"Ambry Genetics"[submitter] AND "ZFP90"[gene] - ClinVar

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Items: 40

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3193222	NM_001305203.2(ZFP90):c.213G>C (p.Glu71Asp)	ZFP90 (E71D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193223	NM_001305203.2(ZFP90):c.220A>G (p.Ile74Val)	ZFP90 (I74V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193224	NM_001305203.2(ZFP90):c.290A>G (p.His97Arg)	ZFP90 (H97R)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2411627	NM_001305203.2(ZFP90):c.347C>G (p.Thr116Arg)	ZFP90 (T116R)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2359861	NM_001305203.2(ZFP90):c.372C>A (p.Ser124Arg)	ZFP90 (S124R)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2334353	NM_001305203.2(ZFP90):c.394G>A (p.Glu132Lys)	ZFP90 (E132K)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2454867	NM_001305203.2(ZFP90):c.449C>T (p.Thr150Ile)	ZFP90 (T150I)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2252713	NM_001305203.2(ZFP90):c.463T>C (p.Phe155Leu)	ZFP90 (F155L)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2247042	NM_001305203.2(ZFP90):c.490T>A (p.Ser164Thr)	ZFP90 (S164T)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3334528	NM_001305203.2(ZFP90):c.506A>T (p.Asn169Ile)	ZFP90 (N169I)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2237990	NM_001305203.2(ZFP90):c.608A>C (p.Asn203Thr)	ZFP90 (N203T)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3193225	NM_001305203.2(ZFP90):c.617C>T (p.Ala206Val)	ZFP90 (A206V)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2306770	NM_001305203.2(ZFP90):c.622A>G (p.Lys208Glu)	ZFP90 (K208E)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2246412	NM_001305203.2(ZFP90):c.670T>C (p.Ser224Pro)	ZFP90 (S224P)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2554718	NM_001305203.2(ZFP90):c.700A>G (p.Lys234Glu)	ZFP90 (K234E)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3193226	NM_001305203.2(ZFP90):c.772G>A (p.Asp258Asn)	ZFP90 (D258N)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2301269	NM_001305203.2(ZFP90):c.775T>C (p.Cys259Arg)	ZFP90 (C259R)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3193227	NM_001305203.2(ZFP90):c.785C>A (p.Thr262Asn)	ZFP90 (T262N)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2401485	NM_001305203.2(ZFP90):c.853A>T (p.Asn285Tyr)	ZFP90 (N285Y)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2551559	NM_001305203.2(ZFP90):c.916G>A (p.Gly306Arg)	ZFP90 (G306R)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2458094	NM_001305203.2(ZFP90):c.951A>C (p.Lys317Asn)	ZFP90 (K317N)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3334527	NM_001305203.2(ZFP90):c.974T>C (p.Leu325Pro)	ZFP90 (L325P)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2546362	NM_001305203.2(ZFP90):c.1130G>A (p.Arg377Gln)	ZFP90 (R377Q)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3193218	NM_001305203.2(ZFP90):c.1277A>G (p.Asn426Ser)	ZFP90 (N426S)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3334530	NM_001305203.2(ZFP90):c.1319A>T (p.Asp440Val)	ZFP90 (D440V)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3334529	NM_001305203.2(ZFP90):c.1319A>G (p.Asp440Gly)	ZFP90 (D440G)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2210776	NM_001305203.2(ZFP90):c.1336G>A (p.Glu446Lys)	ZFP90 (E446K)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2407142	NM_001305203.2(ZFP90):c.1352A>G (p.His451Arg)	ZFP90 (H451R)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3193220	NM_001305203.2(ZFP90):c.1354T>C (p.Cys452Arg)	ZFP90 (C452R)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2539846	NM_001305203.2(ZFP90):c.1403A>G (p.His468Arg)	ZFP90 (H468R)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3334526	NM_001305203.2(ZFP90):c.1444C>G (p.Gln482Glu)	ZFP90 (Q482E)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3193221	NM_001305203.2(ZFP90):c.1487C>T (p.Pro496Leu)	ZFP90 (P496L)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2558793	NM_001305203.2(ZFP90):c.1514C>G (p.Ala505Gly)	ZFP90 (A505G)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2391009	NM_001305203.2(ZFP90):c.1537A>G (p.Ile513Val)	ZFP90 (I513V)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2525113	NM_001305203.2(ZFP90):c.1609C>T (p.Arg537Cys)	ZFP90 (R537C)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2302910	NM_001305203.2(ZFP90):c.1670A>C (p.Asp557Ala)	ZFP90 (D557A)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2385588	NM_001305203.2(ZFP90):c.1781C>A (p.Thr594Asn)	ZFP90 (T594N)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3334525	NM_001305203.2(ZFP90):c.1795C>T (p.His599Tyr)	ZFP90 (H599Y)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2325079	NM_001305203.2(ZFP90):c.1803A>C (p.Arg601Ser)	ZFP90 (R601S)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2260390	NM_001305203.2(ZFP90):c.1808A>G (p.His603Arg)	ZFP90 (H603R)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance

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Items: 40