CCR4[gene] - ClinVar

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Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57397	GRCh38/hg38 3p26.3-22.2(chr3:52266-37148076)x3	LOC129936421, LOC129936422 +962 more	Copy number gain	See cases	GPathogenic
Select item 153415	GRCh38/hg38 3p26.3-22.1(chr3:53308-41381521)x3	ACAA1, ACVR2B +1111 more	Copy number gain	See cases	GPathogenic
Select item 57978	GRCh38/hg38 3p25.3-22.2(chr3:11463328-38919543)x3	LOC132088948, LOC132088950 +730 more	Copy number gain	See cases	GPathogenic
Select item 57769	GRCh38/hg38 3p22.3-22.2(chr3:32322382-36775606)x1	ARPP21, ARPP21-AS1 +87 more	Copy number loss	See cases	GPathogenic
Select item 2470777	NM_005508.5(CCR4):c.43A>G (p.Ile15Val)	CCR4 (I15V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140089	NM_005508.5(CCR4):c.62T>A (p.Leu21Gln)	CCR4 (L21Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140086	NM_005508.5(CCR4):c.204G>T (p.Lys68Asn)	CCR4 (K68N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350713	NM_005508.5(CCR4):c.263T>G (p.Phe88Cys)	CCR4 (F88C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140087	NM_005508.5(CCR4):c.391A>G (p.Met131Val)	CCR4 (M131V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140088	NM_005508.5(CCR4):c.530C>T (p.Thr177Ile)	CCR4 (T177I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246932	NM_005508.5(CCR4):c.624T>G (p.Ile208Met)	CCR4 (I208M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339733	NM_005508.5(CCR4):c.672G>T (p.Met224Ile)	CCR4 (M224I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327418	NM_005508.5(CCR4):c.688C>A (p.Gln230Lys)	CCR4 (Q230K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235300	NM_005508.5(CCR4):c.737C>T (p.Ala246Val)	CCR4 (A246V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217635	NM_005508.5(CCR4):c.745G>A (p.Val249Ile)	CCR4 (V249I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140090	NM_005508.5(CCR4):c.766A>G (p.Thr256Ala)	CCR4 (T256A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222546	NM_005508.5(CCR4):c.778A>G (p.Ile260Val)	CCR4 (I260V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2256545	NM_005508.5(CCR4):c.779T>C (p.Ile260Thr)	CCR4 (I260T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466975	NM_005508.5(CCR4):c.979G>A (p.Val327Met)	CCR4 (V327M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264641	NM_005508.5(CCR4):c.980T>G (p.Val327Gly)	CCR4 (V327G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140091	NM_005508.5(CCR4):c.985T>G (p.Cys329Gly)	CCR4 (C329G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466387	NM_005508.5(CCR4):c.1000C>G (p.Leu334Val)	CCR4 (L334V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3242334	GRCh37/hg19 3p26.3-22.3(chr3:60000-34461438)x3	ANKRD28, ARL8B +145 more	Copy number gain	not provided	GPathogenic
Select item 3062708	GRCh37/hg19 3p26.3-22.3(chr3:61891-33946644)x3	OXTR, PDCD6IP +145 more	Copy number gain	not specified	GPathogenic
Select item 2685913	GRCh37/hg19 3p22.3(chr3:32324460-33982773)x3	CCR4, CLASP2 +13 more	Copy number gain	not provided	GUncertain significance
Select item 1527006	GRCh37/hg19 3p22.3(chr3:32699328-35286114)	CCR4, CLASP2 +9 more	Copy number gain	not specified	GUncertain significance
Select item 1527005	GRCh37/hg19 3p23-22.3(chr3:31859973-33127072)	CCR4, CMTM6 +9 more	Copy number gain	not specified	GUncertain significance
Select item 1526968	GRCh37/hg19 3p26.3-22.2(chr3:61891-36710181)	FANCD2OS, THUMPD3 +148 more	Copy number gain	not specified	GPathogenic
Select item 1455527	NC_000003.11:g.(?_16710965)_(41275270_?)del	ACAA1, ACVR2B +93 more	Deletion	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 443464	GRCh37/hg19 3p26.3-22.2(chr3:61891-37459464)x3	ANKRD28, APRG1 +155 more	Copy number gain	See cases	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 441705	GRCh37/hg19 3p26.3-22.3(chr3:61891-33958201)x3	TRIM71, TRNT1 +145 more	Copy number gain	See cases	GPathogenic
Select item 253599	GRCh37/hg19 3p24.1-22.3(chr3:29689082-34233218)x1	CCR4, CLASP2 +20 more	Copy number loss	See cases	GPathogenic

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Items: 35