| 150472896 | CV1252318 | single nucleotide variant | NM_172217.5(IL16):c.*643T>C | not provided [RCV001671520] | benign | 15 | 81309441 | 81309441 | Human | | name |
| 405870047 | CV2842376 | single nucleotide variant | NM_172217.5(IL16):c.1903-5C>A | EBV-positive nodal T- and NK-cell lymphoma [RCV004557733] | likely benign | 15 | 81296923 | 81296923 | Human | | name |
| 405804460 | CV3270928 | single nucleotide variant | NM_172217.5(IL16):c.8C>T (p.Ser3Leu) | not specified [RCV004404989] | uncertain significance | 15 | 81225407 | 81225407 | Human | | name |
| 156047253 | CV2382423 | single nucleotide variant | NM_172217.5(IL16):c.19G>A (p.Ala7Thr) | not specified [RCV004230762] | likely benign | 15 | 81225418 | 81225418 | Human | | name |
| 405804430 | CV3270912 | single nucleotide variant | NM_172217.5(IL16):c.23G>C (p.Gly8Ala) | not specified [RCV004404973] | uncertain significance | 15 | 81225422 | 81225422 | Human | | name |
| 598207281 | CV3976022 | single nucleotide variant | NM_172217.5(IL16):c.26A>C (p.Lys9Thr) | not specified [RCV005337949] | uncertain significance | 15 | 81225425 | 81225425 | Human | | name |
| 156144540 | CV2292265 | single nucleotide variant | NM_172217.5(IL16):c.29G>T (p.Ser10Ile) | not specified [RCV004148301] | uncertain significance | 15 | 81225428 | 81225428 | Human | | name |
| 407515576 | CV3444487 | single nucleotide variant | NM_172217.5(IL16):c.55A>G (p.Ile19Val) | not specified [RCV004627939] | uncertain significance | 15 | 81225454 | 81225454 | Human | | name |
| 597792942 | CV3690167 | single nucleotide variant | NM_172217.5(IL16):c.49C>T (p.Arg17Trp) | not specified [RCV004934013] | uncertain significance | 15 | 81225448 | 81225448 | Human | | name |
| 156068362 | CV2203668 | single nucleotide variant | NM_172217.5(IL16):c.173A>C (p.His58Pro) | not specified [RCV004074322] | uncertain significance | 15 | 81225572 | 81225572 | Human | | name |
| 401916430 | CV2814415 | single nucleotide variant | NM_172217.5(IL16):c.2199T>C (p.His733=) | not provided [RCV003400983] | likely benign | 15 | 81299525 | 81299525 | Human | | name |
| 405804441 | CV3270918 | single nucleotide variant | NM_172217.5(IL16):c.292A>G (p.Arg98Gly) | not specified [RCV004404979] | uncertain significance | 15 | 81225691 | 81225691 | Human | | name |
| 597792948 | CV3690169 | single nucleotide variant | NM_172217.5(IL16):c.278G>A (p.Arg93Gln) | not specified [RCV004934015] | uncertain significance | 15 | 81225677 | 81225677 | Human | | name |
| 597792982 | CV3690181 | single nucleotide variant | NM_172217.5(IL16):c.148G>A (p.Ala50Thr) | not specified [RCV004934027] | uncertain significance | 15 | 81225547 | 81225547 | Human | | name |
| 597792999 | CV3690188 | single nucleotide variant | NM_172217.5(IL16):c.1200G>C (p.Arg400=) | not specified [RCV004934033] | likely benign | 15 | 81285698 | 81285698 | Human | | name |
| 598179360 | CV3976025 | single nucleotide variant | NM_172217.5(IL16):c.242C>T (p.Ser81Leu) | not specified [RCV005352142] | uncertain significance | 15 | 81225641 | 81225641 | Human | | name |
| 15198088 | CV726296 | single nucleotide variant | NM_172217.5(IL16):c.2814G>A (p.Pro938=) | not provided [RCV000890252] | benign | 15 | 81300140 | 81300140 | Human | | name |
| 15179309 | CV770373 | single nucleotide variant | NM_172217.5(IL16):c.2592C>G (p.Leu864=) | not provided [RCV000929608] | likely benign | 15 | 81299918 | 81299918 | Human | | name |
| 156195581 | CV2223440 | single nucleotide variant | NM_172217.5(IL16):c.936C>A (p.His312Gln) | not specified [RCV004106017] | uncertain significance | 15 | 81279629 | 81279629 | Human | | name |
| 156254884 | CV2229230 | single nucleotide variant | NM_172217.5(IL16):c.943C>T (p.Pro315Ser) | not specified [RCV004101044] | uncertain significance | 15 | 81279636 | 81279636 | Human | | name |
| 156039615 | CV2313752 | single nucleotide variant | NM_172217.5(IL16):c.584G>A (p.Arg195Gln) | not specified [RCV004157663] | uncertain significance | 15 | 81269557 | 81269557 | Human | | name |
| 155923875 | CV2347576 | single nucleotide variant | NM_172217.5(IL16):c.772G>T (p.Asp258Tyr) | not specified [RCV004200514] | uncertain significance | 15 | 81273186 | 81273186 | Human | | name |
| 155925138 | CV2348300 | single nucleotide variant | NM_172217.5(IL16):c.911C>T (p.Thr304Met) | not specified [RCV004193500] | likely benign | 15 | 81279604 | 81279604 | Human | | name |
| 155927281 | CV2365901 | single nucleotide variant | NM_172217.5(IL16):c.947C>T (p.Pro316Leu) | not specified [RCV004214429] | uncertain significance | 15 | 81279640 | 81279640 | Human | | name |
| 329390400 | CV2459185 | single nucleotide variant | NM_172217.5(IL16):c.694G>A (p.Val232Ile) | not specified [RCV004272629] | uncertain significance | 15 | 81273108 | 81273108 | Human | | name |
| 329387707 | CV2470914 | single nucleotide variant | NM_172217.5(IL16):c.617C>A (p.Ser206Tyr) | not specified [RCV004276108] | uncertain significance | 15 | 81269590 | 81269590 | Human | | name |
| 401742407 | CV2715212 | single nucleotide variant | NM_172217.5(IL16):c.413A>T (p.Asn138Ile) | not specified [RCV004324564] | uncertain significance | 15 | 81259872 | 81259872 | Human | | name |
| 401874459 | CV2759220 | single nucleotide variant | NM_172217.5(IL16):c.905G>A (p.Arg302His) | not specified [RCV004342505] | uncertain significance | 15 | 81279598 | 81279598 | Human | | name |
| 401882458 | CV2781635 | single nucleotide variant | NM_172217.5(IL16):c.880C>T (p.Leu294Phe) | not specified [RCV004354839] | uncertain significance | 15 | 81279573 | 81279573 | Human | | name |
| 401916432 | CV2814416 | single nucleotide variant | NM_172217.5(IL16):c.3546C>A (p.Leu1182=) | not provided [RCV003400984] | likely benign | 15 | 81306033 | 81306033 | Human | | name |
| 405804451 | CV3270923 | single nucleotide variant | NM_172217.5(IL16):c.488A>G (p.Asp163Gly) | not specified [RCV004404984] | uncertain significance | 15 | 81265725 | 81265725 | Human | | name |
| 405804453 | CV3270924 | single nucleotide variant | NM_172217.5(IL16):c.541G>A (p.Asp181Asn) | not specified [RCV004404985] | uncertain significance | 15 | 81265778 | 81265778 | Human | | name |
| 405804455 | CV3270925 | single nucleotide variant | NM_172217.5(IL16):c.607G>A (p.Val203Met) | not specified [RCV004404986] | uncertain significance | 15 | 81269580 | 81269580 | Human | | name |
| 405804456 | CV3270926 | single nucleotide variant | NM_172217.5(IL16):c.761C>A (p.Ala254Glu) | not specified [RCV004404987] | uncertain significance | 15 | 81273175 | 81273175 | Human | | name |
| 405804458 | CV3270927 | single nucleotide variant | NM_172217.5(IL16):c.823A>G (p.Met275Val) | not specified [RCV004404988] | uncertain significance | 15 | 81278849 | 81278849 | Human | | name |
| 405804462 | CV3270929 | single nucleotide variant | NM_172217.5(IL16):c.977G>A (p.Cys326Tyr) | not specified [RCV004404990] | uncertain significance | 15 | 81279670 | 81279670 | Human | | name |
| 407515557 | CV3444481 | single nucleotide variant | NM_172217.5(IL16):c.872A>G (p.Lys291Arg) | not specified [RCV004627933] | uncertain significance | 15 | 81279565 | 81279565 | Human | | name |
| 407515573 | CV3444486 | single nucleotide variant | NM_172217.5(IL16):c.721C>T (p.Pro241Ser) | not specified [RCV004627938] | uncertain significance | 15 | 81273135 | 81273135 | Human | | name |
| 407515584 | CV3444489 | single nucleotide variant | NM_172217.5(IL16):c.323C>T (p.Thr108Ile) | not specified [RCV004627941] | uncertain significance | 15 | 81259782 | 81259782 | Human | | name |
| 407515599 | CV3444493 | single nucleotide variant | NM_172217.5(IL16):c.344C>G (p.Pro115Arg) | not specified [RCV004627945] | uncertain significance | 15 | 81259803 | 81259803 | Human | | name |
| 407515602 | CV3444494 | single nucleotide variant | NM_172217.5(IL16):c.322A>G (p.Thr108Ala) | not specified [RCV004627946] | uncertain significance | 15 | 81259781 | 81259781 | Human | | name |
| 597792956 | CV3690172 | single nucleotide variant | NM_172217.5(IL16):c.466A>G (p.Lys156Glu) | not specified [RCV004934018] | uncertain significance | 15 | 81265703 | 81265703 | Human | | name |
| 597792996 | CV3690187 | single nucleotide variant | NM_172217.5(IL16):c.707A>C (p.Asp236Ala) | not specified [RCV004934032] | uncertain significance | 15 | 81273121 | 81273121 | Human | | name |
| 598179335 | CV3976019 | single nucleotide variant | NM_172217.5(IL16):c.955C>T (p.Arg319Cys) | not specified [RCV005352138] | uncertain significance | 15 | 81279648 | 81279648 | Human | | name |
| 598179343 | CV3976020 | single nucleotide variant | NM_172217.5(IL16):c.563C>T (p.Ala188Val) | not specified [RCV005352139] | likely benign | 15 | 81265800 | 81265800 | Human | | name |
| 598179348 | CV3976021 | single nucleotide variant | NM_172217.5(IL16):c.677G>T (p.Gly226Val) | not specified [RCV005352140] | uncertain significance | 15 | 81273091 | 81273091 | Human | | name |
| 598179366 | CV3976027 | single nucleotide variant | NM_172217.5(IL16):c.568A>T (p.Thr190Ser) | not specified [RCV005352143] | uncertain significance | 15 | 81269541 | 81269541 | Human | | name |
| 598179372 | CV3976028 | single nucleotide variant | NM_172217.5(IL16):c.300A>G (p.Ile100Met) | not specified [RCV005352144] | likely benign | 15 | 81225699 | 81225699 | Human | | name |
| 598179404 | CV3976036 | single nucleotide variant | NM_172217.5(IL16):c.770C>A (p.Ala257Asp) | not specified [RCV005352150] | uncertain significance | 15 | 81273184 | 81273184 | Human | | name |
| 598179415 | CV3976038 | single nucleotide variant | NM_172217.5(IL16):c.920C>T (p.Pro307Leu) | not specified [RCV005352152] | uncertain significance | 15 | 81279613 | 81279613 | Human | | name |
| 598207312 | CV3976040 | single nucleotide variant | NM_172217.5(IL16):c.946C>G (p.Pro316Ala) | not specified [RCV005337954] | uncertain significance | 15 | 81279639 | 81279639 | Human | | name |
| 598179424 | CV3976041 | single nucleotide variant | NM_172217.5(IL16):c.406C>T (p.Arg136Cys) | not specified [RCV005352154] | uncertain significance | 15 | 81259865 | 81259865 | Human | | name |
| 15105712 | CV714647 | single nucleotide variant | NM_172217.5(IL16):c.3222C>T (p.Ser1074=) | not provided [RCV000959938] | benign | 15 | 81301416 | 81301416 | Human | | name |
| 15201854 | CV770374 | single nucleotide variant | NM_172217.5(IL16):c.3444G>A (p.Gly1148=) | not provided [RCV000935782] | benign | 15 | 81305931 | 81305931 | Human | | name |
| 156371204 | CV2204498 | single nucleotide variant | NM_172217.5(IL16):c.1975G>A (p.Gly659Ser) | not specified [RCV004079297] | likely benign | 15 | 81297000 | 81297000 | Human | | name |
| 156131611 | CV2206394 | single nucleotide variant | NM_172217.5(IL16):c.2324A>G (p.Asp775Gly) | not specified [RCV004078721] | uncertain significance | 15 | 81299650 | 81299650 | Human | | name |
| 156280374 | CV2206395 | single nucleotide variant | NM_172217.5(IL16):c.2881A>G (p.Ser961Gly) | not specified [RCV004078722] | uncertain significance | 15 | 81300207 | 81300207 | Human | | name |
| 156193591 | CV2223277 | single nucleotide variant | NM_172217.5(IL16):c.1912G>C (p.Glu638Gln) | not specified [RCV004105892] | uncertain significance | 15 | 81296937 | 81296937 | Human | | name |
| 155980041 | CV2243899 | single nucleotide variant | NM_172217.5(IL16):c.1211A>C (p.Glu404Ala) | not specified [RCV004108411] | uncertain significance | 15 | 81285709 | 81285709 | Human | | name |
| 156052833 | CV2246356 | single nucleotide variant | NM_172217.5(IL16):c.2822T>G (p.Leu941Arg) | not specified [RCV004107795] | uncertain significance | 15 | 81300148 | 81300148 | Human | | name |
| 156099096 | CV2250646 | single nucleotide variant | NM_172217.5(IL16):c.1150G>T (p.Val384Phe) | not specified [RCV004129276] | uncertain significance | 15 | 81282707 | 81282707 | Human | | name |
| 156357168 | CV2253860 | single nucleotide variant | NM_172217.5(IL16):c.2821C>A (p.Leu941Ile) | not specified [RCV004127547] | uncertain significance | 15 | 81300147 | 81300147 | Human | | name |
| 156003873 | CV2254229 | single nucleotide variant | NM_172217.5(IL16):c.1996G>C (p.Gly666Arg) | not specified [RCV004129908] | uncertain significance | 15 | 81297021 | 81297021 | Human | | name |
| 156190469 | CV2255159 | single nucleotide variant | NM_172217.5(IL16):c.1036G>T (p.Ala346Ser) | not specified [RCV004115780] | uncertain significance | 15 | 81279729 | 81279729 | Human | | name |
| 155925388 | CV2258527 | single nucleotide variant | NM_172217.5(IL16):c.2185A>G (p.Met729Val) | not specified [RCV004116015] | uncertain significance | 15 | 81299511 | 81299511 | Human | | name |
| 156158909 | CV2262528 | single nucleotide variant | NM_172217.5(IL16):c.2753G>A (p.Gly918Asp) | not specified [RCV004130743] | uncertain significance | 15 | 81300079 | 81300079 | Human | | name |
| 156171087 | CV2312553 | single nucleotide variant | NM_172217.5(IL16):c.1898G>C (p.Gly633Ala) | not specified [RCV004169298] | uncertain significance | 15 | 81293033 | 81293033 | Human | | name |
| 156347489 | CV2315306 | single nucleotide variant | NM_172217.5(IL16):c.1060G>A (p.Val354Met) | not specified [RCV004167291] | uncertain significance | 15 | 81279753 | 81279753 | Human | | name |
| 156156809 | CV2322520 | single nucleotide variant | NM_172217.5(IL16):c.2222A>T (p.Asn741Ile) | not specified [RCV004182682] | uncertain significance | 15 | 81299548 | 81299548 | Human | | name |
| 156293725 | CV2336547 | single nucleotide variant | NM_172217.5(IL16):c.1996G>A (p.Gly666Ser) | not specified [RCV004194752] | uncertain significance | 15 | 81297021 | 81297021 | Human | | name |
| 156264106 | CV2364238 | single nucleotide variant | NM_172217.5(IL16):c.1993A>G (p.Ile665Val) | not specified [RCV004223470] | likely benign | 15 | 81297018 | 81297018 | Human | | name |
| 156387058 | CV2372617 | single nucleotide variant | NM_172217.5(IL16):c.2091G>C (p.Lys697Asn) | not specified [RCV004221822] | uncertain significance | 15 | 81299417 | 81299417 | Human | | name |
| 156387064 | CV2372618 | single nucleotide variant | NM_172217.5(IL16):c.2173T>C (p.Phe725Leu) | not specified [RCV004221823] | uncertain significance | 15 | 81299499 | 81299499 | Human | | name |
| 156258283 | CV2383739 | single nucleotide variant | NM_172217.5(IL16):c.2806C>G (p.Pro936Ala) | not specified [RCV004231620] | uncertain significance | 15 | 81300132 | 81300132 | Human | | name |
| 156006575 | CV2401211 | single nucleotide variant | NM_172217.5(IL16):c.1210G>A (p.Glu404Lys) | not specified [RCV004245765] | uncertain significance | 15 | 81285708 | 81285708 | Human | | name |
| 329359744 | CV2436138 | single nucleotide variant | NM_172217.5(IL16):c.1019C>T (p.Ser340Leu) | not specified [RCV004249381] | uncertain significance | 15 | 81279712 | 81279712 | Human | | name |
| 401757821 | CV2685568 | single nucleotide variant | NM_172217.5(IL16):c.2573G>A (p.Gly858Glu) | not specified [RCV004294579] | uncertain significance | 15 | 81299899 | 81299899 | Human | | name |
| 401735068 | CV2699153 | single nucleotide variant | NM_172217.5(IL16):c.2359C>T (p.Pro787Ser) | not specified [RCV004303653] | uncertain significance | 15 | 81299685 | 81299685 | Human | | name |
| 401770559 | CV2707280 | single nucleotide variant | NM_172217.5(IL16):c.1087G>A (p.Gly363Ser) | not specified [RCV004312686] | uncertain significance | 15 | 81282644 | 81282644 | Human | | name |
| 401724471 | CV2714853 | single nucleotide variant | NM_172217.5(IL16):c.1818A>C (p.Lys606Asn) | not specified [RCV004320405] | uncertain significance | 15 | 81292953 | 81292953 | Human | | name |
| 401777402 | CV2721707 | single nucleotide variant | NM_172217.5(IL16):c.1291G>A (p.Gly431Ser) | not specified [RCV004316186] | uncertain significance | 15 | 81285789 | 81285789 | Human | | name |
| 401861851 | CV2766441 | single nucleotide variant | NM_172217.5(IL16):c.2779C>T (p.Arg927Trp) | not specified [RCV004347071] | uncertain significance | 15 | 81300105 | 81300105 | Human | | name |
| 401863247 | CV2779217 | single nucleotide variant | NM_172217.5(IL16):c.2959C>G (p.Leu987Val) | not specified [RCV004350908] | uncertain significance | 15 | 81300285 | 81300285 | Human | | name |
| 405804366 | CV3270902 | single nucleotide variant | NM_172217.5(IL16):c.1117G>A (p.Val373Ile) | not specified [RCV004404963] | uncertain significance | 15 | 81282674 | 81282674 | Human | | name |
| 405804368 | CV3270903 | single nucleotide variant | NM_172217.5(IL16):c.1306A>G (p.Ile436Val) | not specified [RCV004404964] | uncertain significance | 15 | 81285804 | 81285804 | Human | | name |
| 405804370 | CV3270904 | single nucleotide variant | NM_172217.5(IL16):c.1403A>G (p.His468Arg) | not specified [RCV004404965] | uncertain significance | 15 | 81290523 | 81290523 | Human | | name |
| 405804372 | CV3270905 | single nucleotide variant | NM_172217.5(IL16):c.1564G>C (p.Gly522Arg) | not specified [RCV004404966] | uncertain significance | 15 | 81292699 | 81292699 | Human | | name |
| 405804374 | CV3270906 | single nucleotide variant | NM_172217.5(IL16):c.1648C>T (p.Arg550Trp) | not specified [RCV004404967] | uncertain significance | 15 | 81292783 | 81292783 | Human | | name |
| 405804378 | CV3270908 | single nucleotide variant | NM_172217.5(IL16):c.2069C>T (p.Pro690Leu) | not specified [RCV004404969] | uncertain significance | 15 | 81299395 | 81299395 | Human | | name |
| 405804380 | CV3270909 | single nucleotide variant | NM_172217.5(IL16):c.2101C>T (p.Arg701Trp) | not specified [RCV004404970] | uncertain significance | 15 | 81299427 | 81299427 | Human | | name |
| 405804426 | CV3270910 | single nucleotide variant | NM_172217.5(IL16):c.2184C>G (p.Ile728Met) | not specified [RCV004404971] | uncertain significance | 15 | 81299510 | 81299510 | Human | | name |
| 405804432 | CV3270913 | single nucleotide variant | NM_172217.5(IL16):c.2452C>T (p.Pro818Ser) | not specified [RCV004404974] | uncertain significance | 15 | 81299778 | 81299778 | Human | | name |
| 405804434 | CV3270914 | single nucleotide variant | NM_172217.5(IL16):c.2458C>T (p.Pro820Ser) | not specified [RCV004404975] | uncertain significance | 15 | 81299784 | 81299784 | Human | | name |
| 405804436 | CV3270915 | single nucleotide variant | NM_172217.5(IL16):c.2744G>C (p.Arg915Thr) | not specified [RCV004404976] | uncertain significance | 15 | 81300070 | 81300070 | Human | | name |
| 405804438 | CV3270916 | single nucleotide variant | NM_172217.5(IL16):c.2803C>G (p.Pro935Ala) | not specified [RCV004404977] | uncertain significance | 15 | 81300129 | 81300129 | Human | | name |
| 405804440 | CV3270917 | single nucleotide variant | NM_172217.5(IL16):c.2893C>T (p.Arg965Trp) | not specified [RCV004404978] | uncertain significance | 15 | 81300219 | 81300219 | Human | | name |
| 407515563 | CV3444483 | single nucleotide variant | NM_172217.5(IL16):c.2420G>A (p.Arg807Lys) | not specified [RCV004627935] | uncertain significance | 15 | 81299746 | 81299746 | Human | | name |
| 407515567 | CV3444484 | single nucleotide variant | NM_172217.5(IL16):c.1450G>A (p.Gly484Arg) | not specified [RCV004627936] | uncertain significance | 15 | 81292585 | 81292585 | Human | | name |
| 407515588 | CV3444490 | single nucleotide variant | NM_172217.5(IL16):c.2179C>T (p.Pro727Ser) | not specified [RCV004627942] | uncertain significance | 15 | 81299505 | 81299505 | Human | | name |
| 407515596 | CV3444492 | single nucleotide variant | NM_172217.5(IL16):c.1456C>A (p.Pro486Thr) | not specified [RCV004627944] | uncertain significance | 15 | 81292591 | 81292591 | Human | | name |
| 407515606 | CV3444495 | single nucleotide variant | NM_172217.5(IL16):c.1046A>G (p.Asn349Ser) | not specified [RCV004627947] | uncertain significance | 15 | 81279739 | 81279739 | Human | | name |
| 597792945 | CV3690168 | single nucleotide variant | NM_172217.5(IL16):c.1609G>A (p.Val537Met) | not specified [RCV004934014] | uncertain significance | 15 | 81292744 | 81292744 | Human | | name |
| 597792951 | CV3690170 | single nucleotide variant | NM_172217.5(IL16):c.1702C>T (p.Pro568Ser) | not specified [RCV004934016] | uncertain significance | 15 | 81292837 | 81292837 | Human | | name |
| 597792965 | CV3690175 | single nucleotide variant | NM_172217.5(IL16):c.2115C>G (p.Ser705Arg) | not specified [RCV004934021] | uncertain significance | 15 | 81299441 | 81299441 | Human | | name |
| 597792968 | CV3690176 | single nucleotide variant | NM_172217.5(IL16):c.1773G>C (p.Lys591Asn) | not specified [RCV004934022] | uncertain significance | 15 | 81292908 | 81292908 | Human | | name |
| 597792971 | CV3690177 | single nucleotide variant | NM_172217.5(IL16):c.1268C>T (p.Thr423Met) | not specified [RCV004934023] | uncertain significance | 15 | 81285766 | 81285766 | Human | | name |
| 597792974 | CV3690178 | single nucleotide variant | NM_172217.5(IL16):c.1500T>A (p.His500Gln) | not specified [RCV004934024] | uncertain significance | 15 | 81292635 | 81292635 | Human | | name |
| 597792977 | CV3690179 | single nucleotide variant | NM_172217.5(IL16):c.1454G>A (p.Arg485Gln) | not specified [RCV004934025] | uncertain significance | 15 | 81292589 | 81292589 | Human | | name |
| 597792979 | CV3690180 | single nucleotide variant | NM_172217.5(IL16):c.2196C>A (p.Asn732Lys) | not specified [RCV004934026] | uncertain significance | 15 | 81299522 | 81299522 | Human | | name |
| 597792985 | CV3690182 | single nucleotide variant | NM_172217.5(IL16):c.1144A>T (p.Ile382Phe) | not specified [RCV004934028] | uncertain significance | 15 | 81282701 | 81282701 | Human | | name |
| 597792988 | CV3690183 | single nucleotide variant | NM_172217.5(IL16):c.2774C>G (p.Pro925Arg) | not specified [RCV004934029] | uncertain significance | 15 | 81300100 | 81300100 | Human | | name |
| 597792994 | CV3690185 | single nucleotide variant | NM_172217.5(IL16):c.1730C>T (p.Pro577Leu) | not specified [RCV004934031] | uncertain significance | 15 | 81292865 | 81292865 | Human | | name |
| 597793002 | CV3690189 | single nucleotide variant | NM_172217.5(IL16):c.2266G>A (p.Gly756Arg) | not specified [RCV004934034] | uncertain significance | 15 | 81299592 | 81299592 | Human | | name |
| 597793005 | CV3690190 | single nucleotide variant | NM_172217.5(IL16):c.1733C>T (p.Pro578Leu) | not specified [RCV004934035] | uncertain significance | 15 | 81292868 | 81292868 | Human | | name |
| 598207287 | CV3976023 | single nucleotide variant | NM_172217.5(IL16):c.2780G>A (p.Arg927Gln) | not specified [RCV005337950] | likely benign | 15 | 81300106 | 81300106 | Human | | name |
| 598207293 | CV3976026 | single nucleotide variant | NM_172217.5(IL16):c.2404C>T (p.Arg802Cys) | not specified [RCV005337951] | uncertain significance | 15 | 81299730 | 81299730 | Human | | name |
| 598179383 | CV3976030 | single nucleotide variant | NM_172217.5(IL16):c.1894T>G (p.Cys632Gly) | not specified [RCV005352146] | uncertain significance | 15 | 81293029 | 81293029 | Human | | name |
| 598207306 | CV3976032 | single nucleotide variant | NM_172217.5(IL16):c.2767C>T (p.Pro923Ser) | not specified [RCV005337953] | uncertain significance | 15 | 81300093 | 81300093 | Human | | name |
| 598179394 | CV3976034 | single nucleotide variant | NM_172217.5(IL16):c.2509T>C (p.Ser837Pro) | not specified [RCV005352148] | uncertain significance | 15 | 81299835 | 81299835 | Human | | name |
| 598179410 | CV3976037 | single nucleotide variant | NM_172217.5(IL16):c.2294A>C (p.Asn765Thr) | not specified [RCV005352151] | uncertain significance | 15 | 81299620 | 81299620 | Human | | name |
| 598179420 | CV3976039 | single nucleotide variant | NM_172217.5(IL16):c.2222A>G (p.Asn741Ser) | not specified [RCV005352153] | likely benign | 15 | 81299548 | 81299548 | Human | | name |
| 15139576 | CV714646 | single nucleotide variant | NM_172217.5(IL16):c.2666G>A (p.Arg889Gln) | not provided [RCV000965990] | benign | 15 | 81299992 | 81299992 | Human | | name |
| 15180961 | CV726295 | single nucleotide variant | NM_172217.5(IL16):c.2753G>C (p.Gly918Ala) | not provided [RCV000885653] | benign | 15 | 81300079 | 81300079 | Human | | name |
| 156373619 | CV2201291 | single nucleotide variant | NM_172217.5(IL16):c.3125C>T (p.Ala1042Val) | not specified [RCV004077425] | uncertain significance | 15 | 81300451 | 81300451 | Human | | name |
| 156356621 | CV2257468 | single nucleotide variant | NM_172217.5(IL16):c.3825T>G (p.Ser1275Arg) | not specified [RCV004125539] | uncertain significance | 15 | 81308624 | 81308624 | Human | | name |
| 156172051 | CV2326754 | single nucleotide variant | NM_172217.5(IL16):c.3548G>A (p.Arg1183His) | not specified [RCV004176598] | uncertain significance | 15 | 81306035 | 81306035 | Human | | name |
| 156198202 | CV2334508 | single nucleotide variant | NM_172217.5(IL16):c.3203A>T (p.Asp1068Val) | not specified [RCV004188470] | uncertain significance | 15 | 81301397 | 81301397 | Human | | name |
| 156107113 | CV2355302 | single nucleotide variant | NM_172217.5(IL16):c.3664G>A (p.Val1222Ile) | not specified [RCV004203152] | uncertain significance | 15 | 81306151 | 81306151 | Human | | name |
| 156257901 | CV2369015 | single nucleotide variant | NM_172217.5(IL16):c.3844G>T (p.Asp1282Tyr) | not specified [RCV004207953] | uncertain significance | 15 | 81308643 | 81308643 | Human | | name |
| 401726136 | CV2699113 | single nucleotide variant | NM_172217.5(IL16):c.3613G>T (p.Asp1205Tyr) | not specified [RCV004303621] | uncertain significance | 15 | 81306100 | 81306100 | Human | | name |
| 401862078 | CV2766586 | single nucleotide variant | NM_172217.5(IL16):c.3089A>T (p.Glu1030Val) | not specified [RCV004347203] | uncertain significance | 15 | 81300415 | 81300415 | Human | | name |
| 401880803 | CV2787639 | single nucleotide variant | NM_172217.5(IL16):c.3032G>A (p.Cys1011Tyr) | not specified [RCV004356570] | uncertain significance | 15 | 81300358 | 81300358 | Human | | name |
| 405804443 | CV3270919 | single nucleotide variant | NM_172217.5(IL16):c.3107G>A (p.Gly1036Asp) | not specified [RCV004404980] | uncertain significance | 15 | 81300433 | 81300433 | Human | | name |
| 405804445 | CV3270920 | single nucleotide variant | NM_172217.5(IL16):c.3283G>A (p.Glu1095Lys) | not specified [RCV004404981] | uncertain significance | 15 | 81301477 | 81301477 | Human | | name |
| 405804447 | CV3270921 | single nucleotide variant | NM_172217.5(IL16):c.3692C>T (p.Thr1231Ile) | not specified [RCV004404982] | uncertain significance | 15 | 81306432 | 81306432 | Human | | name |
| 407515560 | CV3444482 | single nucleotide variant | NM_172217.5(IL16):c.3092A>T (p.Asp1031Val) | not specified [RCV004627934] | uncertain significance | 15 | 81300418 | 81300418 | Human | | name |
| 407515570 | CV3444485 | single nucleotide variant | NM_172217.5(IL16):c.3832G>A (p.Val1278Ile) | not specified [RCV004627937] | likely benign | 15 | 81308631 | 81308631 | Human | | name |
| 407515592 | CV3444491 | single nucleotide variant | NM_172217.5(IL16):c.3491C>G (p.Ser1164Cys) | not specified [RCV004627943] | uncertain significance | 15 | 81305978 | 81305978 | Human | | name |
| 597792954 | CV3690171 | single nucleotide variant | NM_172217.5(IL16):c.3276A>T (p.Lys1092Asn) | not specified [RCV004934017] | uncertain significance | 15 | 81301470 | 81301470 | Human | | name |
| 597792959 | CV3690173 | single nucleotide variant | NM_172217.5(IL16):c.3202G>T (p.Asp1068Tyr) | not specified [RCV004934019] | uncertain significance | 15 | 81301396 | 81301396 | Human | | name |
| 597792962 | CV3690174 | single nucleotide variant | NM_172217.5(IL16):c.3043C>G (p.Pro1015Ala) | not specified [RCV004934020] | uncertain significance | 15 | 81300369 | 81300369 | Human | | name |
| 597792991 | CV3690184 | single nucleotide variant | NM_172217.5(IL16):c.3217A>C (p.Ser1073Arg) | not specified [RCV004934030] | uncertain significance | 15 | 81301411 | 81301411 | Human | | name |
| 598179376 | CV3976029 | single nucleotide variant | NM_172217.5(IL16):c.3170A>T (p.Tyr1057Phe) | not specified [RCV005352145] | uncertain significance | 15 | 81301364 | 81301364 | Human | | name |
| 598207300 | CV3976031 | single nucleotide variant | NM_172217.5(IL16):c.3263A>G (p.Glu1088Gly) | not specified [RCV005337952] | uncertain significance | 15 | 81301457 | 81301457 | Human | | name |
| 598179388 | CV3976033 | single nucleotide variant | NM_172217.5(IL16):c.3307G>A (p.Ala1103Thr) | not specified [RCV005352147] | uncertain significance | 15 | 81301501 | 81301501 | Human | | name |
| 598179400 | CV3976035 | single nucleotide variant | NM_172217.5(IL16):c.3211G>T (p.Asp1071Tyr) | not specified [RCV005352149] | uncertain significance | 15 | 81301405 | 81301405 | Human | | name |
| 15171276 | CV703371 | single nucleotide variant | NM_172217.5(IL16):c.3079T>A (p.Ser1027Thr) | not provided [RCV000949802] | benign | 15 | 81300405 | 81300405 | Human | | name |
| 8635596 | CV90818 | single nucleotide variant | NM_001172128.1(IL16):c.3886C>A (p.Arg1296=) | Malignant melanoma [RCV000070916] | not provided | 15 | 81308688 | 81308688 | Human | | name |
