ClinVar for Gene (Select 990) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3265035	NM_001254.4(CDC6):c.271C>G (p.Leu91Val)	CDC6 (L91V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3242217	GRCh37/hg19 17q12-22(chr17:41196270-41277589)	SLC4A1, DCAKD +422 more	Copy number loss	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 3239079	NM_001254.4(CDC6):c.1132C>T (p.Arg378Cys)	CDC6 (R378C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3140977	NM_001254.4(CDC6):c.354C>A (p.Asn118Lys)	CDC6 (N118K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140976	NM_001254.4(CDC6):c.293T>C (p.Phe98Ser)	CDC6 (F98S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140975	NM_001254.4(CDC6):c.148G>A (p.Ala50Thr)	CDC6 (A50T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140974	NM_001254.4(CDC6):c.1273A>G (p.Ile425Val)	CDC6 (I425V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3140973	NM_001254.4(CDC6):c.114T>G (p.Asn38Lys)	CDC6 (N38K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3023681	NM_001254.4(CDC6):c.1342T>C (p.Leu448=)	CDC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3022631	NM_001254.4(CDC6):c.1185-5dup	CDC6	Duplication (intron variant)	not provided	GBenign
Select item 3020977	NM_001254.4(CDC6):c.660G>C (p.Lys220Asn)	CDC6 (K220N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3019832	NM_001254.4(CDC6):c.660+5A>T	CDC6	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3018130	NM_001254.4(CDC6):c.6T>C (p.Pro2=)	CDC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3013341	NM_001254.4(CDC6):c.1249+6T>C	CDC6	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3013191	NM_001254.4(CDC6):c.348C>T (p.His116=)	CDC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3009765	NM_001254.4(CDC6):c.1593+11T>C	CDC6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3006390	NM_001254.4(CDC6):c.1596G>A (p.Val532=)	CDC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3004365	NM_001254.4(CDC6):c.1250-17G>C	CDC6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3002915	NM_001254.4(CDC6):c.1226C>A (p.Thr409Asn)	CDC6 (T409N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2993501	NM_001254.4(CDC6):c.510T>C (p.Asp170=)	CDC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2990674	NM_001254.4(CDC6):c.836+15G>A	CDC6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2975757	NM_001254.4(CDC6):c.723T>C (p.Ala241=)	CDC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2969456	NM_001254.4(CDC6):c.270A>C (p.Thr90=)	CDC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2964242	NM_001254.4(CDC6):c.609T>C (p.Ala203=)	CDC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2963303	NM_001254.4(CDC6):c.1363G>T (p.Asp455Tyr)	CDC6 (D455Y)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2962803	NM_001254.4(CDC6):c.305T>G (p.Leu102Arg)	CDC6 (L102R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2960270	NM_001254.4(CDC6):c.1145C>G (p.Ala382Gly)	CDC6 (A382G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2960023	NM_001254.4(CDC6):c.668T>A (p.Leu223Gln)	CDC6 (L223Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2956033	NM_001254.4(CDC6):c.812_813del (p.Met271fs)	CDC6 (M271fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 2954792	NM_001254.4(CDC6):c.93T>A (p.Asp31Glu)	CDC6 (D31E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2908876	NM_001254.4(CDC6):c.436T>C (p.Cys146Arg)	CDC6 (C146R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2904633	NM_001254.4(CDC6):c.487G>T (p.Val163Phe)	CDC6 (V163F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2896887	NM_001254.4(CDC6):c.733G>C (p.Ala245Pro)	CDC6 (A245P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2894577	NM_001254.4(CDC6):c.161G>A (p.Ser54Asn)	CDC6 (S54N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2893264	NM_001254.4(CDC6):c.685A>G (p.Ile229Val)	CDC6 (I229V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2890229	NM_001254.4(CDC6):c.1185-4A>G	CDC6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2881425	NM_001254.4(CDC6):c.342A>G (p.Lys114=)	CDC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2865259	NM_001254.4(CDC6):c.814A>C (p.Thr272Pro)	CDC6 (T272P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2852824	NM_001254.4(CDC6):c.975A>T (p.Arg325Ser)	CDC6 (R325S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2848302	NM_001254.4(CDC6):c.1393G>A (p.Val465Ile)	CDC6 (V465I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2839998	NM_001254.4(CDC6):c.1312A>G (p.Ile438Val)	CDC6 (I438V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2831900	NM_001254.4(CDC6):c.614G>A (p.Gly205Glu)	CDC6 (G205E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2822103	NM_001254.4(CDC6):c.536T>C (p.Met179Thr)	CDC6 (M179T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2786822	NM_001254.4(CDC6):c.1169C>T (p.Ala390Val)	CDC6 (A390V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2778347	NM_001254.4(CDC6):c.1577A>G (p.Glu526Gly)	CDC6 (E526G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2769129	NM_001254.4(CDC6):c.1397G>A (p.Cys466Tyr)	CDC6 (C466Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2761046	NM_001254.4(CDC6):c.958C>G (p.Leu320Val)	CDC6 (L320V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2759817	NM_001254.4(CDC6):c.1258C>G (p.Pro420Ala)	CDC6 (P420A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2759524	NM_001254.4(CDC6):c.705del (p.Ser235_Leu236insTer)	CDC6	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 2759113	NM_001254.4(CDC6):c.1494G>A (p.Val498=)	CDC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2732245	NM_001254.4(CDC6):c.1253A>G (p.Lys418Arg)	CDC6 (K418R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2727235	NM_001254.4(CDC6):c.944-15del	CDC6	Deletion (intron variant)	not provided	GLikely benign
Select item 2721508	NM_001254.4(CDC6):c.836+17T>A	CDC6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2684849	GRCh37/hg19 17q21.1-21.2(chr17:38390996-38689619)x3	CDC6, GJD3 +5 more	Copy number gain	not provided	GUncertain significance
Select item 2624201	NM_001254.4(CDC6):c.1547G>A (p.Arg516Lys)	CDC6 (R516K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529962	NM_001254.4(CDC6):c.1284G>T (p.Arg428Ser)	CDC6 (R428S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478230	NM_001254.4(CDC6):c.776C>A (p.Ala259Asp)	CDC6 (A259D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477750	NM_001254.4(CDC6):c.188A>G (p.Asn63Ser)	CDC6 (N63S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2424720	NC_000017.10:g.(?_37821613)_(38458253_?)dup	CASC3, CDC6 +20 more	Duplication	Hypertrophic cardiomyopathy 25 +1 more	GUncertain significance
Select item 2420778	NM_001254.4(CDC6):c.1206G>A (p.Glu402=)	CDC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2362724	NM_001254.4(CDC6):c.1583G>A (p.Arg528His)	CDC6 (R528H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2338266	NM_001254.4(CDC6):c.250G>A (p.Gly84Ser)	CDC6 (G84S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309961	NM_001254.4(CDC6):c.1133G>C (p.Arg378Pro)	CDC6 (R378P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255746	NM_001254.4(CDC6):c.1192A>G (p.Ile398Val)	CDC6 (I398V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252935	NM_001254.4(CDC6):c.61C>T (p.Arg21Trp)	CDC6 (R21W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2192644	NM_001254.4(CDC6):c.745G>C (p.Glu249Gln)	CDC6 (E249Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2181834	NM_001254.4(CDC6):c.918A>G (p.Leu306=)	CDC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2181177	NM_001254.4(CDC6):c.865C>G (p.Leu289Val)	CDC6 (L289V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2177973	NM_001254.4(CDC6):c.246G>A (p.Glu82=)	CDC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2175357	NM_001254.4(CDC6):c.62G>A (p.Arg21Gln)	CDC6 (R21Q)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2085910	NM_001254.4(CDC6):c.511C>T (p.Arg171Trp)	CDC6 (R171W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2063859	NM_001254.4(CDC6):c.214C>A (p.Pro72Thr)	CDC6 (P72T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2058656	NM_001254.4(CDC6):c.535A>G (p.Met179Val)	CDC6 (M179V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2049978	NM_001254.4(CDC6):c.1452+12T>C	CDC6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2049354	NM_001254.4(CDC6):c.439G>T (p.Val147Leu)	CDC6 (V147L)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2040489	NM_001254.4(CDC6):c.130_139dup (p.Arg47fs)	CDC6 (R47fs)	Duplication (frameshift variant)	not provided	GUncertain significance
Select item 2033472	NM_001254.4(CDC6):c.1249+11T>A	CDC6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2021190	NM_001254.4(CDC6):c.1083+17T>C	CDC6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2010677	NM_001254.4(CDC6):c.114T>C (p.Asn38=)	CDC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2007305	NM_001254.4(CDC6):c.404A>T (p.Glu135Val)	CDC6 (E135V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1992747	NM_001254.4(CDC6):c.26A>G (p.Gln9Arg)	CDC6 (Q9R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1991465	NM_001254.4(CDC6):c.661-14A>T	CDC6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1989760	NM_001254.4(CDC6):c.1663T>G (p.Leu555Val)	CDC6 (L555V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1981375	NM_001254.4(CDC6):c.1311C>A (p.Val437=)	CDC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1965962	NM_001254.4(CDC6):c.461-19C>A	CDC6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1963990	NM_001254.4(CDC6):c.1652T>C (p.Ile551Thr)	CDC6 (I551T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1962490	NM_001254.4(CDC6):c.461G>T (p.Gly154Val)	CDC6 (G154V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1939856	NM_001254.4(CDC6):c.787A>G (p.Met263Val)	CDC6 (M263V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1939288	NM_001254.4(CDC6):c.969A>C (p.Thr323=)	CDC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1934528	NM_001254.4(CDC6):c.1132C>G (p.Arg378Gly)	CDC6 (R378G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1929740	NM_001254.4(CDC6):c.944-5C>T	CDC6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1927730	NM_001254.4(CDC6):c.1589C>G (p.Thr530Arg)	CDC6 (T530R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1919580	NM_001254.4(CDC6):c.941T>C (p.Ile314Thr)	CDC6 (I314T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1913518	NM_001254.4(CDC6):c.74A>C (p.Lys25Thr)	CDC6 (K25T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1910508	NM_001254.4(CDC6):c.400T>G (p.Ser134Ala)	CDC6 (S134A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1901712	NM_001254.4(CDC6):c.413G>A (p.Cys138Tyr)	CDC6 (C138Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1717760	NM_001254.4(CDC6):c.561G>T (p.Arg187Ser)	CDC6 (R187S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1713665	NM_001254.4(CDC6):c.1226C>T (p.Thr409Ile)	CDC6 (T409I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1690476	NM_001254.4(CDC6):c.1480C>T (p.Arg494Cys)	CDC6 (R494C)	Single nucleotide variant (missense variant)	See cases +1 more	GUncertain significance
Select item 1668001	NM_001254.4(CDC6):c.252T>A (p.Gly84=)	CDC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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