DYRK2[gene] and "single gene"[properties] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3086610	NM_006482.3(DYRK2):c.216C>G (p.His72Gln)	DYRK2 (H72Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3086611	NM_006482.3(DYRK2):c.224A>G (p.Asn75Ser)	DYRK2 (N75S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086612	NM_006482.3(DYRK2):c.314C>T (p.Thr105Met)	DYRK2 (T32M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594743	NM_006482.3(DYRK2):c.374G>A (p.Arg125Gln)	DYRK2 (R125Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511697	NM_006482.3(DYRK2):c.386G>A (p.Ser129Asn)	DYRK2 (S129N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274226	NM_006482.3(DYRK2):c.490A>G (p.Met164Val)	DYRK2 (M91V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086614	NM_006482.3(DYRK2):c.540A>T (p.Glu180Asp)	DYRK2 (E107D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274227	NM_006482.3(DYRK2):c.576G>T (p.Gln192His)	DYRK2 (Q192H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385476	NM_006482.3(DYRK2):c.599A>G (p.Asn200Ser)	DYRK2 (N127S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274224	NM_006482.3(DYRK2):c.602G>A (p.Gly201Asp)	DYRK2 (G201D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251314	NM_006482.3(DYRK2):c.616G>A (p.Asp206Asn)	DYRK2 (D133N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337551	NM_006482.3(DYRK2):c.742G>A (p.Val248Met)	DYRK2 (V175M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254744	NM_006482.3(DYRK2):c.820C>T (p.Arg274Trp)	DYRK2 (R201W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493730	NM_006482.3(DYRK2):c.1193G>C (p.Arg398Thr)	DYRK2 (R325T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274225	NM_006482.3(DYRK2):c.1238C>G (p.Ala413Gly)	DYRK2 (A413G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346898	NM_006482.3(DYRK2):c.1250C>T (p.Thr417Met)	DYRK2 (T344M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242888	NM_006482.3(DYRK2):c.1325C>T (p.Ser442Leu)	DYRK2 (S369L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294306	NM_006482.3(DYRK2):c.1362T>G (p.Asn454Lys)	DYRK2 (N454K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086607	NM_006482.3(DYRK2):c.1408C>G (p.Leu470Val)	DYRK2 (L397V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488376	NM_006482.3(DYRK2):c.1427T>C (p.Val476Ala)	DYRK2 (V403A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298286	NM_006482.3(DYRK2):c.1441C>T (p.Arg481Cys)	DYRK2 (R408C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388200	NM_006482.3(DYRK2):c.1494C>A (p.Asn498Lys)	DYRK2 (N498K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357388	NM_006482.3(DYRK2):c.1496C>T (p.Ala499Val)	DYRK2 (A426V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086608	NM_006482.3(DYRK2):c.1597C>T (p.Pro533Ser)	DYRK2 (P460S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589788	NM_006482.3(DYRK2):c.1702C>T (p.Pro568Ser)	DYRK2 (P495S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25