"Ambry Genetics"[submitter] AND "CDK8"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3141606	NM_001260.3(CDK8):c.29G>A (p.Ser10Asn)	CDK8, LOC130009416 (S10N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2525118	NM_001260.3(CDK8):c.36G>C (p.Glu12Asp)	CDK8, LOC130009416 (E12D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2356496	NM_001260.3(CDK8):c.204A>G (p.Ala68=)	CDK8	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2559620	NM_001260.3(CDK8):c.428A>G (p.His143Arg)	CDK8 (H143R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2247169	NM_001260.3(CDK8):c.733A>G (p.Asn245Asp)	CDK8 (N245D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3141607	NM_001260.3(CDK8):c.866C>A (p.Thr289Asn)	CDK8 (T116N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3141608	NM_001260.3(CDK8):c.998C>T (p.Pro333Leu)	CDK8 (P333L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2230526	NM_001260.3(CDK8):c.1067G>A (p.Arg356Gln)	CDK8 (R183Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2551635	NM_001260.3(CDK8):c.1166G>A (p.Gly389Glu)	CDK8 (G389E +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3265505	NM_001260.3(CDK8):c.1232C>T (p.Thr411Ile)	CDK8 (T410I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2299291	NM_001260.3(CDK8):c.1265A>G (p.Tyr422Cys)	CDK8 (Y249C +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3141605	NM_001260.3(CDK8):c.1320G>T (p.Gln440His)	CDK8 (Q439H +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2489195	NM_001260.3(CDK8):c.1335G>C (p.Met445Ile)	CDK8 (M272I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance