| 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 |
