Rps6ka5 Variant Search Result - Rat Genome Database

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55 records found for search term Rps6ka5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156215983	CV2347934	single nucleotide variant	NM_004755.4(RPS6KA5):c.22A>C (p.Ser8Arg)	not specified [RCV004197624]	uncertain significance	14	91060413	91060413	Human		name
598220492	CV3903043	single nucleotide variant	NM_004755.4(RPS6KA5):c.25G>T (p.Gly9Cys)	not specified [RCV005272482]	uncertain significance	14	91060410	91060410	Human		name
155913925	CV2242541	single nucleotide variant	NM_004755.4(RPS6KA5):c.50A>G (p.Asp17Gly)	not specified [RCV004113610]	uncertain significance	14	91060385	91060385	Human		name
155925321	CV2258506	single nucleotide variant	NM_004755.4(RPS6KA5):c.92A>T (p.Glu31Val)	not specified [RCV004115998]	uncertain significance	14	91060343	91060343	Human		name
329349481	CV2440639	single nucleotide variant	NM_004755.4(RPS6KA5):c.62G>T (p.Gly21Val)	not specified [RCV004256549]	uncertain significance	14	91060373	91060373	Human		name
401747952	CV2712330	single nucleotide variant	NM_004755.4(RPS6KA5):c.56G>T (p.Gly19Val)	not specified [RCV004313818]	uncertain significance	14	91060379	91060379	Human		name
401858149	CV2770713	single nucleotide variant	NM_004755.4(RPS6KA5):c.52G>C (p.Gly18Arg)	not specified [RCV004349757]	uncertain significance	14	91060383	91060383	Human		name
598220500	CV3903044	single nucleotide variant	NM_004755.4(RPS6KA5):c.59A>G (p.Asp20Gly)	not specified [RCV005272483]	uncertain significance	14	91060376	91060376	Human		name
156006050	CV2357727	single nucleotide variant	NM_004755.4(RPS6KA5):c.199C>T (p.Arg67Cys)	not specified [RCV004205022]	uncertain significance	14	90978501	90978501	Human		name
401718098	CV2725309	single nucleotide variant	NM_004755.4(RPS6KA5):c.200G>A (p.Arg67His)	not specified [RCV004319973]	uncertain significance	14	90978500	90978500	Human		name
8635324	CV90546	single nucleotide variant	NM_004755.2(RPS6KA5):c.2394G>A (p.Ser798=)	Malignant melanoma [RCV000070644]	not provided	14	90872089	90872089	Human		name
155995114	CV2258949	single nucleotide variant	NM_004755.4(RPS6KA5):c.737A>G (p.Tyr246Cys)	not specified [RCV004120229]	uncertain significance	14	90920275	90920275	Human		name
156240414	CV2265533	single nucleotide variant	NM_004755.4(RPS6KA5):c.458A>C (p.Glu153Ala)	not specified [RCV004124282]	uncertain significance	14	90947487	90947487	Human		name
156251086	CV2286795	single nucleotide variant	NM_004755.4(RPS6KA5):c.839A>G (p.Gln280Arg)	not specified [RCV004142599]	uncertain significance	14	90906267	90906267	Human		name
156282386	CV2288820	single nucleotide variant	NM_004755.4(RPS6KA5):c.443G>A (p.Arg148His)	not specified [RCV004148029]	uncertain significance	14	90947502	90947502	Human		name
405739155	CV3320289	single nucleotide variant	NM_004755.4(RPS6KA5):c.502C>G (p.Leu168Val)	not specified [RCV004452110]	uncertain significance	14	90947443	90947443	Human		name
405739162	CV3320290	single nucleotide variant	NM_004755.4(RPS6KA5):c.772G>C (p.Asp258His)	not specified [RCV004452111]	uncertain significance	14	90920240	90920240	Human		name
405739171	CV3320291	single nucleotide variant	NM_004755.4(RPS6KA5):c.958A>G (p.Lys320Glu)	not specified [RCV004452112]	uncertain significance	14	90902969	90902969	Human		name
405739179	CV3320292	single nucleotide variant	NM_004755.4(RPS6KA5):c.982G>A (p.Ala328Thr)	not specified [RCV004452113]	uncertain significance	14	90902945	90902945	Human		name
407488139	CV3476234	single nucleotide variant	NM_004755.4(RPS6KA5):c.892C>A (p.Pro298Thr)	RPS6KA5-related disorder [RCV005392843]\|not specified [RCV004665817]	uncertain significance	14	90906214	90906214	Human		name , trait
407513806	CV3476235	single nucleotide variant	NM_004755.4(RPS6KA5):c.298A>G (p.Thr100Ala)	not specified [RCV004674254]	uncertain significance	14	90978402	90978402	Human		name
597710065	CV3594399	single nucleotide variant	NM_004755.4(RPS6KA5):c.549T>G (p.Ile183Met)	not specified [RCV004860914]	uncertain significance	14	90943147	90943147	Human		name
597786139	CV3594401	single nucleotide variant	NM_004755.4(RPS6KA5):c.864C>G (p.Asp288Glu)	not specified [RCV004854925]	uncertain significance	14	90906242	90906242	Human		name
597710085	CV3594404	single nucleotide variant	NM_004755.4(RPS6KA5):c.772G>A (p.Asp258Asn)	not specified [RCV004860916]	uncertain significance	14	90920240	90920240	Human		name
597786144	CV3594406	single nucleotide variant	NM_004755.4(RPS6KA5):c.874C>T (p.Arg292Cys)	not specified [RCV004854926]	uncertain significance	14	90906232	90906232	Human		name
598220485	CV3903042	single nucleotide variant	NM_004755.4(RPS6KA5):c.875G>A (p.Arg292His)	not specified [RCV005272481]	uncertain significance	14	90906231	90906231	Human		name
598220535	CV3903049	single nucleotide variant	NM_004755.4(RPS6KA5):c.928G>A (p.Asp310Asn)	not specified [RCV005272488]	uncertain significance	14	90906178	90906178	Human		name
156108330	CV2304211	single nucleotide variant	NM_004755.4(RPS6KA5):c.2372C>T (p.Pro791Leu)	not specified [RCV004170232]	uncertain significance	14	90872111	90872111	Human		name
156346005	CV2309003	single nucleotide variant	NM_004755.4(RPS6KA5):c.1526G>A (p.Arg509His)	not specified [RCV004171067]	uncertain significance	14	90894531	90894531	Human		name
156265263	CV2329517	single nucleotide variant	NM_004755.4(RPS6KA5):c.1540A>C (p.Lys514Gln)	not specified [RCV004180651]	uncertain significance	14	90894517	90894517	Human		name
156292675	CV2340230	single nucleotide variant	NM_004755.4(RPS6KA5):c.1939T>A (p.Ser647Thr)	not specified [RCV004192461]	uncertain significance	14	90875258	90875258	Human		name
155927537	CV2365944	single nucleotide variant	NM_004755.4(RPS6KA5):c.1838A>G (p.Tyr613Cys)	not specified [RCV004207554]	uncertain significance	14	90875359	90875359	Human		name
156308132	CV2369869	single nucleotide variant	NM_004755.4(RPS6KA5):c.1895C>G (p.Thr632Ser)	not specified [RCV004208340]	uncertain significance	14	90875302	90875302	Human		name
329382487	CV2424415	single nucleotide variant	NM_004755.4(RPS6KA5):c.1322G>A (p.Arg441Gln)	not specified [RCV004252311]	uncertain significance	14	90900165	90900165	Human		name
329389814	CV2441352	single nucleotide variant	NM_004755.4(RPS6KA5):c.1935T>G (p.Asp645Glu)	not specified [RCV004257161]	uncertain significance	14	90875262	90875262	Human		name
329374592	CV2464188	single nucleotide variant	NM_004755.4(RPS6KA5):c.1088C>T (p.Ala363Val)	not specified [RCV004273867]	uncertain significance	14	90902839	90902839	Human		name
401733932	CV2687876	single nucleotide variant	NM_004755.4(RPS6KA5):c.2360A>T (p.Asp787Val)	not specified [RCV004303179]	uncertain significance	14	90872123	90872123	Human		name
401892165	CV2777291	single nucleotide variant	NM_004755.4(RPS6KA5):c.1753A>C (p.Thr585Pro)	not specified [RCV004354307]	uncertain significance	14	90890570	90890570	Human		name
401874963	CV2781366	single nucleotide variant	NM_004755.4(RPS6KA5):c.2002C>A (p.Leu668Ile)	not specified [RCV004352374]	uncertain significance	14	90873790	90873790	Human		name
405739115	CV3320283	single nucleotide variant	NM_004755.4(RPS6KA5):c.1068T>A (p.Asp356Glu)	not specified [RCV004452104]	uncertain significance	14	90902859	90902859	Human		name
405739121	CV3320284	single nucleotide variant	NM_004755.4(RPS6KA5):c.1204C>T (p.Arg402Cys)	not specified [RCV004452105]	uncertain significance	14	90900652	90900652	Human		name
405739132	CV3320285	single nucleotide variant	NM_004755.4(RPS6KA5):c.1891T>C (p.Cys631Arg)	not specified [RCV004452106]	uncertain significance	14	90875306	90875306	Human		name
405739137	CV3320286	single nucleotide variant	NM_004755.4(RPS6KA5):c.2089C>G (p.Pro697Ala)	not specified [RCV004452107]	uncertain significance	14	90873703	90873703	Human		name
405739143	CV3320287	single nucleotide variant	NM_004755.4(RPS6KA5):c.2266C>T (p.Arg756Cys)	not specified [RCV004452108]	uncertain significance	14	90872217	90872217	Human		name
405739149	CV3320288	single nucleotide variant	NM_004755.4(RPS6KA5):c.2362A>G (p.Ser788Gly)	not specified [RCV004452109]	likely benign	14	90872121	90872121	Human		name
407513803	CV3476233	single nucleotide variant	NM_004755.4(RPS6KA5):c.2131G>T (p.Val711Leu)	not specified [RCV004674253]	uncertain significance	14	90873661	90873661	Human		name
597710057	CV3594398	single nucleotide variant	NM_004755.4(RPS6KA5):c.1391A>G (p.Asn464Ser)	not specified [RCV004860913]	uncertain significance	14	90899411	90899411	Human		name
597786135	CV3594400	single nucleotide variant	NM_004755.4(RPS6KA5):c.2051A>G (p.Asn684Ser)	not specified [RCV004854924]	uncertain significance	14	90873741	90873741	Human		name
597710074	CV3594402	single nucleotide variant	NM_004755.4(RPS6KA5):c.2224A>G (p.Lys742Glu)	not specified [RCV004860915]	uncertain significance	14	90872259	90872259	Human		name
597710092	CV3594405	single nucleotide variant	NM_004755.4(RPS6KA5):c.1049A>G (p.Glu350Gly)	not specified [RCV004860917]	uncertain significance	14	90902878	90902878	Human		name
597786148	CV3594407	single nucleotide variant	NM_004755.4(RPS6KA5):c.1992C>G (p.Ile664Met)	not specified [RCV004854927]	uncertain significance	14	90875205	90875205	Human		name
598220507	CV3903045	single nucleotide variant	NM_004755.4(RPS6KA5):c.1564A>G (p.Ser522Gly)	not specified [RCV005272484]	uncertain significance	14	90894493	90894493	Human		name
598220514	CV3903046	single nucleotide variant	NM_004755.4(RPS6KA5):c.2369A>G (p.Asn790Ser)	not specified [RCV005272485]	uncertain significance	14	90872114	90872114	Human		name
598220521	CV3903047	single nucleotide variant	NM_004755.4(RPS6KA5):c.2279G>A (p.Ser760Asn)	not specified [RCV005272486]	uncertain significance	14	90872204	90872204	Human		name
598220529	CV3903048	single nucleotide variant	NM_004755.4(RPS6KA5):c.1598G>A (p.Ser533Asn)	not specified [RCV005272487]	uncertain significance	14	90894459	90894459	Human		name

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