ClinVar for Gene (Select 22900) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 100 of 432

<< First< Prev

Page of 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3902042	NM_001184900.3(CARD8):c.275A>G (p.Asp92Gly)	CARD8 (D42G +3 more)	Single nucleotide variant (missense variant +3 more)	Inflammatory bowel disease 30	GUncertain significance
Select item 3778999	NM_001184900.3(CARD8):c.330A>C (p.Leu110=)	CARD8 (Y19S +1 more)	Single nucleotide variant (synonymous variant +3 more)	Inflammatory bowel disease 30	GUncertain significance
Select item 3730639	NM_001184900.3(CARD8):c.543-18C>T	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3725478	NM_001184900.3(CARD8):c.391G>A (p.Gly131Arg)	CARD8 (G131R +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3715262	NM_001184900.3(CARD8):c.1510A>G (p.Ser504Gly)	CARD8 (S392G +4 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 3715060	NM_001184900.3(CARD8):c.848G>A (p.Arg283Gln)	CARD8 (R171Q +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3712701	NM_001184900.3(CARD8):c.847C>T (p.Arg283Trp)	CARD8 (R171W +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3706591	NM_001184900.3(CARD8):c.213A>G (p.Val71=)	CARD8 (Y4C)	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign
Select item 3699201	NM_001184900.3(CARD8):c.878G>A (p.Ser293Asn)	CARD8 (S187N +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3697468	NM_001184900.3(CARD8):c.242C>T (p.Thr81Ile)	CARD8 (P14S +2 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3693990	NM_001184900.3(CARD8):c.625A>G (p.Ile209Val)	CARD8 (I128V +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3693299	NM_001184900.3(CARD8):c.727G>A (p.Glu243Lys)	CARD8 (E162K +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3692695	NM_001184900.3(CARD8):c.1058G>T (p.Arg353Leu)	CARD8 (R248L +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3690944	NM_001184900.3(CARD8):c.1349-3C>T	CARD8	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3689798	NM_001184900.3(CARD8):c.1541T>C (p.Leu514Pro)	CARD8 (L464P +4 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 3689672	NM_001184900.3(CARD8):c.59+20G>T	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3687817	NM_001184900.3(CARD8):c.1058G>C (p.Arg353Pro)	CARD8 (R272P +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3687799	NM_001184900.3(CARD8):c.542+15T>G	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3685397	NM_001184900.3(CARD8):c.1348+17C>T	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3685290	NM_001184900.3(CARD8):c.682T>C (p.Trp228Arg)	CARD8 (W123R +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3683410	NM_001184900.3(CARD8):c.448T>C (p.Phe150Leu)	CARD8 (F69L +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3680305	NM_001184900.3(CARD8):c.1226A>T (p.Gln409Leu)	CARD8 (Q297L +4 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3680280	NM_001184900.3(CARD8):c.1511G>A (p.Ser504Asn)	CARD8 (S392N +4 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 3679747	NM_001184900.3(CARD8):c.1162-19A>G	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3679580	NM_001184900.3(CARD8):c.439A>G (p.Lys147Glu)	CARD8 (K147E +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3677872	NM_001184900.3(CARD8):c.1169A>G (p.Lys390Arg)	CARD8 (K278R +4 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3674861	NM_001184900.3(CARD8):c.1128G>A (p.Val376=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3674638	NM_001184900.3(CARD8):c.1272G>A (p.Gly424=)	CARD8	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 3670798	NM_001184900.3(CARD8):c.1162-2A>G	CARD8	Single nucleotide variant (splice acceptor variant +1 more)	not provided	GUncertain significance
Select item 3668177	NM_001184900.3(CARD8):c.456C>A (p.Ile152=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3665910	NM_001184900.3(CARD8):c.1270G>A (p.Gly424Arg)	CARD8 (G318R +4 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3665160	NM_001184900.3(CARD8):c.986A>T (p.Asp329Val)	CARD8 (D223V +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3660747	NM_001184900.3(CARD8):c.542+3A>C	CARD8	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3660282	NM_001184900.3(CARD8):c.392-18C>G	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3658953	NM_001184900.3(CARD8):c.773-4_773-3insGGAGGCTGTGGGGGCCGCTGGGGTGCGTGCCGTCTCACTGCTGTTGTGGTTCTCCTGGTGGCTGGGGACAGCAGCAGGGCCTAGGAAGGATGCACGCTCTTTCGCCTCTGCATCTTTGGAGTTCGATACTTTTCTGACCTGGACTTTCCTCACCAGCAGAAAGTGTCTTCTGCTATTTCGGACCAGTAGAAATGTAGGTGCATT	CARD8	Insertion (intron variant)	not provided	GUncertain significance
Select item 3658481	NM_001184900.3(CARD8):c.746del (p.His249fs)	CARD8 (H168fs +4 more)	Deletion (frameshift variant +1 more)	not provided	GUncertain significance
Select item 3656069	NM_001184900.3(CARD8):c.1147_1150del (p.Leu382_Lys383insTer)	CARD8	Deletion (nonsense +1 more)	not provided	GUncertain significance
Select item 3651293	NM_001184900.3(CARD8):c.1035+7T>C	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3650017	NM_001184900.3(CARD8):c.368A>G (p.Glu123Gly)	CARD8 (E123G +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3649839	NM_001184900.3(CARD8):c.40del (p.Glu14fs)	CARD8 (E14fs)	Deletion (frameshift variant +2 more)	not provided	GUncertain significance
Select item 3648215	NM_001184900.3(CARD8):c.773-3C>T	CARD8	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3647448	NM_001184900.3(CARD8):c.688G>A (p.Val230Met)	CARD8 (V118M +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3642291	NM_001184900.3(CARD8):c.434C>A (p.Ala145Asp)	CARD8 (A145D +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3640990	NM_001184900.3(CARD8):c.542+15T>A	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3638167	NM_001184900.3(CARD8):c.1160A>G (p.Lys387Arg)	CARD8 (K275R +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3637374	NM_001184900.3(CARD8):c.913A>T (p.Ile305Phe)	CARD8 (I255F +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3632640	NM_001184900.3(CARD8):c.1207T>A (p.Ser403Thr)	CARD8 (S298T +4 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3632102	NM_001184900.3(CARD8):c.1304-5T>C	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3630779	NM_001184900.3(CARD8):c.51G>A (p.Leu17=)	CARD8	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 3630629	NM_001184900.3(CARD8):c.36C>T (p.Ser12=)	CARD8	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 3628064	NM_001184900.3(CARD8):c.989T>C (p.Ile330Thr)	CARD8 (I218T +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3623048	NM_001184900.3(CARD8):c.542+15T>C	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3622729	NM_001184900.3(CARD8):c.1461G>A (p.Glu487=)	CARD8	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign
Select item 3621950	NM_001184900.3(CARD8):c.1348+18A>C	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3621558	NM_001184900.3(CARD8):c.1431C>G (p.Asp477Glu)	CARD8 (D365E +4 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 3620838	NM_001184900.3(CARD8):c.1456A>G (p.Lys486Glu)	CARD8 (K374E +4 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 3620446	NM_001184900.3(CARD8):c.1462C>T (p.Leu488=)	CARD8	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign
Select item 3618264	NM_001184900.3(CARD8):c.1036-14C>T	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3616671	NM_001184900.3(CARD8):c.1239C>T (p.Pro413=)	CARD8	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 3616376	NM_001184900.3(CARD8):c.1417G>A (p.Asp473Asn)	CARD8 (D361N +4 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 3616187	NM_001184900.3(CARD8):c.542+8T>C	CARD8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3614731	NM_001184900.3(CARD8):c.581C>T (p.Ala194Val)	CARD8 (A113V +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3613377	NM_001184900.3(CARD8):c.1291G>A (p.Glu431Lys)	CARD8 (E319K +4 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3613024	NM_001184900.3(CARD8):c.1349-2A>G	CARD8	Single nucleotide variant (intron variant +1 more)	not provided	GUncertain significance
Select item 3611006	NM_001184900.3(CARD8):c.918C>G (p.Ala306=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3610576	NM_001184900.3(CARD8):c.658C>G (p.Leu220Val)	CARD8 (L108V +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3610212	NM_001184900.3(CARD8):c.802G>T (p.Val268Phe)	CARD8 (V156F +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3608223	NM_001184900.3(CARD8):c.1102C>T (p.Leu368=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3605938	NM_001184900.3(CARD8):c.388dup (p.Ser130fs)	CARD8 (S130fs +2 more)	Duplication (frameshift variant +1 more)	not provided	GUncertain significance
Select item 3603715	NM_001184900.3(CARD8):c.786C>T (p.Asp262=)	CARD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3485001	NM_001184900.3(CARD8):c.457G>C (p.Glu153Gln)	CARD8 (E103Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3485000	NM_001184900.3(CARD8):c.1540C>G (p.Leu514Val)	CARD8 (L408V +4 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3484999	NM_001184900.3(CARD8):c.1274C>G (p.Thr425Ser)	CARD8 (T313S +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3484997	NM_001184900.3(CARD8):c.62A>G (p.Asp21Gly)	CARD8 (D21G)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3393338	NM_001184900.3(CARD8):c.1207T>G (p.Ser403Ala)	CARD8 (S291A +4 more)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease 30	GUncertain significance
Select item 3346470	NM_001184900.3(CARD8):c.350+565_350+569del	CARD8 (T2fs)	Deletion (frameshift variant +2 more)	CARD8-related disorder	GUncertain significance
Select item 3263314	NM_001184900.3(CARD8):c.680A>G (p.Gln227Arg)	CARD8 (Q122R +4 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 3242694	NC_000019.9:g.(?_48744199)_(48822028_?)del	CARD8, ODAD1 +1 more	Deletion	not provided	GUncertain significance
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 (missense 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 +1 more	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 (non-coding transcript 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

<< First< Prev

Page of 5