ClinVar for Gene (Select 285349) - ClinVar

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Links from Gene

Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3259087	NM_173658.4(ZNF660):c.986A>C (p.Glu329Ala)	ZKSCAN7-AS1, ZNF660 +1 more (E329A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3259086	NM_173658.4(ZNF660):c.469A>G (p.Thr157Ala)	ZKSCAN7-AS1, ZNF660 +1 more (T157A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3259085	NM_173658.4(ZNF660):c.493A>G (p.Ile165Val)	ZKSCAN7-AS1, ZNF660 +1 more (I165V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197547	NM_173658.4(ZNF660):c.99G>T (p.Gln33His)	ZKSCAN7-AS1, ZNF660 +1 more (Q33H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197546	NM_173658.4(ZNF660):c.870T>G (p.Ile290Met)	ZKSCAN7-AS1, ZNF660 +1 more (I290M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197545	NM_173658.4(ZNF660):c.681C>A (p.Phe227Leu)	ZKSCAN7-AS1, ZNF660 +1 more (F227L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197544	NM_173658.4(ZNF660):c.664G>A (p.Glu222Lys)	ZKSCAN7-AS1, ZNF660 +1 more (E222K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197543	NM_173658.4(ZNF660):c.583T>C (p.Cys195Arg)	ZKSCAN7-AS1, ZNF660 +1 more (C195R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197542	NM_173658.4(ZNF660):c.537A>C (p.Gln179His)	ZKSCAN7-AS1, ZNF660 +1 more (Q179H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197540	NM_173658.4(ZNF660):c.209G>A (p.Arg70Gln)	ZKSCAN7-AS1, ZNF660 +1 more (R70Q)	Single nucleotide variant (missense variant +1 more)	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 2619719	NM_173658.4(ZNF660):c.127G>C (p.Val43Leu)	ZKSCAN7-AS1, ZNF660 +1 more (V43L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2602889	NM_173658.4(ZNF660):c.367C>T (p.Arg123Trp)	ZKSCAN7-AS1, ZNF660 +1 more (R123W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2525975	NM_173658.4(ZNF660):c.780C>G (p.Asn260Lys)	ZKSCAN7-AS1, ZNF660 +1 more (N260K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2476495	NM_173658.4(ZNF660):c.640G>A (p.Gly214Arg)	ZKSCAN7-AS1, ZNF660 +1 more (G214R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386390	NM_173658.4(ZNF660):c.328G>C (p.Glu110Gln)	ZKSCAN7-AS1, ZNF660 +1 more (E110Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2372284	NM_173658.4(ZNF660):c.434G>A (p.Arg145Gln)	ZKSCAN7-AS1, ZNF660 +1 more (R145Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366702	NM_173658.4(ZNF660):c.722G>A (p.Arg241His)	ZKSCAN7-AS1, ZNF660 +1 more (R241H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2361384	NM_173658.4(ZNF660):c.494T>C (p.Ile165Thr)	ZKSCAN7-AS1, ZNF660 +1 more (I165T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2262661	NM_173658.4(ZNF660):c.538C>T (p.His180Tyr)	ZKSCAN7-AS1, ZNF660 +1 more (H180Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2258027	NM_173658.4(ZNF660):c.662A>C (p.Asp221Ala)	ZKSCAN7-AS1, ZNF660 +1 more (D221A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2225913	NM_173658.4(ZNF660):c.649C>G (p.Pro217Ala)	ZKSCAN7-AS1, ZNF660 +1 more (P217A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 814439	GRCh37/hg19 3p21.31(chr3:44444902-45413927)x1	CDCP1, CLEC3B +16 more	Copy number loss	not provided	GUncertain significance
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 253640	GRCh37/hg19 3p22.1-21.31(chr3:41104508-44636698)x1	HHATL, ZKSCAN7 +29 more	Copy number loss	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
Select item 156210	NM_173658.4(ZNF660):c.721C>T (p.Arg241Cys)	ZKSCAN7-AS1, ZNF660 +1 more (R241C)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance

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Links from Gene

Items: 29