"Ambry Genetics"[submitter] AND "CDK11A"[gene] - ClinVar

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Items: 46

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3141462	NM_024011.4(CDK11A):c.2046C>G (p.Phe682Leu)	CDK11A (F682L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141461	NM_024011.4(CDK11A):c.2021G>C (p.Gly674Ala)	CDK11A (G673A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2469375	NM_024011.4(CDK11A):c.2015G>A (p.Arg672His)	CDK11A (R675H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141459	NM_024011.4(CDK11A):c.2014C>T (p.Arg672Cys)	CDK11A (R675C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141458	NM_024011.4(CDK11A):c.2008C>T (p.Arg670Cys)	CDK11A (R669C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141457	NM_024011.4(CDK11A):c.1853C>T (p.Thr618Ile)	CDK11A (T621I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141456	NM_024011.4(CDK11A):c.1818G>C (p.Met606Ile)	CDK11A (M605I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337185	NM_024011.4(CDK11A):c.1771C>G (p.Pro591Ala)	CDK11A (P594A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2251824	NM_024011.4(CDK11A):c.1768G>A (p.Ala590Thr)	CDK11A (A580T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2554715	NM_024011.4(CDK11A):c.1765C>T (p.Arg589Cys)	CDK11A (R588C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2227540	NM_024011.4(CDK11A):c.1721C>A (p.Ser574Tyr)	CDK11A (S574Y +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2524988	NM_024011.4(CDK11A):c.1709G>A (p.Arg570Gln)	CDK11A (R569Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2468748	NM_024011.4(CDK11A):c.1700G>A (p.Gly567Glu)	CDK11A (G557E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2479151	NM_024011.4(CDK11A):c.1637G>A (p.Arg546His)	CDK11A (R536H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2206824	NM_024011.4(CDK11A):c.1618G>A (p.Asp540Asn)	CDK11A (D543N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141454	NM_024011.4(CDK11A):c.1518C>A (p.His506Gln)	CDK11A (H496Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2520986	NM_024011.4(CDK11A):c.1471G>A (p.Gly491Ser)	CDK11A (G481S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374706	NM_024011.4(CDK11A):c.1463T>C (p.Ile488Thr)	CDK11A (I488T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406348	NM_024011.4(CDK11A):c.1453G>A (p.Val485Ile)	CDK11A (V484I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141453	NM_024011.4(CDK11A):c.1433A>G (p.Gln478Arg)	CDK11A (Q468R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2514977	NM_024011.4(CDK11A):c.1381G>A (p.Glu461Lys)	CDK11A (E451K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2411279	NM_024011.4(CDK11A):c.1358G>A (p.Arg453Gln)	CDK11A (R453Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141451	NM_024011.4(CDK11A):c.1258G>A (p.Val420Ile)	CDK11A (V420I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354148	NM_024011.4(CDK11A):c.1252C>T (p.Arg418Trp)	CDK11A (R417W +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2276715	NM_024011.4(CDK11A):c.1205A>G (p.Glu402Gly)	CDK11A (E392G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305145	NM_024011.4(CDK11A):c.1182C>G (p.Asp394Glu)	CDK11A (D394E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222263	NM_024011.4(CDK11A):c.1174G>A (p.Val392Met)	CDK11A (V391M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533849	NM_024011.4(CDK11A):c.1139C>G (p.Thr380Arg)	CDK11A (T380R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141449	NM_024011.4(CDK11A):c.1087G>A (p.Asp363Asn)	CDK11A (D353N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2343257	NM_024011.4(CDK11A):c.1033G>A (p.Asp345Asn)	CDK11A (D344N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141448	NM_024011.4(CDK11A):c.1007A>T (p.Glu336Val)	CDK11A (E326V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 915402	NM_024011.4(CDK11A):c.740G>A (p.Arg247Gln)	CDK11A (R237Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2494183	NM_024011.4(CDK11A):c.587C>T (p.Ala196Val)	CDK11A (A195V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2355537	NM_024011.4(CDK11A):c.583C>T (p.Arg195Trp)	CDK11A (R194W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2286784	NM_024011.4(CDK11A):c.546G>C (p.Gln182His)	CDK11A (Q172H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306683	NM_024011.4(CDK11A):c.539G>A (p.Arg180Gln)	CDK11A (R179Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141466	NM_024011.4(CDK11A):c.462G>T (p.Met154Ile)	CDK11A (M154I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141465	NM_024011.4(CDK11A):c.391C>T (p.Arg131Cys)	CDK11A (R131C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141464	NM_024011.4(CDK11A):c.359A>C (p.Lys120Thr)	CDK11A (K110T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141463	NM_024011.4(CDK11A):c.302A>G (p.Lys101Arg)	CDK11A (K101R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2365856	NM_024011.4(CDK11A):c.150G>C (p.Glu50Asp)	CDK11A (E50D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141452	NM_024011.4(CDK11A):c.133C>T (p.Arg45Trp)	CDK11A (R45W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2212067	NM_024011.4(CDK11A):c.122G>A (p.Arg41Gln)	CDK11A (R41Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2325513	NM_024011.4(CDK11A):c.121C>T (p.Arg41Trp)	CDK11A (R41W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2479461	NM_024011.4(CDK11A):c.65G>A (p.Arg22Gln)	CDK11A (R22Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2492486	NM_024011.4(CDK11A):c.59A>T (p.Lys20Met)	CDK11A (K20M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 46