ClinVar for Gene (Select 8913) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3069129	NM_018896.5(CACNA1G):c.4926T>C (p.Ala1642=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 3067799	NM_018896.5(CACNA1G):c.580G>C (p.Val194Leu)	CACNA1G (V194L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3066134	NM_018896.5(CACNA1G):c.661G>A (p.Val221Ile)	CACNA1G (V221I)	Single nucleotide variant (missense variant +1 more)	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits	GUncertain significance
Select item 3063747	NM_018896.5(CACNA1G):c.6692del (p.Pro2231fs)	CACNA1G (P2081fs +23 more)	Deletion (frameshift variant +2 more)	not specified	GUncertain significance
Select item 3054884	NM_018896.5(CACNA1G):c.103G>A (p.Gly35Arg)	CACNA1G, CACNA1G-AS1 (G35R)	Single nucleotide variant (missense variant +1 more)	CACNA1G-related condition	GUncertain significance
Select item 3054237	NM_018896.5(CACNA1G):c.2453+10C>A	CACNA1G	Single nucleotide variant (intron variant)	CACNA1G-related condition	GLikely benign
Select item 3047538	NM_018896.5(CACNA1G):c.2755-8G>T	CACNA1G	Single nucleotide variant (intron variant)	CACNA1G-related condition	GLikely benign
Select item 3047084	NM_018896.5(CACNA1G):c.621G>T (p.Thr207=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	CACNA1G-related condition	GLikely benign
Select item 3046754	NM_018896.5(CACNA1G):c.6977G>A (p.Ser2326Asn)	CACNA1G (S2120N +26 more)	Single nucleotide variant (missense variant +1 more)	CACNA1G-related condition	GLikely benign
Select item 3044567	NM_018896.5(CACNA1G):c.5428G>C (p.Asp1810His)	CACNA1G (D1753H +14 more)	Single nucleotide variant (missense variant +1 more)	CACNA1G-related condition	GUncertain significance
Select item 3034778	NM_018896.5(CACNA1G):c.3816C>T (p.Ile1272=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	CACNA1G-related condition	GLikely benign
Select item 3032988	NM_018896.5(CACNA1G):c.586+10C>T	CACNA1G	Single nucleotide variant (intron variant)	CACNA1G-related condition	GLikely benign
Select item 3031933	NM_018896.5(CACNA1G):c.4705+5G>A	CACNA1G	Single nucleotide variant (intron variant +2 more)	CACNA1G-related condition	GLikely benign
Select item 3027376	NM_018896.5(CACNA1G):c.6152G>A (p.Ser2051Asn)	CACNA1G (S1901N +23 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3026741	NM_018896.5(CACNA1G):c.4296+5G>A	CACNA1G	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3026732	NM_018896.5(CACNA1G):c.1765G>T (p.Val589Leu)	CACNA1G (V589L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3026321	NM_018896.5(CACNA1G):c.1580A>G (p.Asn527Ser)	CACNA1G (N527S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3026283	NM_018896.5(CACNA1G):c.2243G>C (p.Gly748Ala)	CACNA1G (G748A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3026084	NM_018896.5(CACNA1G):c.3669C>T (p.Asp1223=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3026065	NM_018896.5(CACNA1G):c.5471C>T (p.Thr1824Met)	CACNA1G (T1767M +14 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3023401	NM_018896.5(CACNA1G):c.6096C>T (p.Asp2032=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3016740	NM_018896.5(CACNA1G):c.2754+5G>A	CACNA1G	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3016698	NM_018896.5(CACNA1G):c.5214G>A (p.Gln1738=)	CACNA1G	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 3013066	NM_018896.5(CACNA1G):c.5984C>T (p.Ser1995Phe)	CACNA1G (S1995F +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3012385	NM_018896.5(CACNA1G):c.488+8C>G	CACNA1G	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3012209	NM_018896.5(CACNA1G):c.1140C>T (p.Ile380=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 3011030	NM_018896.5(CACNA1G):c.4912-17G>T	CACNA1G	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3010711	NM_018896.5(CACNA1G):c.242+19C>G	CACNA1G, CACNA1G-AS1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3005421	NM_018896.5(CACNA1G):c.3915+18C>T	CACNA1G	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3002543	NM_018896.5(CACNA1G):c.1244G>A (p.Arg415Gln)	CACNA1G (R415Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3001813	NM_018896.5(CACNA1G):c.3272G>T (p.Ser1091Ile)	CACNA1G (S1068I +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2997914	NM_018896.5(CACNA1G):c.1236G>A (p.Gln412=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2993893	NM_018896.5(CACNA1G):c.3703C>T (p.Arg1235Trp)	CACNA1G (R1235W +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2992095	NM_018896.5(CACNA1G):c.484G>T (p.Ala162Ser)	CACNA1G (A162S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2991399	NM_018896.5(CACNA1G):c.6964C>T (p.Arg2322Trp)	CACNA1G (R2172W +26 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2989739	NM_018896.5(CACNA1G):c.4047G>T (p.Leu1349=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2985715	NM_018896.5(CACNA1G):c.5747G>T (p.Arg1916Ile)	CACNA1G (R1864I +14 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2984923	NM_018896.5(CACNA1G):c.2787C>T (p.Leu929=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2984426	NM_018896.5(CACNA1G):c.6131C>T (p.Thr2044Met)	CACNA1G (T1915M +23 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2984040	NM_018896.5(CACNA1G):c.3362G>A (p.Arg1121Gln)	CACNA1G (R1098Q +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2979601	NM_018896.5(CACNA1G):c.1864C>T (p.Leu622Phe)	CACNA1G (L622F)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2977017	NM_018896.5(CACNA1G):c.6230-18G>A	CACNA1G	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2976103	NM_018896.5(CACNA1G):c.3475C>T (p.Arg1159Cys)	CACNA1G (R1136C +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2974226	NM_018896.5(CACNA1G):c.6453C>A (p.Asp2151Glu)	CACNA1G (D2033E +23 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2974100	NM_018896.5(CACNA1G):c.2321C>T (p.Ala774Val)	CACNA1G (A774V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2973556	NM_018896.5(CACNA1G):c.192G>A (p.Leu64=)	CACNA1G, CACNA1G-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2973329	NM_018896.5(CACNA1G):c.2684G>A (p.Arg895Gln)	CACNA1G (R895Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2973092	NM_018896.5(CACNA1G):c.3198G>C (p.Ser1066=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2971977	NM_018896.5(CACNA1G):c.6608A>C (p.Asn2203Thr)	CACNA1G (N2058T +23 more)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 2970005	NM_018896.5(CACNA1G):c.3913G>A (p.Ala1305Thr)	CACNA1G (A1282T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2966810	NM_018896.5(CACNA1G):c.3065-7C>T	CACNA1G	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2966343	NM_018896.5(CACNA1G):c.5156-11C>T	CACNA1G	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2965933	NM_018896.5(CACNA1G):c.687C>T (p.Gly229=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2965501	NM_018896.5(CACNA1G):c.4706-17G>A	CACNA1G	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2963925	NM_018896.5(CACNA1G):c.2631C>T (p.Phe877=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2963410	NM_018896.5(CACNA1G):c.3456C>T (p.Ser1152=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2963272	NM_018896.5(CACNA1G):c.5021+6G>A	CACNA1G	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2963117	NM_018896.5(CACNA1G):c.4371G>A (p.Glu1457=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2962641	NM_018896.5(CACNA1G):c.5686G>A (p.Glu1896Lys)	CACNA1G (E1869K +14 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2962272	NM_018896.5(CACNA1G):c.73C>T (p.Leu25=)	CACNA1G, CACNA1G-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2962174	NM_018896.5(CACNA1G):c.7080A>C (p.Lys2360Asn)	CACNA1G (K2210N +26 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2962030	NM_018896.5(CACNA1G):c.1925-11_1925-10del	CACNA1G	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2961920	NM_018896.5(CACNA1G):c.621G>A (p.Thr207=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2961672	NM_018896.5(CACNA1G):c.5305+19G>A	CACNA1G	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2960769	NM_018896.5(CACNA1G):c.1047+8A>G	CACNA1G	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2960128	NM_018896.5(CACNA1G):c.488+6G>A	CACNA1G	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2959811	NM_018896.5(CACNA1G):c.5427+18G>A	CACNA1G	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2958869	NM_018896.5(CACNA1G):c.1577C>T (p.Ala526Val)	CACNA1G (A526V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2957775	NM_018896.5(CACNA1G):c.3915+16C>T	CACNA1G	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2956890	NM_018896.5(CACNA1G):c.2373G>A (p.Leu791=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2956378	NM_018896.5(CACNA1G):c.5226+14G>C	CACNA1G	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2956113	NM_018896.5(CACNA1G):c.3033_3034delinsAT (p.Asp1011_Gly1012delinsGluCys)	CACNA1G	Indel (missense variant +1 more)	not provided	GUncertain significance
Select item 2955757	NM_018896.5(CACNA1G):c.5428-13C>T	CACNA1G	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2955737	NM_018896.5(CACNA1G):c.3430G>A (p.Glu1144Lys)	CACNA1G (E1121K +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2954954	NM_018896.5(CACNA1G):c.6483G>A (p.Pro2161=)	CACNA1G	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 2920371	NM_018896.5(CACNA1G):c.279C>G (p.Leu93=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2920171	NM_018896.5(CACNA1G):c.123G>T (p.Pro41=)	CACNA1G, CACNA1G-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2919049	NM_018896.5(CACNA1G):c.1557G>A (p.Pro519=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2914525	NM_018896.5(CACNA1G):c.6924G>A (p.Pro2308=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2912497	NM_018896.5(CACNA1G):c.2070C>T (p.Ser690=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2909005	NM_018896.5(CACNA1G):c.1451G>A (p.Arg484His)	CACNA1G (R484H)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2907455	NM_018896.5(CACNA1G):c.5793G>A (p.Leu1931=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2906031	NM_018896.5(CACNA1G):c.285C>T (p.Cys95=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2901464	NM_018896.5(CACNA1G):c.3629G>A (p.Arg1210Gln)	CACNA1G (R1187Q +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2899835	NM_018896.5(CACNA1G):c.1776C>T (p.Thr592=)	CACNA1G	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2898097	NM_018896.5(CACNA1G):c.6119G>T (p.Gly2040Val)	CACNA1G (G1890V +23 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2897851	NM_018896.5(CACNA1G):c.6446G>A (p.Arg2149Gln)	CACNA1G (R1999Q +23 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2895072	NM_018896.5(CACNA1G):c.2664C>T (p.Gly888=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2894677	NM_018896.5(CACNA1G):c.1442G>A (p.Ser481Asn)	CACNA1G (S481N)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2894256	NM_018896.5(CACNA1G):c.2109C>T (p.Ser703=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2894008	NM_018896.5(CACNA1G):c.2979+8C>T	CACNA1G	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2892562	NM_018896.5(CACNA1G):c.663C>T (p.Val221=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2891730	NM_018896.5(CACNA1G):c.1407A>C (p.Ala469=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2889816	NM_018896.5(CACNA1G):c.3356T>C (p.Leu1119Pro)	CACNA1G (L1096P +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2889764	NM_018896.5(CACNA1G):c.5985C>T (p.Ser1995=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2889763	NM_018896.5(CACNA1G):c.6946C>G (p.Pro2316Ala)	CACNA1G (P2144A +26 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2889703	NM_018896.5(CACNA1G):c.4785C>G (p.Ser1595=)	CACNA1G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2889050	NM_018896.5(CACNA1G):c.165G>A (p.Ala55=)	CACNA1G, CACNA1G-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2888122	NM_018896.5(CACNA1G):c.89G>A (p.Gly30Asp)	CACNA1G, CACNA1G-AS1 (G30D)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2888106	NM_018896.5(CACNA1G):c.5695G>A (p.Asp1899Asn)	CACNA1G (D1858N +14 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign

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