Tbc1d16 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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115 records found for search term Tbc1d16

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15194353	CV756196	single nucleotide variant	NM_019020.4(TBC1D16):c.66C>A (p.Pro22=)	not provided [RCV000911101]	benign	17	80013482	80013482	Human		name
156327744	CV2217346	single nucleotide variant	NM_019020.4(TBC1D16):c.23G>A (p.Arg8His)	not specified [RCV004087782]	uncertain significance	17	80013525	80013525	Human		name
405780399	CV3335074	single nucleotide variant	NM_019020.4(TBC1D16):c.26G>T (p.Arg9Met)	not specified [RCV004471852]	uncertain significance	17	80013522	80013522	Human		name
329353973	CV2436700	single nucleotide variant	NM_019020.4(TBC1D16):c.58C>T (p.Leu20Phe)	not specified [RCV004258070]	uncertain significance	17	80013490	80013490	Human		name
407512254	CV3475448	single nucleotide variant	NM_019020.4(TBC1D16):c.67G>A (p.Gly23Ser)	not specified [RCV004673383]	uncertain significance	17	80013481	80013481	Human		name
407530607	CV3475450	single nucleotide variant	NM_019020.4(TBC1D16):c.89C>T (p.Pro30Leu)	not specified [RCV004681999]	uncertain significance	17	80013459	80013459	Human		name
597760730	CV3609383	single nucleotide variant	NM_019020.4(TBC1D16):c.38A>G (p.Lys13Arg)	not specified [RCV004869291]	uncertain significance	17	80013510	80013510	Human		name
597760859	CV3609388	single nucleotide variant	NM_019020.4(TBC1D16):c.49C>T (p.Leu17Phe)	not specified [RCV004869296]	uncertain significance	17	80013499	80013499	Human		name
598195983	CV3916621	single nucleotide variant	NM_019020.4(TBC1D16):c.786G>A (p.Pro262=)	not specified [RCV005289342]	likely benign	17	79952812	79952812	Human		name
15173092	CV715774	single nucleotide variant	NM_019020.4(TBC1D16):c.570C>T (p.Val190=)	not provided [RCV000972545]	benign	17	80010369	80010369	Human		name
401896229	CV2773854	single nucleotide variant	NM_019020.4(TBC1D16):c.215T>C (p.Met72Thr)	not specified [RCV004358295]	uncertain significance	17	80010724	80010724	Human		name
401906607	CV2818027	single nucleotide variant	NM_019020.4(TBC1D16):c.1965C>T (p.Asp655=)	not provided [RCV003421531]	likely benign	17	79942150	79942150	Human		name
405780406	CV3335075	single nucleotide variant	NM_019020.4(TBC1D16):c.284T>C (p.Leu95Pro)	not specified [RCV004471853]	uncertain significance	17	80010655	80010655	Human		name
407512363	CV3475446	single nucleotide variant	NM_019020.4(TBC1D16):c.209A>G (p.Asp70Gly)	not specified [RCV004673381]	uncertain significance	17	80010730	80010730	Human		name
407512194	CV3475454	single nucleotide variant	NM_019020.4(TBC1D16):c.110T>C (p.Ile37Thr)	not specified [RCV004673388]	uncertain significance	17	80013438	80013438	Human		name
15174363	CV727492	single nucleotide variant	NM_019020.4(TBC1D16):c.1944C>T (p.Ile648=)	not provided [RCV000884118]	benign	17	79942171	79942171	Human		name
156238019	CV2193604	single nucleotide variant	NM_019020.4(TBC1D16):c.494C>T (p.Ala165Val)	not specified [RCV004074210]	uncertain significance	17	80010445	80010445	Human		name
156190474	CV2226909	single nucleotide variant	NM_019020.4(TBC1D16):c.545G>A (p.Ser182Asn)	not specified [RCV004103881]	uncertain significance	17	80010394	80010394	Human		name
156284551	CV2259355	single nucleotide variant	NM_019020.4(TBC1D16):c.361G>A (p.Ala121Thr)	not specified [RCV004122596]	uncertain significance	17	80010578	80010578	Human		name
156285356	CV2317625	single nucleotide variant	NM_019020.4(TBC1D16):c.380C>A (p.Pro127Gln)	not specified [RCV004172562]	uncertain significance	17	80010559	80010559	Human		name
156038249	CV2332614	single nucleotide variant	NM_019020.4(TBC1D16):c.608G>A (p.Arg203Gln)	not specified [RCV004189295]	uncertain significance	17	80010331	80010331	Human		name
156273432	CV2334020	single nucleotide variant	NM_019020.4(TBC1D16):c.616G>A (p.Ala206Thr)	not specified [RCV004183546]	uncertain significance	17	80010323	80010323	Human		name
156127302	CV2351178	single nucleotide variant	NM_019020.4(TBC1D16):c.734C>T (p.Ala245Val)	not specified [RCV004214030]	uncertain significance	17	80010205	80010205	Human		name
156341969	CV2368488	single nucleotide variant	NM_019020.4(TBC1D16):c.929G>A (p.Arg310His)	not specified [RCV004221289]	uncertain significance	17	79952669	79952669	Human		name
156040668	CV2387631	single nucleotide variant	NM_019020.4(TBC1D16):c.607C>T (p.Arg203Trp)	not specified [RCV004234179]	uncertain significance	17	80010332	80010332	Human		name
156049617	CV2391098	single nucleotide variant	NM_019020.4(TBC1D16):c.809G>A (p.Arg270Gln)	not specified [RCV004235083]	uncertain significance	17	79952789	79952789	Human		name
155998941	CV2396335	single nucleotide variant	NM_019020.4(TBC1D16):c.347C>T (p.Thr116Ile)	not specified [RCV004242063]	uncertain significance	17	80010592	80010592	Human		name
329361291	CV2436863	single nucleotide variant	NM_019020.4(TBC1D16):c.844C>T (p.Arg282Cys)	not specified [RCV004260252]	uncertain significance	17	79952754	79952754	Human		name
329353213	CV2468940	single nucleotide variant	NM_019020.4(TBC1D16):c.425T>C (p.Leu142Pro)	not specified [RCV004274207]	uncertain significance	17	80010514	80010514	Human		name
401751984	CV2672642	single nucleotide variant	NM_019020.4(TBC1D16):c.817G>A (p.Asp273Asn)	not specified [RCV004287665]	uncertain significance	17	79952781	79952781	Human		name
401743861	CV2684797	single nucleotide variant	NM_019020.4(TBC1D16):c.749G>A (p.Arg250His)	not specified [RCV004293872]	uncertain significance	17	80010190	80010190	Human		name
401740779	CV2702627	single nucleotide variant	NM_019020.4(TBC1D16):c.331C>T (p.Pro111Ser)	not specified [RCV004318897]	uncertain significance	17	80010608	80010608	Human		name
401752464	CV2723245	single nucleotide variant	NM_019020.4(TBC1D16):c.367C>T (p.His123Tyr)	not specified [RCV004329479]	uncertain significance	17	80010572	80010572	Human		name
401728907	CV2729897	single nucleotide variant	NM_019020.4(TBC1D16):c.649G>C (p.Ala217Pro)	not specified [RCV004332900]	uncertain significance	17	80010290	80010290	Human		name
401880679	CV2766194	single nucleotide variant	NM_019020.4(TBC1D16):c.796G>A (p.Asp266Asn)	not specified [RCV004340636]	uncertain significance	17	79952802	79952802	Human		name
401876536	CV2767625	single nucleotide variant	NM_019020.4(TBC1D16):c.391C>T (p.Arg131Trp)	not specified [RCV004343769]	uncertain significance	17	80010548	80010548	Human		name
405780414	CV3335076	single nucleotide variant	NM_019020.4(TBC1D16):c.349C>T (p.Arg117Trp)	not specified [RCV004471854]	uncertain significance	17	80010590	80010590	Human		name
405780419	CV3335077	single nucleotide variant	NM_019020.4(TBC1D16):c.380C>T (p.Pro127Leu)	not specified [RCV004471855]	uncertain significance	17	80010559	80010559	Human		name
405780430	CV3335079	single nucleotide variant	NM_019020.4(TBC1D16):c.404C>T (p.Thr135Ile)	not specified [RCV004471857]	likely benign	17	80010535	80010535	Human		name
405780436	CV3335080	single nucleotide variant	NM_019020.4(TBC1D16):c.530C>T (p.Ser177Leu)	not specified [RCV004471858]	uncertain significance	17	80010409	80010409	Human		name
405780442	CV3335081	single nucleotide variant	NM_019020.4(TBC1D16):c.605C>T (p.Pro202Leu)	not specified [RCV004471859]	likely benign	17	80010334	80010334	Human		name
405780455	CV3335083	single nucleotide variant	NM_019020.4(TBC1D16):c.808C>T (p.Arg270Trp)	not specified [RCV004471861]	uncertain significance	17	79952790	79952790	Human		name
405780461	CV3335084	single nucleotide variant	NM_019020.4(TBC1D16):c.887G>A (p.Cys296Tyr)	not specified [RCV004471862]	uncertain significance	17	79952711	79952711	Human		name
405780473	CV3335086	single nucleotide variant	NM_019020.4(TBC1D16):c.889G>A (p.Gly297Ser)	not specified [RCV004471864]	uncertain significance	17	79952709	79952709	Human		name
405780479	CV3335087	single nucleotide variant	NM_019020.4(TBC1D16):c.980G>A (p.Ser327Asn)	not specified [RCV004471865]	uncertain significance	17	79951559	79951559	Human		name
407512367	CV3475445	single nucleotide variant	NM_019020.4(TBC1D16):c.863G>A (p.Arg288Gln)	not specified [RCV004673380]	uncertain significance	17	79952735	79952735	Human		name
407512359	CV3475447	single nucleotide variant	NM_019020.4(TBC1D16):c.757G>A (p.Val253Met)	not specified [RCV004673382]	uncertain significance	17	80010182	80010182	Human		name
407512188	CV3475452	single nucleotide variant	NM_019020.4(TBC1D16):c.983G>A (p.Arg328Gln)	not specified [RCV004673386]	uncertain significance	17	79951556	79951556	Human		name
597760682	CV3609369	single nucleotide variant	NM_019020.4(TBC1D16):c.452G>A (p.Arg151His)	not specified [RCV004869280]	uncertain significance	17	80010487	80010487	Human		name
597760690	CV3609372	single nucleotide variant	NM_019020.4(TBC1D16):c.356C>T (p.Ser119Leu)	not specified [RCV004869282]	uncertain significance	17	80010583	80010583	Human		name
597760726	CV3609382	single nucleotide variant	NM_019020.4(TBC1D16):c.557T>A (p.Ile186Asn)	not specified [RCV004869290]	uncertain significance	17	80010382	80010382	Human		name
597760735	CV3609384	single nucleotide variant	NM_019020.4(TBC1D16):c.990C>G (p.Ser330Arg)	not specified [RCV004869292]	uncertain significance	17	79951549	79951549	Human		name
597760738	CV3609385	single nucleotide variant	NM_019020.4(TBC1D16):c.733G>A (p.Ala245Thr)	not specified [RCV004869293]	uncertain significance	17	80010206	80010206	Human		name
597760854	CV3609387	single nucleotide variant	NM_019020.4(TBC1D16):c.785C>G (p.Pro262Arg)	not specified [RCV004869295]	uncertain significance	17	79952813	79952813	Human		name
598265376	CV3916611	single nucleotide variant	NM_019020.4(TBC1D16):c.719C>T (p.Ser240Leu)	not specified [RCV005280973]	uncertain significance	17	80010220	80010220	Human		name
598265371	CV3916612	single nucleotide variant	NM_019020.4(TBC1D16):c.731C>T (p.Ala244Val)	not specified [RCV005280974]	uncertain significance	17	80010208	80010208	Human		name
598195955	CV3916616	single nucleotide variant	NM_019020.4(TBC1D16):c.340C>T (p.Arg114Trp)	not specified [RCV005289337]	uncertain significance	17	80010599	80010599	Human		name
598195977	CV3916620	single nucleotide variant	NM_019020.4(TBC1D16):c.427G>A (p.Val143Met)	not specified [RCV005289341]	uncertain significance	17	80010512	80010512	Human		name
598195988	CV3916622	single nucleotide variant	NM_019020.4(TBC1D16):c.844C>G (p.Arg282Gly)	not specified [RCV005289343]	uncertain significance	17	79952754	79952754	Human		name
156261301	CV2204889	single nucleotide variant	NM_019020.4(TBC1D16):c.1757C>T (p.Thr586Met)	not specified [RCV004075131]	uncertain significance	17	79945059	79945059	Human		name
156132481	CV2235320	single nucleotide variant	NM_019020.4(TBC1D16):c.1508G>C (p.Arg503Pro)	not specified [RCV004107351]	uncertain significance	17	79948905	79948905	Human		name
156070300	CV2237195	single nucleotide variant	NM_019020.4(TBC1D16):c.1858C>T (p.Pro620Ser)	not specified [RCV004114935]	uncertain significance	17	79944958	79944958	Human		name
155949012	CV2242607	single nucleotide variant	NM_019020.4(TBC1D16):c.1175T>C (p.Met392Thr)	not specified [RCV004113668]	uncertain significance	17	79950493	79950493	Human		name
156209416	CV2250212	single nucleotide variant	NM_019020.4(TBC1D16):c.1741G>A (p.Glu581Lys)	not specified [RCV004117004]	uncertain significance	17	79945075	79945075	Human		name
156197395	CV2259265	single nucleotide variant	NM_019020.4(TBC1D16):c.1739G>A (p.Arg580His)	not specified [RCV004122285]	uncertain significance	17	79945077	79945077	Human		name
156250608	CV2273310	single nucleotide variant	NM_019020.4(TBC1D16):c.1018G>A (p.Gly340Ser)	not specified [RCV004132102]	uncertain significance	17	79951521	79951521	Human		name
156168761	CV2315410	single nucleotide variant	NM_019020.4(TBC1D16):c.2051G>A (p.Arg684Gln)	not specified [RCV004167372]	uncertain significance	17	79942064	79942064	Human		name
156355642	CV2324522	single nucleotide variant	NM_019020.4(TBC1D16):c.1537A>G (p.Met513Val)	not specified [RCV004179001]	uncertain significance	17	79948876	79948876	Human		name
156252819	CV2325437	single nucleotide variant	NM_019020.4(TBC1D16):c.2290G>A (p.Gly764Ser)	not specified [RCV004179892]	uncertain significance	17	79940873	79940873	Human		name
156174962	CV2327029	single nucleotide variant	NM_019020.4(TBC1D16):c.2165C>A (p.Ala722Glu)	not specified [RCV004178618]	uncertain significance	17	79940998	79940998	Human		name
155919336	CV2360227	single nucleotide variant	NM_019020.4(TBC1D16):c.1805T>C (p.Leu602Pro)	not specified [RCV004208575]	uncertain significance	17	79945011	79945011	Human		name
156166759	CV2373628	single nucleotide variant	NM_019020.4(TBC1D16):c.2038G>C (p.Glu680Gln)	not specified [RCV004222719]	uncertain significance	17	79942077	79942077	Human		name
156091305	CV2384660	single nucleotide variant	NM_019020.4(TBC1D16):c.2050C>T (p.Arg684Trp)	not specified [RCV004232437]	uncertain significance	17	79942065	79942065	Human		name
156006948	CV2394279	single nucleotide variant	NM_019020.4(TBC1D16):c.1042G>A (p.Val348Met)	not specified [RCV004238510]	uncertain significance	17	79951497	79951497	Human		name
329367823	CV2427577	single nucleotide variant	NM_019020.4(TBC1D16):c.2093G>A (p.Arg698Gln)	not specified [RCV004250213]	uncertain significance	17	79941070	79941070	Human		name
329395516	CV2458432	single nucleotide variant	NM_019020.4(TBC1D16):c.2227A>G (p.Met743Val)	not specified [RCV004266061]	uncertain significance	17	79940936	79940936	Human		name
329387273	CV2463508	single nucleotide variant	NM_019020.4(TBC1D16):c.2212G>A (p.Gly738Arg)	not specified [RCV004277325]	uncertain significance	17	79940951	79940951	Human		name
329361909	CV2468437	single nucleotide variant	NM_019020.4(TBC1D16):c.2097C>G (p.Ile699Met)	not specified [RCV004277744]	uncertain significance	17	79941066	79941066	Human		name
401739149	CV2673232	single nucleotide variant	NM_019020.4(TBC1D16):c.1222C>A (p.Leu408Met)	not specified [RCV004286039]	uncertain significance	17	79950446	79950446	Human		name
401732825	CV2691121	single nucleotide variant	NM_019020.4(TBC1D16):c.1812G>T (p.Met604Ile)	not specified [RCV004301116]	uncertain significance	17	79945004	79945004	Human		name
401779742	CV2714731	single nucleotide variant	NM_019020.4(TBC1D16):c.1910C>T (p.Thr637Met)	not specified [RCV004320303]	uncertain significance	17	79942205	79942205	Human		name
401862965	CV2755744	single nucleotide variant	NM_019020.4(TBC1D16):c.1738C>T (p.Arg580Cys)	not specified [RCV004342124]	uncertain significance	17	79945078	79945078	Human		name
401864494	CV2760933	single nucleotide variant	NM_019020.4(TBC1D16):c.2191G>A (p.Gly731Ser)	not specified [RCV004336565]	uncertain significance	17	79940972	79940972	Human		name
401865805	CV2786133	single nucleotide variant	NM_019020.4(TBC1D16):c.2035G>A (p.Gly679Arg)	not specified [RCV004359939]	uncertain significance	17	79942080	79942080	Human		name
405780329	CV3324693	single nucleotide variant	NM_019020.4(TBC1D16):c.1380G>T (p.Lys460Asn)	not specified [RCV004471841]	uncertain significance	17	79949743	79949743	Human		name
405780337	CV3324694	single nucleotide variant	NM_019020.4(TBC1D16):c.1462G>A (p.Val488Met)	not specified [RCV004471842]	uncertain significance	17	79948951	79948951	Human		name
405780349	CV3324696	single nucleotide variant	NM_019020.4(TBC1D16):c.1825C>T (p.Arg609Cys)	not specified [RCV004471844]	uncertain significance	17	79944991	79944991	Human		name
405780357	CV3324697	single nucleotide variant	NM_019020.4(TBC1D16):c.1988C>T (p.Thr663Met)	not specified [RCV004471845]	uncertain significance	17	79942127	79942127	Human		name
405780361	CV3324698	single nucleotide variant	NM_019020.4(TBC1D16):c.2011G>A (p.Gly671Arg)	not specified [RCV004471846]	uncertain significance	17	79942104	79942104	Human		name
405780373	CV3335070	single nucleotide variant	NM_019020.4(TBC1D16):c.2113G>A (p.Asp705Asn)	not specified [RCV004471848]	uncertain significance	17	79941050	79941050	Human		name
405780379	CV3335071	single nucleotide variant	NM_019020.4(TBC1D16):c.2180G>A (p.Gly727Asp)	not specified [RCV004471849]	uncertain significance	17	79940983	79940983	Human		name
405780387	CV3335072	single nucleotide variant	NM_019020.4(TBC1D16):c.2276C>T (p.Pro759Leu)	not specified [RCV004471850]	uncertain significance	17	79940887	79940887	Human		name
407512182	CV3475449	single nucleotide variant	NM_019020.4(TBC1D16):c.1862A>G (p.Glu621Gly)	not specified [RCV004673384]	uncertain significance	17	79944954	79944954	Human		name
407512185	CV3475451	single nucleotide variant	NM_019020.4(TBC1D16):c.1129C>A (p.Arg377Ser)	not specified [RCV004673385]	uncertain significance	17	79950539	79950539	Human		name
407512191	CV3475453	single nucleotide variant	NM_019020.4(TBC1D16):c.1973A>G (p.Glu658Gly)	not specified [RCV004673387]	uncertain significance	17	79942142	79942142	Human		name
597760677	CV3609368	single nucleotide variant	NM_019020.4(TBC1D16):c.2176A>G (p.Thr726Ala)	not specified [RCV004869279]	uncertain significance	17	79940987	79940987	Human		name
597760686	CV3609371	single nucleotide variant	NM_019020.4(TBC1D16):c.2092C>T (p.Arg698Trp)	not specified [RCV004869281]	uncertain significance	17	79941071	79941071	Human		name
597760695	CV3609373	single nucleotide variant	NM_019020.4(TBC1D16):c.1508G>A (p.Arg503Gln)	not specified [RCV004869283]	uncertain significance	17	79948905	79948905	Human		name
597794823	CV3609374	single nucleotide variant	NM_019020.4(TBC1D16):c.1871C>T (p.Ala624Val)	not specified [RCV004877987]	uncertain significance	17	79944945	79944945	Human		name
597760700	CV3609375	single nucleotide variant	NM_019020.4(TBC1D16):c.1175T>A (p.Met392Lys)	not specified [RCV004869284]	uncertain significance	17	79950493	79950493	Human		name
597760704	CV3609376	single nucleotide variant	NM_019020.4(TBC1D16):c.1613C>T (p.Ala538Val)	not specified [RCV004869285]	uncertain significance	17	79947760	79947760	Human		name
597760708	CV3609377	single nucleotide variant	NM_019020.4(TBC1D16):c.2014A>G (p.Asn672Asp)	not specified [RCV004869286]	uncertain significance	17	79942101	79942101	Human		name
597760712	CV3609378	single nucleotide variant	NM_019020.4(TBC1D16):c.2230C>A (p.Pro744Thr)	not specified [RCV004869287]	uncertain significance	17	79940933	79940933	Human		name
597760717	CV3609379	single nucleotide variant	NM_019020.4(TBC1D16):c.1032G>C (p.Lys344Asn)	not specified [RCV004869288]	uncertain significance	17	79951507	79951507	Human		name
597760721	CV3609381	single nucleotide variant	NM_019020.4(TBC1D16):c.1385A>C (p.Tyr462Ser)	not specified [RCV004869289]	uncertain significance	17	79949738	79949738	Human		name
597760851	CV3609386	single nucleotide variant	NM_019020.4(TBC1D16):c.1465G>T (p.Asp489Tyr)	not specified [RCV004869294]	uncertain significance	17	79948948	79948948	Human		name
598195946	CV3916613	single nucleotide variant	NM_019020.4(TBC1D16):c.2219C>T (p.Thr740Met)	not specified [RCV005289335]	uncertain significance	17	79940944	79940944	Human		name
598195951	CV3916614	single nucleotide variant	NM_019020.4(TBC1D16):c.1861G>A (p.Glu621Lys)	not specified [RCV005289336]	uncertain significance	17	79944955	79944955	Human		name
598265366	CV3916615	single nucleotide variant	NM_019020.4(TBC1D16):c.1690G>A (p.Val564Ile)	not specified [RCV005280975]	uncertain significance	17	79947683	79947683	Human		name
598195965	CV3916618	single nucleotide variant	NM_019020.4(TBC1D16):c.1162C>A (p.Pro388Thr)	not specified [RCV005289339]	uncertain significance	17	79950506	79950506	Human		name
598195971	CV3916619	single nucleotide variant	NM_019020.4(TBC1D16):c.1936G>A (p.Val646Met)	not specified [RCV005289340]	uncertain significance	17	79942179	79942179	Human		name
598265361	CV3916623	single nucleotide variant	NM_019020.4(TBC1D16):c.1994A>G (p.Gln665Arg)	not specified [RCV005280976]	uncertain significance	17	79942121	79942121	Human		name
598265354	CV3916624	single nucleotide variant	NM_019020.4(TBC1D16):c.1765C>T (p.Arg589Cys)	not specified [RCV005280977]	uncertain significance	17	79945051	79945051	Human		name
598195993	CV3916625	single nucleotide variant	NM_019020.4(TBC1D16):c.1627G>A (p.Glu543Lys)	not specified [RCV005289344]	uncertain significance	17	79947746	79947746	Human		name
8636379	CV91602	single nucleotide variant	NM_019020.3(TBC1D16):c.1306C>T (p.Pro436Ser)	Malignant melanoma [RCV000071700]	not provided	17	79949817	79949817	Human		name

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