| 8579769 | CV114171 | single nucleotide variant | NM_015230.3(ARAP2):c.3264-2753A>G | Lung cancer [RCV000094694] | uncertain significance | 4 | 36136142 | 36136142 | Human | | name |
| 401927997 | CV2822473 | single nucleotide variant | NM_015230.4(ARAP2):c.28G>A (p.Asp10Asn) | not provided [RCV003439283] | likely benign | 4 | 36229459 | 36229459 | Human | | name |
| 156276383 | CV2316534 | single nucleotide variant | NM_015230.4(ARAP2):c.170G>A (p.Arg57His) | not specified [RCV004169999] | uncertain significance | 4 | 36229317 | 36229317 | Human | | name |
| 156015135 | CV2360228 | single nucleotide variant | NM_015230.4(ARAP2):c.110A>G (p.Asp37Gly) | not specified [RCV004208576] | uncertain significance | 4 | 36229377 | 36229377 | Human | | name |
| 401881711 | CV2784789 | single nucleotide variant | NM_015230.4(ARAP2):c.228A>G (p.Ile76Met) | not specified [RCV004352582] | uncertain significance | 4 | 36229259 | 36229259 | Human | | name |
| 401923265 | CV2822471 | single nucleotide variant | NM_015230.4(ARAP2):c.1392C>T (p.Ala464=) | not provided [RCV003434995] | likely benign | 4 | 36210485 | 36210485 | Human | | name |
| 405673977 | CV3286149 | single nucleotide variant | NM_015230.4(ARAP2):c.153A>G (p.Ile51Met) | not specified [RCV004420129] | uncertain significance | 4 | 36229334 | 36229334 | Human | | name |
| 407464849 | CV3467932 | single nucleotide variant | NM_015230.4(ARAP2):c.158C>T (p.Pro53Leu) | not specified [RCV004660053] | uncertain significance | 4 | 36229329 | 36229329 | Human | | name |
| 407464908 | CV3467974 | single nucleotide variant | NM_015230.4(ARAP2):c.131G>A (p.Ser44Asn) | not specified [RCV004660067] | uncertain significance | 4 | 36229356 | 36229356 | Human | | name |
| 597703644 | CV3569472 | single nucleotide variant | NM_015230.4(ARAP2):c.235A>G (p.Asn79Asp) | not specified [RCV004840060] | uncertain significance | 4 | 36229252 | 36229252 | Human | | name |
| 598261364 | CV3999551 | single nucleotide variant | NM_015230.4(ARAP2):c.271A>G (p.Lys91Glu) | not specified [RCV005386877] | uncertain significance | 4 | 36229216 | 36229216 | Human | | name |
| 156183419 | CV2198509 | single nucleotide variant | NM_015230.4(ARAP2):c.521A>G (p.Asp174Gly) | not specified [RCV004075540] | uncertain significance | 4 | 36228966 | 36228966 | Human | | name |
| 155920621 | CV2211887 | single nucleotide variant | NM_015230.4(ARAP2):c.978G>T (p.Glu326Asp) | not specified [RCV004087020] | uncertain significance | 4 | 36213306 | 36213306 | Human | | name |
| 155902964 | CV2274799 | single nucleotide variant | NM_015230.4(ARAP2):c.703G>C (p.Gly235Arg) | not specified [RCV004139141] | uncertain significance | 4 | 36228784 | 36228784 | Human | | name |
| 155901461 | CV2345809 | single nucleotide variant | NM_015230.4(ARAP2):c.811C>T (p.Arg271Cys) | not specified [RCV004205733] | uncertain significance | 4 | 36228676 | 36228676 | Human | | name |
| 156282030 | CV2348825 | single nucleotide variant | NM_015230.4(ARAP2):c.299A>C (p.Gln100Pro) | not specified [RCV004203269] | uncertain significance | 4 | 36229188 | 36229188 | Human | | name |
| 156186008 | CV2377910 | single nucleotide variant | NM_015230.4(ARAP2):c.679A>T (p.Thr227Ser) | not specified [RCV004230478] | uncertain significance | 4 | 36228808 | 36228808 | Human | | name |
| 156171409 | CV2400677 | single nucleotide variant | NM_015230.4(ARAP2):c.805A>G (p.Arg269Gly) | not specified [RCV004242353] | uncertain significance | 4 | 36228682 | 36228682 | Human | | name |
| 329354531 | CV2448361 | single nucleotide variant | NM_015230.4(ARAP2):c.611A>C (p.Glu204Ala) | not specified [RCV004256647] | uncertain significance | 4 | 36228876 | 36228876 | Human | | name |
| 329398011 | CV2464690 | single nucleotide variant | NM_015230.4(ARAP2):c.856C>T (p.His286Tyr) | not specified [RCV004284667] | uncertain significance | 4 | 36228631 | 36228631 | Human | | name |
| 401884572 | CV2761896 | single nucleotide variant | NM_015230.4(ARAP2):c.311T>C (p.Ile104Thr) | not specified [RCV004339533] | uncertain significance | 4 | 36229176 | 36229176 | Human | | name |
| 401889939 | CV2765108 | single nucleotide variant | NM_015230.4(ARAP2):c.506C>G (p.Ser169Cys) | not specified [RCV004337604] | uncertain significance | 4 | 36228981 | 36228981 | Human | | name |
| 401880099 | CV2766125 | single nucleotide variant | NM_015230.4(ARAP2):c.460C>T (p.Pro154Ser) | not specified [RCV004340580] | uncertain significance | 4 | 36229027 | 36229027 | Human | | name |
| 401927992 | CV2822470 | single nucleotide variant | NM_015230.4(ARAP2):c.4422G>A (p.Val1474=) | not provided [RCV003439281] | likely benign | 4 | 36091884 | 36091884 | Human | | name |
| 405673816 | CV3286171 | single nucleotide variant | NM_015230.4(ARAP2):c.479A>G (p.His160Arg) | not specified [RCV004420151] | uncertain significance | 4 | 36229008 | 36229008 | Human | | name |
| 405673831 | CV3286175 | single nucleotide variant | NM_015230.4(ARAP2):c.773A>G (p.Tyr258Cys) | not specified [RCV004420155] | uncertain significance | 4 | 36228714 | 36228714 | Human | | name |
| 405673832 | CV3286176 | single nucleotide variant | NM_015230.4(ARAP2):c.808A>G (p.Ser270Gly) | not specified [RCV004420156] | uncertain significance | 4 | 36228679 | 36228679 | Human | | name |
| 407464735 | CV3467881 | single nucleotide variant | NM_015230.4(ARAP2):c.461C>G (p.Pro154Arg) | not specified [RCV004660027] | uncertain significance | 4 | 36229026 | 36229026 | Human | | name |
| 407529945 | CV3467901 | single nucleotide variant | NM_015230.4(ARAP2):c.310A>G (p.Ile104Val) | not specified [RCV004656348] | uncertain significance | 4 | 36229177 | 36229177 | Human | | name |
| 407529981 | CV3467965 | single nucleotide variant | NM_015230.4(ARAP2):c.771G>T (p.Leu257Phe) | not specified [RCV004656385] | uncertain significance | 4 | 36228716 | 36228716 | Human | | name |
| 597703413 | CV3569438 | single nucleotide variant | NM_015230.4(ARAP2):c.323A>G (p.Asn108Ser) | not specified [RCV004840039] | likely benign | 4 | 36229164 | 36229164 | Human | | name |
| 597767654 | CV3569473 | single nucleotide variant | NM_015230.4(ARAP2):c.533T>C (p.Ile178Thr) | not specified [RCV004850525] | uncertain significance | 4 | 36228954 | 36228954 | Human | | name |
| 597767681 | CV3569530 | single nucleotide variant | NM_015230.4(ARAP2):c.901G>T (p.Gly301Trp) | not specified [RCV004850531] | uncertain significance | 4 | 36228586 | 36228586 | Human | | name |
| 597704474 | CV3569596 | single nucleotide variant | NM_015230.4(ARAP2):c.518G>T (p.Ser173Ile) | not specified [RCV004840142] | uncertain significance | 4 | 36228969 | 36228969 | Human | | name |
| 597705040 | CV3569657 | single nucleotide variant | NM_015230.4(ARAP2):c.601T>A (p.Leu201Met) | not specified [RCV004840197] | uncertain significance | 4 | 36228886 | 36228886 | Human | | name |
| 597767760 | CV3569668 | single nucleotide variant | NM_015230.4(ARAP2):c.708A>T (p.Leu236Phe) | not specified [RCV004850548] | uncertain significance | 4 | 36228779 | 36228779 | Human | | name |
| 598196638 | CV3999570 | single nucleotide variant | NM_015230.4(ARAP2):c.839G>A (p.Arg280Gln) | not specified [RCV005397746] | uncertain significance | 4 | 36228648 | 36228648 | Human | | name |
| 598261488 | CV3999580 | single nucleotide variant | NM_015230.4(ARAP2):c.944A>G (p.Glu315Gly) | not specified [RCV005386898] | likely benign | 4 | 36214442 | 36214442 | Human | | name |
| 598261629 | CV3999613 | single nucleotide variant | NM_015230.4(ARAP2):c.679A>G (p.Thr227Ala) | not specified [RCV005386926] | likely benign | 4 | 36228808 | 36228808 | Human | | name |
| 598196724 | CV3999649 | single nucleotide variant | NM_015230.4(ARAP2):c.299A>G (p.Gln100Arg) | not specified [RCV005397759] | uncertain significance | 4 | 36229188 | 36229188 | Human | | name |
| 598196762 | CV3999682 | single nucleotide variant | NM_015230.4(ARAP2):c.812G>A (p.Arg271His) | not specified [RCV005397767] | uncertain significance | 4 | 36228675 | 36228675 | Human | | name |
| 8625781 | CV80905 | single nucleotide variant | NM_015230.3(ARAP2):c.997C>T (p.Pro333Ser) | Malignant melanoma [RCV000060982] | not provided | 4 | 36213287 | 36213287 | Human | | name |
| 155941681 | CV2229253 | single nucleotide variant | NM_015230.4(ARAP2):c.1775G>A (p.Gly592Glu) | not specified [RCV004101063] | uncertain significance | 4 | 36177909 | 36177909 | Human | | name |
| 156285095 | CV2232772 | single nucleotide variant | NM_015230.4(ARAP2):c.2549C>G (p.Pro850Arg) | not specified [RCV004101410] | uncertain significance | 4 | 36159399 | 36159399 | Human | | name |
| 156200982 | CV2234308 | single nucleotide variant | NM_015230.4(ARAP2):c.2517G>T (p.Met839Ile) | not specified [RCV004100542] | uncertain significance | 4 | 36159431 | 36159431 | Human | | name |
| 156365874 | CV2272192 | single nucleotide variant | NM_015230.4(ARAP2):c.1544A>G (p.Tyr515Cys) | not specified [RCV004124962] | uncertain significance | 4 | 36193591 | 36193591 | Human | | name |
| 156075825 | CV2281545 | single nucleotide variant | NM_015230.4(ARAP2):c.1624A>C (p.Lys542Gln) | not specified [RCV004153855] | uncertain significance | 4 | 36187505 | 36187505 | Human | | name |
| 155939794 | CV2293974 | single nucleotide variant | NM_015230.4(ARAP2):c.1355C>T (p.Pro452Leu) | not specified [RCV004149373] | uncertain significance | 4 | 36210522 | 36210522 | Human | | name |
| 156186533 | CV2324738 | single nucleotide variant | NM_015230.4(ARAP2):c.1410A>G (p.Ile470Met) | not specified [RCV004172977] | uncertain significance | 4 | 36210467 | 36210467 | Human | | name |
| 156178650 | CV2327483 | single nucleotide variant | NM_015230.4(ARAP2):c.2353A>G (p.Lys785Glu) | not specified [RCV004176797] | uncertain significance | 4 | 36160548 | 36160548 | Human | | name |
| 156334726 | CV2333428 | single nucleotide variant | NM_015230.4(ARAP2):c.2204C>T (p.Ser735Phe) | not specified [RCV004190134] | uncertain significance | 4 | 36161520 | 36161520 | Human | | name |
| 156235117 | CV2346333 | single nucleotide variant | NM_015230.4(ARAP2):c.2430A>C (p.Glu810Asp) | not specified [RCV004203817] | uncertain significance | 4 | 36160471 | 36160471 | Human | | name |
| 156130854 | CV2358134 | single nucleotide variant | NM_015230.4(ARAP2):c.1639A>G (p.Thr547Ala) | not specified [RCV004211940] | uncertain significance | 4 | 36187490 | 36187490 | Human | | name |
| 156211073 | CV2378249 | single nucleotide variant | NM_015230.4(ARAP2):c.2404A>T (p.Thr802Ser) | not specified [RCV004226284] | uncertain significance | 4 | 36160497 | 36160497 | Human | | name |
| 156227350 | CV2388216 | single nucleotide variant | NM_015230.4(ARAP2):c.2644G>A (p.Glu882Lys) | not specified [RCV004234674] | uncertain significance | 4 | 36158838 | 36158838 | Human | | name |
| 156047454 | CV2390942 | single nucleotide variant | NM_015230.4(ARAP2):c.1408A>G (p.Ile470Val) | not specified [RCV004234952] | uncertain significance | 4 | 36210469 | 36210469 | Human | | name |
| 329370165 | CV2435496 | single nucleotide variant | NM_015230.4(ARAP2):c.2080A>G (p.Asn694Asp) | not specified [RCV004253140] | uncertain significance | 4 | 36165007 | 36165007 | Human | | name |
| 329361724 | CV2437859 | single nucleotide variant | NM_015230.4(ARAP2):c.2801A>G (p.Tyr934Cys) | not specified [RCV004261148] | uncertain significance | 4 | 36150996 | 36150996 | Human | | name |
| 329380758 | CV2440490 | single nucleotide variant | NM_015230.4(ARAP2):c.2906T>C (p.Phe969Ser) | not specified [RCV004256416] | uncertain significance | 4 | 36148499 | 36148499 | Human | | name |
| 401718967 | CV2679366 | single nucleotide variant | NM_015230.4(ARAP2):c.1796A>G (p.Tyr599Cys) | not specified [RCV004285899] | uncertain significance | 4 | 36177888 | 36177888 | Human | | name |
| 401743310 | CV2687918 | single nucleotide variant | NM_015230.4(ARAP2):c.1001A>G (p.Tyr334Cys) | not specified [RCV004305008] | uncertain significance | 4 | 36213283 | 36213283 | Human | | name |
| 401734451 | CV2709507 | single nucleotide variant | NM_015230.4(ARAP2):c.2921A>G (p.Tyr974Cys) | not specified [RCV004318747] | uncertain significance | 4 | 36148484 | 36148484 | Human | | name |
| 401772290 | CV2712643 | single nucleotide variant | NM_015230.4(ARAP2):c.2081A>T (p.Asn694Ile) | not specified [RCV004307967] | uncertain significance | 4 | 36165006 | 36165006 | Human | | name |
| 401887555 | CV2772011 | single nucleotide variant | NM_015230.4(ARAP2):c.2849A>G (p.Glu950Gly) | not specified [RCV004344689] | uncertain significance | 4 | 36150948 | 36150948 | Human | | name |
| 401893881 | CV2774155 | single nucleotide variant | NM_015230.4(ARAP2):c.2807A>G (p.Asn936Ser) | not specified [RCV004345745] | likely benign | 4 | 36150990 | 36150990 | Human | | name |
| 401927994 | CV2822472 | single nucleotide variant | NM_015230.4(ARAP2):c.1336G>A (p.Val446Ile) | not provided [RCV003439282] | likely benign | 4 | 36210541 | 36210541 | Human | | name |
| 405269389 | CV3187341 | single nucleotide variant | NM_015230.4(ARAP2):c.2698T>G (p.Tyr900Asp) | not provided [RCV003887425] | uncertain significance | 4 | 36158784 | 36158784 | Human | | name |
| 405673987 | CV3286146 | single nucleotide variant | NM_015230.4(ARAP2):c.1274T>C (p.Leu425Ser) | not specified [RCV004420126] | uncertain significance | 4 | 36210603 | 36210603 | Human | | name |
| 405673984 | CV3286147 | single nucleotide variant | NM_015230.4(ARAP2):c.1294G>A (p.Ala432Thr) | not specified [RCV004420127] | uncertain significance | 4 | 36210583 | 36210583 | Human | | name |
| 405673981 | CV3286148 | single nucleotide variant | NM_015230.4(ARAP2):c.1506G>C (p.Lys502Asn) | not specified [RCV004420128] | uncertain significance | 4 | 36193629 | 36193629 | Human | | name |
| 405673973 | CV3286150 | single nucleotide variant | NM_015230.4(ARAP2):c.1550A>T (p.Asn517Ile) | not specified [RCV004420130] | uncertain significance | 4 | 36193585 | 36193585 | Human | | name |
| 405673969 | CV3286151 | single nucleotide variant | NM_015230.4(ARAP2):c.1702A>C (p.Ile568Leu) | not specified [RCV004420131] | uncertain significance | 4 | 36177982 | 36177982 | Human | | name |
| 405673964 | CV3286152 | single nucleotide variant | NM_015230.4(ARAP2):c.2050G>A (p.Asp684Asn) | not specified [RCV004420132] | uncertain significance | 4 | 36165037 | 36165037 | Human | | name |
| 405673962 | CV3286153 | single nucleotide variant | NM_015230.4(ARAP2):c.2282A>G (p.Lys761Arg) | not specified [RCV004420133] | uncertain significance | 4 | 36160619 | 36160619 | Human | | name |
| 405673958 | CV3286154 | single nucleotide variant | NM_015230.4(ARAP2):c.2499C>G (p.Phe833Leu) | not specified [RCV004420134] | uncertain significance | 4 | 36159449 | 36159449 | Human | | name |
| 405673951 | CV3286156 | single nucleotide variant | NM_015230.4(ARAP2):c.2682C>A (p.Phe894Leu) | not specified [RCV004420136] | uncertain significance | 4 | 36158800 | 36158800 | Human | | name |
| 407529938 | CV3467892 | single nucleotide variant | NM_015230.4(ARAP2):c.2569G>A (p.Ala857Thr) | not specified [RCV004656341] | uncertain significance | 4 | 36159379 | 36159379 | Human | | name |
| 407464800 | CV3467911 | single nucleotide variant | NM_015230.4(ARAP2):c.1627T>C (p.Phe543Leu) | not specified [RCV004660041] | uncertain significance | 4 | 36187502 | 36187502 | Human | | name |
| 407529955 | CV3467922 | single nucleotide variant | NM_015230.4(ARAP2):c.2054A>G (p.Tyr685Cys) | not specified [RCV004656359] | uncertain significance | 4 | 36165033 | 36165033 | Human | | name |
| 597703654 | CV3569483 | single nucleotide variant | NM_015230.4(ARAP2):c.2884T>C (p.Tyr962His) | not specified [RCV004840061] | uncertain significance | 4 | 36150913 | 36150913 | Human | | name |
| 597703671 | CV3569497 | single nucleotide variant | NM_015230.4(ARAP2):c.2338G>A (p.Asp780Asn) | not specified [RCV004840063] | uncertain significance | 4 | 36160563 | 36160563 | Human | | name |
| 597767669 | CV3569512 | single nucleotide variant | NM_015230.4(ARAP2):c.2091C>G (p.Asn697Lys) | not specified [RCV004850528] | uncertain significance | 4 | 36164996 | 36164996 | Human | | name |
| 597767673 | CV3569518 | single nucleotide variant | NM_015230.4(ARAP2):c.1591G>A (p.Ala531Thr) | not specified [RCV004850529] | uncertain significance | 4 | 36187538 | 36187538 | Human | | name |
| 597704168 | CV3569563 | single nucleotide variant | NM_015230.4(ARAP2):c.2336T>G (p.Met779Arg) | not specified [RCV004840112] | uncertain significance | 4 | 36160565 | 36160565 | Human | | name |
| 597704370 | CV3569585 | single nucleotide variant | NM_015230.4(ARAP2):c.1895T>C (p.Met632Thr) | not specified [RCV004840132] | uncertain significance | 4 | 36167010 | 36167010 | Human | | name |
| 597704556 | CV3569604 | single nucleotide variant | NM_015230.4(ARAP2):c.1534A>G (p.Ile512Val) | not specified [RCV004840150] | uncertain significance | 4 | 36193601 | 36193601 | Human | | name |
| 597704601 | CV3569608 | single nucleotide variant | NM_015230.4(ARAP2):c.2516T>C (p.Met839Thr) | not specified [RCV004840154] | uncertain significance | 4 | 36159432 | 36159432 | Human | | name |
| 597704699 | CV3569619 | single nucleotide variant | NM_015230.4(ARAP2):c.1090G>A (p.Gly364Arg) | not specified [RCV004840164] | uncertain significance | 4 | 36212439 | 36212439 | Human | | name |
| 597704882 | CV3569639 | single nucleotide variant | NM_015230.4(ARAP2):c.1498T>G (p.Phe500Val) | not specified [RCV004840182] | uncertain significance | 4 | 36193637 | 36193637 | Human | | name |
| 598261670 | CV3999621 | single nucleotide variant | NM_015230.4(ARAP2):c.2012T>C (p.Ile671Thr) | not specified [RCV005386933] | uncertain significance | 4 | 36165075 | 36165075 | Human | | name |
| 598196738 | CV3999658 | single nucleotide variant | NM_015230.4(ARAP2):c.1760C>T (p.Thr587Ile) | not specified [RCV005397762] | uncertain significance | 4 | 36177924 | 36177924 | Human | | name |
| 598261835 | CV3999665 | single nucleotide variant | NM_015230.4(ARAP2):c.1474C>G (p.Leu492Val) | not specified [RCV005386968] | uncertain significance | 4 | 36210403 | 36210403 | Human | | name |
| 598196757 | CV3999674 | single nucleotide variant | NM_015230.4(ARAP2):c.2854A>T (p.Ile952Phe) | not specified [RCV005397766] | uncertain significance | 4 | 36150943 | 36150943 | Human | | name |
| 598261870 | CV3999676 | single nucleotide variant | NM_015230.4(ARAP2):c.1894A>G (p.Met632Val) | not specified [RCV005386977] | uncertain significance | 4 | 36167011 | 36167011 | Human | | name |
| 598261881 | CV3999679 | single nucleotide variant | NM_015230.4(ARAP2):c.2239T>C (p.Trp747Arg) | not specified [RCV005386980] | uncertain significance | 4 | 36161485 | 36161485 | Human | | name |
| 598261920 | CV3999688 | single nucleotide variant | NM_015230.4(ARAP2):c.1927A>T (p.Thr643Ser) | not specified [RCV005386988] | uncertain significance | 4 | 36166978 | 36166978 | Human | | name |
| 598262085 | CV3999729 | single nucleotide variant | NM_015230.4(ARAP2):c.1447A>G (p.Lys483Glu) | not specified [RCV005387021] | uncertain significance | 4 | 36210430 | 36210430 | Human | | name |
| 598196816 | CV3999739 | single nucleotide variant | NM_015230.4(ARAP2):c.1666G>A (p.Val556Ile) | not specified [RCV005397777] | uncertain significance | 4 | 36187463 | 36187463 | Human | | name |
| 598262147 | CV3999745 | single nucleotide variant | NM_015230.4(ARAP2):c.1790G>A (p.Arg597Lys) | not specified [RCV005387032] | uncertain significance | 4 | 36177894 | 36177894 | Human | | name |
| 598196577 | CV4002796 | single nucleotide variant | NM_015230.4(ARAP2):c.1046G>A (p.Arg349Gln) | not specified [RCV005397736] | uncertain significance | 4 | 36212483 | 36212483 | Human | | name |
| 8631163 | CV86319 | single nucleotide variant | NM_015230.3(ARAP2):c.2734G>A (p.Glu912Lys) | Malignant melanoma [RCV000066410] | not provided | 4 | 36158748 | 36158748 | Human | | name |
| 156169320 | CV2197777 | single nucleotide variant | NM_015230.4(ARAP2):c.3557C>T (p.Thr1186Met) | not specified [RCV004074973] | uncertain significance | 4 | 36128616 | 36128616 | Human | | name |
| 156178380 | CV2201587 | single nucleotide variant | NM_015230.4(ARAP2):c.4375C>T (p.Arg1459Trp) | not specified [RCV004080076] | uncertain significance | 4 | 36091931 | 36091931 | Human | | name |
| 156295502 | CV2233737 | single nucleotide variant | NM_015230.4(ARAP2):c.4267A>G (p.Thr1423Ala) | not specified [RCV004100182] | uncertain significance | 4 | 36107583 | 36107583 | Human | | name |
| 156250331 | CV2273268 | single nucleotide variant | NM_015230.4(ARAP2):c.3758G>C (p.Cys1253Ser) | not specified [RCV004132061] | uncertain significance | 4 | 36121315 | 36121315 | Human | | name |
| 155915297 | CV2274083 | single nucleotide variant | NM_015230.4(ARAP2):c.3516C>A (p.Ser1172Arg) | not specified [RCV004134733] | uncertain significance | 4 | 36128657 | 36128657 | Human | | name |
| 155994891 | CV2286465 | single nucleotide variant | NM_015230.4(ARAP2):c.4475G>A (p.Arg1492His) | not specified [RCV004139974] | uncertain significance | 4 | 36083401 | 36083401 | Human | | name |
| 155910922 | CV2303708 | single nucleotide variant | NM_015230.4(ARAP2):c.3710G>A (p.Arg1237Gln) | not specified [RCV004161776] | uncertain significance | 4 | 36124898 | 36124898 | Human | | name |
| 156287009 | CV2327285 | single nucleotide variant | NM_015230.4(ARAP2):c.4538A>G (p.His1513Arg) | not specified [RCV004174729] | uncertain significance | 4 | 36082257 | 36082257 | Human | | name |
| 156034093 | CV2338588 | single nucleotide variant | NM_015230.4(ARAP2):c.4522G>A (p.Ala1508Thr) | not specified [RCV004182179] | uncertain significance | 4 | 36082273 | 36082273 | Human | | name |
| 155921736 | CV2340502 | single nucleotide variant | NM_015230.4(ARAP2):c.4075G>A (p.Asp1359Asn) | not specified [RCV004197224] | uncertain significance | 4 | 36114251 | 36114251 | Human | | name |
| 156012929 | CV2358991 | single nucleotide variant | NM_015230.4(ARAP2):c.3721G>A (p.Ala1241Thr) | not specified [RCV004212319] | uncertain significance | 4 | 36124887 | 36124887 | Human | | name |
| 155991692 | CV2384326 | single nucleotide variant | NM_015230.4(ARAP2):c.4376G>A (p.Arg1459Gln) | not specified [RCV004227707] | uncertain significance | 4 | 36091930 | 36091930 | Human | | name |
| 156250907 | CV2394255 | single nucleotide variant | NM_015230.4(ARAP2):c.4397G>A (p.Gly1466Glu) | not specified [RCV004238488] | uncertain significance | 4 | 36091909 | 36091909 | Human | | name |
| 329371374 | CV2431977 | single nucleotide variant | NM_015230.4(ARAP2):c.4243G>A (p.Val1415Met) | not specified [RCV004249132] | uncertain significance | 4 | 36107607 | 36107607 | Human | | name |
| 329376119 | CV2437980 | single nucleotide variant | NM_015230.4(ARAP2):c.3697C>T (p.Pro1233Ser) | not specified [RCV004263695] | uncertain significance | 4 | 36124911 | 36124911 | Human | | name |
| 329400686 | CV2438656 | single nucleotide variant | NM_015230.4(ARAP2):c.3382G>T (p.Val1128Phe) | not specified [RCV004261819] | uncertain significance | 4 | 36133271 | 36133271 | Human | | name |
| 329369243 | CV2450580 | single nucleotide variant | NM_015230.4(ARAP2):c.4977G>T (p.Lys1659Asn) | not specified [RCV004265482] | uncertain significance | 4 | 36068045 | 36068045 | Human | | name |
| 329369457 | CV2461118 | single nucleotide variant | NM_015230.4(ARAP2):c.4834G>T (p.Val1612Leu) | not specified [RCV004265541] | uncertain significance | 4 | 36068188 | 36068188 | Human | | name |
| 329398165 | CV2464829 | single nucleotide variant | NM_015230.4(ARAP2):c.3478A>C (p.Ser1160Arg) | not specified [RCV004284777] | uncertain significance | 4 | 36128695 | 36128695 | Human | | name |
| 401757046 | CV2678199 | single nucleotide variant | NM_015230.4(ARAP2):c.3709C>G (p.Arg1237Gly) | not specified [RCV004296706] | uncertain significance | 4 | 36124899 | 36124899 | Human | | name |
| 401737849 | CV2680002 | single nucleotide variant | NM_015230.4(ARAP2):c.3278A>G (p.His1093Arg) | not specified [RCV004284272] | uncertain significance | 4 | 36133375 | 36133375 | Human | | name |
| 401737619 | CV2699863 | single nucleotide variant | NM_015230.4(ARAP2):c.3674A>G (p.Tyr1225Cys) | not specified [RCV004308504] | uncertain significance | 4 | 36124934 | 36124934 | Human | | name |
| 401738414 | CV2711868 | single nucleotide variant | NM_015230.4(ARAP2):c.4801G>A (p.Val1601Met) | not specified [RCV004309496] | uncertain significance | 4 | 36068221 | 36068221 | Human | | name |
| 401724323 | CV2714798 | single nucleotide variant | NM_015230.4(ARAP2):c.4036C>T (p.Arg1346Trp) | not specified [RCV004320359] | uncertain significance | 4 | 36117063 | 36117063 | Human | | name |
| 401724625 | CV2714909 | single nucleotide variant | NM_015230.4(ARAP2):c.4103C>A (p.Pro1368His) | not specified [RCV004322243] | uncertain significance | 4 | 36114223 | 36114223 | Human | | name |
| 401779656 | CV2731946 | single nucleotide variant | NM_015230.4(ARAP2):c.3503A>C (p.Lys1168Thr) | not specified [RCV004333186] | uncertain significance | 4 | 36128670 | 36128670 | Human | | name |
| 401861689 | CV2756416 | single nucleotide variant | NM_015230.4(ARAP2):c.3238G>A (p.Val1080Ile) | not specified [RCV004342956] | uncertain significance | 4 | 36147321 | 36147321 | Human | | name |
| 401891729 | CV2780710 | single nucleotide variant | NM_015230.4(ARAP2):c.4585A>G (p.Met1529Val) | not specified [RCV004352049] | uncertain significance | 4 | 36080239 | 36080239 | Human | | name |
| 405673948 | CV3286157 | single nucleotide variant | NM_015230.4(ARAP2):c.3049T>A (p.Leu1017Met) | not specified [RCV004420137] | uncertain significance | 4 | 36147698 | 36147698 | Human | | name |
| 405673943 | CV3286158 | single nucleotide variant | NM_015230.4(ARAP2):c.3259G>A (p.Gly1087Arg) | not specified [RCV004420138] | uncertain significance | 4 | 36147300 | 36147300 | Human | | name |
| 405673941 | CV3286159 | single nucleotide variant | NM_015230.4(ARAP2):c.3311A>G (p.His1104Arg) | not specified [RCV004420139] | uncertain significance | 4 | 36133342 | 36133342 | Human | | name |
| 405673936 | CV3286160 | single nucleotide variant | NM_015230.4(ARAP2):c.3356A>C (p.Gln1119Pro) | not specified [RCV004420140] | uncertain significance | 4 | 36133297 | 36133297 | Human | | name |
| 405673932 | CV3286161 | single nucleotide variant | NM_015230.4(ARAP2):c.3479G>A (p.Ser1160Asn) | not specified [RCV004420141] | uncertain significance | 4 | 36128694 | 36128694 | Human | | name |
| 405673923 | CV3286163 | single nucleotide variant | NM_015230.4(ARAP2):c.3538C>T (p.His1180Tyr) | not specified [RCV004420143] | uncertain significance | 4 | 36128635 | 36128635 | Human | | name |
| 405673920 | CV3286164 | single nucleotide variant | NM_015230.4(ARAP2):c.3782C>T (p.Ala1261Val) | not specified [RCV004420144] | uncertain significance | 4 | 36121291 | 36121291 | Human | | name |
| 405673915 | CV3286165 | single nucleotide variant | NM_015230.4(ARAP2):c.4016C>A (p.Pro1339His) | not specified [RCV004420145] | uncertain significance | 4 | 36117083 | 36117083 | Human | | name |
| 405673798 | CV3286166 | single nucleotide variant | NM_015230.4(ARAP2):c.4058C>A (p.Ala1353Glu) | not specified [RCV004420146] | uncertain significance | 4 | 36114268 | 36114268 | Human | | name |
| 405673801 | CV3286167 | single nucleotide variant | NM_015230.4(ARAP2):c.4123G>C (p.Ala1375Pro) | not specified [RCV004420147] | uncertain significance | 4 | 36114203 | 36114203 | Human | | name |
| 405673805 | CV3286168 | single nucleotide variant | NM_015230.4(ARAP2):c.4237C>G (p.Leu1413Val) | not specified [RCV004420148] | uncertain significance | 4 | 36107613 | 36107613 | Human | | name |
| 405673809 | CV3286169 | single nucleotide variant | NM_015230.4(ARAP2):c.4498C>T (p.Pro1500Ser) | not specified [RCV004420149] | uncertain significance | 4 | 36083378 | 36083378 | Human | | name |
| 405673812 | CV3286170 | single nucleotide variant | NM_015230.4(ARAP2):c.4577C>T (p.Thr1526Met) | not specified [RCV004420150] | likely benign | 4 | 36080247 | 36080247 | Human | | name |
| 405673823 | CV3286173 | single nucleotide variant | NM_015230.4(ARAP2):c.4870C>G (p.Arg1624Gly) | not specified [RCV004420153] | uncertain significance | 4 | 36068152 | 36068152 | Human | | name |
| 405673827 | CV3286174 | single nucleotide variant | NM_015230.4(ARAP2):c.5103G>T (p.Gln1701His) | not specified [RCV004420154] | uncertain significance | 4 | 36067919 | 36067919 | Human | | name |
| 407464669 | CV3467849 | single nucleotide variant | NM_015230.4(ARAP2):c.4261G>A (p.Ala1421Thr) | not specified [RCV004660011] | uncertain significance | 4 | 36107589 | 36107589 | Human | | name |
| 407529922 | CV3467860 | single nucleotide variant | NM_015230.4(ARAP2):c.4772G>A (p.Arg1591Gln) | not specified [RCV004656325] | uncertain significance | 4 | 36068250 | 36068250 | Human | | name |
| 407464711 | CV3467870 | single nucleotide variant | NM_015230.4(ARAP2):c.4201C>T (p.Arg1401Trp) | not specified [RCV004660021] | uncertain significance | 4 | 36107649 | 36107649 | Human | | name |
| 407464871 | CV3467943 | single nucleotide variant | NM_015230.4(ARAP2):c.4175A>G (p.Lys1392Arg) | not specified [RCV004660058] | uncertain significance | 4 | 36107675 | 36107675 | Human | | name |
| 407529971 | CV3467954 | single nucleotide variant | NM_015230.4(ARAP2):c.3146A>G (p.Gln1049Arg) | not specified [RCV004656375] | uncertain significance | 4 | 36147601 | 36147601 | Human | | name |
| 597703525 | CV3569449 | single nucleotide variant | NM_015230.4(ARAP2):c.4037G>A (p.Arg1346Gln) | not specified [RCV004840049] | uncertain significance | 4 | 36117062 | 36117062 | Human | | name |
| 597703632 | CV3569460 | single nucleotide variant | NM_015230.4(ARAP2):c.4729C>T (p.Arg1577Trp) | not specified [RCV004840059] | uncertain significance | 4 | 36073703 | 36073703 | Human | | name |
| 597767659 | CV3569478 | single nucleotide variant | NM_015230.4(ARAP2):c.4937G>T (p.Gly1646Val) | not specified [RCV004850526] | uncertain significance | 4 | 36068085 | 36068085 | Human | | name |
| 597703662 | CV3569491 | single nucleotide variant | NM_015230.4(ARAP2):c.3366G>C (p.Gln1122His) | not specified [RCV004840062] | uncertain significance | 4 | 36133287 | 36133287 | Human | | name |
| 597703682 | CV3569503 | single nucleotide variant | NM_015230.4(ARAP2):c.4355C>A (p.Ser1452Tyr) | not specified [RCV004840064] | uncertain significance | 4 | 36091951 | 36091951 | Human | | name |
| 597703691 | CV3569505 | single nucleotide variant | NM_015230.4(ARAP2):c.3223G>T (p.Gly1075Trp) | not specified [RCV004840065] | uncertain significance | 4 | 36147336 | 36147336 | Human | | name |
| 597703849 | CV3569524 | single nucleotide variant | NM_015230.4(ARAP2):c.3653A>G (p.Asp1218Gly) | not specified [RCV004840080] | uncertain significance | 4 | 36124955 | 36124955 | Human | | name |
| 597767686 | CV3569540 | single nucleotide variant | NM_015230.4(ARAP2):c.4945A>C (p.Lys1649Gln) | not specified [RCV004850532] | uncertain significance | 4 | 36068077 | 36068077 | Human | | name |
| 597767700 | CV3569552 | single nucleotide variant | NM_015230.4(ARAP2):c.4620T>A (p.Asp1540Glu) | not specified [RCV004850535] | uncertain significance | 4 | 36073812 | 36073812 | Human | | name |
| 597704274 | CV3569574 | single nucleotide variant | NM_015230.4(ARAP2):c.3835A>C (p.Thr1279Pro) | not specified [RCV004840123] | uncertain significance | 4 | 36121238 | 36121238 | Human | | name |
| 597704808 | CV3569630 | single nucleotide variant | NM_015230.4(ARAP2):c.4261G>T (p.Ala1421Ser) | not specified [RCV004840174] | uncertain significance | 4 | 36107589 | 36107589 | Human | | name |
| 597704964 | CV3569649 | single nucleotide variant | NM_015230.4(ARAP2):c.4736A>G (p.Asn1579Ser) | not specified [RCV004840190] | uncertain significance | 4 | 36073696 | 36073696 | Human | | name |
| 598261311 | CV3999541 | single nucleotide variant | NM_015230.4(ARAP2):c.3850A>C (p.Asn1284His) | not specified [RCV005386868] | uncertain significance | 4 | 36121223 | 36121223 | Human | | name |
| 598261402 | CV3999561 | single nucleotide variant | NM_015230.4(ARAP2):c.4891C>T (p.Arg1631Trp) | not specified [RCV005386884] | uncertain significance | 4 | 36068131 | 36068131 | Human | | name |
| 598261535 | CV3999589 | single nucleotide variant | NM_015230.4(ARAP2):c.3998A>G (p.Tyr1333Cys) | not specified [RCV005386907] | uncertain significance | 4 | 36117101 | 36117101 | Human | | name |
| 598261755 | CV3999639 | single nucleotide variant | NM_015230.4(ARAP2):c.5014G>A (p.Asp1672Asn) | not specified [RCV005386949] | uncertain significance | 4 | 36068008 | 36068008 | Human | | name |
| 598261851 | CV3999670 | single nucleotide variant | NM_015230.4(ARAP2):c.4475G>T (p.Arg1492Leu) | not specified [RCV005386972] | likely benign | 4 | 36083401 | 36083401 | Human | | name |
| 598196772 | CV3999694 | single nucleotide variant | NM_015230.4(ARAP2):c.5069C>T (p.Ser1690Leu) | not specified [RCV005397769] | uncertain significance | 4 | 36067953 | 36067953 | Human | | name |
| 598261950 | CV3999699 | single nucleotide variant | NM_015230.4(ARAP2):c.3781G>A (p.Ala1261Thr) | not specified [RCV005386994] | uncertain significance | 4 | 36121292 | 36121292 | Human | | name |
| 598261994 | CV3999708 | single nucleotide variant | NM_015230.4(ARAP2):c.5111A>G (p.Lys1704Arg) | not specified [RCV005387003] | uncertain significance | 4 | 36067911 | 36067911 | Human | | name |
| 598262042 | CV3999719 | single nucleotide variant | NM_015230.4(ARAP2):c.4864A>G (p.Lys1622Glu) | not specified [RCV005387013] | uncertain significance | 4 | 36068158 | 36068158 | Human | | name |
| 8631162 | CV86318 | single nucleotide variant | NM_015230.3(ARAP2):c.5053G>A (p.Val1685Met) | Malignant melanoma [RCV000066409] | not provided | 4 | 36067969 | 36067969 | Human | | name |
