"Ambry Genetics"[submitter] AND "DYRK4"[gene] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3086628	NM_001394779.1(DYRK4):c.350C>T (p.Pro117Leu)	DYRK4 (P117L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2546053	NM_001394779.1(DYRK4):c.440A>C (p.Gln147Pro)	DYRK4 (Q141P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2263589	NM_001394779.1(DYRK4):c.458C>T (p.Ala153Val)	DYRK4 (A147V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3086627	NM_001394779.1(DYRK4):c.557A>G (p.Lys186Arg)	DYRK4 (K71R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2248696	NM_001394779.1(DYRK4):c.572C>G (p.Ala191Gly)	DYRK4 (A185G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2209703	NM_001394779.1(DYRK4):c.733G>C (p.Val245Leu)	DYRK4 (V239L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2260293	NM_001394779.1(DYRK4):c.734T>G (p.Val245Gly)	DYRK4 (V130G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354931	NM_001394779.1(DYRK4):c.805G>A (p.Ala269Thr)	DYRK4 (A263T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374880	NM_001394779.1(DYRK4):c.833C>A (p.Thr278Asn)	DYRK4 (T163N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2591032	NM_001394779.1(DYRK4):c.910A>G (p.Asn304Asp)	DYRK4 (N298D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086629	NM_001394779.1(DYRK4):c.1039A>C (p.Lys347Gln)	DYRK4 (K347Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320144	NM_001394779.1(DYRK4):c.1063C>A (p.Gln355Lys)	DYRK4 (Q240K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278446	NM_001394779.1(DYRK4):c.1105A>G (p.Ser369Gly)	DYRK4 (S254G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086630	NM_001394779.1(DYRK4):c.1138A>T (p.Ile380Phe)	DYRK4, LOC130007211 (I265F +2 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2224873	NM_001394779.1(DYRK4):c.1144A>T (p.Ser382Cys)	DYRK4, LOC130007211 (S382C +2 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3086631	NM_001394779.1(DYRK4):c.1333A>G (p.Thr445Ala)	DYRK4 (T330A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086621	NM_001394779.1(DYRK4):c.1403A>C (p.Lys468Thr)	DYRK4 (K462T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086623	NM_001394779.1(DYRK4):c.1438G>A (p.Val480Met)	DYRK4 (V474M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341484	NM_001394779.1(DYRK4):c.1451A>G (p.Tyr484Cys)	DYRK4 (Y83C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474078	NM_001394779.1(DYRK4):c.1472T>C (p.Phe491Ser)	DYRK4 (F491S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086624	NM_001394779.1(DYRK4):c.1491A>G (p.Val497=)	DYRK4	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2347108	NM_001394779.1(DYRK4):c.1534C>A (p.His512Asn)	DYRK4 (H111N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204380	NM_001394779.1(DYRK4):c.1556G>A (p.Arg519Gln)	DYRK4 (R404Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244642	NM_001394779.1(DYRK4):c.1562T>C (p.Leu521Pro)	DYRK4 (L120P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590052	NM_001394779.1(DYRK4):c.1822G>A (p.Gly608Arg)	DYRK4 (G494R +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513510	NM_001394779.1(DYRK4):c.1874A>G (p.Lys625Arg)	DYRK4 (K511R +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086626	NM_001394779.1(DYRK4):c.1885G>A (p.Val629Ile)	DYRK4 (V228I +5 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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Items: 27