Slc9a8 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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40 records found for search term Slc9a8

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8586517	CV121120	single nucleotide variant	NM_001260491.1(SLC9A8):c.761+3648G>T	Lung cancer [RCV000101640]	uncertain significance	20	49859229	49859229	Human		name
401770943	CV2686104	single nucleotide variant	NM_015266.3(SLC9A8):c.59A>G (p.Asn20Ser)	not specified [RCV004297113]	uncertain significance	20	49815040	49815040	Human		name
401754607	CV2722770	single nucleotide variant	NM_015266.3(SLC9A8):c.570T>C (p.Ser190=)	not specified [RCV004325198]	likely benign	20	49855438	49855438	Human		name
597725503	CV3606908	single nucleotide variant	NM_015266.3(SLC9A8):c.89C>T (p.Thr30Met)	not specified [RCV004862440]	uncertain significance	20	49815070	49815070	Human		name
156041701	CV2261398	single nucleotide variant	NM_015266.3(SLC9A8):c.225G>C (p.Leu75Phe)	not specified [RCV004130034]	uncertain significance	20	49823077	49823077	Human		name
401717867	CV2704046	single nucleotide variant	NM_015266.3(SLC9A8):c.253C>T (p.His85Tyr)	not specified [RCV004308929]	uncertain significance	20	49823105	49823105	Human		name
401919786	CV2824477	single nucleotide variant	NM_015266.3(SLC9A8):c.1650C>T (p.His550=)	not provided [RCV003431353]	likely benign	20	49887840	49887840	Human		name
405771470	CV3322423	single nucleotide variant	NM_015266.3(SLC9A8):c.113C>T (p.Pro38Leu)	not specified [RCV004457054]	uncertain significance	20	49815094	49815094	Human		name
405771477	CV3322424	single nucleotide variant	NM_015266.3(SLC9A8):c.133G>A (p.Val45Met)	not specified [RCV004457055]	uncertain significance	20	49815114	49815114	Human		name
597777064	CV3606906	single nucleotide variant	NM_015266.3(SLC9A8):c.290G>A (p.Gly97Asp)	not specified [RCV004872948]	uncertain significance	20	49839541	49839541	Human		name
597777073	CV3606910	single nucleotide variant	NM_015266.3(SLC9A8):c.215G>A (p.Cys72Tyr)	not specified [RCV004872950]	uncertain significance	20	49823067	49823067	Human		name
598260695	CV3922147	single nucleotide variant	NM_015266.3(SLC9A8):c.107C>T (p.Pro36Leu)	not specified [RCV005279832]	uncertain significance	20	49815088	49815088	Human		name
598237716	CV3922149	single nucleotide variant	NM_015266.3(SLC9A8):c.283T>G (p.Ser95Ala)	not specified [RCV005275708]	uncertain significance	20	49823135	49823135	Human		name
156150878	CV2318717	single nucleotide variant	NM_015266.3(SLC9A8):c.620C>T (p.Ala207Val)	not specified [RCV004173608]	uncertain significance	20	49855488	49855488	Human		name
156153389	CV2374842	single nucleotide variant	NM_015266.3(SLC9A8):c.400A>G (p.Ile134Val)	not specified [RCV004227874]	uncertain significance	20	49845087	49845087	Human		name
155962020	CV2388160	single nucleotide variant	NM_015266.3(SLC9A8):c.881C>T (p.Thr294Met)	not specified [RCV004234623]	uncertain significance	20	49864767	49864767	Human		name
329400026	CV2440406	single nucleotide variant	NM_015266.3(SLC9A8):c.727T>A (p.Leu243Ile)	not specified [RCV004256343]	uncertain significance	20	49862942	49862942	Human		name
329354772	CV2449025	single nucleotide variant	NM_015266.3(SLC9A8):c.562A>G (p.Thr188Ala)	not specified [RCV004264100]	uncertain significance	20	49850837	49850837	Human		name
329378179	CV2459061	single nucleotide variant	NM_015266.3(SLC9A8):c.724G>A (p.Gly242Ser)	not specified [RCV004272530]	uncertain significance	20	49862939	49862939	Human		name
401752960	CV2681070	single nucleotide variant	NM_015266.3(SLC9A8):c.796A>G (p.Lys266Glu)	not specified [RCV004296131]	uncertain significance	20	49863011	49863011	Human		name
401734114	CV2697958	single nucleotide variant	NM_015266.3(SLC9A8):c.764A>G (p.Gln255Arg)	not specified [RCV004302446]	uncertain significance	20	49862979	49862979	Human		name
401883672	CV2754552	single nucleotide variant	NM_015266.3(SLC9A8):c.853G>A (p.Val285Met)	not specified [RCV004339231]	uncertain significance	20	49864739	49864739	Human		name
405771494	CV3322427	single nucleotide variant	NM_015266.3(SLC9A8):c.311T>C (p.Ile104Thr)	not specified [RCV004457058]	uncertain significance	20	49839562	49839562	Human		name
405771500	CV3322428	single nucleotide variant	NM_015266.3(SLC9A8):c.567C>G (p.Asp189Glu)	not specified [RCV004457059]	uncertain significance	20	49850842	49850842	Human		name
405771508	CV3322429	single nucleotide variant	NM_015266.3(SLC9A8):c.979T>C (p.Ser327Pro)	not specified [RCV004457060]	uncertain significance	20	49874725	49874725	Human		name
407515884	CV3481191	single nucleotide variant	NM_015266.3(SLC9A8):c.302G>A (p.Gly101Glu)	not specified [RCV004675085]	uncertain significance	20	49839553	49839553	Human		name
597777060	CV3606905	single nucleotide variant	NM_015266.3(SLC9A8):c.452T>C (p.Ile151Thr)	not specified [RCV004872947]	uncertain significance	20	49849598	49849598	Human		name
598260692	CV3922146	single nucleotide variant	NM_015266.3(SLC9A8):c.739A>G (p.Asn247Asp)	not specified [RCV005279831]	uncertain significance	20	49862954	49862954	Human		name
598260705	CV3922150	single nucleotide variant	NM_015266.3(SLC9A8):c.433G>T (p.Gly145Cys)	not specified [RCV005279834]	uncertain significance	20	49849579	49849579	Human		name
155934934	CV2225455	single nucleotide variant	NM_015266.3(SLC9A8):c.1618A>C (p.Thr540Pro)	not specified [RCV004100853]	uncertain significance	20	49886878	49886878	Human		name
156284923	CV2360718	single nucleotide variant	NM_015266.3(SLC9A8):c.1171T>G (p.Phe391Val)	not specified [RCV004213507]	uncertain significance	20	49880936	49880936	Human		name
329394041	CV2450041	single nucleotide variant	NM_015266.3(SLC9A8):c.1334G>A (p.Arg445Gln)	not specified [RCV004269092]	uncertain significance	20	49883909	49883909	Human		name
405771482	CV3322425	single nucleotide variant	NM_015266.3(SLC9A8):c.1465G>A (p.Val489Ile)	not specified [RCV004457056]	uncertain significance	20	49884040	49884040	Human		name
407452088	CV3481189	single nucleotide variant	NM_015266.3(SLC9A8):c.1222C>T (p.Arg408Trp)	not specified [RCV004683883]	uncertain significance	20	49880987	49880987	Human		name
407515879	CV3481190	single nucleotide variant	NM_015266.3(SLC9A8):c.1508C>T (p.Ser503Leu)	not specified [RCV004675084]	uncertain significance	20	49886768	49886768	Human		name
597725497	CV3606907	single nucleotide variant	NM_015266.3(SLC9A8):c.1469A>G (p.Asn490Ser)	not specified [RCV004862439]	uncertain significance	20	49884044	49884044	Human		name
597777069	CV3606909	single nucleotide variant	NM_015266.3(SLC9A8):c.1333C>T (p.Arg445Trp)	not specified [RCV004872949]	uncertain significance	20	49883908	49883908	Human		name
597725510	CV3606911	single nucleotide variant	NM_015266.3(SLC9A8):c.1180G>A (p.Ala394Thr)	not specified [RCV004862441]	uncertain significance	20	49880945	49880945	Human		name
598237709	CV3922145	single nucleotide variant	NM_015266.3(SLC9A8):c.1440G>C (p.Lys480Asn)	not specified [RCV005275707]	uncertain significance	20	49884015	49884015	Human		name
598260700	CV3922148	single nucleotide variant	NM_015266.3(SLC9A8):c.1355C>T (p.Thr452Ile)	not specified [RCV005279833]	uncertain significance	20	49883930	49883930	Human		name

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