Il15 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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48 records found for search term Il15

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8579247	CV113645	single nucleotide variant	NM_000585.4(IL15):c.-1908A>C	Lung cancer [RCV000094168]	uncertain significance	4	141635062	141635062	Human		name
405804346	CV3270891	single nucleotide variant	NM_000585.5(IL15):c.22T>G (p.Leu8Val)	not specified [RCV004404952]	uncertain significance	4	141720478	141720478	Human		name
597792928	CV3690162	single nucleotide variant	NM_000585.5(IL15):c.86C>G (p.Ala29Gly)	not specified [RCV004934008]	uncertain significance	4	141720542	141720542	Human		name
15122046	CV709176	single nucleotide variant	NM_000585.5(IL15):c.349C>T (p.Leu117=)	not provided [RCV000963006]	benign	4	141729955	141729955	Human		name
15177161	CV709177	single nucleotide variant	NM_000585.5(IL15):c.408T>C (p.Cys136=)	not provided [RCV000973357]	likely benign	4	141732767	141732767	Human		name
155955849	CV2281856	single nucleotide variant	NM_000585.5(IL15):c.231T>G (p.Ser77Arg)	not specified [RCV004136857]	uncertain significance	4	141727975	141727975	Human		name
329393595	CV2453457	single nucleotide variant	NM_000585.5(IL15):c.149G>T (p.Trp50Leu)	not specified [RCV004267059]	uncertain significance	4	141721962	141721962	Human		name
401863743	CV2773270	single nucleotide variant	NM_000585.5(IL15):c.238C>T (p.His80Tyr)	not specified [RCV004353941]	uncertain significance	4	141727982	141727982	Human		name
405804344	CV3270890	single nucleotide variant	NM_000585.5(IL15):c.218T>C (p.Leu73Ser)	not specified [RCV004404951]	uncertain significance	4	141727962	141727962	Human		name
156294211	CV2321393	single nucleotide variant	NM_000585.5(IL15):c.361A>C (p.Ser121Arg)	not specified [RCV004177384]	uncertain significance	4	141729967	141729967	Human		name
329353003	CV2468164	single nucleotide variant	NM_000585.5(IL15):c.436G>C (p.Glu146Gln)	not specified [RCV004275751]	uncertain significance	4	141732795	141732795	Human		name
405804349	CV3270893	single nucleotide variant	NM_000585.5(IL15):c.430A>T (p.Ile144Phe)	not specified [RCV004404954]	uncertain significance	4	141732789	141732789	Human		name
156066772	CV2225598	single nucleotide variant	NM_002189.4(IL15RA):c.8C>T (p.Pro3Leu)	not specified [RCV004100971]	uncertain significance	10	5977485	5977485	Human		name
156207736	CV2360459	single nucleotide variant	NM_002189.4(IL15RA):c.19C>T (p.Arg7Cys)	not specified [RCV004208779]	uncertain significance	10	5977474	5977474	Human		name
597792930	CV3690163	single nucleotide variant	NM_002189.4(IL15RA):c.11G>A (p.Arg4Gln)	not specified [RCV004934009]	uncertain significance	10	5977482	5977482	Human		name
401890583	CV2768319	single nucleotide variant	NM_002189.4(IL15RA):c.59T>C (p.Leu20Pro)	not specified [RCV004350300]	uncertain significance	10	5977434	5977434	Human		name
401938100	CV2812983	single nucleotide variant	NM_002189.4(IL15RA):c.750T>C (p.Thr250=)	not provided [RCV003417205]	likely benign	10	5953149	5953149	Human		name
407515553	CV3444480	single nucleotide variant	NM_002189.4(IL15RA):c.74C>T (p.Pro25Leu)	not specified [RCV004627932]	uncertain significance	10	5977419	5977419	Human		name
15186425	CV701387	single nucleotide variant	NM_001256765.1(IL15RA):c.15G>A (p.Gly5=)	not provided [RCV000953278]	likely benign	10	5977583	5977583	Human		name
15121678	CV712409	single nucleotide variant	NM_002189.4(IL15RA):c.513C>G (p.Ser171=)	not provided [RCV000962938]	benign\|likely benign	10	5960437	5960437	Human		name
405804351	CV3270894	single nucleotide variant	NM_002189.4(IL15RA):c.238G>T (p.Ala80Ser)	not specified [RCV004404955]	uncertain significance	10	5966190	5966190	Human		name
405804353	CV3270895	single nucleotide variant	NM_002189.4(IL15RA):c.242C>T (p.Thr81Met)	not specified [RCV004404956]	uncertain significance	10	5966186	5966186	Human		name
407515550	CV3444478	single nucleotide variant	NM_002189.4(IL15RA):c.202G>A (p.Gly68Ser)	not specified [RCV004627931]	uncertain significance	10	5966226	5966226	Human		name
597792933	CV3690164	single nucleotide variant	NM_002189.4(IL15RA):c.250G>A (p.Ala84Thr)	not specified [RCV004934010]	uncertain significance	10	5966178	5966178	Human		name
597792939	CV3690166	single nucleotide variant	NM_002189.4(IL15RA):c.286G>C (p.Asp96His)	not specified [RCV004934012]	uncertain significance	10	5963839	5963839	Human		name
598179324	CV3976017	single nucleotide variant	NM_002189.4(IL15RA):c.176G>A (p.Cys59Tyr)	not specified [RCV005352136]	uncertain significance	10	5966252	5966252	Human		name
150497675	CV1219445	single nucleotide variant	NM_002189.4(IL15RA):c.545A>C (p.Asn182Thr)	not provided [RCV001620114]	benign	10	5960405	5960405	Human	1	name
156180954	CV2353044	single nucleotide variant	NM_002189.4(IL15RA):c.416C>T (p.Thr139Ile)	not specified [RCV004203532]	uncertain significance	10	5960534	5960534	Human		name
156150547	CV2394661	single nucleotide variant	NM_002189.4(IL15RA):c.361A>G (p.Ser121Gly)	not specified [RCV004240998]	uncertain significance	10	5963764	5963764	Human		name
156005363	CV2401083	single nucleotide variant	NM_002189.4(IL15RA):c.704C>T (p.Pro235Leu)	not specified [RCV004245654]	uncertain significance	10	5953195	5953195	Human		name
401747306	CV2698836	single nucleotide variant	NM_002189.4(IL15RA):c.419C>T (p.Ala140Val)	not specified [RCV004301275]	likely benign	10	5960531	5960531	Human		name
401768769	CV2716724	single nucleotide variant	NM_002189.4(IL15RA):c.661G>A (p.Val221Met)	not specified [RCV004327771]	uncertain significance	10	5956410	5956410	Human		name
401883242	CV2760745	single nucleotide variant	NM_002189.4(IL15RA):c.629C>T (p.Thr210Met)	not specified [RCV004336392]	uncertain significance	10	5956442	5956442	Human		name
401859869	CV2765174	single nucleotide variant	NM_002189.4(IL15RA):c.443C>T (p.Pro148Leu)	not specified [RCV004339704]	uncertain significance	10	5960507	5960507	Human		name
401888112	CV2791256	single nucleotide variant	NM_002189.4(IL15RA):c.508T>C (p.Ser170Pro)	not specified [RCV004356889]	likely benign	10	5960442	5960442	Human		name
405804355	CV3270896	single nucleotide variant	NM_002189.4(IL15RA):c.310C>T (p.Pro104Ser)	not specified [RCV004404957]	uncertain significance	10	5963815	5963815	Human		name
405804357	CV3270897	single nucleotide variant	NM_002189.4(IL15RA):c.400C>T (p.Pro134Ser)	not specified [RCV004404958]	likely benign	10	5960550	5960550	Human		name
405804359	CV3270898	single nucleotide variant	NM_002189.4(IL15RA):c.421G>A (p.Ala141Thr)	not specified [RCV004404959]	uncertain significance	10	5960529	5960529	Human		name
405804361	CV3270899	single nucleotide variant	NM_002189.4(IL15RA):c.506A>G (p.Glu169Gly)	not specified [RCV004404960]	uncertain significance	10	5960444	5960444	Human		name
405804363	CV3270900	single nucleotide variant	NM_002189.4(IL15RA):c.665C>T (p.Ser222Phe)	not specified [RCV004404961]	uncertain significance	10	5956406	5956406	Human		name
405804365	CV3270901	single nucleotide variant	NM_002189.4(IL15RA):c.700C>T (p.Pro234Ser)	not specified [RCV004404962]	likely benign	10	5953199	5953199	Human		name
407515540	CV3440966	single nucleotide variant	NM_002189.4(IL15RA):c.364C>T (p.Leu122Phe)	not specified [RCV004627928]	uncertain significance	10	5963761	5963761	Human		name
407515544	CV3440967	single nucleotide variant	NM_002189.4(IL15RA):c.314C>T (p.Ala105Val)	not specified [RCV004627929]	likely benign	10	5963811	5963811	Human		name
407511188	CV3444479	single nucleotide variant	NM_002189.4(IL15RA):c.524C>G (p.Pro175Arg)	not specified [RCV004626383]	uncertain significance	10	5960426	5960426	Human		name
597792936	CV3690165	single nucleotide variant	NM_002189.4(IL15RA):c.490G>A (p.Glu164Lys)	not specified [RCV004934011]	uncertain significance	10	5960460	5960460	Human		name
598179331	CV3976018	single nucleotide variant	NM_002189.4(IL15RA):c.518G>C (p.Gly173Ala)	not specified [RCV005352137]	likely benign	10	5960432	5960432	Human		name
15173172	CV701385	single nucleotide variant	NM_002189.4(IL15RA):c.332C>T (p.Thr111Met)	not provided [RCV000950183]	benign	10	5963793	5963793	Human		name
15155443	CV723978	single nucleotide variant	NM_002189.4(IL15RA):c.715G>A (p.Val239Ile)	not provided [RCV000880418]	benign	10	5953184	5953184	Human		name

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