842.5(CDCP1):c.918G>A (p.Ala306=)	CDCP1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 712052	NM_022842.5(CDCP1):c.1786G>A (p.Gly596Ser)	CDCP1 (G596S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 625696	GRCh37/hg19 3p21.31-21.1(chr3:45153770-53878616)	APEH, HEMK1 +177 more	Copy number gain	not provided	GPathogenic
Select item 562760	GRCh37/hg19 3p24.3-21.31(chr3:16923595-45249923)x2,3	ABHD5, ACAA1 +135 more	Copy number gain	not provided	GPathogenic
Select item 442401	GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3	HHLA2, HIGD1A +1054 more	Copy number gain	See cases	GPathogenic
Select item 442400	GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)	A4GNT, AADAC +1054 more	Copy number gain	See cases	GPathogenic
Select item 253356	GRCh37/hg19 3p22.2-21.31(chr3:37028313-49929220)x3	ABHD5, ACAA1 +177 more	Copy number gain	See cases	GLikely pathogenic

ClinVar

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Germline classification

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Links from Gene

Items: 66