ClinVar for Gene (Select 84630) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3184040	NM_032538.3(TTBK1):c.956T>C (p.Leu319Pro)	TTBK1 (L319P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184038	NM_032538.3(TTBK1):c.3868G>A (p.Gly1290Arg)	TTBK1 (G1290R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184037	NM_032538.3(TTBK1):c.3743C>T (p.Ser1248Phe)	TTBK1 (S1248F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184036	NM_032538.3(TTBK1):c.3671G>A (p.Gly1224Glu)	TTBK1 (G1224E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184035	NM_032538.3(TTBK1):c.3518C>T (p.Pro1173Leu)	TTBK1 (P1173L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3184034	NM_032538.3(TTBK1):c.3487C>T (p.Arg1163Cys)	TTBK1 (R1163C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184033	NM_032538.3(TTBK1):c.3451G>A (p.Ala1151Thr)	TTBK1 (A1151T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184032	NM_032538.3(TTBK1):c.3356G>A (p.Arg1119His)	TTBK1 (R1119H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184031	NM_032538.3(TTBK1):c.3250C>T (p.Arg1084Trp)	TTBK1 (R1084W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184030	NM_032538.3(TTBK1):c.3145G>A (p.Gly1049Ser)	TTBK1 (G1049S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184029	NM_032538.3(TTBK1):c.3131G>A (p.Arg1044His)	TTBK1 (R1044H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3184028	NM_032538.3(TTBK1):c.3089T>C (p.Leu1030Pro)	TTBK1 (L1030P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184027	NM_032538.3(TTBK1):c.3058C>T (p.Leu1020Phe)	TTBK1 (L1020F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184026	NM_032538.3(TTBK1):c.2944G>A (p.Gly982Ser)	TTBK1 (G982S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184025	NM_032538.3(TTBK1):c.2396G>A (p.Arg799Gln)	TTBK1 (R799Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184024	NM_032538.3(TTBK1):c.2341G>C (p.Val781Leu)	TTBK1 (V781L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184023	NM_032538.3(TTBK1):c.2330C>T (p.Ala777Val)	TTBK1 (A777V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184021	NM_032538.3(TTBK1):c.2173G>C (p.Val725Leu)	TTBK1 (V725L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184019	NM_032538.3(TTBK1):c.1853C>T (p.Pro618Leu)	TTBK1 (P618L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184018	NM_032538.3(TTBK1):c.1751G>A (p.Arg584Gln)	TTBK1 (R584Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184017	NM_032538.3(TTBK1):c.1723C>T (p.Arg575Trp)	TTBK1 (R575W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184016	NM_032538.3(TTBK1):c.1576G>A (p.Ala526Thr)	TTBK1 (A526T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184015	NM_032538.3(TTBK1):c.1532G>T (p.Arg511Leu)	TTBK1 (R511L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184014	NM_032538.3(TTBK1):c.1477C>G (p.Pro493Ala)	TTBK1 (P493A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184013	NM_032538.3(TTBK1):c.1419G>C (p.Glu473Asp)	TTBK1 (E473D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184012	NM_032538.3(TTBK1):c.1405G>A (p.Val469Met)	TTBK1 (V469M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184011	NM_032538.3(TTBK1):c.1177G>A (p.Gly393Arg)	TTBK1 (G393R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656593	NM_032538.3(TTBK1):c.3606T>G (p.Thr1202=)	TTBK1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656592	NM_032538.3(TTBK1):c.2099G>A (p.Arg700Gln)	TTBK1 (R700Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2656591	NM_032538.3(TTBK1):c.2080G>A (p.Asp694Asn)	TTBK1 (D694N)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2656590	NM_032538.3(TTBK1):c.1104G>A (p.Glu368=)	TTBK1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656589	NM_032538.3(TTBK1):c.576C>T (p.Pro192=)	TTBK1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2624301	NM_032538.3(TTBK1):c.1171C>A (p.His391Asn)	TTBK1 (H391N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622944	NM_032538.3(TTBK1):c.3001G>C (p.Ala1001Pro)	TTBK1 (A1001P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2618410	NM_032538.3(TTBK1):c.1693G>A (p.Gly565Ser)	TTBK1 (G565S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610168	NM_032538.3(TTBK1):c.3506C>T (p.Ala1169Val)	TTBK1 (A1169V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605231	NM_032538.3(TTBK1):c.3674C>A (p.Ala1225Asp)	TTBK1 (A1225D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602684	NM_032538.3(TTBK1):c.2093G>A (p.Arg698Gln)	TTBK1 (R698Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597255	NM_032538.3(TTBK1):c.3872G>A (p.Gly1291Asp)	TTBK1 (G1291D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596008	NM_032538.3(TTBK1):c.3827T>A (p.Val1276Asp)	TTBK1 (V1276D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594372	NM_032538.3(TTBK1):c.1355G>A (p.Arg452Gln)	TTBK1 (R452Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589559	NM_032538.3(TTBK1):c.1900A>T (p.Thr634Ser)	TTBK1 (T634S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570679	NM_032538.3(TTBK1):c.367C>T (p.Arg123Ter)	TTBK1 (R123*)	Single nucleotide variant (nonsense)	Autism +5 more	GUncertain significance
Select item 2557456	NM_032538.3(TTBK1):c.2087G>C (p.Arg696Pro)	TTBK1 (R696P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550022	NM_032538.3(TTBK1):c.2750C>T (p.Ala917Val)	TTBK1 (A917V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540625	NM_032538.3(TTBK1):c.1514A>G (p.Asp505Gly)	TTBK1 (D505G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532633	NM_032538.3(TTBK1):c.2338G>C (p.Glu780Gln)	TTBK1 (E780Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530108	NM_032538.3(TTBK1):c.2335G>T (p.Gly779Trp)	TTBK1 (G779W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529169	NM_032538.3(TTBK1):c.946G>A (p.Asp316Asn)	TTBK1 (D316N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529106	NM_032538.3(TTBK1):c.640C>T (p.Arg214Trp)	TTBK1 (R214W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525111	NM_032538.3(TTBK1):c.2927G>A (p.Arg976Gln)	TTBK1 (R976Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525035	NM_032538.3(TTBK1):c.1739A>G (p.Glu580Gly)	TTBK1 (E580G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511531	NM_032538.3(TTBK1):c.3043C>A (p.Pro1015Thr)	TTBK1 (P1015T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511530	NM_032538.3(TTBK1):c.2847G>T (p.Leu949Phe)	TTBK1 (L949F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476107	NM_032538.3(TTBK1):c.159C>G (p.Asp53Glu)	TTBK1 (D53E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469256	NM_032538.3(TTBK1):c.3163C>T (p.Arg1055Cys)	TTBK1 (R1055C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468160	NM_032538.3(TTBK1):c.2234A>G (p.Glu745Gly)	TTBK1 (E745G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461986	NM_032538.3(TTBK1):c.3677G>T (p.Arg1226Met)	TTBK1 (R1226M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458310	NM_032538.3(TTBK1):c.3749G>A (p.Arg1250Gln)	TTBK1 (R1250Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2424354	NC_000006.11:g.(?_42162409)_(44154249_?)del	MRPS18A, PEX6 +43 more	Deletion	not provided	GUncertain significance
Select item 2422887	NC_000006.11:g.(?_41126341)_(43737486_?)dup	ABCC10, BICRAL +57 more	Duplication	PRPH2-related disorder	GUncertain significance
Select item 2422814	NC_000006.11:g.(?_41126341)_(43752536_?)del	ABCC10, BICRAL +58 more	Deletion	Peroxisome biogenesis disorder	GPathogenic
Select item 2394269	NM_032538.3(TTBK1):c.2600C>T (p.Pro867Leu)	TTBK1 (P867L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392670	NM_032538.3(TTBK1):c.1354C>T (p.Arg452Trp)	TTBK1 (R452W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385292	NM_032538.3(TTBK1):c.3670G>A (p.Gly1224Arg)	TTBK1 (G1224R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368591	NM_032538.3(TTBK1):c.280A>G (p.Ile94Val)	TTBK1 (I94V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366931	NM_032538.3(TTBK1):c.3008G>A (p.Arg1003Gln)	TTBK1 (R1003Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364351	NM_032538.3(TTBK1):c.2030G>A (p.Arg677Gln)	TTBK1 (R677Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357780	NM_032538.3(TTBK1):c.3416C>G (p.Ala1139Gly)	TTBK1 (A1139G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352470	NM_032538.3(TTBK1):c.2455C>T (p.Arg819Trp)	TTBK1 (R819W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351247	NM_032538.3(TTBK1):c.2866G>A (p.Ala956Thr)	TTBK1 (A956T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2348979	NM_032538.3(TTBK1):c.1315C>G (p.Pro439Ala)	TTBK1 (P439A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343478	NM_032538.3(TTBK1):c.1243G>A (p.Gly415Ser)	TTBK1 (G415S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340989	NM_032538.3(TTBK1):c.3820C>T (p.Arg1274Trp)	TTBK1 (R1274W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340352	NM_032538.3(TTBK1):c.1777G>A (p.Val593Ile)	TTBK1 (V593I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336511	NM_032538.3(TTBK1):c.191T>C (p.Val64Ala)	TTBK1 (V64A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333976	NM_032538.3(TTBK1):c.31G>A (p.Glu11Lys)	TTBK1 (E11K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323189	NM_032538.3(TTBK1):c.28G>C (p.Asp10His)	TTBK1 (D10H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314438	NM_032538.3(TTBK1):c.1876C>T (p.Arg626Cys)	TTBK1 (R626C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299820	NM_032538.3(TTBK1):c.3727C>T (p.Arg1243Cys)	TTBK1 (R1243C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299819	NM_032538.3(TTBK1):c.2607T>G (p.His869Gln)	TTBK1 (H869Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2288297	NM_032538.3(TTBK1):c.2089G>A (p.Glu697Lys)	TTBK1 (E697K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285788	NM_032538.3(TTBK1):c.2962C>A (p.Leu988Met)	TTBK1 (L988M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279089	NM_032538.3(TTBK1):c.2104C>T (p.Leu702Phe)	TTBK1 (L702F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271936	NM_032538.3(TTBK1):c.3776G>T (p.Ser1259Ile)	TTBK1 (S1259I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268495	NM_032538.3(TTBK1):c.629C>T (p.Ala210Val)	TTBK1 (A210V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249437	NM_032538.3(TTBK1):c.3233G>A (p.Arg1078Gln)	TTBK1 (R1078Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237468	NM_032538.3(TTBK1):c.2005C>T (p.Pro669Ser)	TTBK1 (P669S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228349	NM_032538.3(TTBK1):c.1277G>A (p.Arg426Gln)	TTBK1 (R426Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222194	NM_032538.3(TTBK1):c.3380C>T (p.Thr1127Met)	TTBK1 (T1127M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219791	NM_032538.3(TTBK1):c.2542C>T (p.Pro848Ser)	TTBK1 (P848S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214918	NM_032538.3(TTBK1):c.3254C>T (p.Pro1085Leu)	TTBK1 (P1085L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2212970	NM_032538.3(TTBK1):c.2719G>A (p.Gly907Arg)	TTBK1 (G907R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207468	NM_032538.3(TTBK1):c.1939C>T (p.Pro647Ser)	TTBK1 (P647S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206595	NM_032538.3(TTBK1):c.3247G>T (p.Ala1083Ser)	TTBK1 (A1083S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1341645	NM_032538.3(TTBK1):c.1868G>C (p.Gly623Ala)	TTBK1 (G623A)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1328717	NM_032538.3(TTBK1):c.3551T>C (p.Leu1184Ser)	TTBK1 (L1184S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1328716	NM_032538.3(TTBK1):c.3434A>G (p.Lys1145Arg)	TTBK1 (K1145R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1072088	NC_000006.11:g.(?_42928506)_(43737486_?)del	KLHDC3, LRRC73 +27 more	Deletion	not provided	GPathogenic
Select item 984591	NM_032538.3(TTBK1):c.735+1G>T	TTBK1	Single nucleotide variant (splice donor variant)	Neurodevelopmental abnormality	GLikely benign

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