ClinVar for Gene (Select 23242) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3147039	NM_015198.5(COBL):c.811T>C (p.Ser271Pro)	COBL (S271P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147038	NM_015198.5(COBL):c.508C>T (p.Arg170Cys)	COBL (R170C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147037	NM_015198.5(COBL):c.443C>T (p.Pro148Leu)	COBL (P148L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147036	NM_015198.5(COBL):c.3598C>T (p.Leu1200Phe)	COBL (L1282F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3147035	NM_015198.5(COBL):c.3544G>A (p.Asp1182Asn)	COBL (D1182N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3147034	NM_015198.5(COBL):c.3433G>A (p.Glu1145Lys)	COBL (E1227K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147033	NM_015198.5(COBL):c.3388G>T (p.Ala1130Ser)	COBL (A1187S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147031	NM_015198.5(COBL):c.3118T>G (p.Ser1040Ala)	COBL (S1097A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147030	NM_015198.5(COBL):c.3103G>A (p.Glu1035Lys)	COBL (E1035K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147029	NM_015198.5(COBL):c.3095G>A (p.Cys1032Tyr)	COBL (C1089Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147028	NM_015198.5(COBL):c.2957G>T (p.Arg986Leu)	COBL (R1068L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147027	NM_015198.5(COBL):c.2853G>T (p.Arg951Ser)	COBL (R1008S +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3147026	NM_015198.5(COBL):c.2804C>T (p.Thr935Ile)	COBL (T992I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147025	NM_015198.5(COBL):c.2699C>T (p.Ala900Val)	COBL (A957V +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3147024	NM_015198.5(COBL):c.2684G>T (p.Gly895Val)	COBL (G895V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147023	NM_015198.5(COBL):c.2530G>A (p.Val844Met)	COBL (V901M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147021	NM_015198.5(COBL):c.2203G>A (p.Glu735Lys)	COBL (E735K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147020	NM_015198.5(COBL):c.212G>C (p.Ser71Thr)	COBL (S71T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147019	NM_015198.5(COBL):c.20C>T (p.Ser7Leu)	COBL (S7L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147018	NM_015198.5(COBL):c.1996G>A (p.Val666Met)	COBL (V666M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147017	NM_015198.5(COBL):c.1756C>T (p.His586Tyr)	COBL (H586Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147016	NM_015198.5(COBL):c.1558G>C (p.Gly520Arg)	COBL (G520R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147015	NM_015198.5(COBL):c.1549T>G (p.Ser517Ala)	COBL (S517A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147014	NM_015198.5(COBL):c.146A>G (p.Gln49Arg)	COBL (Q49R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147013	NM_015198.5(COBL):c.1468C>T (p.Arg490Cys)	COBL (R490C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147012	NM_015198.5(COBL):c.121C>T (p.His41Tyr)	COBL (H41Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3147011	NM_015198.5(COBL):c.1027C>T (p.Pro343Ser)	COBL (P368S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2921024	NM_015198.5(COBL):c.2440A>G (p.Ile814Val)	COBL (I896V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2685240	GRCh37/hg19 7p12.1(chr7:50617859-52201563)x1	COBL, DDC +1 more	Copy number loss	not provided	GUncertain significance
Select item 2657506	NM_015198.5(COBL):c.1974G>A (p.Glu658=)	COBL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2657505	NM_015198.5(COBL):c.2672A>G (p.Tyr891Cys)	COBL (Y891C +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2657504	NM_015198.5(COBL):c.3729C>T (p.Asp1243=)	COBL	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2611208	NM_015198.5(COBL):c.1968C>G (p.Asp656Glu)	COBL (D656E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599997	NM_015198.5(COBL):c.121C>G (p.His41Asp)	COBL (H41D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599926	NM_015198.5(COBL):c.3139G>A (p.Gly1047Ser)	COBL (G1047S +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2598463	NM_015198.5(COBL):c.40G>C (p.Gly14Arg)	COBL (G14R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595322	NM_015198.5(COBL):c.898C>T (p.Arg300Cys)	COBL (R325C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594433	NM_015198.5(COBL):c.1001G>A (p.Arg334Gln)	COBL (R334Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592840	NM_015198.5(COBL):c.2705T>C (p.Val902Ala)	COBL (V959A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2587932	NM_015198.5(COBL):c.950C>T (p.Ser317Leu)	COBL (S317L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568811	NM_015198.5(COBL):c.1969G>A (p.Gly657Arg)	COBL (G657R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553057	NM_015198.5(COBL):c.2230G>A (p.Ala744Thr)	COBL (A826T +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2548407	NM_015198.5(COBL):c.3067C>G (p.Pro1023Ala)	COBL (P1023A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548007	NM_015198.5(COBL):c.2888C>T (p.Thr963Ile)	COBL (T1020I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545003	NM_015198.5(COBL):c.3041G>A (p.Arg1014His)	COBL (R1014H +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2540545	NM_015198.5(COBL):c.376A>G (p.Thr126Ala)	COBL (T126A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533451	NM_015198.5(COBL):c.779G>A (p.Ser260Asn)	COBL (S260N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533015	NM_015198.5(COBL):c.2535G>T (p.Arg845Ser)	COBL (R845S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525936	NM_015198.5(COBL):c.877G>A (p.Val293Met)	COBL (V293M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518605	NM_015198.5(COBL):c.602A>G (p.Asn201Ser)	COBL (N201S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518521	NM_015198.5(COBL):c.187A>G (p.Met63Val)	COBL (M63V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2517419	NM_015198.5(COBL):c.3709G>A (p.Ala1237Thr)	COBL (A1190T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2514897	NM_015198.5(COBL):c.2776A>G (p.Lys926Glu)	COBL (K1008E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512689	NM_015198.5(COBL):c.1958G>A (p.Gly653Asp)	COBL (G710D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509889	NM_015198.5(COBL):c.3205A>G (p.Lys1069Glu)	COBL (K1069E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509163	NM_015198.5(COBL):c.1706C>T (p.Ser569Leu)	COBL (S626L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508243	NM_015198.5(COBL):c.2956C>T (p.Arg986Cys)	COBL (R986C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486920	NM_015198.5(COBL):c.187A>T (p.Met63Leu)	COBL (M63L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484173	NM_015198.5(COBL):c.3622C>T (p.Pro1208Ser)	COBL (P1208S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2477629	NM_015198.5(COBL):c.2978G>A (p.Cys993Tyr)	COBL (C1050Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477171	NM_015198.5(COBL):c.1817A>G (p.Asp606Gly)	COBL (D663G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467112	NM_015198.5(COBL):c.2132T>C (p.Ile711Thr)	COBL (I768T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466793	NM_015198.5(COBL):c.2276C>G (p.Ala759Gly)	COBL (A841G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454210	NM_015198.5(COBL):c.3400G>A (p.Gly1134Arg)	COBL (G1134R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411615	NM_015198.5(COBL):c.2261C>T (p.Ser754Leu)	COBL (S754L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410510	NM_015198.5(COBL):c.2375C>T (p.Pro792Leu)	COBL (P792L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409448	NM_015198.5(COBL):c.1631T>C (p.Ile544Thr)	COBL (I544T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403764	NM_015198.5(COBL):c.1568A>G (p.Asn523Ser)	COBL (N523S +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2400554	NM_015198.5(COBL):c.3505G>T (p.Val1169Leu)	COBL (V1169L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393818	NM_015198.5(COBL):c.2853G>C (p.Arg951Ser)	COBL (R1008S +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2369035	NM_015198.5(COBL):c.889A>G (p.Met297Val)	COBL (M322V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368431	NM_015198.5(COBL):c.3074A>C (p.His1025Pro)	COBL (H1082P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366062	NM_015198.5(COBL):c.2236G>A (p.Gly746Ser)	COBL (G746S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363360	NM_015198.5(COBL):c.2957G>A (p.Arg986His)	COBL (R1043H +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2360436	NM_015198.5(COBL):c.2161G>C (p.Asp721His)	COBL (D721H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359888	NM_015198.5(COBL):c.3550G>A (p.Ala1184Thr)	COBL (A1184T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2358867	NM_015198.5(COBL):c.2517G>A (p.Met839Ile)	COBL (M839I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356845	NM_015198.5(COBL):c.1469G>A (p.Arg490His)	COBL (R490H +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2351361	NM_015198.5(COBL):c.3056C>T (p.Thr1019Ile)	COBL (T1019I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349415	NM_015198.5(COBL):c.1126T>G (p.Cys376Gly)	COBL (C376G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322539	NM_015198.5(COBL):c.884C>T (p.Ser295Leu)	COBL (S295L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321312	NM_015198.5(COBL):c.2330A>T (p.Glu777Val)	COBL (E834V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307729	NM_015198.5(COBL):c.3199G>C (p.Glu1067Gln)	COBL (E1067Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288367	NM_015198.5(COBL):c.1273A>G (p.Ser425Gly)	COBL (S425G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276140	NM_015198.5(COBL):c.251C>T (p.Ala84Val)	COBL (A84V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276080	NM_015198.5(COBL):c.11C>G (p.Pro4Arg)	COBL (P4R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272249	NM_015198.5(COBL):c.1230G>A (p.Met410Ile)	COBL (M467I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258445	NM_015198.5(COBL):c.2855G>T (p.Gly952Val)	COBL (G1009V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255494	NM_015198.5(COBL):c.2378C>A (p.Ser793Tyr)	COBL (S793Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253709	NM_015198.5(COBL):c.385G>A (p.Val129Met)	COBL (V129M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235237	NM_015198.5(COBL):c.372T>G (p.Ile124Met)	COBL (I124M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223566	NM_015198.5(COBL):c.1828G>A (p.Gly610Arg)	COBL (G610R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219905	NM_015198.5(COBL):c.394G>A (p.Val132Met)	COBL (V132M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217267	NM_015198.5(COBL):c.3628C>T (p.Pro1210Ser)	COBL (P1210S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2211271	NM_015198.5(COBL):c.2393C>G (p.Thr798Arg)	COBL (T798R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1708459	GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1	AASS, ABCA13 +896 more	Copy number loss	See cases	GUncertain significance
Select item 1703560	Single allele	CACNA2D1, CADPS2 +896 more	Complex	Ring chromosome 7	GPathogenic
Select item 1340646	GRCh37/hg19 7p12.1(chr7:51217906-51328561)x1	COBL	Copy number loss	not provided	GUncertain significance
Select item 1340467	GRCh37/hg19 7p12.1(chr7:51142796-51440184)x3	COBL	Copy number gain	not provided	GUncertain significance
Select item 1273872	NM_015198.5(COBL):c.1963G>C (p.Ala655Pro)	COBL (A655P +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign

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