ClinVar for Gene (Select 64759) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3180871	NM_022748.12(TNS3):c.775C>T (p.Arg259Cys)	TNS3 (R259C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180870	NM_022748.12(TNS3):c.640G>C (p.Gly214Arg)	TNS3 (G214R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180869	NM_022748.12(TNS3):c.574G>A (p.Asp192Asn)	TNS3 (D192N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180868	NM_022748.12(TNS3):c.560G>A (p.Gly187Asp)	TNS3 (G187D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180867	NM_022748.12(TNS3):c.472C>T (p.Arg158Trp)	TNS3 (R272W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180866	NM_022748.12(TNS3):c.4288A>G (p.Ile1430Val)	TNS3 (I1533V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180865	NM_022748.12(TNS3):c.4129A>G (p.Ser1377Gly)	TNS3 (S1377G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180864	NM_022748.12(TNS3):c.3613G>T (p.Ala1205Ser)	TNS3 (A1205S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180863	NM_022748.12(TNS3):c.3449C>T (p.Pro1150Leu)	TNS3 (P1264L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180862	NM_022748.12(TNS3):c.3418G>A (p.Asp1140Asn)	TNS3 (D1140N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180861	NM_022748.12(TNS3):c.3368G>T (p.Ser1123Ile)	TNS3 (S1123I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180860	NM_022748.12(TNS3):c.3082G>A (p.Gly1028Arg)	TNS3 (G1028R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180859	NM_022748.12(TNS3):c.3035C>T (p.Ala1012Val)	TNS3 (A1012V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180858	NM_022748.12(TNS3):c.2890G>T (p.Gly964Cys)	TNS3 (G1078C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180857	NM_022748.12(TNS3):c.2788A>G (p.Ile930Val)	TNS3 (I930V +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3180856	NM_022748.12(TNS3):c.2710G>A (p.Gly904Arg)	TNS3 (G1018R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180855	NM_022748.12(TNS3):c.2474A>G (p.Gln825Arg)	TNS3 (Q928R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180854	NM_022748.12(TNS3):c.2443G>A (p.Val815Ile)	TNS3 (V815I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180852	NM_022748.12(TNS3):c.2253G>C (p.Glu751Asp)	TNS3 (E854D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180851	NM_022748.12(TNS3):c.2231G>A (p.Ser744Asn)	TNS3 (S744N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180850	NM_022748.12(TNS3):c.2221C>T (p.Arg741Trp)	TNS3 (R855W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180849	NM_022748.12(TNS3):c.2158A>G (p.Met720Val)	TNS3 (M823V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180848	NM_022748.12(TNS3):c.1829G>C (p.Arg610Pro)	TNS3 (R713P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180847	NM_022748.12(TNS3):c.136G>A (p.Gly46Arg)	TNS3 (G46R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180845	NM_022748.12(TNS3):c.104A>G (p.Gln35Arg)	TNS3 (Q138R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180844	NM_022748.12(TNS3):c.1005C>G (p.Asn335Lys)	TNS3 (N449K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2657455	NM_022748.12(TNS3):c.327C>T (p.Gly109=)	TNS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2657454	NM_022748.12(TNS3):c.1638C>T (p.Asp546=)	TNS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2657453	NM_022748.12(TNS3):c.1817A>G (p.Asp606Gly)	TNS3 (D606G +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2657452	NM_022748.12(TNS3):c.3378C>T (p.Ser1126=)	TNS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2657451	NM_022748.12(TNS3):c.4181G>A (p.Gly1394Asp)	TNS3 (G1394D +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2624238	NM_022748.12(TNS3):c.2732G>T (p.Arg911Leu)	TNS3 (R1014L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600396	NM_022748.12(TNS3):c.1912A>G (p.Ser638Gly)	TNS3 (S638G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597793	NM_022748.12(TNS3):c.3314C>T (p.Ser1105Leu)	TNS3 (S1105L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592542	NM_022748.12(TNS3):c.2164G>A (p.Ala722Thr)	TNS3 (A825T +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2590038	NM_022748.12(TNS3):c.2639A>G (p.Lys880Arg)	TNS3 (K994R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588461	NM_022748.12(TNS3):c.841A>C (p.Asn281His)	TNS3 (N384H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588038	NM_022748.12(TNS3):c.1834G>A (p.Val612Met)	TNS3 (V715M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570539	NM_022748.12(TNS3):c.2761C>A (p.Gln921Lys)	TNS3 (Q1024K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557219	NM_022748.12(TNS3):c.2894G>T (p.Arg965Leu)	TNS3 (R1079L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555993	NM_022748.12(TNS3):c.1646A>G (p.Tyr549Cys)	TNS3 (Y652C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554313	NM_022748.12(TNS3):c.4153C>T (p.Pro1385Ser)	TNS3 (P1488S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541398	NM_022748.12(TNS3):c.3809C>T (p.Thr1270Met)	TNS3 (T1373M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529617	NM_022748.12(TNS3):c.4282A>G (p.Ser1428Gly)	TNS3 (S1542G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518850	NM_022748.12(TNS3):c.1616C>T (p.Pro539Leu)	TNS3 (P642L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516263	NM_022748.12(TNS3):c.811G>A (p.Gly271Arg)	TNS3 (G385R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515767	NM_022748.12(TNS3):c.939C>A (p.Asn313Lys)	TNS3 (N313K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511972	NM_022748.12(TNS3):c.3220G>A (p.Ala1074Thr)	TNS3 (A1188T +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2491698	NM_022748.12(TNS3):c.3027C>A (p.Asp1009Glu)	TNS3 (D1123E +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2486749	NM_022748.12(TNS3):c.947G>A (p.Gly316Asp)	TNS3 (G316D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479404	NM_022748.12(TNS3):c.3782C>T (p.Thr1261Met)	TNS3 (T1364M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475776	NM_022748.12(TNS3):c.1064C>T (p.Ala355Val)	TNS3 (A458V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473538	NM_022748.12(TNS3):c.1441G>A (p.Glu481Lys)	TNS3 (E595K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472645	NM_022748.12(TNS3):c.1417C>T (p.Arg473Trp)	TNS3 (R473W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463775	NM_022748.12(TNS3):c.2762A>G (p.Gln921Arg)	TNS3 (Q921R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461781	NM_022748.12(TNS3):c.1888C>T (p.Pro630Ser)	TNS3 (P630S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459135	NM_022748.12(TNS3):c.2170G>A (p.Gly724Ser)	TNS3 (G724S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455406	NM_022748.12(TNS3):c.2420C>T (p.Pro807Leu)	TNS3 (P921L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454987	NM_022748.12(TNS3):c.1810G>A (p.Ala604Thr)	TNS3 (A604T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401137	NM_022748.12(TNS3):c.592C>T (p.Arg198Trp)	TNS3 (R198W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399681	NM_022748.12(TNS3):c.1016A>G (p.Asp339Gly)	TNS3 (D442G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398001	NM_022748.12(TNS3):c.3550G>A (p.Ala1184Thr)	TNS3 (A1287T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396724	NM_022748.12(TNS3):c.2581C>T (p.Arg861Cys)	TNS3 (R975C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395904	NM_022748.12(TNS3):c.2608C>A (p.Pro870Thr)	TNS3 (P870T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395449	NM_022748.12(TNS3):c.3976G>A (p.Gly1326Ser)	TNS3 (G1326S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389832	NM_022748.12(TNS3):c.3221C>T (p.Ala1074Val)	TNS3 (A1074V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386696	NM_022748.12(TNS3):c.1508A>C (p.Gln503Pro)	TNS3 (Q503P +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2386644	NM_022748.12(TNS3):c.2343C>G (p.Asp781Glu)	TNS3 (D781E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381785	NM_022748.12(TNS3):c.2659A>G (p.Ser887Gly)	TNS3 (S1001G +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2369302	NM_022748.12(TNS3):c.2375A>G (p.Lys792Arg)	TNS3 (K906R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369301	NM_022748.12(TNS3):c.116G>A (p.Arg39His)	TNS3 (R142H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366642	NM_022748.12(TNS3):c.1957C>A (p.Pro653Thr)	TNS3 (P653T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364939	NM_022748.12(TNS3):c.1343G>A (p.Arg448Gln)	TNS3 (R551Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361689	NM_022748.12(TNS3):c.569A>G (p.Asn190Ser)	TNS3 (N293S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358401	NM_022748.12(TNS3):c.2095A>T (p.Ile699Phe)	TNS3 (I699F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357886	NM_022748.12(TNS3):c.2327G>A (p.Ser776Asn)	TNS3 (S776N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356307	NM_022748.12(TNS3):c.3184G>A (p.Asp1062Asn)	TNS3 (D1062N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353182	NM_022748.12(TNS3):c.2452A>G (p.Thr818Ala)	TNS3 (T818A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348491	NM_022748.12(TNS3):c.2438C>T (p.Ala813Val)	TNS3 (A916V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345785	NM_022748.12(TNS3):c.1598C>T (p.Pro533Leu)	TNS3 (P533L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344179	NM_022748.12(TNS3):c.596C>T (p.Pro199Leu)	TNS3 (P199L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332284	NM_022748.12(TNS3):c.3452T>A (p.Leu1151Gln)	TNS3 (L1254Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331240	NM_022748.12(TNS3):c.1818T>A (p.Asp606Glu)	TNS3 (D606E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329137	NM_022748.12(TNS3):c.2731C>T (p.Arg911Trp)	TNS3 (R1025W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326479	NM_022748.12(TNS3):c.396C>A (p.Asp132Glu)	TNS3 (D246E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320689	NM_022748.12(TNS3):c.3106G>A (p.Asp1036Asn)	TNS3 (D1036N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320556	NM_022748.12(TNS3):c.2295A>C (p.Glu765Asp)	TNS3 (E765D +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2316263	NM_022748.12(TNS3):c.1064C>G (p.Ala355Gly)	TNS3 (A355G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302905	NM_022748.12(TNS3):c.3091C>T (p.Leu1031Phe)	TNS3 (L1145F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300060	NM_022748.12(TNS3):c.2446A>C (p.Lys816Gln)	TNS3 (K816Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275063	NM_022748.12(TNS3):c.1862G>A (p.Gly621Asp)	TNS3 (G724D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264341	NM_022748.12(TNS3):c.1201A>G (p.Arg401Gly)	TNS3 (R401G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262005	NM_022748.12(TNS3):c.2855G>A (p.Ser952Asn)	TNS3 (S1066N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247869	NM_022748.12(TNS3):c.1055G>A (p.Ser352Asn)	TNS3 (S466N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236137	NM_022748.12(TNS3):c.442G>A (p.Val148Ile)	TNS3 (V251I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233135	NM_022748.12(TNS3):c.1490C>T (p.Ser497Phe)	TNS3 (S497F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230401	NM_022748.12(TNS3):c.2131C>G (p.Pro711Ala)	TNS3 (P825A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214481	NM_022748.12(TNS3):c.1829G>A (p.Arg610Gln)	TNS3 (R724Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1708459	GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1	AASS, ABCA13 +896 more	Copy number loss	See cases	GUncertain significance
Select item 1703560	Single allele	CACNA2D1, CADPS2 +896 more	Complex	Ring chromosome 7	GPathogenic

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