Slc9a5 Variant Search Result - Rat Genome Database

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77 records found for search term Slc9a5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155981290	CV2233061	single nucleotide variant	NM_004594.3(SLC9A5):c.10G>T (p.Ala4Ser)	not specified [RCV004103694]	uncertain significance	16	67249024	67249024	Human		name
156227753	CV2388302	single nucleotide variant	NM_004594.3(SLC9A5):c.41C>T (p.Ala14Val)	not specified [RCV004234755]	uncertain significance	16	67249055	67249055	Human		name
597777009	CV3606887	single nucleotide variant	NM_004594.3(SLC9A5):c.98G>A (p.Gly33Asp)	not specified [RCV004872935]	uncertain significance	16	67249112	67249112	Human		name
598260661	CV3922136	single nucleotide variant	NM_004594.3(SLC9A5):c.47C>G (p.Ala16Gly)	not specified [RCV005279825]	uncertain significance	16	67249061	67249061	Human		name
156052264	CV2388451	single nucleotide variant	NM_004594.3(SLC9A5):c.202C>G (p.Arg68Gly)	not specified [RCV004237311]	uncertain significance	16	67252556	67252556	Human		name
401903332	CV2808030	single nucleotide variant	NM_004594.3(SLC9A5):c.1737G>A (p.Ala579=)	not provided [RCV003419362]	likely benign	16	67259841	67259841	Human		name
401934500	CV2808033	single nucleotide variant	NM_004594.3(SLC9A5):c.2457A>G (p.Pro819=)	not provided [RCV003411369]	likely benign	16	67270976	67270976	Human		name
405771420	CV3322415	single nucleotide variant	NM_004594.3(SLC9A5):c.292G>C (p.Ala98Pro)	not specified [RCV004457046]	uncertain significance	16	67252646	67252646	Human		name
597725451	CV3606890	single nucleotide variant	NM_004594.3(SLC9A5):c.296A>G (p.Glu99Gly)	not specified [RCV004862433]	uncertain significance	16	67252650	67252650	Human		name
598260651	CV3922133	single nucleotide variant	NM_004594.3(SLC9A5):c.257T>C (p.Val86Ala)	not specified [RCV005279823]	uncertain significance	16	67252611	67252611	Human		name
155741747	CV1770535	deletion	NM_004594.3(SLC9A5):c.2270del (p.Cys757fs)	Hepatocellular carcinoma [RCV002302760]	pathogenic	16	67270789	67270789	Human	1	name
156224981	CV2219488	single nucleotide variant	NM_004594.3(SLC9A5):c.823G>A (p.Val275Ile)	not specified [RCV004095247]	uncertain significance	16	67255842	67255842	Human		name
155902943	CV2301545	single nucleotide variant	NM_004594.3(SLC9A5):c.970T>A (p.Ser324Thr)	not specified [RCV004162458]	uncertain significance	16	67256527	67256527	Human		name
156279303	CV2338301	single nucleotide variant	NM_004594.3(SLC9A5):c.865G>A (p.Ala289Thr)	not specified [RCV004186356]	uncertain significance	16	67255884	67255884	Human		name
156284317	CV2349014	single nucleotide variant	NM_004594.3(SLC9A5):c.895C>G (p.Leu299Val)	not specified [RCV004203440]	uncertain significance	16	67255914	67255914	Human		name
401885374	CV2783275	single nucleotide variant	NM_004594.3(SLC9A5):c.652G>A (p.Val218Met)	not specified [RCV004363887]	uncertain significance	16	67255182	67255182	Human		name
405771426	CV3322416	single nucleotide variant	NM_004594.3(SLC9A5):c.592G>A (p.Val198Ile)	not specified [RCV004457047]	uncertain significance	16	67255122	67255122	Human		name
405771432	CV3322417	single nucleotide variant	NM_004594.3(SLC9A5):c.615C>G (p.Ile205Met)	not specified [RCV004457048]	uncertain significance	16	67255145	67255145	Human		name
405771439	CV3322418	single nucleotide variant	NM_004594.3(SLC9A5):c.712A>T (p.Thr238Ser)	not specified [RCV004457049]	uncertain significance	16	67255450	67255450	Human		name
407452078	CV3481181	single nucleotide variant	NM_004594.3(SLC9A5):c.827G>A (p.Arg276His)	not specified [RCV004683880]	uncertain significance	16	67255846	67255846	Human		name
597777001	CV3606885	single nucleotide variant	NM_004594.3(SLC9A5):c.832A>G (p.Ile278Val)	not specified [RCV004872933]	uncertain significance	16	67255851	67255851	Human		name
597777016	CV3606889	single nucleotide variant	NM_004594.3(SLC9A5):c.835G>C (p.Glu279Gln)	not specified [RCV004872937]	uncertain significance	16	67255854	67255854	Human		name
155741746	CV1770534	single nucleotide variant	NM_004594.3(SLC9A5):c.2261C>G (p.Ser754Cys)	Hepatocellular carcinoma [RCV002302759]	pathogenic	16	67270780	67270780	Human	1	name
156284308	CV2231188	single nucleotide variant	NM_004594.3(SLC9A5):c.2027C>T (p.Ala676Val)	not specified [RCV004094390]	uncertain significance	16	67265053	67265053	Human		name
155911870	CV2235445	single nucleotide variant	NM_004594.3(SLC9A5):c.1321A>G (p.Thr441Ala)	not specified [RCV004109493]	uncertain significance	16	67257099	67257099	Human		name
155965784	CV2261838	single nucleotide variant	NM_004594.3(SLC9A5):c.1204A>T (p.Met402Leu)	not specified [RCV004126108]	uncertain significance	16	67256982	67256982	Human		name
155915103	CV2264889	single nucleotide variant	NM_004594.3(SLC9A5):c.1589G>A (p.Arg530Lys)	not specified [RCV004134638]	uncertain significance	16	67258410	67258410	Human		name
156333422	CV2266753	single nucleotide variant	NM_004594.3(SLC9A5):c.1562G>A (p.Arg521Gln)	not specified [RCV004137580]	uncertain significance	16	67258383	67258383	Human		name
156364926	CV2272020	single nucleotide variant	NM_004594.3(SLC9A5):c.2266A>G (p.Thr756Ala)	not specified [RCV004124825]	uncertain significance	16	67270785	67270785	Human		name
155928018	CV2280987	single nucleotide variant	NM_004594.3(SLC9A5):c.2234G>C (p.Cys745Ser)	not specified [RCV004145488]	uncertain significance	16	67270753	67270753	Human		name
155928200	CV2281040	single nucleotide variant	NM_004594.3(SLC9A5):c.1927C>T (p.Arg643Trp)	not specified [RCV004147317]	uncertain significance	16	67264436	67264436	Human		name
156238921	CV2285923	single nucleotide variant	NM_004594.3(SLC9A5):c.1669A>G (p.Met557Val)	not specified [RCV004143848]	uncertain significance	16	67259615	67259615	Human		name
156168684	CV2299479	single nucleotide variant	NM_004594.3(SLC9A5):c.2495C>G (p.Pro832Arg)	not specified [RCV004154554]	uncertain significance	16	67271014	67271014	Human		name
156211598	CV2306213	single nucleotide variant	NM_004594.3(SLC9A5):c.1925A>C (p.Lys642Thr)	not specified [RCV004162953]	uncertain significance	16	67264434	67264434	Human		name
156296813	CV2310455	single nucleotide variant	NM_004594.3(SLC9A5):c.2197C>T (p.Leu733Phe)	not specified [RCV004163488]	uncertain significance	16	67266204	67266204	Human		name
156275555	CV2330680	single nucleotide variant	NM_004594.3(SLC9A5):c.1861C>T (p.Arg621Cys)	not specified [RCV004185751]	uncertain significance	16	67264370	67264370	Human		name
155923025	CV2347428	single nucleotide variant	NM_004594.3(SLC9A5):c.1330G>A (p.Val444Met)	not specified [RCV004207262]	uncertain significance	16	67257108	67257108	Human		name
156132404	CV2365780	single nucleotide variant	NM_004594.3(SLC9A5):c.2542G>T (p.Ala848Ser)	not specified [RCV004214319]	uncertain significance	16	67271061	67271061	Human		name
156134944	CV2379754	single nucleotide variant	NM_004594.3(SLC9A5):c.2469A>C (p.Glu823Asp)	not specified [RCV004219873]	uncertain significance	16	67270988	67270988	Human		name
156270831	CV2398739	single nucleotide variant	NM_004594.3(SLC9A5):c.1555C>T (p.Arg519Cys)	not specified [RCV004240078]	uncertain significance	16	67258376	67258376	Human		name
329361568	CV2437649	single nucleotide variant	NM_004594.3(SLC9A5):c.2648C>T (p.Thr883Ile)	not specified [RCV004260967]	uncertain significance	16	67271167	67271167	Human		name
329396197	CV2451953	single nucleotide variant	NM_004594.3(SLC9A5):c.1838G>A (p.Arg613His)	not specified [RCV004276615]	uncertain significance	16	67259942	67259942	Human		name
329402228	CV2454070	single nucleotide variant	NM_004594.3(SLC9A5):c.1246G>A (p.Val416Ile)	not specified [RCV004265579]	uncertain significance	16	67257024	67257024	Human		name
329364178	CV2460281	single nucleotide variant	NM_004594.3(SLC9A5):c.2258C>G (p.Pro753Arg)	not specified [RCV004266829]	uncertain significance	16	67270777	67270777	Human		name
401772403	CV2687515	single nucleotide variant	NM_004594.3(SLC9A5):c.2006G>A (p.Arg669His)	not specified [RCV004300748]	uncertain significance	16	67264515	67264515	Human		name
401767413	CV2729644	single nucleotide variant	NM_004594.3(SLC9A5):c.2318T>C (p.Val773Ala)	not specified [RCV004331906]	uncertain significance	16	67270837	67270837	Human		name
401856021	CV2764271	single nucleotide variant	NM_004594.3(SLC9A5):c.2292G>C (p.Trp764Cys)	not specified [RCV004336803]	uncertain significance	16	67270811	67270811	Human		name
401883828	CV2764673	single nucleotide variant	NM_004594.3(SLC9A5):c.1054G>A (p.Val352Met)	not specified [RCV004341474]	uncertain significance	16	67256611	67256611	Human		name
401864382	CV2777819	single nucleotide variant	NM_004594.3(SLC9A5):c.1768C>T (p.Arg590Cys)	not specified [RCV004346008]	uncertain significance	16	67259872	67259872	Human		name
401900093	CV2780400	single nucleotide variant	NM_004594.3(SLC9A5):c.1952C>T (p.Thr651Ile)	not specified [RCV004357795]	uncertain significance	16	67264461	67264461	Human		name
401911726	CV2808032	single nucleotide variant	NM_004594.3(SLC9A5):c.2206G>C (p.Gly736Arg)	not provided [RCV003426741]	uncertain significance	16	67266213	67266213	Human		name
405771414	CV3322414	single nucleotide variant	NM_004594.3(SLC9A5):c.1837C>T (p.Arg613Cys)	not specified [RCV004457045]	uncertain significance	16	67259941	67259941	Human		name
407452075	CV3481179	single nucleotide variant	NM_004594.3(SLC9A5):c.1649C>T (p.Thr550Ile)	not specified [RCV004683879]	uncertain significance	16	67259595	67259595	Human		name
407515862	CV3481180	single nucleotide variant	NM_004594.3(SLC9A5):c.1394A>T (p.Lys465Ile)	not specified [RCV004675078]	uncertain significance	16	67257403	67257403	Human		name
407515865	CV3481182	single nucleotide variant	NM_004594.3(SLC9A5):c.1956G>T (p.Lys652Asn)	not specified [RCV004675079]	uncertain significance	16	67264465	67264465	Human		name
407515871	CV3481184	single nucleotide variant	NM_004594.3(SLC9A5):c.1719G>T (p.Arg573Ser)	not specified [RCV004675081]	uncertain significance	16	67259823	67259823	Human		name
597776986	CV3606881	single nucleotide variant	NM_004594.3(SLC9A5):c.1892G>A (p.Arg631Gln)	not specified [RCV004872930]	uncertain significance	16	67264401	67264401	Human		name
597776993	CV3606882	single nucleotide variant	NM_004594.3(SLC9A5):c.1678C>T (p.Arg560Cys)	not specified [RCV004872931]	uncertain significance	16	67259624	67259624	Human		name
597776997	CV3606883	single nucleotide variant	NM_004594.3(SLC9A5):c.1955A>G (p.Lys652Arg)	not specified [RCV004872932]	uncertain significance	16	67264464	67264464	Human		name
597725444	CV3606884	single nucleotide variant	NM_004594.3(SLC9A5):c.2500G>A (p.Asp834Asn)	not specified [RCV004862432]	uncertain significance	16	67271019	67271019	Human		name
597777005	CV3606886	single nucleotide variant	NM_004594.3(SLC9A5):c.2360T>C (p.Met787Thr)	not specified [RCV004872934]	uncertain significance	16	67270879	67270879	Human		name
597777012	CV3606888	single nucleotide variant	NM_004594.3(SLC9A5):c.2462G>A (p.Gly821Asp)	not specified [RCV004872936]	uncertain significance	16	67270981	67270981	Human		name
597777022	CV3606891	single nucleotide variant	NM_004594.3(SLC9A5):c.1600C>T (p.Arg534Trp)	not specified [RCV004872938]	uncertain significance	16	67258421	67258421	Human		name
597725457	CV3606892	single nucleotide variant	NM_004594.3(SLC9A5):c.2298T>A (p.Ser766Arg)	not specified [RCV004862434]	uncertain significance	16	67270817	67270817	Human		name
597777026	CV3606893	single nucleotide variant	NM_004594.3(SLC9A5):c.2632A>G (p.Ser878Gly)	not specified [RCV004872939]	uncertain significance	16	67271151	67271151	Human		name
597725465	CV3606894	single nucleotide variant	NM_004594.3(SLC9A5):c.1990C>T (p.Pro664Ser)	not specified [RCV004862435]	uncertain significance	16	67264499	67264499	Human		name
597725473	CV3606895	single nucleotide variant	NM_004594.3(SLC9A5):c.2194G>A (p.Val732Ile)	not specified [RCV004862436]	uncertain significance	16	67266201	67266201	Human		name
598237686	CV3922134	single nucleotide variant	NM_004594.3(SLC9A5):c.1784G>A (p.Arg595His)	not specified [RCV005275703]	uncertain significance	16	67259888	67259888	Human		name
598260656	CV3922135	single nucleotide variant	NM_004594.3(SLC9A5):c.1769G>A (p.Arg590His)	not specified [RCV005279824]	uncertain significance	16	67259873	67259873	Human		name
598260665	CV3922137	single nucleotide variant	NM_004594.3(SLC9A5):c.2518G>A (p.Ala840Thr)	not specified [RCV005279826]	uncertain significance	16	67271037	67271037	Human		name
598260670	CV3922138	single nucleotide variant	NM_004594.3(SLC9A5):c.1430T>C (p.Phe477Ser)	not specified [RCV005279827]	uncertain significance	16	67257535	67257535	Human		name
598237693	CV3922139	single nucleotide variant	NM_004594.3(SLC9A5):c.1601G>A (p.Arg534Gln)	not specified [RCV005275704]	uncertain significance	16	67258422	67258422	Human		name
155741660	CV1770468	microsatellite	NM_004594.3(SLC9A5):c.2107GAG[5] (p.Glu708del)	Hepatocellular carcinoma [RCV002302692]	pathogenic	16	67266114	67266116	Human		name
155741623	CV1770437	deletion	NM_004594.3(SLC9A5):c.2277_2279del (p.Lys760del)	Hepatocellular carcinoma [RCV002302661]	pathogenic	16	67270795	67270797	Human	1	name
401903334	CV2808031	deletion	NM_004594.3(SLC9A5):c.2146_2148del (p.Lys716del)	not provided [RCV003419363]	uncertain significance	16	67266151	67266153	Human		name
155741624	CV1770438	insertion	NM_004594.3(SLC9A5):c.2287_2288insTTT (p.Pro763delinsLeuSer)	Hepatocellular carcinoma [RCV002302662]	pathogenic	16	67270806	67270807	Human	1	name
155741625	CV1770439	insertion	NM_004594.3(SLC9A5):c.2291_2292insCACAGGTTGGGGAGGGGG (p.Trp764delinsCysThrGlyTrpGlyGlyGly)	Hepatocellular carcinoma [RCV002302663]	pathogenic	16	67270809	67270810	Human	1	name

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