ZNF567[gene] and "single gene"[properties] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2606102	NM_001322917.1(ZNF567):c.147G>A (p.Met49Ile)	ZNF567 (M41I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601449	NM_001322917.1(ZNF567):c.265G>A (p.Glu89Lys)	ZNF567 (E112K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258702	NM_001322917.1(ZNF567):c.428A>G (p.Asn143Ser)	ZNF567 (N112S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543458	NM_001322917.1(ZNF567):c.503C>T (p.Ser168Leu)	ZNF567 (S168L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402438	NM_001322917.1(ZNF567):c.608C>T (p.Thr203Met)	ZNF567 (T226M +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2407831	NM_001322917.1(ZNF567):c.671G>A (p.Gly224Asp)	ZNF567 (G193D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521216	NM_001322917.1(ZNF567):c.955C>T (p.Arg319Cys)	ZNF567 (R342C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299400	NM_001322917.1(ZNF567):c.1228G>C (p.Val410Leu)	ZNF567 (V379L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196777	NM_001322917.1(ZNF567):c.1237A>G (p.Arg413Gly)	ZNF567 (R382G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386255	NM_001322917.1(ZNF567):c.1238G>T (p.Arg413Ile)	ZNF567 (R436I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242461	NM_001322917.1(ZNF567):c.1241C>T (p.Thr414Ile)	ZNF567 (T406I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196778	NM_001322917.1(ZNF567):c.1310C>T (p.Ala437Val)	ZNF567 (A437V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258703	NM_001322917.1(ZNF567):c.1586G>A (p.Gly529Glu)	ZNF567 (G498E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267359	NM_001322917.1(ZNF567):c.1598A>G (p.Tyr533Cys)	ZNF567 (Y502C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388057	NM_001322917.1(ZNF567):c.1627C>T (p.Arg543Cys)	ZNF567 (R535C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258700	NM_001322917.1(ZNF567):c.1628G>A (p.Arg543His)	ZNF567 (R512H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258699	NM_001322917.1(ZNF567):c.1784G>A (p.Gly595Glu)	ZNF567 (G587E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455191	NM_001322917.1(ZNF567):c.1788G>C (p.Lys596Asn)	ZNF567 (K565N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196779	NM_001322917.1(ZNF567):c.1802A>C (p.Lys601Thr)	ZNF567 (K601T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208209	NM_001322917.1(ZNF567):c.1868G>A (p.Gly623Asp)	ZNF567 (G646D +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 20