EXOSC10[gene] and "single gene"[properties] - ClinVar

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Items: 53

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2383402	NM_001001998.3(EXOSC10):c.2642A>G (p.Asn881Ser)	EXOSC10 (N856S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3276822	NM_001001998.3(EXOSC10):c.2614G>A (p.Gly872Arg)	EXOSC10 (G847R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091188	NM_001001998.3(EXOSC10):c.2596A>G (p.Ser866Gly)	EXOSC10 (S866G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621773	NM_001001998.3(EXOSC10):c.2593A>C (p.Lys865Gln)	EXOSC10 (K840Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269349	NM_001001998.3(EXOSC10):c.2555G>A (p.Cys852Tyr)	EXOSC10 (C852Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477927	NM_001001998.3(EXOSC10):c.2504A>G (p.Lys835Arg)	EXOSC10 (K810R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3276824	NM_001001998.3(EXOSC10):c.2449C>G (p.Pro817Ala)	EXOSC10 (P792A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2638217	NM_001001998.3(EXOSC10):c.2303G>A (p.Arg768Gln)	EXOSC10 (R743Q +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2458050	NM_001001998.3(EXOSC10):c.2299G>A (p.Val767Ile)	EXOSC10 (V742I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091186	NM_001001998.3(EXOSC10):c.2273A>G (p.Lys758Arg)	EXOSC10 (K733R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520102	NM_001001998.3(EXOSC10):c.2240C>G (p.Thr747Arg)	EXOSC10 (T747R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3024718	NM_001001998.3(EXOSC10):c.2157+7G>A	EXOSC10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2638218	NM_001001998.3(EXOSC10):c.2143A>G (p.Thr715Ala)	EXOSC10 (T715A)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2321381	NM_001001998.3(EXOSC10):c.2119C>G (p.Gln707Glu)	EXOSC10 (Q707E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3276827	NM_001001998.3(EXOSC10):c.2110C>G (p.Pro704Ala)	EXOSC10 (P704A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3091185	NM_001001998.3(EXOSC10):c.2041G>A (p.Ala681Thr)	EXOSC10 (A681T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513257	NM_001001998.3(EXOSC10):c.1975A>T (p.Thr659Ser)	EXOSC10 (T659S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322739	NM_001001998.3(EXOSC10):c.1868T>C (p.Ile623Thr)	EXOSC10 (I623T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590909	NM_001001998.3(EXOSC10):c.1831G>C (p.Asp611His)	EXOSC10 (D611H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474145	NM_001001998.3(EXOSC10):c.1804T>A (p.Leu602Met)	EXOSC10 (L602M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091183	NM_001001998.3(EXOSC10):c.1768G>A (p.Val590Met)	EXOSC10 (V590M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3276825	NM_001001998.3(EXOSC10):c.1726G>A (p.Ala576Thr)	EXOSC10 (A576T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091182	NM_001001998.3(EXOSC10):c.1681C>A (p.Leu561Ile)	EXOSC10 (L561I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401983	NM_001001998.3(EXOSC10):c.1484A>G (p.Tyr495Cys)	EXOSC10 (Y495C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385119	NM_001001998.3(EXOSC10):c.1423G>A (p.Asp475Asn)	EXOSC10 (D475N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091181	NM_001001998.3(EXOSC10):c.1390G>A (p.Val464Met)	EXOSC10 (V464M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217832	NM_001001998.3(EXOSC10):c.1375G>A (p.Gly459Ser)	EXOSC10 (G459S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091180	NM_001001998.3(EXOSC10):c.1373G>A (p.Arg458His)	EXOSC10 (R458H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3276823	NM_001001998.3(EXOSC10):c.1291G>A (p.Glu431Lys)	EXOSC10 (E431K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091179	NM_001001998.3(EXOSC10):c.1237G>A (p.Val413Met)	EXOSC10 (V413M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249537	NM_001001998.3(EXOSC10):c.1090G>A (p.Val364Ile)	EXOSC10 (V364I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225204	NM_001001998.3(EXOSC10):c.1046T>C (p.Met349Thr)	EXOSC10 (M349T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609745	NM_001001998.3(EXOSC10):c.1039A>G (p.Ser347Gly)	EXOSC10 (S347G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 786450	NM_001001998.3(EXOSC10):c.1029C>T (p.Leu343=)	EXOSC10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3091178	NM_001001998.3(EXOSC10):c.1000C>T (p.Arg334Trp)	EXOSC10 (R334W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3276826	NM_001001998.3(EXOSC10):c.962G>C (p.Ser321Thr)	EXOSC10 (S321T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570246	NM_001001998.3(EXOSC10):c.930T>G (p.Phe310Leu)	EXOSC10 (F310L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328480	NM_001001998.3(EXOSC10):c.904G>A (p.Glu302Lys)	EXOSC10 (E302K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311679	NM_001001998.3(EXOSC10):c.904G>C (p.Glu302Gln)	EXOSC10 (E302Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297082	NM_001001998.3(EXOSC10):c.892G>A (p.Val298Met)	EXOSC10 (V298M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528466	NM_001001998.3(EXOSC10):c.850G>C (p.Glu284Gln)	EXOSC10 (E284Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469821	NM_001001998.3(EXOSC10):c.697G>A (p.Val233Ile)	EXOSC10 (V233I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385200	NM_001001998.3(EXOSC10):c.518G>A (p.Arg173Gln)	EXOSC10 (R173Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091190	NM_001001998.3(EXOSC10):c.445C>T (p.Pro149Ser)	EXOSC10 (P149S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091189	NM_001001998.3(EXOSC10):c.438G>T (p.Leu146Phe)	EXOSC10 (L146F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249829	NM_001001998.3(EXOSC10):c.406A>C (p.Lys136Gln)	EXOSC10 (K136Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462126	NM_001001998.3(EXOSC10):c.298C>G (p.Arg100Gly)	EXOSC10 (R100G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274747	NM_001001998.3(EXOSC10):c.281G>A (p.Arg94His)	EXOSC10 (R94H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377632	NM_001001998.3(EXOSC10):c.278G>T (p.Cys93Phe)	EXOSC10 (C93F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476785	NM_001001998.3(EXOSC10):c.268T>G (p.Tyr90Asp)	EXOSC10 (Y90D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3276828	NM_001001998.3(EXOSC10):c.260T>A (p.Val87Glu)	EXOSC10 (V87E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091184	NM_001001998.3(EXOSC10):c.191G>A (p.Arg64Gln)	EXOSC10 (R64Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333811	NM_001001998.3(EXOSC10):c.127G>A (p.Val43Met)	EXOSC10 (V43M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 53