"Ambry Genetics"[submitter] AND "PKNOX2"[gene] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2236499	NM_001382323.2(PKNOX2):c.121C>G (p.Gln41Glu)	PKNOX2 (Q12E +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3307085	NM_001382323.2(PKNOX2):c.140C>A (p.Ala47Asp)	PKNOX2 (A18D +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2409801	NM_001382323.2(PKNOX2):c.167T>C (p.Val56Ala)	PKNOX2 (V56A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2295723	NM_001382323.2(PKNOX2):c.181A>C (p.Ile61Leu)	PKNOX2 (I61L +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3213977	NM_001382323.2(PKNOX2):c.206C>A (p.Ala69Asp)	PKNOX2 (A40D +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2518313	NM_001382323.2(PKNOX2):c.215G>A (p.Arg72Gln)	PKNOX2 (R72Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2283365	NM_001382323.2(PKNOX2):c.332A>C (p.Asn111Thr)	PKNOX2 (N111T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2301774	NM_001382323.2(PKNOX2):c.392A>G (p.Asp131Gly)	PKNOX2 (D102G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3213979	NM_001382323.2(PKNOX2):c.535G>T (p.Asp179Tyr)	PKNOX2 (D115Y +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3307086	NM_001382323.2(PKNOX2):c.665C>T (p.Ala222Val)	PKNOX2 (A158V +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2528412	NM_001382323.2(PKNOX2):c.668T>A (p.Leu223His)	PKNOX2 (L159H +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2358952	NM_001382323.2(PKNOX2):c.697G>A (p.Val233Ile)	PKNOX2 (V204I +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2556256	NM_001382323.2(PKNOX2):c.727T>G (p.Leu243Val)	PKNOX2 (L214V +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2554925	NM_001382323.2(PKNOX2):c.790G>A (p.Gly264Arg)	PKNOX2 (G264R +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2589566	NM_001382323.2(PKNOX2):c.904A>C (p.Ile302Leu)	PKNOX2 (I226L +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2354241	NM_001382323.2(PKNOX2):c.1168G>A (p.Gly390Ser)	PKNOX2 (G274S +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2221050	NM_001382323.2(PKNOX2):c.1193G>T (p.Gly398Val)	PKNOX2 (G282V +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392247	NM_001382323.2(PKNOX2):c.1198A>G (p.Ile400Val)	PKNOX2 (I255V +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2269180	NM_001382323.2(PKNOX2):c.1207G>A (p.Asp403Asn)	PKNOX2 (D258N +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3307087	NM_001382323.2(PKNOX2):c.1309G>A (p.Glu437Lys)	PKNOX2 (E408K +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 20