INO80E[gene] and "single gene"[properties] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3109772	NM_173618.3(INO80E):c.137T>G (p.Val46Gly)	INO80E (V46G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2328892	NM_173618.3(INO80E):c.163G>C (p.Asp55His)	INO80E (D55H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2308397	NM_173618.3(INO80E):c.181G>C (p.Glu61Gln)	INO80E (E61Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109773	NM_173618.3(INO80E):c.196G>A (p.Asp66Asn)	INO80E (D66N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109774	NM_173618.3(INO80E):c.241A>G (p.Thr81Ala)	INO80E (T81A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2221477	NM_173618.3(INO80E):c.242C>T (p.Thr81Met)	INO80E (T81M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109775	NM_173618.3(INO80E):c.251C>T (p.Thr84Ile)	INO80E (T84I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109776	NM_173618.3(INO80E):c.272C>T (p.Pro91Leu)	INO80E (P91L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363947	NM_173618.3(INO80E):c.280A>G (p.Lys94Glu)	INO80E (K94E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2646377	NM_173618.3(INO80E):c.309C>T (p.Gly103=)	INO80E	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2212041	NM_173618.3(INO80E):c.310G>T (p.Ala104Ser)	INO80E (A104S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2230249	NM_173618.3(INO80E):c.311C>T (p.Ala104Val)	INO80E (A104V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2210396	NM_173618.3(INO80E):c.376C>G (p.Pro126Ala)	INO80E (P126A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2476014	NM_173618.3(INO80E):c.383C>G (p.Pro128Arg)	INO80E (P128R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2548615	NM_173618.3(INO80E):c.404C>T (p.Ser135Phe)	INO80E (S135F)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2392742	NM_173618.3(INO80E):c.409C>T (p.Arg137Cys)	INO80E (R137C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3109777	NM_173618.3(INO80E):c.425C>T (p.Pro142Leu)	INO80E (P142L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3109778	NM_173618.3(INO80E):c.473C>A (p.Pro158His)	INO80E (P158H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2299024	NM_173618.3(INO80E):c.488G>A (p.Arg163Gln)	INO80E (R163Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3109779	NM_173618.3(INO80E):c.589G>A (p.Gly197Arg)	INO80E (G158R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2518656	NM_173618.3(INO80E):c.601A>G (p.Thr201Ala)	INO80E (T162A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2319729	NM_173618.3(INO80E):c.626C>T (p.Pro209Leu)	INO80E (P170L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2223348	NM_173618.3(INO80E):c.628C>G (p.Pro210Ala)	INO80E (P210A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2353312	NM_173618.3(INO80E):c.631C>A (p.Pro211Thr)	INO80E (P172T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3109780	NM_173618.3(INO80E):c.656G>A (p.Arg219Gln)	INO80E (R180Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2489584	NM_173618.3(INO80E):c.667A>G (p.Ser223Gly)	INO80E (S184G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 26