"Ambry Genetics"[submitter] AND "CDC14A"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2410994	NM_003672.4(CDC14A):c.203A>G (p.Asn68Ser)	CDC14A (N68S +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2300227	NM_003672.4(CDC14A):c.254C>G (p.Thr85Ser)	CDC14A (T27S +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2602571	NM_003672.4(CDC14A):c.302C>T (p.Ala101Val)	CDC14A (A43V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2540396	NM_003672.4(CDC14A):c.340G>A (p.Ala114Thr)	CDC14A (A114T +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2373955	NM_003672.4(CDC14A):c.374C>A (p.Pro125His)	CDC14A (P125H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2475620	NM_003672.4(CDC14A):c.523G>A (p.Val175Ile)	CDC14A (V117I +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2255882	NM_003672.4(CDC14A):c.782G>A (p.Arg261Gln)	CDC14A (R203Q +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2255563	NM_003672.4(CDC14A):c.1175G>A (p.Gly392Asp)	CDC14A (G99D +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1327802	NM_003672.4(CDC14A):c.1268G>A (p.Gly423Glu)	CDC14A (G130E +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2473573	NM_003672.4(CDC14A):c.1429A>G (p.Ile477Val)	CDC14A (I477V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2262672	NM_003672.4(CDC14A):c.1447A>G (p.Ser483Gly)	CDC14A (S425G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2298471	NM_003672.4(CDC14A):c.1544A>G (p.Asn515Ser)	CDC14A (N222S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2300226	NM_003672.4(CDC14A):c.1546C>T (p.Leu516Phe)	CDC14A (L223F +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2531655	NM_003672.4(CDC14A):c.1576A>G (p.Arg526Gly)	CDC14A (R233G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2184836	NM_003672.4(CDC14A):c.1640T>G (p.Leu547Arg)	CDC14A (L254R +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2395825	NM_003672.4(CDC14A):c.1655G>T (p.Gly552Val)	CDC14A (G259V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2326235	NM_003672.4(CDC14A):c.1705T>C (p.Tyr569His)	CDC14A (Y276H +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2301758	NM_003672.4(CDC14A):c.1755+91T>C	CDC14A (F558L +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance