"Ambry Genetics"[submitter] AND "ZNF556"[gene] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2557226	NM_024967.3(ZNF556):c.59T>C (p.Leu20Ser)	ZNF556 (L20S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620203	NM_024967.3(ZNF556):c.80A>G (p.Lys27Arg)	ZNF556 (K27R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2250989	NM_024967.3(ZNF556):c.117C>G (p.His39Gln)	ZNF556 (H39Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2399623	NM_024967.3(ZNF556):c.163A>C (p.Ile55Leu)	ZNF556 (I55L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3196672	NM_024967.3(ZNF556):c.298A>G (p.Lys100Glu)	ZNF556 (K100E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3196673	NM_024967.3(ZNF556):c.340T>C (p.Cys114Arg)	ZNF556 (C113R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528327	NM_024967.3(ZNF556):c.365G>A (p.Arg122His)	ZNF556 (R121H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2343009	NM_024967.3(ZNF556):c.400C>T (p.Arg134Cys)	ZNF556 (R133C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3258655	NM_024967.3(ZNF556):c.410G>A (p.Arg137His)	ZNF556 (R136H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3196674	NM_024967.3(ZNF556):c.437G>A (p.Arg146Gln)	ZNF556 (R146Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3258657	NM_024967.3(ZNF556):c.557G>A (p.Arg186His)	ZNF556 (R185H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3196675	NM_024967.3(ZNF556):c.562T>G (p.Ser188Ala)	ZNF556 (S187A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2293843	NM_024967.3(ZNF556):c.563C>T (p.Ser188Phe)	ZNF556 (S188F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2485758	NM_024967.3(ZNF556):c.608A>G (p.Tyr203Cys)	ZNF556 (Y202C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2356370	NM_024967.3(ZNF556):c.625G>A (p.Gly209Arg)	ZNF556 (G208R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2388973	NM_024967.3(ZNF556):c.740G>A (p.Arg247His)	ZNF556 (R246H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3196676	NM_024967.3(ZNF556):c.788A>G (p.His263Arg)	ZNF556 (H262R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2459894	NM_024967.3(ZNF556):c.857C>A (p.Pro286Gln)	ZNF556 (P285Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2391577	NM_024967.3(ZNF556):c.872A>T (p.Gln291Leu)	ZNF556 (Q290L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3196678	NM_024967.3(ZNF556):c.926A>G (p.His309Arg)	ZNF556 (H308R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359749	NM_024967.3(ZNF556):c.944A>G (p.Tyr315Cys)	ZNF556 (Y315C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2384287	NM_024967.3(ZNF556):c.967G>C (p.Ala323Pro)	ZNF556 (A322P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3196679	NM_024967.3(ZNF556):c.976T>C (p.Trp326Arg)	ZNF556 (W325R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597860	NM_024967.3(ZNF556):c.1001C>T (p.Ala334Val)	ZNF556 (A333V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3258656	NM_024967.3(ZNF556):c.1007C>T (p.Thr336Met)	ZNF556 (T335M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3258658	NM_024967.3(ZNF556):c.1027G>A (p.Val343Met)	ZNF556 (V342M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366639	NM_024967.3(ZNF556):c.1042G>A (p.Val348Met)	ZNF556 (V347M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2387528	NM_024967.3(ZNF556):c.1067G>A (p.Arg356His)	ZNF556 (R355H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2292425	NM_024967.3(ZNF556):c.1184A>T (p.Glu395Val)	ZNF556 (E394V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363568	NM_024967.3(ZNF556):c.1225G>A (p.Gly409Arg)	ZNF556 (G408R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545865	NM_024967.3(ZNF556):c.1292G>A (p.Gly431Glu)	ZNF556 (G430E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512187	NM_024967.3(ZNF556):c.1355C>T (p.Ser452Phe)	ZNF556 (S451F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 32