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

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2392961	NM_005931.5(MICB):c.11G>A (p.Gly4Asp)	MICB (G4D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126290	NM_005931.5(MICB):c.65C>A (p.Ala22Asp)	MICB (A22D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 726697	NM_005931.5(MICB):c.66C>T (p.Ala22=)	MICB	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2255586	NM_005931.5(MICB):c.107C>T (p.Ser36Phe)	MICB (S36F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126285	NM_005931.5(MICB):c.139G>A (p.Ala47Thr)	MICB (A15T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126286	NM_005931.5(MICB):c.173G>A (p.Arg58His)	MICB (R58H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2223651	NM_005931.5(MICB):c.191G>A (p.Arg64His)	MICB (R32H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126287	NM_005931.5(MICB):c.250A>G (p.Thr84Ala)	MICB (T52A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406351	NM_005931.5(MICB):c.259G>A (p.Glu87Lys)	MICB (E55K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337133	NM_005931.5(MICB):c.277G>A (p.Gly93Arg)	MICB (G61R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126288	NM_005931.5(MICB):c.326G>A (p.Gly109Asp)	MICB (G77D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2460005	NM_005931.5(MICB):c.391C>T (p.Arg131Trp)	MICB (R131W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3294796	NM_005931.5(MICB):c.392G>A (p.Arg131Gln)	MICB (R131Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2380728	NM_005931.5(MICB):c.449C>T (p.Ser150Leu)	MICB (S118L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374911	NM_005931.5(MICB):c.493G>A (p.Val165Ile)	MICB (V133I +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2549361	NM_005931.5(MICB):c.536A>G (p.His179Arg)	MICB (H179R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462309	NM_005931.5(MICB):c.542G>A (p.Arg181His)	MICB (R138H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126289	NM_005931.5(MICB):c.595G>T (p.Val199Leu)	MICB (V167L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408811	NM_005931.5(MICB):c.667G>A (p.Val223Met)	MICB (V223M +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3126291	NM_005931.5(MICB):c.718C>T (p.Arg240Cys)	MICB (R208C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271441	NM_005931.5(MICB):c.791A>G (p.Tyr264Cys)	MICB (Y232C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126292	NM_005931.5(MICB):c.813G>C (p.Arg271Ser)	MICB (R228S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530874	NM_005931.5(MICB):c.826G>A (p.Glu276Lys)	MICB (E244K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619053	NM_005931.5(MICB):c.912G>C (p.Gln304His)	MICB (Q261H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209181	NM_005931.5(MICB):c.919C>T (p.Arg307Trp)	MICB (R264W +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2341684	NM_005931.5(MICB):c.1061T>C (p.Val354Ala)	MICB (V354A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 713467	NM_005931.5(MICB):c.1134T>C (p.Gly378=)	MICB	Single nucleotide variant (synonymous variant)	not provided	GBenign

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Items: 27