MID2[gene] and "single gene"[properties] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2339011	NM_012216.4(MID2):c.167G>A (p.Arg56His)	MID2 (R36H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126342	NM_012216.4(MID2):c.175G>A (p.Val59Ile)	MID2 (V39I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1321169	NM_012216.4(MID2):c.180A>C (p.Ser60=)	MID2	Single nucleotide variant (synonymous variant)	Intellectual disability, X-linked 101	GBenign
Select item 2442092	NM_012216.4(MID2):c.308T>G (p.Ile103Ser)	MID2 (I103S +1 more)	Single nucleotide variant (missense variant)	Intellectual disability, X-linked 101	GUncertain significance
Select item 3126343	NM_012216.4(MID2):c.314G>C (p.Arg105Pro)	MID2 (R85P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126344	NM_012216.4(MID2):c.361C>T (p.Arg121Cys)	MID2 (R121C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2661155	NM_012216.4(MID2):c.362G>A (p.Arg121His)	MID2 (R101H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2244034	NM_012216.4(MID2):c.362G>T (p.Arg121Leu)	MID2 (R121L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1301698	NM_012216.4(MID2):c.373A>G (p.Thr125Ala)	MID2 (T105A +1 more)	Single nucleotide variant (missense variant)	Intellectual disability, X-linked 101	GUncertain significance
Select item 1696300	NM_012216.4(MID2):c.397T>A (p.Ser133Thr)	MID2 (S113T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1683338	NM_012216.4(MID2):c.402C>G (p.Ser134Arg)	MID2 (S114R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 224103	NM_012216.4(MID2):c.448G>T (p.Ala150Ser)	MID2 (A150S)	Single nucleotide variant (missense variant)	Intellectual disability, X-linked 101 +1 more	GUncertain significance
Select item 3126345	NM_012216.4(MID2):c.490C>T (p.Arg164Cys)	MID2 (R164C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 807797	NM_012216.4(MID2):c.490C>G (p.Arg164Gly)	MID2 (R164G)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 548625	NM_012216.4(MID2):c.491G>A (p.Arg164His)	MID2 (R164H)	Single nucleotide variant (missense variant)	Intellectual disability, X-linked 101	GUncertain significance
Select item 2335598	NM_012216.4(MID2):c.560A>G (p.Asp187Gly)	MID2 (D187G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 794087	NM_012216.4(MID2):c.582C>A (p.Thr194=)	MID2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 425513	NM_012216.4(MID2):c.667C>T (p.Arg223Cys)	MID2 (R223C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 445781	NM_012216.4(MID2):c.720+17G>A	MID2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 435870	NM_012216.4(MID2):c.758G>A (p.Arg253His)	MID2 (R253H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 20