ClinVar for Gene (Select 81603) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3182830	NM_030912.3(TRIM8):c.1359G>C (p.Gln453His)	TRIM8 (Q421H +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3182829	NM_030912.3(TRIM8):c.1294G>A (p.Ala432Thr)	TRIM8 (A400T +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 3182828	NM_030912.3(TRIM8):c.119G>C (p.Gly40Ala)	LOC130004618, TRIM8 (G40A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3182827	NM_030912.3(TRIM8):c.1162T>C (p.Phe388Leu)	TRIM8 (F356L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3063164	GRCh37/hg19 10q23.33-26.3(chr10:95078198-135427143)x3	ABCC2, ABLIM1 +293 more	Copy number gain	not specified	GPathogenic
Select item 3022561	NM_030912.3(TRIM8):c.1299A>G (p.Gln433=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3022159	NM_030912.3(TRIM8):c.565A>T (p.Ile189Phe)	TRIM8 (I189F)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 3021854	NM_030912.3(TRIM8):c.768G>A (p.Lys256=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3018278	NM_030912.3(TRIM8):c.1555C>T (p.Leu519=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3013901	NM_030912.3(TRIM8):c.667-7C>T	TRIM8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3009706	NM_030912.3(TRIM8):c.1496C>G (p.Ser499Trp)	TRIM8 (S499W +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3005459	NM_030912.3(TRIM8):c.218A>G (p.Asn73Ser)	LOC130004618, TRIM8 (N73S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2999814	NM_030912.3(TRIM8):c.354C>T (p.His118=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2999393	NM_030912.3(TRIM8):c.1302A>G (p.Pro434=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2998420	NM_030912.3(TRIM8):c.1105G>A (p.Val369Met)	TRIM8 (V369M +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2996831	NM_030912.3(TRIM8):c.528A>T (p.Gly176=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2994762	NM_030912.3(TRIM8):c.1376A>T (p.Gln459Leu)	TRIM8 (Q427L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2992535	NM_030912.3(TRIM8):c.54C>T (p.Cys18=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2992115	NM_030912.3(TRIM8):c.861G>C (p.Gln287His)	TRIM8 (Q255H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2991058	NM_030912.3(TRIM8):c.546G>A (p.Val182=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2990177	NM_030912.3(TRIM8):c.1275G>A (p.Leu425=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2989831	NM_030912.3(TRIM8):c.883G>A (p.Asp295Asn)	TRIM8 (D263N +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2987996	NM_030912.3(TRIM8):c.1609T>C (p.Tyr537His)	TRIM8 (Y505H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2987949	NM_030912.3(TRIM8):c.796G>A (p.Ala266Thr)	TRIM8 (A266T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2983379	NM_030912.3(TRIM8):c.806C>T (p.Ala269Val)	TRIM8 (A269V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2982825	NM_030912.3(TRIM8):c.1071C>T (p.Pro357=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2981963	NM_030912.3(TRIM8):c.742C>G (p.Arg248Gly)	TRIM8 (R216G +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 2978871	NM_030912.3(TRIM8):c.1341C>T (p.Pro447=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2978379	NM_030912.3(TRIM8):c.655C>T (p.Arg219Cys)	TRIM8 (R219C)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2976882	NM_030912.3(TRIM8):c.900+16G>A	TRIM8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2976414	NM_030912.3(TRIM8):c.191G>C (p.Gly64Ala)	LOC130004618, TRIM8 (G64A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2974305	NM_030912.3(TRIM8):c.426C>T (p.Ala142=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2974067	NM_030912.3(TRIM8):c.828G>A (p.Met276Ile)	TRIM8 (M276I +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2973687	NM_030912.3(TRIM8):c.400C>A (p.Leu134Met)	TRIM8 (L134M)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2967205	NM_030912.3(TRIM8):c.1470C>T (p.Ser490=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2966658	NM_030912.3(TRIM8):c.357G>A (p.Val119=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	TRIM8-related disorder +1 more	GLikely benign
Select item 2964991	NM_030912.3(TRIM8):c.1466G>A (p.Arg489His)	TRIM8 (R457H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2964450	NM_030912.3(TRIM8):c.742C>T (p.Arg248Trp)	TRIM8 (R216W +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2962889	NM_030912.3(TRIM8):c.1383C>T (p.Gly461=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2955878	NM_030912.3(TRIM8):c.1191C>T (p.Gly397=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2920183	NM_030912.3(TRIM8):c.1064C>T (p.Pro355Leu)	TRIM8 (P355L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2917699	NM_030912.3(TRIM8):c.817G>A (p.Gly273Arg)	TRIM8 (G241R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2909466	NM_030912.3(TRIM8):c.1102G>A (p.Gly368Ser)	TRIM8 (G336S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2906136	NM_030912.3(TRIM8):c.1518C>T (p.Leu506=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2903238	NM_030912.3(TRIM8):c.519G>C (p.Ala173=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2903237	NM_030912.3(TRIM8):c.417C>T (p.Asp139=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2901769	NM_030912.3(TRIM8):c.1649C>G (p.Thr550Arg)	TRIM8 (T518R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2900805	NM_030912.3(TRIM8):c.1014C>T (p.Ala338=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2900015	NM_030912.3(TRIM8):c.996C>T (p.Leu332=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2895075	NM_030912.3(TRIM8):c.415G>A (p.Asp139Asn)	TRIM8 (D139N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2895054	NM_030912.3(TRIM8):c.1062G>A (p.Thr354=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2893774	NM_030912.3(TRIM8):c.1200C>T (p.Tyr400=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2893773	NM_030912.3(TRIM8):c.531C>T (p.His177=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2890556	NM_030912.3(TRIM8):c.1209G>A (p.Ala403=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2889597	NM_030912.3(TRIM8):c.1042C>T (p.Leu348=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2889517	NM_030912.3(TRIM8):c.1291G>A (p.Gly431Ser)	TRIM8 (G431S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2886022	NM_030912.3(TRIM8):c.1179G>A (p.Ser393=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2883041	NM_030912.3(TRIM8):c.1332G>T (p.Ser444=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 2881678	NM_030912.3(TRIM8):c.1305G>A (p.Val435=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2872417	NM_030912.3(TRIM8):c.1282C>T (p.Leu428=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2871192	NM_030912.3(TRIM8):c.691G>A (p.Glu231Lys)	TRIM8 (E199K +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2870250	NM_030912.3(TRIM8):c.667-4G>A	TRIM8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2868681	NM_030912.3(TRIM8):c.448G>T (p.Ala150Ser)	TRIM8 (A150S)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2864800	NM_030912.3(TRIM8):c.486C>A (p.Ala162=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2859125	NM_030912.3(TRIM8):c.32A>T (p.Glu11Val)	TRIM8 (E11V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2846656	NM_030912.3(TRIM8):c.527G>T (p.Gly176Val)	TRIM8 (G176V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2841861	NM_030912.3(TRIM8):c.544G>C (p.Val182Leu)	TRIM8 (V182L)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2836463	NM_030912.3(TRIM8):c.1616T>C (p.Val539Ala)	TRIM8 (V507A +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2835582	NM_030912.3(TRIM8):c.1218C>T (p.Ala406=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2831773	NM_030912.3(TRIM8):c.346C>T (p.Gln116Ter)	TRIM8 (Q116*)	Single nucleotide variant (nonsense +1 more)	not provided	GUncertain significance
Select item 2829926	NM_030912.3(TRIM8):c.1100G>C (p.Cys367Ser)	TRIM8 (C335S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2829247	NM_030912.3(TRIM8):c.295C>T (p.Pro99Ser)	TRIM8 (P99S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2824142	NM_030912.3(TRIM8):c.1089C>G (p.Pro363=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 2815448	NM_030912.3(TRIM8):c.643G>A (p.Glu215Lys)	TRIM8 (E215K)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 2813823	NM_030912.3(TRIM8):c.1471G>T (p.Gly491Cys)	TRIM8 (G459C +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2807761	NM_030912.3(TRIM8):c.1441C>T (p.His481Tyr)	TRIM8 (H449Y +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2806427	NM_030912.3(TRIM8):c.1012G>T (p.Ala338Ser)	TRIM8 (A306S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2806350	NM_030912.3(TRIM8):c.547G>C (p.Glu183Gln)	TRIM8 (E183Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2804735	NM_030912.3(TRIM8):c.1048+14G>A	TRIM8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2803022	NM_030912.3(TRIM8):c.147C>T (p.Leu49=)	LOC130004618, TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2802504	NM_030912.3(TRIM8):c.1167A>G (p.Leu389=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2801542	NM_030912.3(TRIM8):c.964C>A (p.Pro322Thr)	TRIM8 (P322T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2798948	NM_030912.3(TRIM8):c.1185T>C (p.Pro395=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2796831	NM_030912.3(TRIM8):c.246C>T (p.His82=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2795691	NM_030912.3(TRIM8):c.1392G>A (p.Lys464=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2792545	NM_030912.3(TRIM8):c.1563C>G (p.Val521=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2790998	NM_030912.3(TRIM8):c.603G>A (p.Glu201=)	TRIM8	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2786789	NM_030912.3(TRIM8):c.1039A>C (p.Met347Leu)	TRIM8 (M315L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2785628	NM_030912.3(TRIM8):c.608G>A (p.Arg203Gln)	TRIM8 (R203Q)	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign
Select item 2785034	NM_030912.3(TRIM8):c.1630T>C (p.Ser544Pro)	TRIM8 (S544P +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2780907	NM_030912.3(TRIM8):c.822G>A (p.Glu274=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2777887	NM_030912.3(TRIM8):c.1301C>T (p.Pro434Leu)	TRIM8 (P434L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2776968	NM_030912.3(TRIM8):c.450C>T (p.Ala150=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2776337	NM_030912.3(TRIM8):c.90C>T (p.Cys30=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2770952	NM_030912.3(TRIM8):c.1352C>T (p.Ala451Val)	TRIM8 (A419V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2766442	NM_030912.3(TRIM8):c.422G>C (p.Arg141Pro)	TRIM8 (R141P)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2765980	NM_030912.3(TRIM8):c.471_472delinsTA (p.Glu157_Ala158delinsAspThr)	TRIM8	Indel (missense variant +1 more)	not provided	GUncertain significance
Select item 2765777	NM_030912.3(TRIM8):c.796G>T (p.Ala266Ser)	TRIM8 (A234S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2755255	NM_030912.3(TRIM8):c.1127A>T (p.Lys376Met)	TRIM8 (K344M +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2748562	NM_030912.3(TRIM8):c.570+7A>G	TRIM8	Single nucleotide variant (intron variant)	not provided	GLikely benign

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