ClinVar for Gene (Select 10131) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3356972	NM_016292.3(TRAP1):c.1166-4C>T	TRAP1	Single nucleotide variant (intron variant)	TRAP1-related disorder	GLikely benign
Select item 3352366	NM_016292.3(TRAP1):c.1086C>T (p.Ser362=)	TRAP1	Single nucleotide variant (synonymous variant)	TRAP1-related disorder	GLikely benign
Select item 3351598	NM_016292.3(TRAP1):c.1938_1940+8dup	DNASE1, TRAP1	Duplication (intron variant +1 more)	TRAP1-related disorder	GUncertain significance
Select item 3348712	NM_016292.3(TRAP1):c.1483C>T (p.Arg495Cys)	DNASE1, TRAP1 (R442C +1 more)	Single nucleotide variant (missense variant +1 more)	TRAP1-related disorder	GUncertain significance
Select item 3328513	NM_016292.3(TRAP1):c.678C>G (p.Ser226Arg)	TRAP1 (S173R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328512	NM_016292.3(TRAP1):c.1703C>T (p.Ser568Phe)	DNASE1, TRAP1 (S515F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3328510	NM_016292.3(TRAP1):c.1715A>T (p.Glu572Val)	DNASE1, TRAP1 (E519V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3328509	NM_016292.3(TRAP1):c.2041G>A (p.Gly681Arg)	DNASE1, TRAP1 (G681R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3328508	NM_016292.3(TRAP1):c.1493A>G (p.Tyr498Cys)	DNASE1, TRAP1 (Y498C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3328507	NM_016292.3(TRAP1):c.1612C>G (p.His538Asp)	DNASE1, TRAP1 (H538D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3328506	NM_016292.3(TRAP1):c.277G>C (p.Glu93Gln)	TRAP1 (E40Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328505	NM_016292.3(TRAP1):c.190G>A (p.Ala64Thr)	TRAP1 (A64T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3328504	NM_016292.3(TRAP1):c.148G>T (p.Ala50Ser)	TRAP1 (A50S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3328503	NM_016292.3(TRAP1):c.724G>A (p.Ala242Thr)	TRAP1 (A242T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328501	NM_016292.3(TRAP1):c.594C>G (p.Ile198Met)	TRAP1 (I198M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328500	NM_016292.3(TRAP1):c.521C>T (p.Thr174Met)	TRAP1 (T174M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328499	NM_016292.3(TRAP1):c.140G>A (p.Arg47Gln)	TRAP1 (R47Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3328498	NM_016292.3(TRAP1):c.766C>A (p.His256Asn)	TRAP1 (H203N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3243654	NC_000016.9:g.(?_3705375)_(3741006_?)del	DNASE1, TRAP1	Deletion	not provided	GUncertain significance
Select item 3243653	NC_000016.9:g.(?_3708774)_(3716139_?)del	TRAP1	Deletion	not provided	GUncertain significance
Select item 3243652	NC_000016.9:g.(?_3726017)_(3726166_?)del	TRAP1	Deletion	not provided	GUncertain significance
Select item 3243222	NC_000016.9:g.(?_339420)_(3767509_?)dup	ABCA3, AMDHD2 +142 more	Duplication	Idiopathic generalized epilepsy +2 more	GUncertain significance
Select item 3181935	NM_016292.3(TRAP1):c.875T>C (p.Met292Thr)	TRAP1 (M292T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181934	NM_016292.3(TRAP1):c.760A>G (p.Ile254Val)	TRAP1 (I254V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181932	NM_016292.3(TRAP1):c.481A>G (p.Ile161Val)	TRAP1 (I161V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181931	NM_016292.3(TRAP1):c.475A>G (p.Thr159Ala)	TRAP1 (T159A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181930	NM_016292.3(TRAP1):c.382C>T (p.Arg128Cys)	TRAP1 (R128C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181929	NM_016292.3(TRAP1):c.356A>G (p.Asn119Ser)	TRAP1 (N119S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181928	NM_016292.3(TRAP1):c.266A>T (p.Glu89Val)	TRAP1 (E89V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181927	NM_016292.3(TRAP1):c.215A>C (p.His72Pro)	TRAP1 (H72P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181926	NM_016292.3(TRAP1):c.214C>T (p.His72Tyr)	TRAP1 (H72Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181925	NM_016292.3(TRAP1):c.2005G>C (p.Val669Leu)	DNASE1, TRAP1 (V616L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181924	NM_016292.3(TRAP1):c.1894G>C (p.Glu632Gln)	DNASE1, TRAP1 (E579Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181923	NM_016292.3(TRAP1):c.1871T>C (p.Met624Thr)	TRAP1, DNASE1 (M624T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181922	NM_016292.3(TRAP1):c.1795G>A (p.Val599Met)	DNASE1, TRAP1 (V546M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181921	NM_016292.3(TRAP1):c.1783A>G (p.Thr595Ala)	DNASE1, TRAP1 (T542A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181919	NM_016292.3(TRAP1):c.1394C>G (p.Ala465Gly)	DNASE1, TRAP1 (A412G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181918	NM_016292.3(TRAP1):c.1334G>A (p.Gly445Asp)	TRAP1 (G392D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181917	NM_016292.3(TRAP1):c.1207G>A (p.Glu403Lys)	TRAP1 (E403K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3060936	NM_016292.3(TRAP1):c.1940+8C>T	DNASE1, TRAP1	Single nucleotide variant (intron variant)	TRAP1-related disorder	GLikely benign
Select item 3058630	NM_016292.3(TRAP1):c.330+4C>T	TRAP1	Single nucleotide variant (intron variant)	TRAP1-related disorder	GLikely benign
Select item 3058013	NM_016292.3(TRAP1):c.472-6C>T	TRAP1	Single nucleotide variant (intron variant)	TRAP1-related disorder	GLikely benign
Select item 3054502	NM_016292.3(TRAP1):c.1242C>G (p.Leu414=)	TRAP1	Single nucleotide variant (synonymous variant)	TRAP1-related disorder	GLikely benign
Select item 3053516	NM_016292.3(TRAP1):c.252C>A (p.Ser84=)	TRAP1	Single nucleotide variant (synonymous variant)	TRAP1-related disorder	GLikely benign
Select item 3052737	NM_016292.3(TRAP1):c.1233C>T (p.Ile411=)	TRAP1	Single nucleotide variant (synonymous variant)	TRAP1-related disorder	GLikely benign
Select item 3051937	NM_016292.3(TRAP1):c.966C>T (p.His322=)	TRAP1	Single nucleotide variant (synonymous variant)	TRAP1-related disorder	GLikely benign
Select item 3047096	NM_016292.3(TRAP1):c.1775C>T (p.Ser592Leu)	DNASE1, TRAP1 (S539L +1 more)	Single nucleotide variant (missense variant +1 more)	TRAP1-related disorder	GUncertain significance
Select item 3036941	NM_016292.3(TRAP1):c.1394C>A (p.Ala465Glu)	DNASE1, TRAP1 (A412E +1 more)	Single nucleotide variant (missense variant +1 more)	TRAP1-related disorder	GLikely benign
Select item 3032495	NM_016292.3(TRAP1):c.189C>T (p.Thr63=)	TRAP1	Single nucleotide variant (synonymous variant +1 more)	TRAP1-related disorder	GLikely benign
Select item 3031018	NM_016292.3(TRAP1):c.90A>G (p.Gly30=)	TRAP1	Single nucleotide variant (synonymous variant +1 more)	TRAP1-related disorder	GLikely benign
Select item 3024595	GRCh37/hg19 16p13.3(chr16:2990033-4837646)x1	CORO7, CORO7-PAM16 +52 more	Copy number loss	not provided	GPathogenic
Select item 3017584	NM_016292.3(TRAP1):c.1045-10T>A	TRAP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3011022	NM_016292.3(TRAP1):c.1916A>T (p.Gln639Leu)	DNASE1, TRAP1 (Q586L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3009129	NM_016292.3(TRAP1):c.789G>A (p.Glu263=)	TRAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3008016	NM_016292.3(TRAP1):c.1617T>C (p.Leu539=)	DNASE1, TRAP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3002701	NM_016292.3(TRAP1):c.948C>T (p.Arg316=)	TRAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2985801	NM_016292.3(TRAP1):c.3G>A (p.Met1Ile)	LOC130058352, TRAP1 (M1I)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2979460	NM_016292.3(TRAP1):c.2099C>T (p.Ala700Val)	DNASE1, TRAP1 (A647V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2979164	NM_016292.3(TRAP1):c.1518C>T (p.His506=)	DNASE1, TRAP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2978693	NM_016292.3(TRAP1):c.1901G>A (p.Arg634His)	DNASE1, TRAP1 (R581H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2977823	NM_016292.3(TRAP1):c.621A>G (p.Ser207=)	TRAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2976973	NM_016292.3(TRAP1):c.2113T>C (p.Ter705Arg)	DNASE1, TRAP1	Single nucleotide variant (stop lost +1 more)	not provided	GUncertain significance
Select item 2972276	NM_016292.3(TRAP1):c.391C>G (p.Leu131Val)	TRAP1 (L78V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2972168	NM_016292.3(TRAP1):c.734C>T (p.Ser245Leu)	TRAP1 (S192L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2970771	NM_016292.3(TRAP1):c.952G>A (p.Val318Ile)	TRAP1 (V265I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2967360	NM_016292.3(TRAP1):c.1235+15G>A	TRAP1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2965415	NM_016292.3(TRAP1):c.89-14A>G	TRAP1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2963917	NM_016292.3(TRAP1):c.1125G>A (p.Lys375=)	TRAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2963657	NM_016292.3(TRAP1):c.1398G>A (p.Lys466=)	DNASE1, TRAP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2961399	NM_016292.3(TRAP1):c.2014-8C>T	DNASE1, TRAP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2961036	NM_016292.3(TRAP1):c.55C>T (p.Leu19=)	LOC130058352, TRAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2957041	NM_016292.3(TRAP1):c.48G>A (p.Arg16=)	LOC130058352, TRAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2955380	NM_016292.3(TRAP1):c.814+15G>A	TRAP1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2916688	NM_016292.3(TRAP1):c.1018C>T (p.Arg340Cys)	TRAP1 (R340C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2914767	NM_016292.3(TRAP1):c.726C>T (p.Ala242=)	TRAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2911220	NM_016292.3(TRAP1):c.799G>A (p.Glu267Lys)	TRAP1 (E267K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2909724	NM_016292.3(TRAP1):c.1710C>T (p.Ala570=)	DNASE1, TRAP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2908367	NM_016292.3(TRAP1):c.704+9C>T	TRAP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2903673	NM_016292.3(TRAP1):c.1404G>A (p.Leu468=)	DNASE1, TRAP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2903534	NM_016292.3(TRAP1):c.1345C>T (p.Arg449Trp)	TRAP1 (R396W +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2902027	NM_016292.3(TRAP1):c.1778G>C (p.Arg593Pro)	DNASE1, TRAP1 (R593P +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2900753	NM_016292.3(TRAP1):c.1799C>T (p.Thr600Ile)	DNASE1, TRAP1 (T600I +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2895249	NM_016292.3(TRAP1):c.748G>A (p.Gly250Arg)	TRAP1 (G197R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2893507	NM_016292.3(TRAP1):c.1914G>A (p.Leu638=)	TRAP1, DNASE1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2892442	NM_016292.3(TRAP1):c.1106A>G (p.Lys369Arg)	TRAP1 (K316R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2888975	NM_016292.3(TRAP1):c.309G>A (p.Arg103=)	TRAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2884997	NM_016292.3(TRAP1):c.981C>T (p.Tyr327=)	TRAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2884261	NM_016292.3(TRAP1):c.713T>C (p.Val238Ala)	TRAP1 (V185A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2820017	NM_016292.3(TRAP1):c.197A>G (p.Asp66Gly)	TRAP1 (D66G)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2811758	NM_016292.3(TRAP1):c.410C>T (p.Ala137Val)	TRAP1 (A137V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2804664	NM_016292.3(TRAP1):c.351C>A (p.Ile117=)	TRAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2804181	NM_016292.3(TRAP1):c.777C>G (p.Ser259=)	TRAP1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2800352	NM_016292.3(TRAP1):c.704+5G>C	TRAP1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2797717	NM_016292.3(TRAP1):c.1045-3C>G	TRAP1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2796848	NM_016292.3(TRAP1):c.1462A>C (p.Ser488Arg)	DNASE1, TRAP1 (S435R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2791761	NM_016292.3(TRAP1):c.363C>T (p.Ser121=)	TRAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2767645	NM_016292.3(TRAP1):c.889-4C>T	TRAP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2757287	NM_016292.3(TRAP1):c.404G>A (p.Gly135Asp)	TRAP1 (G82D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2756415	NM_016292.3(TRAP1):c.786G>A (p.Lys262=)	TRAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2756026	NM_016292.3(TRAP1):c.663G>T (p.Ser221=)	TRAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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