| 8574894 | CV109233 | single nucleotide variant | NM_001122965.1(RPTN):c.-1787G>T | Lung cancer [RCV000089758] | uncertain significance | 1 | 152160950 | 152160950 | Human | | name |
| 156261001 | CV2287461 | single nucleotide variant | NM_001122965.1(RPTN):c.94G>A (p.Glu32Lys) | not specified [RCV004140931] | uncertain significance | 1 | 152157796 | 152157796 | Human | | name |
| 401932816 | CV2809273 | single nucleotide variant | NM_001122965.1(RPTN):c.474T>C (p.His158=) | not provided [RCV003408889] | likely benign | 1 | 152156625 | 152156625 | Human | | name |
| 405739662 | CV3320362 | single nucleotide variant | NM_001122965.1(RPTN):c.52T>C (p.Tyr18His) | not specified [RCV004452183] | uncertain significance | 1 | 152157838 | 152157838 | Human | | name |
| 401733512 | CV2713115 | single nucleotide variant | NM_001122965.1(RPTN):c.122T>C (p.Phe41Ser) | not specified [RCV004316666] | uncertain significance | 1 | 152157768 | 152157768 | Human | | name |
| 405739621 | CV3320355 | single nucleotide variant | NM_001122965.1(RPTN):c.150C>A (p.Asp50Glu) | not specified [RCV004452176] | uncertain significance | 1 | 152156949 | 152156949 | Human | | name |
| 405739625 | CV3320356 | single nucleotide variant | NM_001122965.1(RPTN):c.173T>C (p.Leu58Ser) | not specified [RCV004452177] | uncertain significance | 1 | 152156926 | 152156926 | Human | | name |
| 597786355 | CV3594457 | single nucleotide variant | NM_001122965.1(RPTN):c.291G>T (p.Arg97Ser) | not specified [RCV004854958] | uncertain significance | 1 | 152156808 | 152156808 | Human | | name |
| 38468458 | CV920625 | single nucleotide variant | NM_001122965.1(RPTN):c.1494T>C (p.His498=) | not provided [RCV001200364] | likely benign | 1 | 152155605 | 152155605 | Human | | name |
| 155987204 | CV2259448 | single nucleotide variant | NM_001122965.1(RPTN):c.691T>C (p.Cys231Arg) | not specified [RCV004122657] | uncertain significance | 1 | 152156408 | 152156408 | Human | | name |
| 155984945 | CV2270636 | single nucleotide variant | NM_001122965.1(RPTN):c.644C>T (p.Thr215Ile) | not specified [RCV004137850] | uncertain significance | 1 | 152156455 | 152156455 | Human | | name |
| 156346703 | CV2375290 | single nucleotide variant | NM_001122965.1(RPTN):c.367C>G (p.Gln123Glu) | not specified [RCV004232700] | uncertain significance | 1 | 152156732 | 152156732 | Human | | name |
| 156144487 | CV2383933 | single nucleotide variant | NM_001122965.1(RPTN):c.689G>A (p.Arg230Gln) | not specified [RCV004231785] | likely benign | 1 | 152156410 | 152156410 | Human | | name |
| 329376149 | CV2431746 | single nucleotide variant | NM_001122965.1(RPTN):c.331T>C (p.Cys111Arg) | not specified [RCV004248908] | likely benign | 1 | 152156768 | 152156768 | Human | | name |
| 329402417 | CV2454201 | single nucleotide variant | NM_001122965.1(RPTN):c.547A>C (p.Asn183His) | not specified [RCV004265684] | uncertain significance | 1 | 152156552 | 152156552 | Human | | name |
| 401783220 | CV2703887 | single nucleotide variant | NM_001122965.1(RPTN):c.655G>A (p.Ala219Thr) | not specified [RCV004306746] | likely benign | 1 | 152156444 | 152156444 | Human | | name |
| 405739645 | CV3320359 | single nucleotide variant | NM_001122965.1(RPTN):c.431C>T (p.Ser144Phe) | not specified [RCV004452180] | uncertain significance | 1 | 152156668 | 152156668 | Human | | name |
| 405739650 | CV3320360 | single nucleotide variant | NM_001122965.1(RPTN):c.453A>T (p.Arg151Ser) | not specified [RCV004452181] | uncertain significance | 1 | 152156646 | 152156646 | Human | | name |
| 405739658 | CV3320361 | single nucleotide variant | NM_001122965.1(RPTN):c.473A>G (p.His158Arg) | not specified [RCV004452182] | uncertain significance | 1 | 152156626 | 152156626 | Human | | name |
| 405739681 | CV3320365 | single nucleotide variant | NM_001122965.1(RPTN):c.679G>C (p.Ala227Pro) | not specified [RCV004452186] | uncertain significance | 1 | 152156420 | 152156420 | Human | | name |
| 405739684 | CV3320366 | single nucleotide variant | NM_001122965.1(RPTN):c.965C>T (p.Thr322Met) | not specified [RCV004452187] | uncertain significance | 1 | 152156134 | 152156134 | Human | | name |
| 407488271 | CV3476269 | single nucleotide variant | NM_001122965.1(RPTN):c.469C>T (p.His157Tyr) | not specified [RCV004665840] | uncertain significance | 1 | 152156630 | 152156630 | Human | | name |
| 597710202 | CV3594451 | single nucleotide variant | NM_001122965.1(RPTN):c.315G>T (p.Gln105His) | not specified [RCV004860930] | uncertain significance | 1 | 152156784 | 152156784 | Human | | name |
| 597710209 | CV3594453 | single nucleotide variant | NM_001122965.1(RPTN):c.893C>T (p.Thr298Met) | not specified [RCV004860931] | uncertain significance | 1 | 152156206 | 152156206 | Human | | name |
| 597786351 | CV3594456 | single nucleotide variant | NM_001122965.1(RPTN):c.706C>A (p.Gln236Lys) | not specified [RCV004854957] | uncertain significance | 1 | 152156393 | 152156393 | Human | | name |
| 155901130 | CV2241923 | single nucleotide variant | NM_001122965.1(RPTN):c.1321C>G (p.Gln441Glu) | not specified [RCV004106833] | uncertain significance | 1 | 152155778 | 152155778 | Human | | name |
| 156218543 | CV2253961 | single nucleotide variant | NM_001122965.1(RPTN):c.2291A>T (p.Asp764Val) | not specified [RCV004127635] | uncertain significance | 1 | 152154808 | 152154808 | Human | | name |
| 155961467 | CV2285534 | single nucleotide variant | NM_001122965.1(RPTN):c.2249A>G (p.His750Arg) | not specified [RCV004141416] | uncertain significance | 1 | 152154850 | 152154850 | Human | | name |
| 156103713 | CV2291633 | single nucleotide variant | NM_001122965.1(RPTN):c.1868C>T (p.Thr623Ile) | not specified [RCV004155923] | uncertain significance | 1 | 152155231 | 152155231 | Human | | name |
| 156292546 | CV2296818 | single nucleotide variant | NM_001122965.1(RPTN):c.2110T>C (p.Trp704Arg) | not specified [RCV004148707] | uncertain significance | 1 | 152154989 | 152154989 | Human | | name |
| 156293673 | CV2321337 | single nucleotide variant | NM_001122965.1(RPTN):c.2167G>A (p.Glu723Lys) | not specified [RCV004177341] | uncertain significance | 1 | 152154932 | 152154932 | Human | | name |
| 156053420 | CV2329091 | single nucleotide variant | NM_001122965.1(RPTN):c.1127G>T (p.Ser376Ile) | not specified [RCV004180361] | uncertain significance | 1 | 152155972 | 152155972 | Human | | name |
| 155970913 | CV2334159 | single nucleotide variant | NM_001122965.1(RPTN):c.1436A>C (p.Asp479Ala) | not specified [RCV004186149] | uncertain significance | 1 | 152155663 | 152155663 | Human | | name |
| 155978808 | CV2335200 | single nucleotide variant | NM_001122965.1(RPTN):c.2158G>A (p.Glu720Lys) | not specified [RCV004186773] | uncertain significance | 1 | 152154941 | 152154941 | Human | | name |
| 156268986 | CV2372141 | single nucleotide variant | NM_001122965.1(RPTN):c.1211G>A (p.Gly404Asp) | not specified [RCV004223665] | uncertain significance | 1 | 152155888 | 152155888 | Human | | name |
| 156043684 | CV2397032 | single nucleotide variant | NM_001122965.1(RPTN):c.1745A>G (p.His582Arg) | not specified [RCV004236549] | uncertain significance | 1 | 152155354 | 152155354 | Human | | name |
| 156007299 | CV2401298 | single nucleotide variant | NM_001122965.1(RPTN):c.1721C>G (p.Thr574Arg) | not specified [RCV004245839] | uncertain significance | 1 | 152155378 | 152155378 | Human | | name |
| 329376142 | CV2431743 | single nucleotide variant | NM_001122965.1(RPTN):c.1157A>G (p.Asp386Gly) | not specified [RCV004248905] | likely benign | 1 | 152155942 | 152155942 | Human | | name |
| 329376145 | CV2431744 | single nucleotide variant | NM_001122965.1(RPTN):c.1352A>G (p.Tyr451Cys) | not specified [RCV004248906] | uncertain significance | 1 | 152155747 | 152155747 | Human | | name |
| 329376148 | CV2431745 | single nucleotide variant | NM_001122965.1(RPTN):c.2203A>G (p.Lys735Glu) | not specified [RCV004248907] | likely benign | 1 | 152154896 | 152154896 | Human | | name |
| 329377050 | CV2456868 | single nucleotide variant | NM_001122965.1(RPTN):c.1484A>G (p.Gln495Arg) | not specified [RCV004270829] | uncertain significance | 1 | 152155615 | 152155615 | Human | | name |
| 329392961 | CV2469108 | single nucleotide variant | NM_001122965.1(RPTN):c.1325C>T (p.Pro442Leu) | not specified [RCV004274340] | uncertain significance | 1 | 152155774 | 152155774 | Human | | name |
| 401736589 | CV2688828 | single nucleotide variant | NM_001122965.1(RPTN):c.2149C>T (p.His717Tyr) | not specified [RCV004303846] | uncertain significance | 1 | 152154950 | 152154950 | Human | | name |
| 401719215 | CV2705008 | single nucleotide variant | NM_001122965.1(RPTN):c.1897G>A (p.Gly633Arg) | not specified [RCV004309608] | uncertain significance | 1 | 152155202 | 152155202 | Human | | name |
| 401730368 | CV2711248 | single nucleotide variant | NM_001122965.1(RPTN):c.2258G>A (p.Ser753Asn) | not specified [RCV004313036] | likely benign | 1 | 152154841 | 152154841 | Human | | name |
| 401784063 | CV2721004 | single nucleotide variant | NM_001122965.1(RPTN):c.1381T>C (p.Ser461Pro) | not specified [RCV004328294] | uncertain significance | 1 | 152155718 | 152155718 | Human | | name |
| 401769421 | CV2735022 | single nucleotide variant | NM_001122965.1(RPTN):c.1432C>A (p.Pro478Thr) | not specified [RCV004333722] | likely benign | 1 | 152155667 | 152155667 | Human | | name |
| 401885552 | CV2768246 | single nucleotide variant | NM_001122965.1(RPTN):c.2195G>A (p.Arg732Gln) | not specified [RCV004350241] | likely benign | 1 | 152154904 | 152154904 | Human | | name |
| 401891540 | CV2779238 | single nucleotide variant | NM_001122965.1(RPTN):c.1637A>G (p.His546Arg) | not specified [RCV004350923] | uncertain significance | 1 | 152155462 | 152155462 | Human | | name |
| 405739591 | CV3320351 | single nucleotide variant | NM_001122965.1(RPTN):c.1174G>A (p.Gly392Ser) | not specified [RCV004452172] | uncertain significance | 1 | 152155925 | 152155925 | Human | | name |
| 405739599 | CV3320352 | single nucleotide variant | NM_001122965.1(RPTN):c.1244A>G (p.Tyr415Cys) | not specified [RCV004452173] | uncertain significance | 1 | 152155855 | 152155855 | Human | | name |
| 405739608 | CV3320353 | single nucleotide variant | NM_001122965.1(RPTN):c.1334A>C (p.Gln445Pro) | not specified [RCV004452174] | uncertain significance | 1 | 152155765 | 152155765 | Human | | name |
| 405739615 | CV3320354 | single nucleotide variant | NM_001122965.1(RPTN):c.1442A>T (p.Gln481Leu) | not specified [RCV004452175] | uncertain significance | 1 | 152155657 | 152155657 | Human | | name |
| 405739630 | CV3320357 | single nucleotide variant | NM_001122965.1(RPTN):c.1837T>C (p.Ser613Pro) | not specified [RCV004452178] | uncertain significance | 1 | 152155262 | 152155262 | Human | | name |
| 405739638 | CV3320358 | single nucleotide variant | NM_001122965.1(RPTN):c.1933G>A (p.Gly645Ser) | not specified [RCV004452179] | likely benign | 1 | 152155166 | 152155166 | Human | | name |
| 407513834 | CV3476266 | single nucleotide variant | NM_001122965.1(RPTN):c.1012G>T (p.Gly338Cys) | not specified [RCV004674264] | uncertain significance | 1 | 152156087 | 152156087 | Human | | name |
| 407513836 | CV3476267 | single nucleotide variant | NM_001122965.1(RPTN):c.2191A>G (p.Arg731Gly) | not specified [RCV004674265] | uncertain significance | 1 | 152154908 | 152154908 | Human | | name |
| 407488266 | CV3476268 | single nucleotide variant | NM_001122965.1(RPTN):c.1942G>C (p.Val648Leu) | not specified [RCV004665839] | uncertain significance | 1 | 152155157 | 152155157 | Human | | name |
| 597786341 | CV3594449 | single nucleotide variant | NM_001122965.1(RPTN):c.1679G>A (p.Gly560Asp) | not specified [RCV004854954] | uncertain significance | 1 | 152155420 | 152155420 | Human | | name |
| 597786345 | CV3594450 | single nucleotide variant | NM_001122965.1(RPTN):c.1274C>T (p.Ser425Phe) | not specified [RCV004854955] | uncertain significance | 1 | 152155825 | 152155825 | Human | | name |
| 597786347 | CV3594452 | single nucleotide variant | NM_001122965.1(RPTN):c.1165T>A (p.Ser389Thr) | not specified [RCV004854956] | uncertain significance | 1 | 152155934 | 152155934 | Human | | name |
| 597710218 | CV3594454 | single nucleotide variant | NM_001122965.1(RPTN):c.2138C>G (p.Thr713Ser) | not specified [RCV004860932] | likely benign | 1 | 152154961 | 152154961 | Human | | name |
| 597710227 | CV3594458 | single nucleotide variant | NM_001122965.1(RPTN):c.1750A>C (p.Ile584Leu) | not specified [RCV004860933] | uncertain significance | 1 | 152155349 | 152155349 | Human | | name |
| 597710235 | CV3594459 | single nucleotide variant | NM_001122965.1(RPTN):c.1227A>C (p.Gln409His) | not specified [RCV004860934] | uncertain significance | 1 | 152155872 | 152155872 | Human | | name |
| 597786359 | CV3594460 | single nucleotide variant | NM_001122965.1(RPTN):c.1771A>T (p.Ile591Leu) | not specified [RCV004854959] | uncertain significance | 1 | 152155328 | 152155328 | Human | | name |
| 598222000 | CV3903080 | single nucleotide variant | NM_001122965.1(RPTN):c.1474A>G (p.Arg492Gly) | not specified [RCV005272519] | uncertain significance | 1 | 152155625 | 152155625 | Human | | name |
| 598221994 | CV3903081 | single nucleotide variant | NM_001122965.1(RPTN):c.2173C>G (p.Pro725Ala) | not specified [RCV005272520] | uncertain significance | 1 | 152154926 | 152154926 | Human | | name |
| 598221988 | CV3903082 | single nucleotide variant | NM_001122965.1(RPTN):c.1883G>T (p.Gly628Val) | not specified [RCV005272521] | likely benign | 1 | 152155216 | 152155216 | Human | | name |
| 598221984 | CV3903083 | single nucleotide variant | NM_001122965.1(RPTN):c.2113G>A (p.Ala705Thr) | not specified [RCV005272522] | uncertain significance | 1 | 152154986 | 152154986 | Human | | name |
| 598221978 | CV3903084 | single nucleotide variant | NM_001122965.1(RPTN):c.1637A>C (p.His546Pro) | not specified [RCV005272523] | uncertain significance | 1 | 152155462 | 152155462 | Human | | name |
| 598221974 | CV3903085 | single nucleotide variant | NM_001122965.1(RPTN):c.1351T>C (p.Tyr451His) | not specified [RCV005272524] | uncertain significance | 1 | 152155748 | 152155748 | Human | | name |
| 8628925 | CV84068 | single nucleotide variant | NM_001122965.1(RPTN):c.1533T>A (p.Tyr511Ter) | Malignant melanoma [RCV000064149] | not provided | 1 | 152155566 | 152155566 | Human | | name |
| 15155470 | CV696101 | deletion | NM_001122965.1(RPTN):c.474_509del (p.Gly159_His170del) | not provided [RCV000946497] | benign | 1 | 152156590 | 152156625 | Human | | name |
