Slc9a4 Variant Search Result - Rat Genome Database

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102 records found for search term Slc9a4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150339102	CV1108822	single nucleotide variant	NM_001011552.4(SLC9A4):c.256+2039C>T	Ascending aortic dissection [RCV001543144]	association	2	102476054	102476054	Human	2	name
150339099	CV1108824	single nucleotide variant	NM_001011552.4(SLC9A4):c.1488+592C>T	Ascending aortic dissection [RCV001543141]	association	2	102509525	102509525	Human	2	name
150339100	CV1108825	single nucleotide variant	NM_001011552.4(SLC9A4):c.2038+354T>G	Ascending aortic dissection [RCV001543142]	association	2	102526700	102526700	Human	2	name
598260586	CV3922119	single nucleotide variant	NM_001011552.4(SLC9A4):c.23C>G (p.Thr8Ser)	not specified [RCV005279810]	uncertain significance	2	102473782	102473782	Human		name
150339104	CV1108823	single nucleotide variant	NM_001011552.4(SLC9A4):c.363G>A (p.Ser121=)	Ascending aortic dissection [RCV001543146]	association	2	102478945	102478945	Human	3	name
150339104	CV1108823	single nucleotide variant	NM_001011552.4(SLC9A4):c.363G>A (p.Ser121=)	Ascending aortic dissection [RCV001543146]	association	2	102478945	102478946	Human	3	name
156249944	CV2215597	single nucleotide variant	NM_001011552.4(SLC9A4):c.41G>A (p.Cys14Tyr)	not specified [RCV004089358]	uncertain significance	2	102473800	102473800	Human		name
405771398	CV3322411	single nucleotide variant	NM_001011552.4(SLC9A4):c.77C>T (p.Ala26Val)	not specified [RCV004457042]	uncertain significance	2	102473836	102473836	Human		name
15180131	CV707636	single nucleotide variant	NM_001011552.4(SLC9A4):c.50T>C (p.Leu17Pro)	not provided [RCV000974076]	benign	2	102473809	102473809	Human		name
8629762	CV84909	single nucleotide variant	NM_001011552.3(SLC9A4):c.85G>A (p.Asp29Asn)	Malignant melanoma [RCV000064991]	not provided	2	102473844	102473844	Human		name
156353425	CV2327535	single nucleotide variant	NM_001011552.4(SLC9A4):c.169A>G (p.Ile57Val)	not specified [RCV004176840]	uncertain significance	2	102473928	102473928	Human		name
156196577	CV2337991	single nucleotide variant	NM_001011552.4(SLC9A4):c.109A>G (p.Thr37Ala)	not specified [RCV004186035]	uncertain significance	2	102473868	102473868	Human		name
405771357	CV3322404	single nucleotide variant	NM_001011552.4(SLC9A4):c.157C>T (p.Pro53Ser)	not specified [RCV004457035]	uncertain significance	2	102473916	102473916	Human		name
405771376	CV3322407	single nucleotide variant	NM_001011552.4(SLC9A4):c.212A>C (p.Tyr71Ser)	not specified [RCV004457038]	uncertain significance	2	102473971	102473971	Human		name
405771386	CV3322409	single nucleotide variant	NM_001011552.4(SLC9A4):c.254T>C (p.Ile85Thr)	not specified [RCV004457040]	uncertain significance	2	102474013	102474013	Human		name
407515850	CV3481174	single nucleotide variant	NM_001011552.4(SLC9A4):c.130G>A (p.Ala44Thr)	not specified [RCV004675074]	uncertain significance	2	102473889	102473889	Human		name
597776966	CV3606869	single nucleotide variant	NM_001011552.4(SLC9A4):c.265C>T (p.Leu89Phe)	not specified [RCV004872925]	uncertain significance	2	102478847	102478847	Human		name
597776974	CV3606874	single nucleotide variant	NM_001011552.4(SLC9A4):c.124T>C (p.Ser42Pro)	not specified [RCV004872927]	likely benign	2	102473883	102473883	Human		name
8629763	CV84910	single nucleotide variant	NM_001011552.3(SLC9A4):c.242C>T (p.Ser81Phe)	Malignant melanoma [RCV000064992]	not provided	2	102474001	102474001	Human		name
8629766	CV84913	single nucleotide variant	NM_001011552.3(SLC9A4):c.1882C>T (p.Leu628=)	Malignant melanoma [RCV000064995]	not provided	2	102525087	102525087	Human		name
156154541	CV2209534	single nucleotide variant	NM_001011552.4(SLC9A4):c.707A>T (p.Asp236Val)	not specified [RCV004093650]	uncertain significance	2	102479289	102479289	Human		name
156156437	CV2238470	single nucleotide variant	NM_001011552.4(SLC9A4):c.809T>C (p.Phe270Ser)	not specified [RCV004113524]	uncertain significance	2	102503536	102503536	Human		name
156041378	CV2261375	single nucleotide variant	NM_001011552.4(SLC9A4):c.676A>G (p.Met226Val)	not specified [RCV004130015]	uncertain significance	2	102479258	102479258	Human		name
156334287	CV2267111	single nucleotide variant	NM_001011552.4(SLC9A4):c.488T>C (p.Val163Ala)	not specified [RCV004131730]	uncertain significance	2	102479070	102479070	Human		name
155998122	CV2288703	single nucleotide variant	NM_001011552.4(SLC9A4):c.451T>C (p.Phe151Leu)	not specified [RCV004153994]	uncertain significance	2	102479033	102479033	Human		name
156327514	CV2332114	single nucleotide variant	NM_001011552.4(SLC9A4):c.359A>C (p.Lys120Thr)	not specified [RCV004189154]	uncertain significance	2	102478941	102478941	Human		name
156220522	CV2393745	single nucleotide variant	NM_001011552.4(SLC9A4):c.704A>G (p.Asn235Ser)	not specified [RCV004231540]	uncertain significance	2	102479286	102479286	Human		name
156159163	CV2398089	single nucleotide variant	NM_001011552.4(SLC9A4):c.628G>A (p.Ala210Thr)	not specified [RCV004241675]	uncertain significance	2	102479210	102479210	Human		name
401777913	CV2718385	single nucleotide variant	NM_001011552.4(SLC9A4):c.814G>A (p.Val272Ile)	not specified [RCV004318213]	likely benign	2	102503541	102503541	Human		name
401751875	CV2727437	single nucleotide variant	NM_001011552.4(SLC9A4):c.989C>T (p.Ala330Val)	not specified [RCV004327524]	uncertain significance	2	102505262	102505262	Human		name
401879501	CV2773134	single nucleotide variant	NM_001011552.4(SLC9A4):c.476T>G (p.Leu159Arg)	not specified [RCV004351558]	uncertain significance	2	102479058	102479058	Human		name
405771391	CV3322410	single nucleotide variant	NM_001011552.4(SLC9A4):c.546G>C (p.Gln182His)	not specified [RCV004457041]	uncertain significance	2	102479128	102479128	Human		name
405771403	CV3322412	single nucleotide variant	NM_001011552.4(SLC9A4):c.854G>T (p.Gly285Val)	not specified [RCV004457043]	uncertain significance	2	102503581	102503581	Human		name
405771408	CV3322413	single nucleotide variant	NM_001011552.4(SLC9A4):c.890A>G (p.Asn297Ser)	not specified [RCV004457044]	uncertain significance	2	102503617	102503617	Human		name
407452066	CV3481171	single nucleotide variant	NM_001011552.4(SLC9A4):c.497C>A (p.Ala166Asp)	not specified [RCV004683876]	uncertain significance	2	102479079	102479079	Human		name
407452072	CV3481175	single nucleotide variant	NM_001011552.4(SLC9A4):c.728A>G (p.Tyr243Cys)	not specified [RCV004683878]	uncertain significance	2	102503455	102503455	Human		name
407515859	CV3481178	single nucleotide variant	NM_001011552.4(SLC9A4):c.659T>C (p.Val220Ala)	not specified [RCV004675077]	uncertain significance	2	102479241	102479241	Human		name
597725355	CV3606863	single nucleotide variant	NM_001011552.4(SLC9A4):c.576C>A (p.Asn192Lys)	not specified [RCV004862421]	uncertain significance	2	102479158	102479158	Human		name
597776958	CV3606865	single nucleotide variant	NM_001011552.4(SLC9A4):c.784G>A (p.Asp262Asn)	not specified [RCV004872923]	uncertain significance	2	102503511	102503511	Human		name
597725371	CV3606867	single nucleotide variant	NM_001011552.4(SLC9A4):c.571G>A (p.Val191Ile)	not specified [RCV004862423]	uncertain significance	2	102479153	102479153	Human		name
597776978	CV3606877	single nucleotide variant	NM_001011552.4(SLC9A4):c.401T>G (p.Leu134Arg)	not specified [RCV004872928]	uncertain significance	2	102478983	102478983	Human		name
598260591	CV3922120	single nucleotide variant	NM_001011552.4(SLC9A4):c.878G>A (p.Arg293His)	not specified [RCV005279811]	uncertain significance	2	102503605	102503605	Human		name
598260612	CV3922124	single nucleotide variant	NM_001011552.4(SLC9A4):c.632T>C (p.Val211Ala)	not specified [RCV005279815]	uncertain significance	2	102479214	102479214	Human		name
598260623	CV3922126	single nucleotide variant	NM_001011552.4(SLC9A4):c.368C>T (p.Pro123Leu)	not specified [RCV005279817]	uncertain significance	2	102478950	102478950	Human		name
8629764	CV84911	single nucleotide variant	NM_001011552.3(SLC9A4):c.956C>T (p.Thr319Ile)	Malignant melanoma [RCV000064993]	not provided	2	102503683	102503683	Human		name
156166667	CV2200935	single nucleotide variant	NM_001011552.4(SLC9A4):c.1492A>G (p.Met498Val)	not specified [RCV004081548]	uncertain significance	2	102512206	102512206	Human		name
156178001	CV2201556	single nucleotide variant	NM_001011552.4(SLC9A4):c.1051A>G (p.Ile351Val)	not specified [RCV004080047]	uncertain significance	2	102505324	102505324	Human		name
155927023	CV2230720	single nucleotide variant	NM_001011552.4(SLC9A4):c.1750C>A (p.Leu584Ile)	not specified [RCV004097662]	uncertain significance	2	102519887	102519887	Human		name
156261490	CV2282404	single nucleotide variant	NM_001011552.4(SLC9A4):c.2321G>A (p.Arg774Gln)	not specified [RCV004133218]	likely benign	2	102532612	102532612	Human		name
155956562	CV2304050	single nucleotide variant	NM_001011552.4(SLC9A4):c.2192C>T (p.Thr731Ile)	not specified [RCV004170099]	uncertain significance	2	102532483	102532483	Human		name
156348794	CV2309079	single nucleotide variant	NM_001011552.4(SLC9A4):c.1955G>T (p.Gly652Val)	not specified [RCV004171441]	uncertain significance	2	102526263	102526263	Human		name
155917367	CV2362284	single nucleotide variant	NM_001011552.4(SLC9A4):c.1811G>T (p.Arg604Leu)	not specified [RCV004212926]	uncertain significance	2	102519948	102519948	Human		name
156264478	CV2364323	single nucleotide variant	NM_001011552.4(SLC9A4):c.1589G>A (p.Arg530Gln)	not specified [RCV004223543]	uncertain significance	2	102514119	102514119	Human		name
329391750	CV2445004	single nucleotide variant	NM_001011552.4(SLC9A4):c.1234C>T (p.Arg412Trp)	not specified [RCV004261622]	uncertain significance	2	102508114	102508114	Human		name
329394749	CV2457627	single nucleotide variant	NM_001011552.4(SLC9A4):c.1749A>C (p.Arg583Ser)	not specified [RCV004269484]	uncertain significance	2	102519886	102519886	Human		name
401755901	CV2675577	single nucleotide variant	NM_001011552.4(SLC9A4):c.1087G>A (p.Glu363Lys)	not specified [RCV004295190]	uncertain significance	2	102505360	102505360	Human		name
401771377	CV2675578	single nucleotide variant	NM_001011552.4(SLC9A4):c.1811G>A (p.Arg604Gln)	not specified [RCV004297239]	uncertain significance	2	102519948	102519948	Human		name
401739852	CV2684193	single nucleotide variant	NM_001011552.4(SLC9A4):c.1820C>A (p.Thr607Asn)	not specified [RCV004288863]	uncertain significance	2	102525025	102525025	Human		name
401741344	CV2690473	single nucleotide variant	NM_001011552.4(SLC9A4):c.2228T>A (p.Val743Glu)	not specified [RCV004304240]	uncertain significance	2	102532519	102532519	Human		name
401720828	CV2702137	single nucleotide variant	NM_001011552.4(SLC9A4):c.1917G>A (p.Met639Ile)	not specified [RCV004314491]	uncertain significance	2	102525122	102525122	Human		name
401721767	CV2710151	single nucleotide variant	NM_001011552.4(SLC9A4):c.1537A>T (p.Ser513Cys)	not specified [RCV004315200]	uncertain significance	2	102512251	102512251	Human		name
401783025	CV2716093	single nucleotide variant	NM_001011552.4(SLC9A4):c.2285G>C (p.Gly762Ala)	not specified [RCV004323338]	uncertain significance	2	102532576	102532576	Human		name
401749585	CV2719331	single nucleotide variant	NM_001011552.4(SLC9A4):c.2266G>A (p.Glu756Lys)	not specified [RCV004324966]	uncertain significance	2	102532557	102532557	Human		name
401859867	CV2765173	single nucleotide variant	NM_001011552.4(SLC9A4):c.2092C>T (p.Arg698Trp)	not specified [RCV004339703]	uncertain significance	2	102532383	102532383	Human		name
401893362	CV2765269	single nucleotide variant	NM_001011552.4(SLC9A4):c.2218G>A (p.Val740Ile)	not specified [RCV004339791]	uncertain significance	2	102532509	102532509	Human		name
401882247	CV2774754	single nucleotide variant	NM_001011552.4(SLC9A4):c.1193C>T (p.Ala398Val)	not specified [RCV004343854]	uncertain significance	2	102505466	102505466	Human		name
405771328	CV3322399	single nucleotide variant	NM_001011552.4(SLC9A4):c.1015G>A (p.Val339Met)	not specified [RCV004457030]	uncertain significance	2	102505288	102505288	Human		name
405771335	CV3322400	single nucleotide variant	NM_001011552.4(SLC9A4):c.1084A>G (p.Ser362Gly)	not specified [RCV004457031]	uncertain significance	2	102505357	102505357	Human		name
405771341	CV3322401	single nucleotide variant	NM_001011552.4(SLC9A4):c.1319T>C (p.Leu440Ser)	not specified [RCV004457032]	uncertain significance	2	102508199	102508199	Human		name
405771353	CV3322403	single nucleotide variant	NM_001011552.4(SLC9A4):c.1343G>A (p.Arg448Lys)	not specified [RCV004457034]	uncertain significance	2	102508223	102508223	Human		name
405771363	CV3322405	single nucleotide variant	NM_001011552.4(SLC9A4):c.1666A>T (p.Ile556Phe)	not specified [RCV004457036]	uncertain significance	2	102514196	102514196	Human		name
405771370	CV3322406	single nucleotide variant	NM_001011552.4(SLC9A4):c.1859G>A (p.Ser620Asn)	not specified [RCV004457037]	uncertain significance	2	102525064	102525064	Human		name
407452069	CV3481172	single nucleotide variant	NM_001011552.4(SLC9A4):c.1892G>A (p.Arg631His)	not specified [RCV004683877]	uncertain significance	2	102525097	102525097	Human		name
407515853	CV3481176	single nucleotide variant	NM_001011552.4(SLC9A4):c.2357A>T (p.Asp786Val)	not specified [RCV004675075]	uncertain significance	2	102532648	102532648	Human		name
407515856	CV3481177	single nucleotide variant	NM_001011552.4(SLC9A4):c.1770G>C (p.Glu590Asp)	not specified [RCV004675076]	uncertain significance	2	102519907	102519907	Human		name
597776952	CV3606861	single nucleotide variant	NM_001011552.4(SLC9A4):c.1469A>G (p.Asn490Ser)	not specified [RCV004872922]	uncertain significance	2	102508914	102508914	Human		name
597725346	CV3606862	single nucleotide variant	NM_001011552.4(SLC9A4):c.1588C>T (p.Arg530Trp)	not specified [RCV004862420]	uncertain significance	2	102514118	102514118	Human		name
597725364	CV3606864	single nucleotide variant	NM_001011552.4(SLC9A4):c.1241T>A (p.Phe414Tyr)	not specified [RCV004862422]	uncertain significance	2	102508121	102508121	Human		name
597776962	CV3606866	single nucleotide variant	NM_001011552.4(SLC9A4):c.1267A>G (p.Ile423Val)	not specified [RCV004872924]	uncertain significance	2	102508147	102508147	Human		name
597725380	CV3606868	single nucleotide variant	NM_001011552.4(SLC9A4):c.1143G>T (p.Trp381Cys)	not specified [RCV004862424]	uncertain significance	2	102505416	102505416	Human		name
597725389	CV3606870	single nucleotide variant	NM_001011552.4(SLC9A4):c.2311G>C (p.Val771Leu)	not specified [RCV004862425]	uncertain significance	2	102532602	102532602	Human		name
597725398	CV3606871	single nucleotide variant	NM_001011552.4(SLC9A4):c.2222G>A (p.Arg741Lys)	not specified [RCV004862426]	uncertain significance	2	102532513	102532513	Human		name
597776970	CV3606872	single nucleotide variant	NM_001011552.4(SLC9A4):c.1669G>A (p.Glu557Lys)	not specified [RCV004872926]	uncertain significance	2	102514199	102514199	Human		name
597725406	CV3606873	single nucleotide variant	NM_001011552.4(SLC9A4):c.1711A>G (p.Ile571Val)	not specified [RCV004862427]	likely benign	2	102514241	102514241	Human		name
597725411	CV3606875	single nucleotide variant	NM_001011552.4(SLC9A4):c.1966A>G (p.Ile656Val)	not specified [RCV004862428]	likely benign	2	102526274	102526274	Human		name
597725418	CV3606876	single nucleotide variant	NM_001011552.4(SLC9A4):c.1754C>A (p.Ser585Tyr)	not specified [RCV004862429]	uncertain significance	2	102519891	102519891	Human		name
597725427	CV3606878	single nucleotide variant	NM_001011552.4(SLC9A4):c.1202T>C (p.Val401Ala)	not specified [RCV004862430]	uncertain significance	2	102508082	102508082	Human		name
597725436	CV3606879	single nucleotide variant	NM_001011552.4(SLC9A4):c.1256A>G (p.Lys419Arg)	not specified [RCV004862431]	uncertain significance	2	102508136	102508136	Human		name
597776982	CV3606880	single nucleotide variant	NM_001011552.4(SLC9A4):c.1969C>T (p.Arg657Cys)	not specified [RCV004872929]	uncertain significance	2	102526277	102526277	Human		name
598260596	CV3922121	single nucleotide variant	NM_001011552.4(SLC9A4):c.2026G>T (p.Ala676Ser)	not specified [RCV005279812]	uncertain significance	2	102526334	102526334	Human		name
598260602	CV3922122	single nucleotide variant	NM_001011552.4(SLC9A4):c.1028T>C (p.Val343Ala)	not specified [RCV005279813]	uncertain significance	2	102505301	102505301	Human		name
598260606	CV3922123	single nucleotide variant	NM_001011552.4(SLC9A4):c.2099G>A (p.Gly700Glu)	not specified [RCV005279814]	uncertain significance	2	102532390	102532390	Human		name
598260619	CV3922125	single nucleotide variant	NM_001011552.4(SLC9A4):c.1724C>A (p.Ala575Asp)	not specified [RCV005279816]	uncertain significance	2	102519861	102519861	Human		name
598237682	CV3922127	single nucleotide variant	NM_001011552.4(SLC9A4):c.1253T>C (p.Ile418Thr)	not specified [RCV005275702]	uncertain significance	2	102508133	102508133	Human		name
598260628	CV3922128	single nucleotide variant	NM_001011552.4(SLC9A4):c.1520A>G (p.Asp507Gly)	not specified [RCV005279818]	uncertain significance	2	102512234	102512234	Human		name
598260633	CV3922129	single nucleotide variant	NM_001011552.4(SLC9A4):c.1666A>G (p.Ile556Val)	not specified [RCV005279819]	uncertain significance	2	102514196	102514196	Human		name
598260637	CV3922130	single nucleotide variant	NM_001011552.4(SLC9A4):c.1886T>A (p.Ile629Asn)	not specified [RCV005279820]	uncertain significance	2	102525091	102525091	Human		name
598260642	CV3922131	single nucleotide variant	NM_001011552.4(SLC9A4):c.1403G>T (p.Gly468Val)	not specified [RCV005279821]	uncertain significance	2	102508848	102508848	Human		name
598260647	CV3922132	single nucleotide variant	NM_001011552.4(SLC9A4):c.1694G>A (p.Ser565Asn)	not specified [RCV005279822]	uncertain significance	2	102514224	102514224	Human		name
8625088	CV80207	single nucleotide variant	NM_001011552.3(SLC9A4):c.1546C>G (p.Gln516Glu)	Malignant melanoma [RCV000060283]	not provided	2	102512260	102512260	Human		name
8625089	CV80208	single nucleotide variant	NM_001011552.4(SLC9A4):c.2320C>T (p.Arg774Trp)	not specified [RCV004675073]	uncertain significance\|not provided	2	102532611	102532611	Human		name
8629765	CV84912	single nucleotide variant	NM_001011552.3(SLC9A4):c.1634C>T (p.Ser545Phe)	Malignant melanoma [RCV000064994]	not provided	2	102514164	102514164	Human		name

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