ClinVar for Gene (Select 7584) - ClinVar

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Links from Gene

Items: 37

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3335575	NM_003420.4(ZNF35):c.833A>G (p.Tyr278Cys)	ZKSCAN7-AS1, ZNF35 (Y278C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335574	NM_003420.4(ZNF35):c.214A>G (p.Met72Val)	ZKSCAN7-AS1, ZNF35 (M72V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335573	NM_003420.4(ZNF35):c.559A>G (p.Ser187Gly)	ZKSCAN7-AS1, ZNF35 (S187G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335572	NM_003420.4(ZNF35):c.796G>A (p.Val266Ile)	ZKSCAN7-AS1, ZNF35 (V266I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195349	NM_003420.4(ZNF35):c.713T>C (p.Val238Ala)	ZKSCAN7-AS1, ZNF35 (V238A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195348	NM_003420.4(ZNF35):c.505A>G (p.Arg169Gly)	ZKSCAN7-AS1, ZNF35 (R169G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195347	NM_003420.4(ZNF35):c.385T>C (p.Cys129Arg)	ZKSCAN7-AS1, ZNF35 (C129R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195346	NM_003420.4(ZNF35):c.173G>A (p.Gly58Glu)	ZKSCAN7-AS1, ZNF35 (G58E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195345	NM_003420.4(ZNF35):c.1580A>G (p.Glu527Gly)	ZKSCAN7-AS1, ZNF35 (E527G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195344	NM_003420.4(ZNF35):c.1480A>G (p.Arg494Gly)	ZKSCAN7-AS1, ZNF35 (R494G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195342	NM_003420.4(ZNF35):c.1471G>A (p.Val491Met)	ZKSCAN7-AS1, ZNF35 (V491M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195341	NM_003420.4(ZNF35):c.1292C>G (p.Ser431Cys)	ZKSCAN7-AS1, ZNF35 (S431C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195340	NM_003420.4(ZNF35):c.1009A>C (p.Asn337His)	ZKSCAN7-AS1, ZNF35 (N337H)	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 2600696	NM_003420.4(ZNF35):c.1133T>C (p.Ile378Thr)	ZKSCAN7-AS1, ZNF35 (I378T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593455	NM_003420.4(ZNF35):c.456A>C (p.Leu152Phe)	ZKSCAN7-AS1, ZNF35 (L152F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531257	NM_003420.4(ZNF35):c.605A>C (p.Lys202Thr)	ZKSCAN7-AS1, ZNF35 (K202T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507870	NM_003420.4(ZNF35):c.1567A>G (p.Thr523Ala)	ZKSCAN7-AS1, ZNF35 (T523A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493058	NM_003420.4(ZNF35):c.676G>A (p.Val226Met)	ZKSCAN7-AS1, ZNF35 (V226M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490435	NM_003420.4(ZNF35):c.1407T>G (p.Asn469Lys)	ZKSCAN7-AS1, ZNF35 (N469K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473306	NM_003420.4(ZNF35):c.1264G>A (p.Glu422Lys)	ZKSCAN7-AS1, ZNF35 (E422K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462007	NM_003420.4(ZNF35):c.479A>T (p.Asn160Ile)	ZKSCAN7-AS1, ZNF35 (N160I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455665	NM_003420.4(ZNF35):c.308T>C (p.Leu103Pro)	ZKSCAN7-AS1, ZNF35 (L103P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365289	NM_003420.4(ZNF35):c.1019G>A (p.Gly340Glu)	ZKSCAN7-AS1, ZNF35 (G340E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358343	NM_003420.4(ZNF35):c.786T>G (p.Ser262Arg)	ZKSCAN7-AS1, ZNF35 (S262R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342934	NM_003420.4(ZNF35):c.578A>C (p.Asn193Thr)	ZKSCAN7-AS1, ZNF35 (N193T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330727	NM_003420.4(ZNF35):c.133G>A (p.Val45Ile)	ZKSCAN7-AS1, ZNF35 (V45I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319509	NM_003420.4(ZNF35):c.1300A>C (p.Ile434Leu)	ZKSCAN7-AS1, ZNF35 (I434L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309330	NM_003420.4(ZNF35):c.725G>A (p.Arg242Gln)	ZKSCAN7-AS1, ZNF35 (R242Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294215	NM_003420.4(ZNF35):c.121G>A (p.Glu41Lys)	ZKSCAN7-AS1, ZNF35 (E41K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247473	NM_003420.4(ZNF35):c.565A>G (p.Lys189Glu)	ZKSCAN7-AS1, ZNF35 (K189E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233179	NM_003420.4(ZNF35):c.608A>G (p.Tyr203Cys)	ZKSCAN7-AS1, ZNF35 (Y203C)	Single nucleotide variant (missense variant)	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 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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Links from Gene

Items: 37