Slc9a9 Variant Search Result - Rat Genome Database

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113 records found for search term Slc9a9

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
151353402	CV1326512	single nucleotide variant	NM_173653.4(SLC9A9):c.456+6T>C	not provided [RCV001816368]	likely benign	3	143796820	143796820	Human		name
408365692	CV3508985	single nucleotide variant	NM_173653.4(SLC9A9):c.894+4T>C	SLC9A9-related disorder [RCV004755181]	uncertain significance	3	143578581	143578581	Human		name , trait , alternate_id
15191982	CV730192	single nucleotide variant	NM_173653.4(SLC9A9):c.378+6G>T	not provided [RCV000888533]	benign	3	143832013	143832013	Human		name
15190201	CV777357	deletion	NM_173653.4(SLC9A9):c.176-3del	not provided [RCV000954404]	benign	3	143832224	143832224	Human		name
401924727	CV2805092	single nucleotide variant	NM_173653.4(SLC9A9):c.1000+4A>T	not specified [RCV003404911]	uncertain significance	3	143574084	143574084	Human		name
401925002	CV2805185	single nucleotide variant	NM_173653.4(SLC9A9):c.533+19T>G	not specified [RCV003405006]	likely benign	3	143794982	143794982	Human		name
15097824	CV730191	single nucleotide variant	NM_173653.4(SLC9A9):c.533+10A>G	not provided [RCV000891592]	benign	3	143794991	143794991	Human		name
42723687	CV984561	single nucleotide variant	NM_173653.4(SLC9A9):c.1203+1G>A	Autism, susceptibility to, 16 [RCV001291679]	uncertain significance	3	143495334	143495334	Human	1	name
405654479	CV3228156	single nucleotide variant	NM_173653.4(SLC9A9):c.1604+10G>C	not specified [RCV003994891]	likely benign	3	143363474	143363474	Human		name
8578090	CV112468	single nucleotide variant	NM_173653.3(SLC9A9):c.650-2446G>T	Lung cancer [RCV000092991]	uncertain significance	3	143654806	143654806	Human		name
8578085	CV112463	single nucleotide variant	NM_173653.3(SLC9A9):c.1605-3294C>T	Lung cancer [RCV000092986]	uncertain significance	3	143272274	143272274	Human		name
8578086	CV112464	single nucleotide variant	NM_173653.3(SLC9A9):c.1605-15908A>G	Lung cancer [RCV000092987]	uncertain significance	3	143284888	143284888	Human		name
8578087	CV112465	single nucleotide variant	NM_173653.3(SLC9A9):c.1604+36809A>G	Lung cancer [RCV000092988]	uncertain significance	3	143326675	143326675	Human		name
8578088	CV112466	single nucleotide variant	NM_173653.3(SLC9A9):c.1470-37834C>T	Lung cancer [RCV000092989]	uncertain significance	3	143419948	143419948	Human		name
8578089	CV112467	single nucleotide variant	NM_173653.3(SLC9A9):c.1000+10567T>C	Lung cancer [RCV000092990]	uncertain significance	3	143563521	143563521	Human		name
408380506	CV3517897	single nucleotide variant	NM_173653.4(SLC9A9):c.171G>T (p.Val57=)	SLC9A9-related disorder [RCV004754219]	likely benign	3	143848152	143848152	Human		name , trait , alternate_id
15164879	CV708620	single nucleotide variant	NM_173653.4(SLC9A9):c.147G>A (p.Leu49=)	not provided [RCV000970827]	benign	3	143848176	143848176	Human		name
150336562	CV1165655	single nucleotide variant	NM_173653.4(SLC9A9):c.846C>T (p.Phe282=)	not provided [RCV001532009]	likely benign	3	143578633	143578633	Human		name
156085942	CV2249369	single nucleotide variant	NM_173653.4(SLC9A9):c.55C>G (p.Gln19Glu)	not specified [RCV004118381]	uncertain significance	3	143848268	143848268	Human		name
243063689	CV2405141	deletion	NM_173653.4(SLC9A9):c.119del (p.Leu40fs)	Autism, susceptibility to, 16 [RCV003142273]	uncertain significance	3	143848204	143848204	Human	1	name
401829753	CV2743950	single nucleotide variant	NM_173653.4(SLC9A9):c.723G>A (p.Val241=)	SLC9A9-related disorder [RCV003919053]\|not provided [RCV003327127]	likely benign	3	143652287	143652287	Human	1	name , trait , alternate_id
405264949	CV3185408	single nucleotide variant	NM_173653.4(SLC9A9):c.576C>A (p.Gly192=)	not provided [RCV003885972]	likely benign	3	143693265	143693265	Human		name
405293145	CV3221297	single nucleotide variant	NM_173653.4(SLC9A9):c.702A>G (p.Thr234=)	SLC9A9-related disorder [RCV003966818]	likely benign	3	143652308	143652308	Human		name , trait , alternate_id
12840048	CV368245	single nucleotide variant	NM_173653.4(SLC9A9):c.918T>C (p.Cys306=)	not provided [RCV004716423]\|not specified [RCV000429957]	benign	3	143574170	143574170	Human		name
15168491	CV697871	single nucleotide variant	NM_173653.4(SLC9A9):c.831T>C (p.Asn277=)	not provided [RCV000949268]	benign	3	143578648	143578648	Human		name
15186835	CV733848	single nucleotide variant	NM_173653.4(SLC9A9):c.861A>C (p.Ala287=)	not provided [RCV000908917]	benign	3	143578618	143578618	Human		name
15165183	CV733849	single nucleotide variant	NM_173653.4(SLC9A9):c.684C>T (p.Val228=)	not provided [RCV000904166]	likely benign	3	143652326	143652326	Human		name
15107486	CV748058	single nucleotide variant	NM_173653.4(SLC9A9):c.828G>A (p.Gly276=)	not provided [RCV000915964]	benign	3	143578651	143578651	Human		name
15197932	CV763674	single nucleotide variant	NM_173653.4(SLC9A9):c.759T>C (p.Ser253=)	SLC9A9-related disorder [RCV003960507]\|not provided [RCV000934659]	benign\|likely benign	3	143578720	143578720	Human	1	name , trait , alternate_id
156382540	CV2223520	single nucleotide variant	NM_173653.4(SLC9A9):c.129T>A (p.Asn43Lys)	not specified [RCV004091902]	uncertain significance	3	143848194	143848194	Human		name
11643034	CV269409	deletion	NM_173653.4(SLC9A9):c.540del (p.Met181fs)	not provided [RCV000385425]	uncertain significance	3	143693301	143693301	Human		name
401944690	CV2840481	single nucleotide variant	NM_173653.4(SLC9A9):c.1719A>G (p.Leu573=)	SLC9A9-related disorder [RCV003908980]\|not provided [RCV003457396]	likely benign	3	143266921	143266921	Human	1	name , trait , alternate_id
404993849	CV2851073	single nucleotide variant	NM_173653.4(SLC9A9):c.1450T>C (p.Leu484=)	not provided [RCV003491522]	uncertain significance	3	143467056	143467056	Human		name
405293339	CV3207364	single nucleotide variant	NM_173653.4(SLC9A9):c.1674G>A (p.Pro558=)	SLC9A9-related disorder [RCV003931748]	likely benign	3	143268911	143268911	Human		name , trait , alternate_id
405294978	CV3215025	single nucleotide variant	NM_173653.4(SLC9A9):c.1575C>T (p.Leu525=)	SLC9A9-related disorder [RCV003936874]	likely benign	3	143363513	143363513	Human		name , trait , alternate_id
15156813	CV697870	single nucleotide variant	NM_173653.4(SLC9A9):c.1572G>C (p.Arg524=)	not provided [RCV000946769]	benign	3	143363516	143363516	Human		name
15164876	CV708617	single nucleotide variant	NM_173653.4(SLC9A9):c.1824C>T (p.Asp608=)	not provided [RCV000970826]	benign	3	143266816	143266816	Human		name
15169060	CV708618	single nucleotide variant	NM_173653.4(SLC9A9):c.1641G>A (p.Pro547=)	not provided [RCV000971738]	likely benign	3	143268944	143268944	Human		name
15158196	CV708619	single nucleotide variant	NM_173653.4(SLC9A9):c.283G>A (p.Val95Ile)	SLC9A9-related disorder [RCV003905976]\|not provided [RCV000969460]	benign\|likely benign	3	143832114	143832114	Human	1	name , trait , alternate_id
15156145	CV720229	single nucleotide variant	NM_173653.4(SLC9A9):c.1428T>C (p.Phe476=)	not provided [RCV000880565]	benign	3	143467078	143467078	Human		name
15175959	CV720230	single nucleotide variant	NM_173653.4(SLC9A9):c.1425A>C (p.Val475=)	not provided [RCV000884482]	benign	3	143467081	143467081	Human		name
15150376	CV748057	single nucleotide variant	NM_173653.4(SLC9A9):c.1476C>T (p.Gly492=)	not provided [RCV000923463]	likely benign	3	143382108	143382108	Human		name
15197929	CV763673	single nucleotide variant	NM_173653.4(SLC9A9):c.1158G>A (p.Thr386=)	not provided [RCV000934658]	likely benign	3	143495380	143495380	Human		name
126729561	CV985854	deletion	NM_173653.4(SLC9A9):c.587del (p.Asn196fs)	Colorectal cancer [RCV001293845]	pathogenic	3	143693254	143693254	Human	2	name
126911613	CV1037328	single nucleotide variant	NM_173653.4(SLC9A9):c.545A>T (p.Tyr182Phe)	not provided [RCV001355564]	uncertain significance	3	143693296	143693296	Human		name
156028363	CV2195760	single nucleotide variant	NM_173653.4(SLC9A9):c.805G>A (p.Ala269Thr)	not specified [RCV004076113]	uncertain significance	3	143578674	143578674	Human		name
156318734	CV2260735	single nucleotide variant	NM_173653.4(SLC9A9):c.886A>G (p.Thr296Ala)	not specified [RCV004125660]	uncertain significance	3	143578593	143578593	Human		name
156273273	CV2283817	single nucleotide variant	NM_173653.4(SLC9A9):c.751A>C (p.Thr251Pro)	not specified [RCV004142332]	uncertain significance	3	143652259	143652259	Human		name
156187275	CV2332739	single nucleotide variant	NM_173653.4(SLC9A9):c.847G>A (p.Ala283Thr)	not specified [RCV004189412]	uncertain significance	3	143578632	143578632	Human		name
156207580	CV2382388	single nucleotide variant	NM_173653.4(SLC9A9):c.491C>T (p.Thr164Met)	not specified [RCV004230727]	uncertain significance	3	143795043	143795043	Human		name
329393779	CV2449852	single nucleotide variant	NM_173653.4(SLC9A9):c.529A>G (p.Ile177Val)	not specified [RCV004268945]	uncertain significance	3	143795005	143795005	Human		name
401896400	CV2781258	single nucleotide variant	NM_173653.4(SLC9A9):c.838G>A (p.Gly280Arg)	not specified [RCV004352291]	uncertain significance	3	143578641	143578641	Human		name
401897286	CV2789984	single nucleotide variant	NM_173653.4(SLC9A9):c.436G>A (p.Ala146Thr)	not specified [RCV004363946]	uncertain significance	3	143796846	143796846	Human		name
404993840	CV2851072	single nucleotide variant	NM_173653.4(SLC9A9):c.554T>G (p.Val185Gly)	not provided [RCV003491521]\|not specified [RCV004867877]	uncertain significance	3	143693287	143693287	Human		name
405654189	CV3228157	single nucleotide variant	NM_173653.4(SLC9A9):c.998C>T (p.Thr333Ile)	not specified [RCV003994892]	uncertain significance	3	143574090	143574090	Human		name
405771550	CV3322436	single nucleotide variant	NM_173653.4(SLC9A9):c.850G>A (p.Gly284Ser)	not specified [RCV004457067]	uncertain significance	3	143578629	143578629	Human		name
405771555	CV3322437	single nucleotide variant	NM_173653.4(SLC9A9):c.926C>T (p.Pro309Leu)	not specified [RCV004457068]	uncertain significance	3	143574162	143574162	Human		name
407427129	CV3410466	single nucleotide variant	NM_173653.4(SLC9A9):c.456G>C (p.Lys152Asn)	not specified [RCV004586113]	uncertain significance	3	143796826	143796826	Human		name
407515896	CV3481194	single nucleotide variant	NM_173653.4(SLC9A9):c.793G>A (p.Ala265Thr)	not specified [RCV004675088]	likely benign	3	143578686	143578686	Human		name
597725524	CV3606913	single nucleotide variant	NM_173653.4(SLC9A9):c.562A>G (p.Met188Val)	not specified [RCV004862443]	uncertain significance	3	143693279	143693279	Human		name
597854236	CV3762456	single nucleotide variant	NM_173653.4(SLC9A9):c.504G>C (p.Leu168Phe)	not specified [RCV005088372]	uncertain significance	3	143795030	143795030	Human		name
598260715	CV3922152	single nucleotide variant	NM_173653.4(SLC9A9):c.409G>A (p.Val137Ile)	not specified [RCV005279836]	uncertain significance	3	143796873	143796873	Human		name
598260724	CV3922154	single nucleotide variant	NM_173653.4(SLC9A9):c.581T>C (p.Leu194Pro)	not specified [RCV005279838]	uncertain significance	3	143693260	143693260	Human		name
15108294	CV720231	single nucleotide variant	NM_173653.4(SLC9A9):c.707T>C (p.Leu236Ser)	not provided [RCV000893642]	benign\|likely benign	3	143652303	143652303	Human		name
126735970	CV1000380	single nucleotide variant	NM_173653.4(SLC9A9):c.1808C>A (p.Ala603Glu)	not provided [RCV001311628]\|not specified [RCV004034240]	likely benign\|uncertain significance	3	143266832	143266832	Human		name
153000618	CV1683756	single nucleotide variant	NM_173653.4(SLC9A9):c.1268G>A (p.Arg423Gln)	Autism, susceptibility to, 16 [RCV002254375]	uncertain significance	3	143493700	143493700	Human	1	name
8556766	CV17402	single nucleotide variant	NM_173653.4(SLC9A9):c.1267C>T (p.Arg423Ter)	Autism, susceptibility to, 16 [RCV000002459]	risk factor	3	143493701	143493701	Human	1	name
156234500	CV2193312	single nucleotide variant	NM_173653.4(SLC9A9):c.1397T>C (p.Leu466Pro)	not specified [RCV004072818]	uncertain significance	3	143467109	143467109	Human		name
156400866	CV2217336	single nucleotide variant	NM_173653.4(SLC9A9):c.1345G>A (p.Ala449Thr)	not specified [RCV004087774]	uncertain significance	3	143467161	143467161	Human		name
156247196	CV2263844	single nucleotide variant	NM_173653.4(SLC9A9):c.1214T>G (p.Phe405Cys)	not specified [RCV004137903]	uncertain significance	3	143493754	143493754	Human		name
156043550	CV2268458	single nucleotide variant	NM_173653.4(SLC9A9):c.1328C>T (p.Ala443Val)	not specified [RCV004130155]	uncertain significance	3	143467178	143467178	Human		name
156135763	CV2284764	single nucleotide variant	NM_173653.4(SLC9A9):c.1730A>G (p.Asp577Gly)	not specified [RCV004142949]	uncertain significance	3	143266910	143266910	Human		name
156288306	CV2309533	single nucleotide variant	NM_173653.4(SLC9A9):c.1593C>G (p.Ser531Arg)	not specified [RCV004158922]	uncertain significance	3	143363495	143363495	Human		name
156165252	CV2330035	single nucleotide variant	NM_173653.4(SLC9A9):c.1706A>T (p.Tyr569Phe)	not specified [RCV004185527]	uncertain significance	3	143268879	143268879	Human		name
155977701	CV2342920	single nucleotide variant	NM_173653.4(SLC9A9):c.1879G>A (p.Gly627Ser)	not specified [RCV004189952]	uncertain significance	3	143266761	143266761	Human		name
155926900	CV2345291	single nucleotide variant	NM_173653.4(SLC9A9):c.1852A>G (p.Lys618Glu)	not specified [RCV004196026]	uncertain significance	3	143266788	143266788	Human		name
156194325	CV2398222	single nucleotide variant	NM_173653.4(SLC9A9):c.1766T>C (p.Ile589Thr)	not specified [RCV004235136]	uncertain significance	3	143266874	143266874	Human		name
329383640	CV2425052	single nucleotide variant	NM_173653.4(SLC9A9):c.1865A>G (p.Tyr622Cys)	not specified [RCV004250708]	uncertain significance	3	143266775	143266775	Human		name
329376417	CV2425130	single nucleotide variant	NM_173653.4(SLC9A9):c.1351C>T (p.Arg451Trp)	not specified [RCV004249022]	uncertain significance	3	143467155	143467155	Human		name
329357393	CV2427701	single nucleotide variant	NM_173653.4(SLC9A9):c.1003A>T (p.Ile335Leu)	not specified [RCV004252486]	uncertain significance	3	143552448	143552448	Human		name
329359769	CV2462276	single nucleotide variant	NM_173653.4(SLC9A9):c.1528G>A (p.Ala510Thr)	not specified [RCV004266269]	uncertain significance	3	143363560	143363560	Human		name
11525937	CV246940	single nucleotide variant	NM_173653.4(SLC9A9):c.1486G>A (p.Asp496Asn)	Autism, susceptibility to, 16 [RCV002487110]\|not provided [RCV004597768]\|not specified [RCV000239045]	likely benign	3	143382098	143382098	Human	1	name
329952809	CV2670158	single nucleotide variant	NM_173653.4(SLC9A9):c.1321C>T (p.Arg441Ter)	SLC9A9-related disorder [RCV003396967]\|not provided [RCV003233368]	uncertain significance	3	143467185	143467185	Human	1	name , trait , alternate_id
401764486	CV2705035	single nucleotide variant	NM_173653.4(SLC9A9):c.1657C>T (p.Pro553Ser)	not specified [RCV004309955]	uncertain significance	3	143268928	143268928	Human		name
401830131	CV2744120	single nucleotide variant	NM_173653.4(SLC9A9):c.1380G>T (p.Met460Ile)	Autism, susceptibility to, 16 [RCV003327317]	uncertain significance	3	143467126	143467126	Human	1	name
401908381	CV2801274	single nucleotide variant	NM_173653.4(SLC9A9):c.1336T>C (p.Phe446Leu)	SLC9A9-related disorder [RCV003397514]	uncertain significance	3	143467170	143467170	Human		name , trait , alternate_id
401906100	CV2804860	single nucleotide variant	NM_173653.4(SLC9A9):c.1426T>C (p.Phe476Leu)	SLC9A9-related disorder [RCV003420966]	uncertain significance	3	143467080	143467080	Human		name , trait , alternate_id
401926533	CV2824991	single nucleotide variant	NM_173653.4(SLC9A9):c.1390A>G (p.Thr464Ala)	not provided [RCV003437956]	uncertain significance	3	143467116	143467116	Human		name
405771515	CV3322430	single nucleotide variant	NM_173653.4(SLC9A9):c.1378A>G (p.Met460Val)	not specified [RCV004457061]	uncertain significance	3	143467128	143467128	Human		name
405771520	CV3322431	single nucleotide variant	NM_173653.4(SLC9A9):c.1478T>C (p.Val493Ala)	not specified [RCV004457062]	uncertain significance	3	143382106	143382106	Human		name
405771525	CV3322432	single nucleotide variant	NM_173653.4(SLC9A9):c.1482C>A (p.Asp494Glu)	not specified [RCV004457063]	uncertain significance	3	143382102	143382102	Human		name
405771532	CV3322433	single nucleotide variant	NM_173653.4(SLC9A9):c.1634G>A (p.Gly545Asp)	not specified [RCV004457064]	uncertain significance	3	143268951	143268951	Human		name
405771538	CV3322434	single nucleotide variant	NM_173653.4(SLC9A9):c.1666T>C (p.Cys556Arg)	not specified [RCV004457065]	uncertain significance	3	143268919	143268919	Human		name
405771544	CV3322435	single nucleotide variant	NM_173653.4(SLC9A9):c.1801C>T (p.Pro601Ser)	not specified [RCV004457066]	uncertain significance	3	143266839	143266839	Human		name
407515892	CV3481193	single nucleotide variant	NM_173653.4(SLC9A9):c.1667G>A (p.Cys556Tyr)	not specified [RCV004675087]	uncertain significance	3	143268918	143268918	Human		name
407452091	CV3481195	single nucleotide variant	NM_173653.4(SLC9A9):c.1601A>C (p.His534Pro)	not specified [RCV004683884]	uncertain significance	3	143363487	143363487	Human		name
407515901	CV3481196	single nucleotide variant	NM_173653.4(SLC9A9):c.1892A>G (p.Tyr631Cys)	not specified [RCV004675089]	uncertain significance	3	143266748	143266748	Human		name
407515909	CV3481197	single nucleotide variant	NM_173653.4(SLC9A9):c.1574T>C (p.Leu525Pro)	not specified [RCV004675090]	uncertain significance	3	143363514	143363514	Human		name
407515916	CV3481198	single nucleotide variant	NM_173653.4(SLC9A9):c.1556A>G (p.Lys519Arg)	not specified [RCV004675091]	uncertain significance	3	143363532	143363532	Human		name
407452096	CV3481199	single nucleotide variant	NM_173653.4(SLC9A9):c.1518A>C (p.Gln506His)	not specified [RCV004683885]	uncertain significance	3	143382066	143382066	Human		name
407515918	CV3481200	single nucleotide variant	NM_173653.4(SLC9A9):c.1837C>T (p.Pro613Ser)	not specified [RCV004675092]	uncertain significance	3	143266803	143266803	Human		name
408380421	CV3517218	single nucleotide variant	NM_173653.4(SLC9A9):c.1046C>T (p.Thr349Ile)	SLC9A9-related disorder [RCV004754172]	uncertain significance	3	143552405	143552405	Human		name , trait , alternate_id
12741022	CV359390	single nucleotide variant	NM_173653.4(SLC9A9):c.1082C>G (p.Thr361Ser)	not specified [RCV000413852]	uncertain significance	3	143552369	143552369	Human		name
597725517	CV3606912	single nucleotide variant	NM_173653.4(SLC9A9):c.1934A>T (p.Asn645Ile)	not specified [RCV004862442]	uncertain significance	3	143266706	143266706	Human		name
597777077	CV3606914	single nucleotide variant	NM_173653.4(SLC9A9):c.1135T>A (p.Tyr379Asn)	not specified [RCV004872951]	uncertain significance	3	143495403	143495403	Human		name
597725533	CV3606915	single nucleotide variant	NM_173653.4(SLC9A9):c.1388C>A (p.Thr463Asn)	not specified [RCV004862444]	uncertain significance	3	143467118	143467118	Human		name
598260710	CV3922151	single nucleotide variant	NM_173653.4(SLC9A9):c.1288A>G (p.Asn430Asp)	not specified [RCV005279835]	uncertain significance	3	143493680	143493680	Human		name
598260721	CV3922153	single nucleotide variant	NM_173653.4(SLC9A9):c.1053C>G (p.Asn351Lys)	not specified [RCV005279837]	uncertain significance	3	143552398	143552398	Human		name
12906795	CV414913	single nucleotide variant	NM_173653.4(SLC9A9):c.1742T>C (p.Ile581Thr)	not provided [RCV000489661]	uncertain significance	3	143266898	143266898	Human		name
15184593	CV720228	single nucleotide variant	NM_173653.4(SLC9A9):c.1618A>G (p.Ile540Val)	not provided [RCV000886484]	benign	3	143268967	143268967	Human		name
8625528	CV80651	single nucleotide variant	NM_173653.3(SLC9A9):c.1436G>A (p.Gly479Glu)	Malignant melanoma [RCV000060728]	not provided	3	143467070	143467070	Human		name
8630631	CV85786	single nucleotide variant	NM_173653.3(SLC9A9):c.1104G>A (p.Met368Ile)	Malignant melanoma [RCV000065869]	not provided	3	143495434	143495434	Human		name
617153287	CV3544514	microsatellite	NM_173653.4(SLC9A9):c.250_251del (p.Val84fs)	See cases [RCV005415501]	uncertain significance	3	143832146	143832147	Human		name

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