"Ambry Genetics"[submitter] AND "PBX3"[gene] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3209029	NM_006195.6(PBX3):c.22C>G (p.Leu8Val)	LOC130002608, PBX3 (L8V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3304506	NM_006195.6(PBX3):c.91C>T (p.Pro31Ser)	LOC130002608, PBX3 (P31S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2556464	NM_006195.6(PBX3):c.166A>G (p.Ile56Val)	LOC130002608, PBX3 (I56V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209028	NM_006195.6(PBX3):c.172G>C (p.Asp58His)	LOC130002608, PBX3 (D58H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2538579	NM_006195.6(PBX3):c.221A>G (p.His74Arg)	PBX3 (H74R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2488748	NM_006195.6(PBX3):c.236C>T (p.Ala79Val)	PBX3 (A4V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2390990	NM_006195.6(PBX3):c.236C>G (p.Ala79Gly)	PBX3 (A4G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370763	NM_006195.6(PBX3):c.389C>T (p.Ala130Val)	PBX3 (A130V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590815	NM_006195.6(PBX3):c.406G>A (p.Ala136Thr)	PBX3 (A136T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209032	NM_006195.6(PBX3):c.413C>T (p.Ala138Val)	PBX3 (A63V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258315	NM_006195.6(PBX3):c.572C>T (p.Thr191Ile)	PBX3 (T116I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3304507	NM_006195.6(PBX3):c.885G>T (p.Lys295Asn)	PBX3 (K220N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2215890	NM_006195.6(PBX3):c.1064A>G (p.Gln355Arg)	PBX3 (Q376R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3209027	NM_006195.6(PBX3):c.1088A>C (p.Gln363Pro)	PBX3 (Q288P +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2255037	NM_006195.6(PBX3):c.1102G>A (p.Gly368Arg)	PBX3 (G293R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2215765	NM_006195.6(PBX3):c.1136G>A (p.Arg379His)	PBX3 (R379H +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2539603	NM_006195.6(PBX3):c.1139A>G (p.His380Arg)	PBX3 (H380R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3304505	NM_006195.6(PBX3):c.1154C>T (p.Thr385Met)	PBX3 (T385M +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2604744	NM_006195.6(PBX3):c.1286A>G (p.His429Arg)	PBX3 (H354R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2276270	NM_006195.6(PBX3):c.1289C>T (p.Ser430Leu)	PBX3 (S430L +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 20