"Ambry Genetics"[submitter] AND "ZNF74"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2395041	NM_003426.4(ZNF74):c.16C>T (p.Pro6Ser)	ZNF74 (P6S)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2519364	NM_003426.4(ZNF74):c.55G>A (p.Ala19Thr)	ZNF74 (A19T)	Single nucleotide variant (missense variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 2372209	NM_003426.4(ZNF74):c.76C>G (p.Leu26Val)	ZNF74 (L26V)	Single nucleotide variant (missense variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 2411264	NM_003426.4(ZNF74):c.194G>A (p.Arg65Lys)	ZNF74 (R65K)	Single nucleotide variant (synonymous variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 2263529	NM_003426.4(ZNF74):c.205C>T (p.Arg69Trp)	ZNF74 (P40L +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2289371	NM_003426.4(ZNF74):c.234C>A (p.Asn78Lys)	ZNF74 (N78K +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2559947	NM_003426.4(ZNF74):c.290G>A (p.Arg97Gln)	ZNF74 (R26Q +1 more)	Single nucleotide variant (synonymous variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2507705	NM_003426.4(ZNF74):c.359C>T (p.Ala120Val)	LOC132090920, ZNF74 (A120V +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2538512	NM_003426.4(ZNF74):c.408G>T (p.Glu136Asp)	LOC132090920, ZNF74 (A108S +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2306355	NM_003426.4(ZNF74):c.412A>C (p.Ile138Leu)	LOC132090920, ZNF74 (H109P +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2327711	NM_003426.4(ZNF74):c.422G>T (p.Arg141Leu)	LOC132090920, ZNF74 (R141L +1 more)	Single nucleotide variant (synonymous variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2410798	NM_003426.4(ZNF74):c.497C>T (p.Pro166Leu)	ZNF74 (P166L +1 more)	Single nucleotide variant (synonymous variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2621641	NM_003426.4(ZNF74):c.499G>C (p.Ala167Pro)	ZNF74 (R138P +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2256736	NM_003426.4(ZNF74):c.571G>T (p.Val191Phe)	ZNF74 (R162L +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2408643	NM_003426.4(ZNF74):c.680G>A (p.Ser227Asn)	ZNF74 (S227N +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2376879	NM_003426.4(ZNF74):c.697C>T (p.Pro233Ser)	ZNF74 (P233S +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2338884	NM_003426.4(ZNF74):c.730G>A (p.Gly244Arg)	ZNF74 (G173R +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2285359	NM_003426.4(ZNF74):c.754G>A (p.Glu252Lys)	ZNF74 (E252K +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2459449	NM_003426.4(ZNF74):c.1136A>G (p.His379Arg)	ZNF74 (H308R +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2356405	NM_003426.4(ZNF74):c.1193C>A (p.Thr398Asn)	ZNF74 (T327N +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2240348	NM_003426.4(ZNF74):c.1224G>T (p.Lys408Asn)	ZNF74 (K337N +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2337231	NM_003426.4(ZNF74):c.1321G>A (p.Glu441Lys)	ZNF74 (E441K +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2472409	NM_003426.4(ZNF74):c.1370C>A (p.Ala457Glu)	ZNF74 (A386E +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2210275	NM_003426.4(ZNF74):c.1376T>C (p.Leu459Pro)	ZNF74 (L388P +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2495683	NM_003426.4(ZNF74):c.1523C>T (p.Ala508Val)	ZNF74 (A437V +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2540389	NM_003426.4(ZNF74):c.1558C>G (p.Arg520Gly)	ZNF74 (R520G +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2486907	NM_003426.4(ZNF74):c.1570G>A (p.Gly524Ser)	ZNF74 (G453S +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2458558	NM_003426.4(ZNF74):c.1600G>A (p.Gly534Ser)	ZNF74 (G463S +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2516308	NM_003426.4(ZNF74):c.1766A>G (p.Asn589Ser)	ZNF74 (N518S +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2252719	NM_003426.4(ZNF74):c.1769A>C (p.Lys590Thr)	ZNF74 (K519T +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2412319	NM_003426.4(ZNF74):c.1861G>A (p.Val621Met)	ZNF74 (V621M +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 31