| 597634497 | CV3702437 | single nucleotide variant | NM_152611.5(LRRN4):c.26T>G (p.Leu9Arg) | not specified [RCV004940435] | uncertain significance | 20 | 6052774 | 6052774 | Human | | name |
| 401764408 | CV2725627 | single nucleotide variant | NM_152611.5(LRRN4):c.29T>A (p.Leu10Gln) | not specified [RCV004322007] | uncertain significance | 20 | 6052771 | 6052771 | Human | | name |
| 401930445 | CV2827093 | single nucleotide variant | NM_152611.5(LRRN4):c.726G>A (p.Thr242=) | not provided [RCV003440341] | likely benign | 20 | 6050913 | 6050913 | Human | | name |
| 598223481 | CV3985005 | single nucleotide variant | NM_152611.5(LRRN4):c.861C>T (p.Asn287=) | not specified [RCV005380057] | likely benign | 20 | 6044680 | 6044680 | Human | | name |
| 8628561 | CV83705 | single nucleotide variant | NM_152611.4(LRRN4):c.708G>A (p.Arg236=) | Malignant melanoma [RCV000063786] | not provided | 20 | 6050931 | 6050931 | Human | | name |
| 41405324 | CV982223 | single nucleotide variant | NM_152611.5(LRRN4):c.88G>A (p.Val30Ile) | not provided [RCV001812931] | uncertain significance | 20 | 6052712 | 6052712 | Human | | name |
| 329359944 | CV2446487 | single nucleotide variant | NM_152611.5(LRRN4):c.249C>A (p.Ser83Arg) | not specified [RCV004251391] | uncertain significance | 20 | 6052551 | 6052551 | Human | | name |
| 329377931 | CV2460682 | single nucleotide variant | NM_152611.5(LRRN4):c.203G>T (p.Arg68Leu) | not specified [RCV004271030] | uncertain significance | 20 | 6052597 | 6052597 | Human | | name |
| 329394413 | CV2469859 | single nucleotide variant | NM_152611.5(LRRN4):c.274A>G (p.Thr92Ala) | not specified [RCV004285337] | likely benign | 20 | 6052526 | 6052526 | Human | | name |
| 401898602 | CV2782531 | single nucleotide variant | NM_152611.5(LRRN4):c.221C>A (p.Pro74Gln) | not specified [RCV004359570] | uncertain significance | 20 | 6052579 | 6052579 | Human | | name |
| 401919624 | CV2827092 | single nucleotide variant | NM_152611.5(LRRN4):c.1437C>T (p.Ala479=) | not provided [RCV003431255] | likely benign | 20 | 6041808 | 6041808 | Human | | name |
| 597634491 | CV3702436 | single nucleotide variant | NM_152611.5(LRRN4):c.190C>G (p.Arg64Gly) | not specified [RCV004940434] | uncertain significance | 20 | 6052610 | 6052610 | Human | | name |
| 597634506 | CV3702439 | single nucleotide variant | NM_152611.5(LRRN4):c.221C>T (p.Pro74Leu) | not specified [RCV004940437] | uncertain significance | 20 | 6052579 | 6052579 | Human | | name |
| 597634517 | CV3702441 | single nucleotide variant | NM_152611.5(LRRN4):c.103C>G (p.Pro35Ala) | not specified [RCV004940439] | uncertain significance | 20 | 6052697 | 6052697 | Human | | name |
| 8628559 | CV83703 | single nucleotide variant | NM_152611.4(LRRN4):c.1959G>A (p.Ala653=) | Malignant melanoma [RCV000063784] | not provided | 20 | 6041286 | 6041286 | Human | | name |
| 156398970 | CV2194902 | single nucleotide variant | NM_152611.5(LRRN4):c.575A>G (p.Glu192Gly) | not specified [RCV004075432] | uncertain significance | 20 | 6052225 | 6052225 | Human | | name |
| 156129644 | CV2209850 | single nucleotide variant | NM_152611.5(LRRN4):c.478G>T (p.Ala160Ser) | not specified [RCV004076312] | uncertain significance | 20 | 6052322 | 6052322 | Human | | name |
| 156113170 | CV2228650 | single nucleotide variant | NM_152611.5(LRRN4):c.328C>A (p.Arg110Ser) | not specified [RCV004092873] | uncertain significance | 20 | 6052472 | 6052472 | Human | | name |
| 156204459 | CV2234724 | single nucleotide variant | NM_152611.5(LRRN4):c.463G>C (p.Gly155Arg) | not specified [RCV004102668] | uncertain significance | 20 | 6052337 | 6052337 | Human | | name |
| 155900798 | CV2275266 | single nucleotide variant | NM_152611.5(LRRN4):c.397C>A (p.Gln133Lys) | not specified [RCV004137045] | uncertain significance | 20 | 6052403 | 6052403 | Human | | name |
| 156000595 | CV2287403 | single nucleotide variant | NM_152611.5(LRRN4):c.637G>C (p.Gly213Arg) | not specified [RCV004147010] | uncertain significance | 20 | 6052163 | 6052163 | Human | | name |
| 156190309 | CV2301721 | single nucleotide variant | NM_152611.5(LRRN4):c.479C>A (p.Ala160Glu) | not specified [RCV004156540] | uncertain significance | 20 | 6052321 | 6052321 | Human | | name |
| 156005137 | CV2357632 | single nucleotide variant | NM_152611.5(LRRN4):c.656T>C (p.Val219Ala) | not specified [RCV004202893] | uncertain significance | 20 | 6050983 | 6050983 | Human | | name |
| 155929095 | CV2369658 | single nucleotide variant | NM_152611.5(LRRN4):c.440G>C (p.Ser147Thr) | not specified [RCV004215062] | uncertain significance | 20 | 6052360 | 6052360 | Human | | name |
| 156183106 | CV2382200 | single nucleotide variant | NM_152611.5(LRRN4):c.536G>A (p.Cys179Tyr) | not specified [RCV004228151] | uncertain significance | 20 | 6052264 | 6052264 | Human | | name |
| 401764608 | CV2705144 | single nucleotide variant | NM_152611.5(LRRN4):c.509C>T (p.Pro170Leu) | not specified [RCV004310040] | uncertain significance | 20 | 6052291 | 6052291 | Human | | name |
| 401866674 | CV2758965 | single nucleotide variant | NM_152611.5(LRRN4):c.452T>C (p.Leu151Pro) | not specified [RCV004342280] | uncertain significance | 20 | 6052348 | 6052348 | Human | | name |
| 401856972 | CV2759899 | single nucleotide variant | NM_152611.5(LRRN4):c.327C>A (p.Asn109Lys) | not specified [RCV004345326] | uncertain significance | 20 | 6052473 | 6052473 | Human | | name |
| 405810561 | CV3284321 | single nucleotide variant | NM_152611.5(LRRN4):c.353C>G (p.Pro118Arg) | not specified [RCV004408049] | uncertain significance | 20 | 6052447 | 6052447 | Human | | name |
| 405810564 | CV3284322 | single nucleotide variant | NM_152611.5(LRRN4):c.449C>T (p.Ala150Val) | not specified [RCV004408050] | likely benign | 20 | 6052351 | 6052351 | Human | | name |
| 405810565 | CV3284323 | single nucleotide variant | NM_152611.5(LRRN4):c.488C>A (p.Pro163His) | not specified [RCV004408051] | uncertain significance | 20 | 6052312 | 6052312 | Human | | name |
| 405810569 | CV3284325 | single nucleotide variant | NM_152611.5(LRRN4):c.889A>G (p.Thr297Ala) | not specified [RCV004408053] | uncertain significance | 20 | 6044652 | 6044652 | Human | | name |
| 407482376 | CV3453021 | single nucleotide variant | NM_152611.5(LRRN4):c.421A>C (p.Thr141Pro) | not specified [RCV004640121] | uncertain significance | 20 | 6052379 | 6052379 | Human | | name |
| 407482382 | CV3453022 | single nucleotide variant | NM_152611.5(LRRN4):c.712A>G (p.Met238Val) | not specified [RCV004640122] | uncertain significance | 20 | 6050927 | 6050927 | Human | | name |
| 407482399 | CV3453025 | single nucleotide variant | NM_152611.5(LRRN4):c.917T>G (p.Ile306Ser) | not specified [RCV004640125] | uncertain significance | 20 | 6044624 | 6044624 | Human | | name |
| 597634443 | CV3702427 | single nucleotide variant | NM_152611.5(LRRN4):c.562G>C (p.Gly188Arg) | not specified [RCV004940425] | uncertain significance | 20 | 6052238 | 6052238 | Human | | name |
| 597634451 | CV3702429 | single nucleotide variant | NM_152611.5(LRRN4):c.416C>A (p.Pro139Gln) | not specified [RCV004940427] | uncertain significance | 20 | 6052384 | 6052384 | Human | | name |
| 598251677 | CV3985001 | single nucleotide variant | NM_152611.5(LRRN4):c.758C>T (p.Pro253Leu) | not specified [RCV005366738] | uncertain significance | 20 | 6050881 | 6050881 | Human | | name |
| 598223472 | CV3985004 | single nucleotide variant | NM_152611.5(LRRN4):c.463G>A (p.Gly155Arg) | not specified [RCV005380056] | uncertain significance | 20 | 6052337 | 6052337 | Human | | name |
| 598251697 | CV3985008 | single nucleotide variant | NM_152611.5(LRRN4):c.725C>T (p.Thr242Met) | not specified [RCV005366741] | uncertain significance | 20 | 6050914 | 6050914 | Human | | name |
| 156067995 | CV2193667 | single nucleotide variant | NM_152611.5(LRRN4):c.1811A>G (p.Asn604Ser) | not specified [RCV004074264] | uncertain significance | 20 | 6041434 | 6041434 | Human | | name |
| 156240419 | CV2221336 | single nucleotide variant | NM_152611.5(LRRN4):c.1705C>T (p.Arg569Trp) | not specified [RCV004094757] | uncertain significance | 20 | 6041540 | 6041540 | Human | | name |
| 156208704 | CV2250141 | single nucleotide variant | NM_152611.5(LRRN4):c.1693C>T (p.Arg565Trp) | not specified [RCV004116949] | uncertain significance | 20 | 6041552 | 6041552 | Human | | name |
| 156104923 | CV2260617 | single nucleotide variant | NM_152611.5(LRRN4):c.2093C>T (p.Thr698Ile) | not specified [RCV004123379] | uncertain significance | 20 | 6041152 | 6041152 | Human | | name |
| 156017628 | CV2262919 | single nucleotide variant | NM_152611.5(LRRN4):c.1747C>T (p.Pro583Ser) | not specified [RCV004125059] | uncertain significance | 20 | 6041498 | 6041498 | Human | | name |
| 156341730 | CV2268307 | single nucleotide variant | NM_152611.5(LRRN4):c.2041G>A (p.Ala681Thr) | not specified [RCV004138596] | uncertain significance | 20 | 6041204 | 6041204 | Human | | name |
| 156051032 | CV2269329 | single nucleotide variant | NM_152611.5(LRRN4):c.1138C>T (p.Arg380Cys) | not specified [RCV004130730] | uncertain significance | 20 | 6042107 | 6042107 | Human | | name |
| 155925295 | CV2277274 | single nucleotide variant | NM_152611.5(LRRN4):c.1333G>A (p.Val445Ile) | not specified [RCV004142889] | uncertain significance | 20 | 6041912 | 6041912 | Human | | name |
| 156001651 | CV2296431 | single nucleotide variant | NM_152611.5(LRRN4):c.1720A>T (p.Ser574Cys) | not specified [RCV004148174] | uncertain significance | 20 | 6041525 | 6041525 | Human | | name |
| 155902384 | CV2356450 | single nucleotide variant | NM_152611.5(LRRN4):c.1156G>C (p.Gly386Arg) | not specified [RCV004199371] | uncertain significance | 20 | 6042089 | 6042089 | Human | | name |
| 156282280 | CV2363112 | single nucleotide variant | NM_152611.5(LRRN4):c.1759G>C (p.Gly587Arg) | not specified [RCV004211237] | uncertain significance | 20 | 6041486 | 6041486 | Human | | name |
| 329380173 | CV2444252 | single nucleotide variant | NM_152611.5(LRRN4):c.1925C>G (p.Ser642Trp) | not specified [RCV004263020] | uncertain significance | 20 | 6041320 | 6041320 | Human | | name |
| 329388533 | CV2447618 | single nucleotide variant | NM_152611.5(LRRN4):c.1105A>C (p.Thr369Pro) | not specified [RCV004258421] | uncertain significance | 20 | 6042140 | 6042140 | Human | | name |
| 329387216 | CV2463452 | single nucleotide variant | NM_152611.5(LRRN4):c.2128C>A (p.Gln710Lys) | not specified [RCV004277283] | uncertain significance | 20 | 6041117 | 6041117 | Human | | name |
| 329375422 | CV2468584 | single nucleotide variant | NM_152611.5(LRRN4):c.1258T>C (p.Trp420Arg) | not specified [RCV004278148] | uncertain significance | 20 | 6041987 | 6041987 | Human | | name |
| 401754244 | CV2685208 | single nucleotide variant | NM_152611.5(LRRN4):c.2050C>T (p.Leu684Phe) | not specified [RCV004289764] | likely benign | 20 | 6041195 | 6041195 | Human | | name |
| 401764655 | CV2705185 | single nucleotide variant | NM_152611.5(LRRN4):c.1903C>A (p.Gln635Lys) | not specified [RCV004310073] | uncertain significance | 20 | 6041342 | 6041342 | Human | | name |
| 401752783 | CV2707125 | single nucleotide variant | NM_152611.5(LRRN4):c.2048T>G (p.Leu683Arg) | not specified [RCV004315493] | uncertain significance | 20 | 6041197 | 6041197 | Human | | name |
| 401872251 | CV2754317 | single nucleotide variant | NM_152611.5(LRRN4):c.1700G>A (p.Arg567Gln) | not specified [RCV004334493] | uncertain significance | 20 | 6041545 | 6041545 | Human | | name |
| 401867701 | CV2767061 | single nucleotide variant | NM_152611.5(LRRN4):c.1156G>T (p.Gly386Cys) | not specified [RCV004347467] | uncertain significance | 20 | 6042089 | 6042089 | Human | | name |
| 401873461 | CV2776604 | single nucleotide variant | NM_152611.5(LRRN4):c.1178C>A (p.Ala393Glu) | not specified [RCV004357481] | uncertain significance | 20 | 6042067 | 6042067 | Human | | name |
| 401872697 | CV2779866 | single nucleotide variant | NM_152611.5(LRRN4):c.1945G>A (p.Val649Met) | not specified [RCV004353485] | uncertain significance | 20 | 6041300 | 6041300 | Human | | name |
| 405810546 | CV3284313 | single nucleotide variant | NM_152611.5(LRRN4):c.1297A>G (p.Thr433Ala) | not specified [RCV004408041] | uncertain significance | 20 | 6041948 | 6041948 | Human | | name |
| 405810548 | CV3284314 | single nucleotide variant | NM_152611.5(LRRN4):c.1375G>A (p.Gly459Arg) | not specified [RCV004408042] | uncertain significance | 20 | 6041870 | 6041870 | Human | | name |
| 405810549 | CV3284315 | single nucleotide variant | NM_152611.5(LRRN4):c.1553A>C (p.Glu518Ala) | not specified [RCV004408043] | uncertain significance | 20 | 6041692 | 6041692 | Human | | name |
| 405810551 | CV3284316 | single nucleotide variant | NM_152611.5(LRRN4):c.1573G>T (p.Asp525Tyr) | not specified [RCV004408044] | uncertain significance | 20 | 6041672 | 6041672 | Human | | name |
| 405810553 | CV3284317 | single nucleotide variant | NM_152611.5(LRRN4):c.1577A>C (p.Asp526Ala) | not specified [RCV004408045] | uncertain significance | 20 | 6041668 | 6041668 | Human | | name |
| 405810555 | CV3284318 | single nucleotide variant | NM_152611.5(LRRN4):c.1650T>A (p.His550Gln) | not specified [RCV004408046] | uncertain significance | 20 | 6041595 | 6041595 | Human | | name |
| 405810557 | CV3284319 | single nucleotide variant | NM_152611.5(LRRN4):c.2020T>C (p.Phe674Leu) | not specified [RCV004408047] | uncertain significance | 20 | 6041225 | 6041225 | Human | | name |
| 405810559 | CV3284320 | single nucleotide variant | NM_152611.5(LRRN4):c.2087C>T (p.Ala696Val) | not specified [RCV004408048] | likely benign | 20 | 6041158 | 6041158 | Human | | name |
| 407482369 | CV3453020 | single nucleotide variant | NM_152611.5(LRRN4):c.1781C>A (p.Thr594Lys) | not specified [RCV004640120] | uncertain significance | 20 | 6041464 | 6041464 | Human | | name |
| 407482388 | CV3453023 | single nucleotide variant | NM_152611.5(LRRN4):c.1495C>A (p.Pro499Thr) | not specified [RCV004640123] | uncertain significance | 20 | 6041750 | 6041750 | Human | | name |
| 407468425 | CV3453026 | single nucleotide variant | NM_152611.5(LRRN4):c.1031G>T (p.Gly344Val) | not specified [RCV004636276] | uncertain significance | 20 | 6042214 | 6042214 | Human | | name |
| 597634447 | CV3702428 | single nucleotide variant | NM_152611.5(LRRN4):c.1241C>T (p.Ser414Phe) | not specified [RCV004940426] | uncertain significance | 20 | 6042004 | 6042004 | Human | | name |
| 597634457 | CV3702430 | single nucleotide variant | NM_152611.5(LRRN4):c.2197C>T (p.Pro733Ser) | not specified [RCV004940428] | uncertain significance | 20 | 6041048 | 6041048 | Human | | name |
| 597634463 | CV3702431 | single nucleotide variant | NM_152611.5(LRRN4):c.1216G>A (p.Val406Ile) | not specified [RCV004940429] | uncertain significance | 20 | 6042029 | 6042029 | Human | | name |
| 597634469 | CV3702432 | single nucleotide variant | NM_152611.5(LRRN4):c.1670C>A (p.Thr557Asn) | not specified [RCV004940430] | uncertain significance | 20 | 6041575 | 6041575 | Human | | name |
| 597634475 | CV3702433 | single nucleotide variant | NM_152611.5(LRRN4):c.2156C>A (p.Thr719Lys) | not specified [RCV004940431] | uncertain significance | 20 | 6041089 | 6041089 | Human | | name |
| 597634481 | CV3702434 | single nucleotide variant | NM_152611.5(LRRN4):c.1454C>T (p.Pro485Leu) | not specified [RCV004940432] | likely benign | 20 | 6041791 | 6041791 | Human | | name |
| 597634486 | CV3702435 | single nucleotide variant | NM_152611.5(LRRN4):c.1733C>G (p.Thr578Ser) | not specified [RCV004940433] | uncertain significance | 20 | 6041512 | 6041512 | Human | | name |
| 597634501 | CV3702438 | single nucleotide variant | NM_152611.5(LRRN4):c.1751G>C (p.Arg584Thr) | not specified [RCV004940436] | uncertain significance | 20 | 6041494 | 6041494 | Human | | name |
| 597634512 | CV3702440 | single nucleotide variant | NM_152611.5(LRRN4):c.1717C>A (p.Leu573Ile) | not specified [RCV004940438] | uncertain significance | 20 | 6041528 | 6041528 | Human | | name |
| 597634522 | CV3702442 | single nucleotide variant | NM_152611.5(LRRN4):c.2044C>G (p.Leu682Val) | not specified [RCV004940440] | uncertain significance | 20 | 6041201 | 6041201 | Human | | name |
| 598223447 | CV3984997 | single nucleotide variant | NM_152611.5(LRRN4):c.2158C>T (p.His720Tyr) | not specified [RCV005380052] | uncertain significance | 20 | 6041087 | 6041087 | Human | | name |
| 598223453 | CV3984998 | single nucleotide variant | NM_152611.5(LRRN4):c.2083C>T (p.Leu695Phe) | not specified [RCV005380053] | uncertain significance | 20 | 6041162 | 6041162 | Human | | name |
| 598251671 | CV3984999 | single nucleotide variant | NM_152611.5(LRRN4):c.2171A>G (p.Tyr724Cys) | not specified [RCV005366737] | likely benign | 20 | 6041074 | 6041074 | Human | | name |
| 598223459 | CV3985000 | single nucleotide variant | NM_152611.5(LRRN4):c.2151C>G (p.Cys717Trp) | not specified [RCV005380054] | uncertain significance | 20 | 6041094 | 6041094 | Human | | name |
| 598251684 | CV3985002 | single nucleotide variant | NM_152611.5(LRRN4):c.1063C>T (p.Leu355Phe) | not specified [RCV005366739] | uncertain significance | 20 | 6042182 | 6042182 | Human | | name |
| 598223465 | CV3985003 | single nucleotide variant | NM_152611.5(LRRN4):c.1722C>A (p.Ser574Arg) | not specified [RCV005380055] | uncertain significance | 20 | 6041523 | 6041523 | Human | | name |
| 598251692 | CV3985007 | single nucleotide variant | NM_152611.5(LRRN4):c.1313C>A (p.Ala438Glu) | not specified [RCV005366740] | uncertain significance | 20 | 6041932 | 6041932 | Human | | name |
| 8628560 | CV83704 | single nucleotide variant | NM_152611.4(LRRN4):c.1678G>A (p.Ala560Thr) | Malignant melanoma [RCV000063785] | not provided | 20 | 6041567 | 6041567 | Human | | name |
| 8637416 | CV92642 | single nucleotide variant | NM_152611.4(LRRN4):c.1960G>T (p.Ala654Ser) | Malignant melanoma [RCV000072740] | not provided | 20 | 6041285 | 6041285 | Human | | name |
| 401782673 | CV2719932 | single nucleotide variant | NM_203422.4(LRRN4CL):c.70G>A (p.Ala24Thr) | not specified [RCV004329324] | uncertain significance | 11 | 62688439 | 62688439 | Human | | name |
| 156089938 | CV2206531 | single nucleotide variant | NM_203422.4(LRRN4CL):c.152A>G (p.Asp51Gly) | not specified [RCV004080883] | uncertain significance | 11 | 62688357 | 62688357 | Human | | name |
| 401725635 | CV2721867 | single nucleotide variant | NM_203422.4(LRRN4CL):c.212G>A (p.Cys71Tyr) | not specified [RCV004326378] | uncertain significance | 11 | 62688297 | 62688297 | Human | | name |
| 405810571 | CV3284326 | single nucleotide variant | NM_203422.4(LRRN4CL):c.199G>C (p.Gly67Arg) | not specified [RCV004408054] | uncertain significance | 11 | 62688310 | 62688310 | Human | | name |
| 405810574 | CV3284327 | single nucleotide variant | NM_203422.4(LRRN4CL):c.252C>G (p.Asp84Glu) | not specified [RCV004408055] | uncertain significance | 11 | 62688257 | 62688257 | Human | | name |
| 405810575 | CV3284328 | single nucleotide variant | NM_203422.4(LRRN4CL):c.262A>T (p.Met88Leu) | not specified [RCV004408056] | likely benign | 11 | 62688247 | 62688247 | Human | | name |
| 597634542 | CV3702446 | single nucleotide variant | NM_203422.4(LRRN4CL):c.101A>G (p.Asp34Gly) | not specified [RCV004940444] | uncertain significance | 11 | 62688408 | 62688408 | Human | | name |
| 156078231 | CV2248472 | single nucleotide variant | NM_203422.4(LRRN4CL):c.625C>G (p.Leu209Val) | not specified [RCV004119604] | uncertain significance | 11 | 62687884 | 62687884 | Human | | name |
| 156078240 | CV2248473 | single nucleotide variant | NM_203422.4(LRRN4CL):c.668G>C (p.Arg223Pro) | not specified [RCV004119605] | uncertain significance | 11 | 62687841 | 62687841 | Human | | name |
| 156316431 | CV2250907 | single nucleotide variant | NM_203422.4(LRRN4CL):c.409A>G (p.Arg137Gly) | not specified [RCV004123490] | uncertain significance | 11 | 62688100 | 62688100 | Human | | name |
| 156151303 | CV2268940 | single nucleotide variant | NM_203422.4(LRRN4CL):c.589C>G (p.His197Asp) | not specified [RCV004128345] | uncertain significance | 11 | 62687920 | 62687920 | Human | | name |
| 156350738 | CV2316262 | single nucleotide variant | NM_203422.4(LRRN4CL):c.692C>G (p.Ala231Gly) | not specified [RCV004174291] | uncertain significance | 11 | 62687817 | 62687817 | Human | | name |
| 156336664 | CV2342934 | single nucleotide variant | NM_203422.4(LRRN4CL):c.707G>A (p.Gly236Glu) | not specified [RCV004192543] | uncertain significance | 11 | 62687802 | 62687802 | Human | | name |
| 329381281 | CV2440763 | single nucleotide variant | NM_203422.4(LRRN4CL):c.433C>A (p.Pro145Thr) | not specified [RCV004258707] | uncertain significance | 11 | 62688076 | 62688076 | Human | | name |
| 329354880 | CV2449152 | single nucleotide variant | NM_203422.4(LRRN4CL):c.638C>T (p.Ala213Val) | not specified [RCV004264210] | uncertain significance | 11 | 62687871 | 62687871 | Human | | name |
| 401726250 | CV2695623 | single nucleotide variant | NM_203422.4(LRRN4CL):c.326C>T (p.Ser109Phe) | not specified [RCV004299441] | uncertain significance | 11 | 62688183 | 62688183 | Human | | name |
| 401759901 | CV2701774 | single nucleotide variant | NM_203422.4(LRRN4CL):c.385C>G (p.Pro129Ala) | not specified [RCV004314170] | uncertain significance | 11 | 62688124 | 62688124 | Human | | name |
| 405810578 | CV3284329 | single nucleotide variant | NM_203422.4(LRRN4CL):c.419T>G (p.Leu140Arg) | not specified [RCV004408057] | uncertain significance | 11 | 62688090 | 62688090 | Human | | name |
| 405810580 | CV3284330 | single nucleotide variant | NM_203422.4(LRRN4CL):c.552C>A (p.Ser184Arg) | not specified [RCV004408058] | uncertain significance | 11 | 62687957 | 62687957 | Human | | name |
| 405810581 | CV3284331 | single nucleotide variant | NM_203422.4(LRRN4CL):c.661C>G (p.Arg221Gly) | not specified [RCV004408059] | uncertain significance | 11 | 62687848 | 62687848 | Human | | name |
| 405810583 | CV3284332 | single nucleotide variant | NM_203422.4(LRRN4CL):c.686G>T (p.Arg229Leu) | not specified [RCV004408060] | uncertain significance | 11 | 62687823 | 62687823 | Human | | name |
| 597634826 | CV3702443 | single nucleotide variant | NM_203422.4(LRRN4CL):c.676T>C (p.Cys226Arg) | not specified [RCV004940441] | uncertain significance | 11 | 62687833 | 62687833 | Human | | name |
| 597634532 | CV3702444 | single nucleotide variant | NM_203422.4(LRRN4CL):c.661C>T (p.Arg221Cys) | not specified [RCV004940442] | uncertain significance | 11 | 62687848 | 62687848 | Human | | name |
| 597634536 | CV3702445 | single nucleotide variant | NM_203422.4(LRRN4CL):c.710C>G (p.Ala237Gly) | not specified [RCV004940443] | likely benign | 11 | 62687799 | 62687799 | Human | | name |
| 598223492 | CV3985009 | single nucleotide variant | NM_203422.4(LRRN4CL):c.364A>G (p.Ser122Gly) | not specified [RCV005380059] | uncertain significance | 11 | 62688145 | 62688145 | Human | | name |
| 598223498 | CV3985010 | single nucleotide variant | NM_203422.4(LRRN4CL):c.442A>G (p.Ile148Val) | not specified [RCV005380060] | likely benign | 11 | 62688067 | 62688067 | Human | | name |
| 598251704 | CV3985011 | single nucleotide variant | NM_203422.4(LRRN4CL):c.643G>A (p.Val215Met) | not specified [RCV005366742] | uncertain significance | 11 | 62687866 | 62687866 | Human | | name |
| 598223506 | CV3985012 | single nucleotide variant | NM_203422.4(LRRN4CL):c.598G>T (p.Val200Phe) | not specified [RCV005380061] | uncertain significance | 11 | 62687911 | 62687911 | Human | | name |
| 598223513 | CV3985013 | single nucleotide variant | NM_203422.4(LRRN4CL):c.466G>C (p.Ala156Pro) | not specified [RCV005380062] | uncertain significance | 11 | 62688043 | 62688043 | Human | | name |
