"Ambry Genetics"[submitter] AND "TAOK3"[gene] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2606550	NM_016281.4(TAOK3):c.2636G>A (p.Ser879Asn)	TAOK3 (S419N +4 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2216276	NM_016281.4(TAOK3):c.2569C>T (p.Arg857Cys)	TAOK3 (R687C +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2482034	NM_016281.4(TAOK3):c.2000T>C (p.Leu667Ser)	TAOK3 (L506S +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2527738	NM_016281.4(TAOK3):c.1873G>A (p.Glu625Lys)	TAOK3 (E464K +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2516541	NM_016281.4(TAOK3):c.1832A>G (p.Asn611Ser)	TAOK3 (N450S +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2357811	NM_016281.4(TAOK3):c.1739A>G (p.Glu580Gly)	TAOK3 (E580G +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2298747	NM_016281.4(TAOK3):c.1679A>C (p.Lys560Thr)	TAOK3 (K390T +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2477876	NM_016281.4(TAOK3):c.1622A>G (p.Gln541Arg)	TAOK3 (Q371R +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2292575	NM_016281.4(TAOK3):c.1574T>C (p.Val525Ala)	TAOK3 (V364A +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2287526	NM_016281.4(TAOK3):c.1402C>T (p.Arg468Trp)	TAOK3 (R468W +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2234021	NM_016281.4(TAOK3):c.1310C>T (p.Thr437Met)	TAOK3 (T276M +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2530655	NM_016281.4(TAOK3):c.1147G>A (p.Asp383Asn)	TAOK3 (D383N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2290766	NM_016281.4(TAOK3):c.970T>C (p.Ser324Pro)	TAOK3 (S154P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2282349	NM_016281.4(TAOK3):c.924G>T (p.Met308Ile)	TAOK3 (M138I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2245696	NM_016281.4(TAOK3):c.892C>A (p.Arg298Ser)	TAOK3 (R298S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2534846	NM_016281.4(TAOK3):c.725A>C (p.Gln242Pro)	TAOK3 (Q72P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2534845	NM_016281.4(TAOK3):c.724C>A (p.Gln242Lys)	TAOK3 (Q242K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2491358	NM_016281.4(TAOK3):c.387T>A (p.His129Gln)	TAOK3 (H129Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2480270	NM_016281.4(TAOK3):c.382A>G (p.Thr128Ala)	TAOK3 (T128A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2248784	NM_016281.4(TAOK3):c.302T>C (p.Met101Thr)	TAOK3 (M101T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2382231	NM_016281.4(TAOK3):c.230G>A (p.Arg77Gln)	TAOK3 (R77Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2308876	NM_016281.4(TAOK3):c.206T>G (p.Ile69Ser)	TAOK3 (I69S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2301909	NM_016281.4(TAOK3):c.32T>C (p.Ile11Thr)	TAOK3 (I11T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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Items: 23