| 405693333 | CV3362400 | single nucleotide variant | NM_002523.3(NPTX2):c.29C>T (p.Ala10Val) | not specified [RCV004491148] | likely benign | 7 | 98617490 | 98617490 | Human | | name |
| 597642703 | CV3566570 | single nucleotide variant | NM_002523.3(NPTX2):c.98C>G (p.Pro33Arg) | not specified [RCV004832488] | uncertain significance | 7 | 98617559 | 98617559 | Human | | name |
| 597685670 | CV3566571 | single nucleotide variant | NM_002523.3(NPTX2):c.95T>C (p.Leu32Pro) | not specified [RCV004838121] | uncertain significance | 7 | 98617556 | 98617556 | Human | | name |
| 598219360 | CV3997877 | single nucleotide variant | NM_002523.3(NPTX2):c.60C>G (p.Ser20Arg) | not specified [RCV005379329] | uncertain significance | 7 | 98617521 | 98617521 | Human | | name |
| 156304952 | CV2338593 | single nucleotide variant | NM_002523.3(NPTX2):c.242G>T (p.Arg81Leu) | not specified [RCV004182182] | uncertain significance | 7 | 98617703 | 98617703 | Human | | name |
| 155913940 | CV2341890 | single nucleotide variant | NM_002523.3(NPTX2):c.241C>G (p.Arg81Gly) | not specified [RCV004184837] | uncertain significance | 7 | 98617702 | 98617702 | Human | | name |
| 405693299 | CV3362394 | single nucleotide variant | NM_002523.3(NPTX2):c.143T>G (p.Met48Arg) | not specified [RCV004491142] | uncertain significance | 7 | 98617604 | 98617604 | Human | | name |
| 405693306 | CV3362395 | single nucleotide variant | NM_002523.3(NPTX2):c.188T>C (p.Val63Ala) | not specified [RCV004491143] | uncertain significance | 7 | 98617649 | 98617649 | Human | | name |
| 405693311 | CV3362396 | single nucleotide variant | NM_002523.3(NPTX2):c.202G>C (p.Glu68Gln) | not specified [RCV004491144] | uncertain significance | 7 | 98617663 | 98617663 | Human | | name |
| 405693317 | CV3362397 | single nucleotide variant | NM_002523.3(NPTX2):c.227C>T (p.Thr76Met) | not specified [RCV004491145] | uncertain significance | 7 | 98617688 | 98617688 | Human | | name |
| 405693328 | CV3362399 | single nucleotide variant | NM_002523.3(NPTX2):c.284A>C (p.Glu95Ala) | not specified [RCV004491147] | uncertain significance | 7 | 98617745 | 98617745 | Human | | name |
| 597685699 | CV3566574 | single nucleotide variant | NM_002523.3(NPTX2):c.266G>A (p.Gly89Asp) | not specified [RCV004838124] | uncertain significance | 7 | 98617727 | 98617727 | Human | | name |
| 598219395 | CV3997883 | single nucleotide variant | NM_002523.3(NPTX2):c.138G>T (p.Met46Ile) | not specified [RCV005379334] | uncertain significance | 7 | 98617599 | 98617599 | Human | | name |
| 156181261 | CV2201799 | single nucleotide variant | NM_002523.3(NPTX2):c.337A>G (p.Met113Val) | not specified [RCV004082236] | uncertain significance | 7 | 98617798 | 98617798 | Human | | name |
| 156249011 | CV2222059 | single nucleotide variant | NM_002523.3(NPTX2):c.524G>A (p.Arg175His) | not specified [RCV004103038] | uncertain significance | 7 | 98619740 | 98619740 | Human | | name |
| 156170964 | CV2247416 | single nucleotide variant | NM_002523.3(NPTX2):c.857A>G (p.Asn286Ser) | not specified [RCV004108747] | uncertain significance | 7 | 98625135 | 98625135 | Human | | name |
| 156299766 | CV2248697 | single nucleotide variant | NM_002523.3(NPTX2):c.445G>A (p.Val149Met) | not specified [RCV004121866] | uncertain significance | 7 | 98619661 | 98619661 | Human | | name |
| 156093964 | CV2300263 | single nucleotide variant | NM_002523.3(NPTX2):c.406G>A (p.Asp136Asn) | not specified [RCV004153224] | uncertain significance | 7 | 98617867 | 98617867 | Human | | name |
| 156085066 | CV2331032 | single nucleotide variant | NM_002523.3(NPTX2):c.756C>G (p.Ile252Met) | not specified [RCV004188070] | uncertain significance | 7 | 98625034 | 98625034 | Human | | name |
| 155968428 | CV2337844 | single nucleotide variant | NM_002523.3(NPTX2):c.919G>A (p.Gly307Ser) | not specified [RCV004183855] | uncertain significance | 7 | 98627195 | 98627195 | Human | | name |
| 155932850 | CV2372177 | single nucleotide variant | NM_002523.3(NPTX2):c.466G>A (p.Gly156Ser) | not specified [RCV004216959] | likely benign | 7 | 98619682 | 98619682 | Human | | name |
| 156147022 | CV2381826 | single nucleotide variant | NM_002523.3(NPTX2):c.322A>G (p.Thr108Ala) | not specified [RCV004232269] | uncertain significance | 7 | 98617783 | 98617783 | Human | | name |
| 329366058 | CV2438051 | single nucleotide variant | NM_002523.3(NPTX2):c.547G>A (p.Glu183Lys) | not specified [RCV004256844] | uncertain significance | 7 | 98619763 | 98619763 | Human | | name |
| 329361663 | CV2468182 | single nucleotide variant | NM_002523.3(NPTX2):c.841C>A (p.Leu281Met) | not specified [RCV004275765] | uncertain significance | 7 | 98625119 | 98625119 | Human | | name |
| 401770257 | CV2715102 | single nucleotide variant | NM_002523.3(NPTX2):c.410G>A (p.Arg137His) | not specified [RCV004322684] | uncertain significance | 7 | 98617871 | 98617871 | Human | | name |
| 405693338 | CV3362401 | single nucleotide variant | NM_002523.3(NPTX2):c.433C>T (p.Leu145Phe) | not specified [RCV004491149] | uncertain significance | 7 | 98619649 | 98619649 | Human | | name |
| 405693342 | CV3362402 | single nucleotide variant | NM_002523.3(NPTX2):c.452A>G (p.Asn151Ser) | not specified [RCV004491150] | uncertain significance | 7 | 98619668 | 98619668 | Human | | name |
| 405693349 | CV3362403 | single nucleotide variant | NM_002523.3(NPTX2):c.668A>G (p.Asp223Gly) | not specified [RCV004491151] | uncertain significance | 7 | 98624946 | 98624946 | Human | | name |
| 405693355 | CV3362404 | single nucleotide variant | NM_002523.3(NPTX2):c.728C>T (p.Thr243Met) | not specified [RCV004491152] | uncertain significance | 7 | 98625006 | 98625006 | Human | | name |
| 405693362 | CV3362405 | single nucleotide variant | NM_002523.3(NPTX2):c.838G>A (p.Val280Met) | not specified [RCV004491153] | uncertain significance | 7 | 98625116 | 98625116 | Human | | name |
| 407476635 | CV3465710 | single nucleotide variant | NM_002523.3(NPTX2):c.445G>T (p.Val149Leu) | not specified [RCV004638632] | uncertain significance | 7 | 98619661 | 98619661 | Human | | name |
| 407516602 | CV3465713 | single nucleotide variant | NM_002523.3(NPTX2):c.682T>G (p.Ser228Ala) | not specified [RCV004650334] | uncertain significance | 7 | 98624960 | 98624960 | Human | | name |
| 597685636 | CV3566566 | single nucleotide variant | NM_002523.3(NPTX2):c.772T>C (p.Ser258Pro) | not specified [RCV004838117] | uncertain significance | 7 | 98625050 | 98625050 | Human | | name |
| 597685651 | CV3566568 | single nucleotide variant | NM_002523.3(NPTX2):c.482T>A (p.Val161Glu) | not specified [RCV004838119] | uncertain significance | 7 | 98619698 | 98619698 | Human | | name |
| 597685676 | CV3566572 | single nucleotide variant | NM_002523.3(NPTX2):c.344A>C (p.Asp115Ala) | not specified [RCV004838122] | uncertain significance | 7 | 98617805 | 98617805 | Human | | name |
| 597685708 | CV3566575 | single nucleotide variant | NM_002523.3(NPTX2):c.769C>T (p.Arg257Trp) | not specified [RCV004838125] | uncertain significance | 7 | 98625047 | 98625047 | Human | | name |
| 597685725 | CV3566577 | single nucleotide variant | NM_002523.3(NPTX2):c.739C>A (p.Leu247Met) | not specified [RCV004838127] | uncertain significance | 7 | 98625017 | 98625017 | Human | | name |
| 597685734 | CV3566578 | single nucleotide variant | NM_002523.3(NPTX2):c.988G>A (p.Glu330Lys) | not specified [RCV004838128] | uncertain significance | 7 | 98627264 | 98627264 | Human | | name |
| 598219374 | CV3997879 | single nucleotide variant | NM_002523.3(NPTX2):c.785C>G (p.Pro262Arg) | not specified [RCV005379331] | uncertain significance | 7 | 98625063 | 98625063 | Human | | name |
| 598219381 | CV3997880 | single nucleotide variant | NM_002523.3(NPTX2):c.412C>A (p.Leu138Met) | not specified [RCV005379332] | uncertain significance | 7 | 98617873 | 98617873 | Human | | name |
| 598264361 | CV3997881 | single nucleotide variant | NM_002523.3(NPTX2):c.311G>A (p.Gly104Asp) | not specified [RCV005387740] | uncertain significance | 7 | 98617772 | 98617772 | Human | | name |
| 598219388 | CV3997882 | single nucleotide variant | NM_002523.3(NPTX2):c.695G>A (p.Arg232His) | not specified [RCV005379333] | uncertain significance | 7 | 98624973 | 98624973 | Human | | name |
| 15177157 | CV736374 | single nucleotide variant | NM_002523.3(NPTX2):c.574T>A (p.Ser192Thr) | not provided [RCV000906585] | likely benign | 7 | 98619790 | 98619790 | Human | | name |
| 156132904 | CV2195913 | single nucleotide variant | NM_002523.3(NPTX2):c.1157A>G (p.Gln386Arg) | not specified [RCV004072173] | uncertain significance | 7 | 98628490 | 98628490 | Human | | name |
| 401768160 | CV2675074 | single nucleotide variant | NM_002523.3(NPTX2):c.1039G>A (p.Gly347Arg) | not specified [RCV004289855] | uncertain significance | 7 | 98627315 | 98627315 | Human | | name |
| 405693279 | CV3362390 | single nucleotide variant | NM_002523.3(NPTX2):c.1000A>G (p.Thr334Ala) | not specified [RCV004491138] | uncertain significance | 7 | 98627276 | 98627276 | Human | | name |
| 405693284 | CV3362391 | single nucleotide variant | NM_002523.3(NPTX2):c.1144G>A (p.Val382Ile) | not specified [RCV004491139] | uncertain significance | 7 | 98628477 | 98628477 | Human | | name |
| 405693288 | CV3362392 | single nucleotide variant | NM_002523.3(NPTX2):c.1173C>G (p.Ile391Met) | not specified [RCV004491140] | uncertain significance | 7 | 98628506 | 98628506 | Human | | name |
| 405693293 | CV3362393 | single nucleotide variant | NM_002523.3(NPTX2):c.1211C>T (p.Pro404Leu) | not specified [RCV004491141] | uncertain significance | 7 | 98628544 | 98628544 | Human | | name |
| 407476631 | CV3465709 | single nucleotide variant | NM_002523.3(NPTX2):c.1154C>T (p.Ala385Val) | not specified [RCV004638631] | uncertain significance | 7 | 98628487 | 98628487 | Human | | name |
| 407476639 | CV3465711 | single nucleotide variant | NM_002523.3(NPTX2):c.1051A>G (p.Ile351Val) | not specified [RCV004638633] | uncertain significance | 7 | 98627327 | 98627327 | Human | | name |
| 407516598 | CV3465712 | single nucleotide variant | NM_002523.3(NPTX2):c.1174G>A (p.Ala392Thr) | not specified [RCV004650333] | uncertain significance | 7 | 98628507 | 98628507 | Human | | name |
| 597685644 | CV3566567 | single nucleotide variant | NM_002523.3(NPTX2):c.1045G>A (p.Val349Met) | not specified [RCV004838118] | uncertain significance | 7 | 98627321 | 98627321 | Human | | name |
| 597685661 | CV3566569 | single nucleotide variant | NM_002523.3(NPTX2):c.1085G>A (p.Arg362Lys) | not specified [RCV004838120] | uncertain significance | 7 | 98628418 | 98628418 | Human | | name |
| 597685689 | CV3566573 | single nucleotide variant | NM_002523.3(NPTX2):c.1075G>A (p.Val359Met) | not specified [RCV004838123] | uncertain significance | 7 | 98628408 | 98628408 | Human | | name |
| 597685715 | CV3566576 | single nucleotide variant | NM_002523.3(NPTX2):c.1202A>G (p.Asn401Ser) | not specified [RCV004838126] | uncertain significance | 7 | 98628535 | 98628535 | Human | | name |
| 597642709 | CV3566579 | single nucleotide variant | NM_002523.3(NPTX2):c.1189A>G (p.Asn397Asp) | not specified [RCV004832489] | uncertain significance | 7 | 98628522 | 98628522 | Human | | name |
| 598219366 | CV3997878 | single nucleotide variant | NM_002523.3(NPTX2):c.1228G>A (p.Val410Ile) | not specified [RCV005379330] | uncertain significance | 7 | 98628561 | 98628561 | Human | | name |
| 8626482 | CV81626 | single nucleotide variant | NM_002523.2(NPTX2):c.1006G>A (p.Glu336Lys) | Malignant melanoma [RCV000061704] | not provided | 7 | 98627282 | 98627282 | Human | | name |
