ClinVar for Gene (Select 22900) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3137344	NM_001184900.3(CARD8):c.1391G>T (p.Arg464Met)	CARD8 (R189M +5 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3064763	NM_001184900.3(CARD8):c.1015A>G (p.Ser339Gly)	CARD8 (S227G +6 more)	Single nucleotide variant (missense variant +1 more)	Inflammatory bowel disease 30	GLikely benign
Select item 3023729	NM_001184900.3(CARD8):c.59G>A (p.Arg20Gln)	CARD8 (R20Q)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3021197	NM_001184900.3(CARD8):c.1556G>T (p.Arg519Ile)	CARD8 (R407I +5 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 3015328	NM_001184900.3(CARD8):c.1073G>A (p.Arg358His)	CARD8 (R83H +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3007848	NM_001184900.3(CARD8):c.879C>T (p.Ser293=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3007707	NM_001184900.3(CARD8):c.772+17G>A	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3000905	NM_001184900.3(CARD8):c.1546G>A (p.Val516Met)	CARD8 (V466M +5 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 2998789	NM_001184900.3(CARD8):c.1047T>A (p.Asp349Glu)	CARD8 (D74E +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2998204	NM_001184900.3(CARD8):c.34A>G (p.Ser12Gly)	CARD8 (S12G)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2995975	NM_001184900.3(CARD8):c.1360G>A (p.Val454Met)	CARD8 (V179M +5 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 2994801	NM_001184900.3(CARD8):c.1476A>G (p.Glu492=)	CARD8	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign
Select item 2994691	NM_001184900.3(CARD8):c.909G>A (p.Leu303=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2992208	NM_001184900.3(CARD8):c.542+16G>A	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2991131	NM_001184900.3(CARD8):c.273A>T (p.Glu91Asp)	CARD8 (E91D +2 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GUncertain significance
Select item 2990635	NM_001184900.3(CARD8):c.1161G>T (p.Lys387Asn)	CARD8 (K112N +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2985783	NM_001184900.3(CARD8):c.713C>G (p.Thr238Ser)	CARD8 (T188S +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2984485	NM_001184900.3(CARD8):c.271G>A (p.Glu91Lys)	CARD8 (E41K +1 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 2983092	NM_001184900.3(CARD8):c.1346C>T (p.Ser449Leu)	CARD8 (S449L +5 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2982569	NM_001184900.3(CARD8):c.230G>C (p.Cys77Ser)	CARD8 (C27S +2 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2980981	NM_001184900.3(CARD8):c.1002G>T (p.Leu334Phe)	CARD8 (L284F +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2976994	NM_001184900.3(CARD8):c.412A>T (p.Asn138Tyr)	CARD8 (N26Y +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2975340	NM_001184900.3(CARD8):c.403T>C (p.Ser135Pro)	CARD8 (S23P +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2973424	NM_001184900.3(CARD8):c.559G>A (p.Ala187Thr)	CARD8 (A82T +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2973188	NM_001184900.3(CARD8):c.1304-11C>T	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2971837	NM_001184900.3(CARD8):c.351-15G>A	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2971521	NM_001184900.3(CARD8):c.466del (p.Tyr156fs)	CARD8 (Y156fs +4 more)	Deletion (frameshift variant +1 more)	not provided	GUncertain significance
Select item 2970419	NM_001184900.3(CARD8):c.8A>G (p.Lys3Arg)	CARD8 (K3R)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2970144	NM_001184900.3(CARD8):c.1423C>T (p.Leu475Phe)	CARD8 (L200F +5 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 2969793	NM_001184900.3(CARD8):c.1502C>A (p.Ala501Asp)	CARD8 (A396D +5 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 2966984	NM_001184900.3(CARD8):c.456C>T (p.Ile152=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2966026	NM_001184900.3(CARD8):c.974C>T (p.Pro325Leu)	CARD8 (P50L +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2966022	NM_001184900.3(CARD8):c.476G>A (p.Arg159His)	CARD8 (R109H +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2963425	NM_001184900.3(CARD8):c.54G>A (p.Pro18=)	CARD8	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2961707	NM_001184900.3(CARD8):c.360A>G (p.Glu120=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2958578	NM_001184900.3(CARD8):c.1002del (p.Leu334fs)	CARD8 (L229fs +5 more)	Deletion (frameshift variant +1 more)	not provided	GUncertain significance
Select item 2956802	NM_001184900.3(CARD8):c.383A>G (p.Gln128Arg)	CARD8 (Q128R +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2911589	NM_001184900.3(CARD8):c.447T>A (p.Cys149Ter)	CARD8 (C149* +4 more)	Single nucleotide variant (nonsense +1 more)	not provided	GUncertain significance
Select item 2906422	NM_001184900.3(CARD8):c.738C>T (p.Ala246=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2902467	NM_001184900.3(CARD8):c.915C>G (p.Ile305Met)	CARD8 (I305M +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2900410	NM_001184900.3(CARD8):c.351-10C>T	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2883584	NM_001184900.3(CARD8):c.340dup (p.Asp114fs)	CARD8 (T47fs +3 more)	Duplication (frameshift variant +2 more)	not provided	GUncertain significance
Select item 2882724	NM_001184900.3(CARD8):c.537A>G (p.Arg179=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 2881654	NM_001184900.3(CARD8):c.1262A>G (p.Lys421Arg)	CARD8 (K309R +5 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2873536	NM_001184900.3(CARD8):c.334G>T (p.Gly112Trp)	CARD8 (G112W +1 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 2871437	NM_001184900.3(CARD8):c.621G>A (p.Val207=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 2870042	NM_001184900.3(CARD8):c.1474G>T (p.Glu492Ter)	CARD8 (E386* +5 more)	Single nucleotide variant (nonsense +3 more)	not provided	GUncertain significance
Select item 2869593	NM_001184900.3(CARD8):c.840T>C (p.His280=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2867996	NM_001184900.3(CARD8):c.773-20C>T	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2867756	NM_001184900.3(CARD8):c.1493A>G (p.Lys498Arg)	CARD8 (K393R +5 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 2867442	NM_001184900.3(CARD8):c.574_575del (p.Trp192fs)	CARD8 (W192fs +4 more)	Microsatellite (frameshift variant +1 more)	not provided	GUncertain significance
Select item 2864486	NM_001184900.3(CARD8):c.998A>G (p.His333Arg)	CARD8 (H228R +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2864120	NM_001184900.3(CARD8):c.256T>G (p.Ser86Ala)	CARD8 (S86A +1 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 2862306	NM_001184900.3(CARD8):c.1040T>C (p.Ile347Thr)	CARD8 (I241T +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2860620	NM_001184900.3(CARD8):c.748C>T (p.Leu250Phe)	CARD8 (L138F +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2859619	NM_001184900.3(CARD8):c.426C>T (p.Ser142=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2851437	NM_001184900.3(CARD8):c.1348+2dup	CARD8	Duplication (splice donor variant)	not provided	GUncertain significance
Select item 2848613	NM_001184900.3(CARD8):c.1009G>A (p.Val337Ile)	CARD8 (V62I +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2842596	NM_001184900.3(CARD8):c.1036-5C>T	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2841638	NM_001184900.3(CARD8):c.704T>C (p.Phe235Ser)	CARD8 (F185S +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2834866	NM_001184900.3(CARD8):c.248G>A (p.Cys83Tyr)	CARD8 (C83Y +2 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2833849	NM_001184900.3(CARD8):c.863A>C (p.Tyr288Ser)	CARD8 (Y238S +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2831540	NM_001184900.3(CARD8):c.1349G>T (p.Gly450Val)	CARD8 (G175V +5 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 2830528	NM_001184900.3(CARD8):c.479A>G (p.Gln160Arg)	CARD8 (Q55R +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2829896	NM_001184900.3(CARD8):c.534C>A (p.Asn178Lys)	CARD8 (N178K +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2829221	NM_001184900.3(CARD8):c.1245A>C (p.Gln415His)	CARD8 (Q309H +5 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2829165	NM_001184900.3(CARD8):c.1116del (p.Ser373fs)	CARD8 (S268fs +5 more)	Deletion (frameshift variant +1 more)	not provided	GUncertain significance
Select item 2828947	NM_001184900.3(CARD8):c.1059C>T (p.Arg353=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2827879	NM_001184900.3(CARD8):c.468T>C (p.Tyr156=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2819365	NM_001184900.3(CARD8):c.831C>T (p.Val277=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2809756	NM_001184900.3(CARD8):c.1304-14del	CARD8	Deletion (intron variant)	not provided	GBenign
Select item 2808394	NM_001184900.3(CARD8):c.456C>G (p.Ile152Met)	CARD8 (I102M +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2804630	NM_001184900.3(CARD8):c.473A>G (p.Asn158Ser)	CARD8 (N108S +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2799434	NM_001184900.3(CARD8):c.282G>C (p.Glu94Asp)	CARD8 (E94D +3 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2797229	NM_001184900.3(CARD8):c.1592A>G (p.Tyr531Cys)	CARD8 (Y256C +5 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 2793548	NM_001184900.3(CARD8):c.869T>C (p.Val290Ala)	CARD8 (V178A +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2788605	NM_001184900.3(CARD8):c.787G>A (p.Val263Ile)	CARD8 (V157I +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2788418	NM_001184900.3(CARD8):c.1368G>C (p.Glu456Asp)	CARD8 (E350D +5 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 2782348	NM_001184900.3(CARD8):c.363G>A (p.Glu121=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2780554	NM_001184900.3(CARD8):c.590T>C (p.Leu197Pro)	CARD8 (L85P +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2777839	NM_001184900.3(CARD8):c.1036-10_1036-9delinsGT	CARD8	Indel (intron variant)	not provided	GUncertain significance
Select item 2776779	NM_001184900.3(CARD8):c.762C>G (p.Ile254Met)	CARD8 (I149M +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2776008	NM_001184900.3(CARD8):c.339G>A (p.Gly113=)	CARD8 (G22E +1 more)	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign
Select item 2766133	NM_001184900.3(CARD8):c.706G>T (p.Asp236Tyr)	CARD8 (D131Y +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2762800	NM_001184900.3(CARD8):c.486G>C (p.Leu162=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2760175	NM_001184900.3(CARD8):c.543-16C>T	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2752129	NM_001184900.3(CARD8):c.391+9C>A	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2746677	NM_001184900.3(CARD8):c.772+10G>A	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2745584	NM_001184900.3(CARD8):c.290C>T (p.Ala97Val)	CARD8 (A47V +3 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 2745243	NM_001184900.3(CARD8):c.878G>T (p.Ser293Ile)	CARD8 (S18I +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2738302	NM_001184900.3(CARD8):c.900C>T (p.Gly300=)	CARD8	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2731329	NM_001184900.3(CARD8):c.850G>T (p.Val284Leu)	CARD8 (V203L +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2720792	NM_001184900.3(CARD8):c.287_288del (p.Glu96fs)	CARD8 (R5fs +3 more)	Microsatellite (frameshift variant +2 more)	not provided	GUncertain significance
Select item 2714157	NM_001184900.3(CARD8):c.1438G>C (p.Val480Leu)	CARD8 (V375L +5 more)	Single nucleotide variant (3 prime UTR variant +3 more)	not provided	GUncertain significance
Select item 2713737	NM_001184900.3(CARD8):c.223C>T (p.Leu75=)	CARD8	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2707397	NM_001184900.3(CARD8):c.630G>T (p.Ala210=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 2707166	NM_001184900.3(CARD8):c.1288A>G (p.Thr430Ala)	CARD8 (T318A +5 more)	Single nucleotide variant (intron variant +2 more)	not provided	GUncertain significance
Select item 2706716	NM_001184900.3(CARD8):c.1029A>G (p.Leu343=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2706181	NM_001184900.3(CARD8):c.849G>T (p.Arg283=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2702627	NM_001184900.3(CARD8):c.505G>A (p.Asp169Asn)	CARD8 (D57N +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance

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