Related gene-specific medical variations for Gene (Select 114884) - ClinVar

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Links from Gene

Items: 46

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3259812	NM_001137674.3(ZNF860):c.109G>A (p.Glu37Lys)	OSBPL10, ZNF860 (E37K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259811	NM_001137674.3(ZNF860):c.596C>T (p.Pro199Leu)	OSBPL10, ZNF860 (P199L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259809	NM_001137674.3(ZNF860):c.1289A>G (p.Lys430Arg)	OSBPL10, ZNF860 (K430R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259808	NM_001137674.3(ZNF860):c.764G>A (p.Gly255Glu)	OSBPL10, ZNF860 (G255E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259807	NM_001137674.3(ZNF860):c.131C>A (p.Thr44Lys)	OSBPL10, ZNF860 (T44K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259806	NM_001137674.3(ZNF860):c.1349G>A (p.Gly450Glu)	OSBPL10, ZNF860 (G450E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258043	NM_017784.5(OSBPL10):c.192C>G (p.Ser64Arg)	OSBPL10, LOC129936413 (S64R)	Single nucleotide variant (missense variant)	Neoplasm	OUncertain significance
Select item 3198871	NM_001137674.3(ZNF860):c.973C>T (p.Arg325Cys)	OSBPL10, ZNF860 (R325C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198870	NM_001137674.3(ZNF860):c.496C>G (p.Leu166Val)	OSBPL10, ZNF860 (L166V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198869	NM_001137674.3(ZNF860):c.210G>A (p.Met70Ile)	OSBPL10, ZNF860 (M70I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198868	NM_001137674.3(ZNF860):c.1841G>T (p.Arg614Ile)	OSBPL10, ZNF860 (R614I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198867	NM_001137674.3(ZNF860):c.1703G>A (p.Cys568Tyr)	OSBPL10, ZNF860 (C568Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198866	NM_001137674.3(ZNF860):c.1013G>A (p.Gly338Glu)	OSBPL10, ZNF860 (G338E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608540	NM_001137674.3(ZNF860):c.898A>C (p.Asn300His)	OSBPL10, ZNF860 (N300H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600718	NM_001137674.3(ZNF860):c.415G>A (p.Asp139Asn)	OSBPL10, ZNF860 (D139N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559217	NM_001137674.3(ZNF860):c.209T>G (p.Met70Arg)	OSBPL10, ZNF860 (M70R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551591	NM_001137674.3(ZNF860):c.1504G>T (p.Ala502Ser)	OSBPL10, ZNF860 (A502S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538685	NM_001137674.3(ZNF860):c.833G>C (p.Arg278Thr)	OSBPL10, ZNF860 (R278T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507814	NM_001137674.3(ZNF860):c.1874A>G (p.His625Arg)	OSBPL10, ZNF860 (H625R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495792	NM_001137674.3(ZNF860):c.818T>G (p.Leu273Arg)	OSBPL10, ZNF860 (L273R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485633	NM_001137674.3(ZNF860):c.812G>A (p.Arg271Gln)	OSBPL10, ZNF860 (R271Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478219	NM_001137674.3(ZNF860):c.122T>C (p.Leu41Pro)	OSBPL10, ZNF860 (L41P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456297	NM_001137674.3(ZNF860):c.1313G>A (p.Arg438His)	OSBPL10, ZNF860 (R438H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455072	NM_001137674.3(ZNF860):c.1579C>T (p.Arg527Cys)	OSBPL10, ZNF860 (R527C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409830	NM_001137674.3(ZNF860):c.649C>T (p.Leu217Phe)	OSBPL10, ZNF860 (L217F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403327	NM_001137674.3(ZNF860):c.424G>A (p.Asp142Asn)	OSBPL10, ZNF860 (D142N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400993	NM_001137674.3(ZNF860):c.1337G>A (p.Arg446Gln)	OSBPL10, ZNF860 (R446Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391668	NM_001137674.3(ZNF860):c.167A>G (p.Asn56Ser)	OSBPL10, ZNF860 (N56S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377798	NM_001137674.3(ZNF860):c.1825C>T (p.Arg609Cys)	OSBPL10, ZNF860 (R609C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365493	NM_017784.5(OSBPL10):c.199G>C (p.Gly67Arg)	LOC129936413, OSBPL10 (G67R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335185	NM_001137674.3(ZNF860):c.1263T>A (p.Asn421Lys)	OSBPL10, ZNF860 (N421K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325420	NM_001137674.3(ZNF860):c.933G>T (p.Glu311Asp)	OSBPL10, ZNF860 (E311D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303551	NM_001137674.3(ZNF860):c.746A>C (p.Gln249Pro)	OSBPL10, ZNF860 (Q249P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281434	NM_001137674.3(ZNF860):c.1852G>A (p.Gly618Arg)	OSBPL10, ZNF860 (G618R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273603	NM_001137674.3(ZNF860):c.456A>C (p.Lys152Asn)	OSBPL10, ZNF860 (K152N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268776	NM_001137674.3(ZNF860):c.995A>G (p.His332Arg)	OSBPL10, ZNF860 (H332R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268053	NM_001137674.3(ZNF860):c.1673G>T (p.Arg558Ile)	OSBPL10, ZNF860 (R558I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255059	NM_001137674.3(ZNF860):c.496C>T (p.Leu166Phe)	OSBPL10, ZNF860 (L166F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254233	NM_001137674.3(ZNF860):c.1256T>G (p.Ile419Ser)	OSBPL10, ZNF860 (I419S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239209	NM_001137674.3(ZNF860):c.845G>C (p.Gly282Ala)	OSBPL10, ZNF860 (G282A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232722	NM_001137674.3(ZNF860):c.1352A>T (p.Glu451Val)	OSBPL10, ZNF860 (E451V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231285	NM_001137674.3(ZNF860):c.131C>T (p.Thr44Met)	OSBPL10, ZNF860 (T44M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229724	NM_001137674.3(ZNF860):c.233C>G (p.Ala78Gly)	OSBPL10, ZNF860 (A78G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 775196	NM_001137674.3(ZNF860):c.1880G>A (p.Arg627His)	OSBPL10, ZNF860 (R627H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 775195	NM_001137674.3(ZNF860):c.1071C>T (p.Leu357=)	OSBPL10, ZNF860	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 775194	NM_001137674.3(ZNF860):c.573G>A (p.Thr191=)	OSBPL10, ZNF860	Single nucleotide variant (synonymous variant)	not provided	GBenign

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Links from Gene

Items: 46