"Ambry Genetics"[submitter] AND "CDK14"[gene] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2318148	NM_001287135.2(CDK14):c.140T>C (p.Met47Thr)	CDK14 (M1T +2 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2605320	NM_001287135.2(CDK14):c.172G>A (p.Val58Met)	CDK14 (V12M +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2482788	NM_001287135.2(CDK14):c.235A>G (p.Thr79Ala)	CDK14 (T33A +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2395440	NM_001287135.2(CDK14):c.304A>G (p.Asn102Asp)	CDK14 (N56D +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2224421	NM_001287135.2(CDK14):c.359G>A (p.Ser120Asn)	CDK14 (S102N +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2489113	NM_001287135.2(CDK14):c.386T>G (p.Phe129Cys)	CDK14 (F83C +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2297507	NM_001287135.2(CDK14):c.433T>A (p.Ser145Thr)	CDK14 (S127T +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2246113	NM_001287135.2(CDK14):c.800C>T (p.Thr267Met)	CDK14 (T249M +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2537873	NM_001287135.2(CDK14):c.1004T>C (p.Met335Thr)	CDK14 (M317T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2478033	NM_001287135.2(CDK14):c.1005G>A (p.Met335Ile)	CDK14 (M206I +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2361390	NM_001287135.2(CDK14):c.1108C>A (p.Arg370Ser)	CDK14 (R370S +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2607687	NM_001287135.2(CDK14):c.1123A>G (p.Ser375Gly)	CDK14 (S246G +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2599900	NM_001287135.2(CDK14):c.1141C>G (p.Gln381Glu)	CDK14 (Q252E +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2513011	NM_001287135.2(CDK14):c.1163A>G (p.Tyr388Cys)	CDK14 (Y259C +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2355931	NM_001287135.2(CDK14):c.1354C>T (p.Arg452Trp)	CDK14 (R406W +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2231208	NM_001287135.2(CDK14):c.1400G>A (p.Ser467Asn)	CDK14 (S467N +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance