Related gene-specific medical variations for Gene (Select 79413) - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3333810	NM_024508.5(ZBED2):c.94G>A (p.Gly32Arg)	CD96, ZBED2 (G32R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3333809	NM_024508.5(ZBED2):c.412A>T (p.Asn138Tyr)	CD96, ZBED2 (N138Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3333807	NM_024508.5(ZBED2):c.382G>A (p.Gly128Arg)	CD96, ZBED2 (G128R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3191799	NM_024508.5(ZBED2):c.509G>T (p.Arg170Leu)	CD96, ZBED2 (R170L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3191798	NM_024508.5(ZBED2):c.362G>A (p.Arg121His)	CD96, ZBED2 (R121H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3191797	NM_024508.5(ZBED2):c.157C>T (p.Arg53Trp)	CD96, ZBED2 (R53W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3191796	NM_024508.5(ZBED2):c.124A>T (p.Met42Leu)	CD96, ZBED2 (M42L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2624013	NM_024508.5(ZBED2):c.41T>C (p.Met14Thr)	CD96, ZBED2 (M14T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2605195	NM_024508.5(ZBED2):c.513G>C (p.Glu171Asp)	CD96, ZBED2 (E171D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2598079	NM_024508.5(ZBED2):c.124A>G (p.Met42Val)	CD96, ZBED2 (M42V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550698	NM_024508.5(ZBED2):c.590C>T (p.Ala197Val)	CD96, ZBED2 (A197V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2486901	NM_024508.5(ZBED2):c.209A>G (p.His70Arg)	CD96, ZBED2 (H70R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473217	NM_024508.5(ZBED2):c.110C>G (p.Pro37Arg)	CD96, ZBED2 (P37R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374755	NM_024508.5(ZBED2):c.361C>G (p.Arg121Gly)	CD96, ZBED2 (R121G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261919	NM_024508.5(ZBED2):c.409G>A (p.Gly137Ser)	CD96, ZBED2 (G137S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239912	NM_024508.5(ZBED2):c.353C>A (p.Ala118Asp)	CD96, ZBED2 (A118D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2221817	NM_024508.5(ZBED2):c.481C>A (p.Leu161Ile)	CD96, ZBED2 (L161I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance