| 401911105 | CV2826314 | single nucleotide variant | NM_153366.4(SVEP1):c.1484-4G>A | not provided [RCV003425754] | likely benign | 9 | 110499242 | 110499242 | Human | | name |
| 8650974 | CV127549 | single nucleotide variant | NM_153366.3(SVEP1):c.2765-59C>G | Lung cancer [RCV000108036] | uncertain significance | 9 | 110471656 | 110471656 | Human | | name |
| 8650973 | CV127548 | single nucleotide variant | NM_153366.3(SVEP1):c.2999-669A>G | Lung cancer [RCV000108035] | uncertain significance | 9 | 110469770 | 110469770 | Human | | name |
| 401911108 | CV2826318 | single nucleotide variant | NM_153366.4(SVEP1):c.12C>T (p.Arg4=) | not provided [RCV003425757] | likely benign | 9 | 110579532 | 110579532 | Human | | name |
| 401911107 | CV2826316 | single nucleotide variant | NM_153366.4(SVEP1):c.198G>A (p.Gln66=) | not provided [RCV003425756] | likely benign | 9 | 110579346 | 110579346 | Human | | name |
| 401918391 | CV2826317 | single nucleotide variant | NM_153366.4(SVEP1):c.129C>T (p.Pro43=) | not provided [RCV003430200] | likely benign | 9 | 110579415 | 110579415 | Human | | name |
| 401911106 | CV2826315 | single nucleotide variant | NM_153366.4(SVEP1):c.483C>G (p.Ser161=) | not provided [RCV003425755] | likely benign | 9 | 110579061 | 110579061 | Human | | name |
| 405707875 | CV3323900 | single nucleotide variant | NM_153366.4(SVEP1):c.47C>T (p.Ser16Leu) | not specified [RCV004461330] | uncertain significance | 9 | 110579497 | 110579497 | Human | | name |
| 598222640 | CV3912677 | single nucleotide variant | NM_153366.4(SVEP1):c.97C>G (p.Arg33Gly) | not specified [RCV005293828] | uncertain significance | 9 | 110579447 | 110579447 | Human | | name |
| 401911103 | CV2826312 | single nucleotide variant | NM_153366.4(SVEP1):c.2805A>G (p.Glu935=) | not provided [RCV003425752] | likely benign | 9 | 110471557 | 110471557 | Human | | name |
| 401911104 | CV2826313 | single nucleotide variant | NM_153366.4(SVEP1):c.2322C>T (p.Gly774=) | not provided [RCV003425753] | likely benign | 9 | 110481285 | 110481285 | Human | | name |
| 405707691 | CV3323873 | single nucleotide variant | NM_153366.4(SVEP1):c.231G>T (p.Glu77Asp) | not specified [RCV004461303] | uncertain significance | 9 | 110579313 | 110579313 | Human | | name |
| 597769906 | CV3608869 | single nucleotide variant | NM_153366.4(SVEP1):c.173G>A (p.Gly58Glu) | not specified [RCV004871347] | likely benign | 9 | 110579371 | 110579371 | Human | | name |
| 156172340 | CV2247511 | single nucleotide variant | NM_153366.4(SVEP1):c.506C>T (p.Thr169Ile) | not specified [RCV004108829] | uncertain significance | 9 | 110579038 | 110579038 | Human | | name |
| 155948334 | CV2272090 | single nucleotide variant | NM_153366.4(SVEP1):c.353C>G (p.Thr118Arg) | not specified [RCV004124879] | uncertain significance | 9 | 110579191 | 110579191 | Human | | name |
| 156137099 | CV2365126 | single nucleotide variant | NM_153366.4(SVEP1):c.686G>C (p.Arg229Pro) | not specified [RCV004224280] | uncertain significance | 9 | 110549950 | 110549950 | Human | | name |
| 156211147 | CV2378257 | single nucleotide variant | NM_153366.4(SVEP1):c.397G>A (p.Val133Met) | not specified [RCV004226292] | uncertain significance | 9 | 110579147 | 110579147 | Human | | name |
| 401733353 | CV2691277 | single nucleotide variant | NM_153366.4(SVEP1):c.686G>A (p.Arg229Gln) | not specified [RCV004303038] | uncertain significance | 9 | 110549950 | 110549950 | Human | | name |
| 401748348 | CV2696604 | single nucleotide variant | NM_153366.4(SVEP1):c.394T>A (p.Tyr132Asn) | not specified [RCV004312631] | likely benign | 9 | 110579150 | 110579150 | Human | | name |
| 401772891 | CV2698020 | single nucleotide variant | NM_153366.4(SVEP1):c.611C>T (p.Pro204Leu) | not specified [RCV004302824] | uncertain significance | 9 | 110550025 | 110550025 | Human | | name |
| 401723990 | CV2725114 | single nucleotide variant | NM_153366.4(SVEP1):c.803G>A (p.Ser268Asn) | not specified [RCV004319859] | uncertain significance | 9 | 110546276 | 110546276 | Human | | name |
| 401890193 | CV2763684 | single nucleotide variant | NM_153366.4(SVEP1):c.905A>G (p.His302Arg) | not specified [RCV004343186] | uncertain significance | 9 | 110546174 | 110546174 | Human | | name |
| 401861343 | CV2779651 | single nucleotide variant | NM_153366.4(SVEP1):c.741C>A (p.His247Gln) | not specified [RCV004351350] | uncertain significance | 9 | 110549895 | 110549895 | Human | | name |
| 401911099 | CV2826306 | single nucleotide variant | NM_153366.4(SVEP1):c.7332G>A (p.Glu2444=) | not provided [RCV003425748] | likely benign | 9 | 110408268 | 110408268 | Human | | name |
| 401918389 | CV2826307 | single nucleotide variant | NM_153366.4(SVEP1):c.6960T>G (p.Pro2320=) | not provided [RCV003430198] | likely benign | 9 | 110408640 | 110408640 | Human | | name |
| 401911100 | CV2826308 | single nucleotide variant | NM_153366.4(SVEP1):c.6444G>A (p.Glu2148=) | not provided [RCV003425749] | likely benign | 9 | 110411267 | 110411267 | Human | | name |
| 401918390 | CV2826309 | single nucleotide variant | NM_153366.4(SVEP1):c.5586A>C (p.Ala1862=) | not provided [RCV003430199] | likely benign | 9 | 110429949 | 110429949 | Human | | name |
| 405707785 | CV3323887 | single nucleotide variant | NM_153366.4(SVEP1):c.349C>G (p.Pro117Ala) | not specified [RCV004461317] | uncertain significance | 9 | 110579195 | 110579195 | Human | | name |
| 405707833 | CV3323894 | single nucleotide variant | NM_153366.4(SVEP1):c.4464C>G (p.Gly1488=) | not specified [RCV004461324] | likely benign | 9 | 110443720 | 110443720 | Human | | name |
| 405707906 | CV3323905 | single nucleotide variant | NM_153366.4(SVEP1):c.601G>A (p.Gly201Arg) | not specified [RCV004461335] | uncertain significance | 9 | 110550035 | 110550035 | Human | | name |
| 405707996 | CV3323918 | single nucleotide variant | NM_153366.4(SVEP1):c.794C>A (p.Pro265His) | not specified [RCV004461348] | uncertain significance | 9 | 110546285 | 110546285 | Human | | name |
| 405708036 | CV3323923 | single nucleotide variant | NM_153366.4(SVEP1):c.869G>A (p.Arg290Gln) | not specified [RCV004461353] | likely benign | 9 | 110546210 | 110546210 | Human | | name |
| 405708087 | CV3323930 | single nucleotide variant | NM_153366.4(SVEP1):c.979A>G (p.Thr327Ala) | not specified [RCV004461360] | uncertain significance | 9 | 110514092 | 110514092 | Human | | name |
| 597770014 | CV3608893 | single nucleotide variant | NM_153366.4(SVEP1):c.623C>T (p.Ala208Val) | not specified [RCV004871367] | uncertain significance | 9 | 110550013 | 110550013 | Human | | name |
| 598222502 | CV3912641 | single nucleotide variant | NM_153366.4(SVEP1):c.847G>A (p.Glu283Lys) | not specified [RCV005293806] | uncertain significance | 9 | 110546232 | 110546232 | Human | | name |
| 598222583 | CV3912660 | single nucleotide variant | NM_153366.4(SVEP1):c.667A>C (p.Ile223Leu) | not specified [RCV005293818] | uncertain significance | 9 | 110549969 | 110549969 | Human | | name |
| 598263693 | CV3912667 | single nucleotide variant | NM_153366.4(SVEP1):c.716A>T (p.Lys239Met) | not specified [RCV005280583] | uncertain significance | 9 | 110549920 | 110549920 | Human | | name |
| 156316263 | CV2193030 | single nucleotide variant | NM_153366.4(SVEP1):c.1813G>A (p.Val605Ile) | not specified [RCV004069578] | uncertain significance | 9 | 110489767 | 110489767 | Human | | name |
| 156331115 | CV2218113 | single nucleotide variant | NM_153366.4(SVEP1):c.1130A>T (p.His377Leu) | not specified [RCV004086542] | uncertain significance | 9 | 110513099 | 110513099 | Human | | name |
| 155980226 | CV2263631 | single nucleotide variant | NM_153366.4(SVEP1):c.1754A>C (p.Asn585Thr) | not specified [RCV004135633] | uncertain significance | 9 | 110496861 | 110496861 | Human | | name |
| 156038076 | CV2278897 | single nucleotide variant | NM_153366.4(SVEP1):c.1325G>A (p.Arg442His) | not specified [RCV004145597] | uncertain significance | 9 | 110503196 | 110503196 | Human | | name |
| 156259815 | CV2322259 | single nucleotide variant | NM_153366.4(SVEP1):c.1735G>A (p.Glu579Lys) | not specified [RCV004176027] | uncertain significance | 9 | 110496880 | 110496880 | Human | | name |
| 156068219 | CV2341028 | single nucleotide variant | NM_153366.4(SVEP1):c.2206G>C (p.Gly736Arg) | not specified [RCV004181517] | uncertain significance | 9 | 110481401 | 110481401 | Human | | name |
| 156150002 | CV2359573 | single nucleotide variant | NM_153366.4(SVEP1):c.2762C>T (p.Thr921Ile) | not specified [RCV004214876] | uncertain significance | 9 | 110472161 | 110472161 | Human | | name |
| 155909402 | CV2359718 | single nucleotide variant | NM_153366.4(SVEP1):c.1717A>G (p.Ile573Val) | not specified [RCV004210537] | uncertain significance | 9 | 110496898 | 110496898 | Human | | name |
| 155937852 | CV2364927 | single nucleotide variant | NM_153366.4(SVEP1):c.1372T>C (p.Tyr458His) | not specified [RCV004222223] | uncertain significance | 9 | 110503149 | 110503149 | Human | | name |
| 329367507 | CV2427300 | single nucleotide variant | NM_153366.4(SVEP1):c.1534C>G (p.His512Asp) | not specified [RCV004248162] | uncertain significance | 9 | 110499188 | 110499188 | Human | | name |
| 329367490 | CV2427308 | single nucleotide variant | NM_153366.4(SVEP1):c.1684G>A (p.Val562Met) | not specified [RCV004248168] | uncertain significance | 9 | 110496931 | 110496931 | Human | | name |
| 329367883 | CV2427624 | single nucleotide variant | NM_153366.4(SVEP1):c.1754A>G (p.Asn585Ser) | not specified [RCV004250255] | uncertain significance | 9 | 110496861 | 110496861 | Human | | name |
| 329375708 | CV2431616 | single nucleotide variant | NM_153366.4(SVEP1):c.2102T>C (p.Ile701Thr) | not specified [RCV004254761] | uncertain significance | 9 | 110482429 | 110482429 | Human | | name |
| 329362734 | CV2439178 | single nucleotide variant | NM_153366.4(SVEP1):c.1916A>G (p.His639Arg) | not specified [RCV004266454] | uncertain significance | 9 | 110489664 | 110489664 | Human | | name |
| 329400051 | CV2440448 | single nucleotide variant | NM_153366.4(SVEP1):c.2768G>A (p.Ser923Asn) | not specified [RCV004256381] | uncertain significance | 9 | 110471594 | 110471594 | Human | | name |
| 329399982 | CV2444482 | single nucleotide variant | NM_153366.4(SVEP1):c.2950G>C (p.Ala984Pro) | not specified [RCV004263212] | uncertain significance | 9 | 110471412 | 110471412 | Human | | name |
| 329380635 | CV2464265 | single nucleotide variant | NM_153366.4(SVEP1):c.2270A>G (p.Tyr757Cys) | not specified [RCV004276226] | uncertain significance | 9 | 110481337 | 110481337 | Human | | name |
| 401757609 | CV2675412 | single nucleotide variant | NM_153366.4(SVEP1):c.1324C>T (p.Arg442Cys) | not specified [RCV004292213] | uncertain significance | 9 | 110503197 | 110503197 | Human | | name |
| 401743181 | CV2677787 | single nucleotide variant | NM_153366.4(SVEP1):c.2375T>C (p.Phe792Ser) | not specified [RCV004291857] | uncertain significance | 9 | 110479747 | 110479747 | Human | | name |
| 401775589 | CV2692427 | single nucleotide variant | NM_153366.4(SVEP1):c.1177A>G (p.Thr393Ala) | not specified [RCV004312187] | uncertain significance | 9 | 110513052 | 110513052 | Human | | name |
| 401758947 | CV2694357 | single nucleotide variant | NM_153366.4(SVEP1):c.1136C>T (p.Pro379Leu) | not specified [RCV004304548] | uncertain significance | 9 | 110513093 | 110513093 | Human | | name |
| 401861745 | CV2756473 | single nucleotide variant | NM_153366.4(SVEP1):c.2747T>C (p.Leu916Ser) | not specified [RCV004343004] | uncertain significance | 9 | 110472176 | 110472176 | Human | | name |
| 401889629 | CV2766769 | single nucleotide variant | NM_153366.4(SVEP1):c.1486C>T (p.Arg496Cys) | not specified [RCV004349158] | uncertain significance | 9 | 110499236 | 110499236 | Human | | name |
| 401885463 | CV2768185 | single nucleotide variant | NM_153366.4(SVEP1):c.2722C>T (p.Pro908Ser) | not specified [RCV004350190] | uncertain significance | 9 | 110472201 | 110472201 | Human | | name |
| 401876323 | CV2770516 | single nucleotide variant | NM_153366.4(SVEP1):c.2950G>T (p.Ala984Ser) | not specified [RCV004347802] | uncertain significance | 9 | 110471412 | 110471412 | Human | | name |
| 401895736 | CV2771091 | single nucleotide variant | NM_153366.4(SVEP1):c.1847C>T (p.Pro616Leu) | not specified [RCV004346096] | uncertain significance | 9 | 110489733 | 110489733 | Human | | name |
| 401911097 | CV2826303 | single nucleotide variant | NM_153366.4(SVEP1):c.10521C>T (p.Pro3507=) | not provided [RCV003425746] | likely benign | 9 | 110375447 | 110375447 | Human | | name |
| 401918388 | CV2826304 | single nucleotide variant | NM_153366.4(SVEP1):c.10092C>T (p.Pro3364=) | not provided [RCV003430197] | likely benign | 9 | 110386043 | 110386043 | Human | | name |
| 405707621 | CV3323863 | single nucleotide variant | NM_153366.4(SVEP1):c.1021A>G (p.Ile341Val) | not specified [RCV004461293] | uncertain significance | 9 | 110514050 | 110514050 | Human | | name |
| 405707651 | CV3323867 | single nucleotide variant | NM_153366.4(SVEP1):c.1548G>T (p.Lys516Asn) | not specified [RCV004461297] | uncertain significance | 9 | 110499174 | 110499174 | Human | | name |
| 405707656 | CV3323868 | single nucleotide variant | NM_153366.4(SVEP1):c.1928T>C (p.Ile643Thr) | not specified [RCV004461298] | uncertain significance | 9 | 110489652 | 110489652 | Human | | name |
| 405707661 | CV3323869 | single nucleotide variant | NM_153366.4(SVEP1):c.1998T>G (p.His666Gln) | not specified [RCV004461299] | uncertain significance | 9 | 110483626 | 110483626 | Human | | name |
| 405707668 | CV3323870 | single nucleotide variant | NM_153366.4(SVEP1):c.2069C>T (p.Thr690Ile) | not specified [RCV004461300] | uncertain significance | 9 | 110482462 | 110482462 | Human | | name |
| 405707676 | CV3323871 | single nucleotide variant | NM_153366.4(SVEP1):c.2236G>A (p.Gly746Arg) | not specified [RCV004461301] | uncertain significance | 9 | 110481371 | 110481371 | Human | | name |
| 405707698 | CV3323874 | single nucleotide variant | NM_153366.4(SVEP1):c.2323G>A (p.Val775Ile) | not specified [RCV004461304] | likely benign | 9 | 110481284 | 110481284 | Human | | name |
| 405707705 | CV3323875 | single nucleotide variant | NM_153366.4(SVEP1):c.2429A>G (p.Asp810Gly) | not specified [RCV004461305] | uncertain significance | 9 | 110479693 | 110479693 | Human | | name |
| 405707711 | CV3323876 | single nucleotide variant | NM_153366.4(SVEP1):c.2770G>A (p.Val924Met) | not specified [RCV004461306] | uncertain significance | 9 | 110471592 | 110471592 | Human | | name |
| 405707724 | CV3323878 | single nucleotide variant | NM_153366.4(SVEP1):c.2817G>T (p.Gln939His) | not specified [RCV004461308] | uncertain significance | 9 | 110471545 | 110471545 | Human | | name |
| 405707729 | CV3323879 | single nucleotide variant | NM_153366.4(SVEP1):c.2894T>C (p.Phe965Ser) | not specified [RCV004461309] | uncertain significance | 9 | 110471468 | 110471468 | Human | | name |
| 405707735 | CV3323880 | single nucleotide variant | NM_153366.4(SVEP1):c.2917A>G (p.Ile973Val) | not specified [RCV004461310] | likely benign | 9 | 110471445 | 110471445 | Human | | name |
| 405707743 | CV3323881 | single nucleotide variant | NM_153366.4(SVEP1):c.2994G>A (p.Met998Ile) | not specified [RCV004461311] | uncertain significance | 9 | 110471368 | 110471368 | Human | | name |
| 407505074 | CV3481998 | single nucleotide variant | NM_153366.4(SVEP1):c.1867G>A (p.Val623Ile) | not specified [RCV004670738] | uncertain significance | 9 | 110489713 | 110489713 | Human | | name |
| 407530230 | CV3482000 | single nucleotide variant | NM_153366.4(SVEP1):c.1428T>A (p.Asp476Glu) | not specified [RCV004681777] | uncertain significance | 9 | 110503093 | 110503093 | Human | | name |
| 407505088 | CV3482004 | single nucleotide variant | NM_153366.4(SVEP1):c.1067C>T (p.Ser356Phe) | not specified [RCV004670742] | uncertain significance | 9 | 110514004 | 110514004 | Human | | name |
| 407505111 | CV3482012 | single nucleotide variant | NM_153366.4(SVEP1):c.2554T>G (p.Tyr852Asp) | not specified [RCV004670749] | uncertain significance | 9 | 110476249 | 110476249 | Human | | name |
| 407530234 | CV3482016 | single nucleotide variant | NM_153366.4(SVEP1):c.2372G>A (p.Arg791His) | not specified [RCV004681781] | uncertain significance | 9 | 110479750 | 110479750 | Human | | name |
| 407505124 | CV3482019 | single nucleotide variant | NM_153366.4(SVEP1):c.2483A>T (p.Lys828Ile) | not specified [RCV004670753] | uncertain significance | 9 | 110479639 | 110479639 | Human | | name |
| 597769776 | CV3608838 | single nucleotide variant | NM_153366.4(SVEP1):c.1268A>G (p.Asn423Ser) | not specified [RCV004871320] | likely benign | 9 | 110512961 | 110512961 | Human | | name |
| 597769857 | CV3608857 | single nucleotide variant | NM_153366.4(SVEP1):c.2033A>G (p.Asn678Ser) | not specified [RCV004871337] | uncertain significance | 9 | 110483591 | 110483591 | Human | | name |
| 597769861 | CV3608858 | single nucleotide variant | NM_153366.4(SVEP1):c.1307G>A (p.Arg436Lys) | not specified [RCV004871338] | uncertain significance | 9 | 110503214 | 110503214 | Human | | name |
| 597769911 | CV3608871 | single nucleotide variant | NM_153366.4(SVEP1):c.1367T>A (p.Met456Lys) | not specified [RCV004871348] | uncertain significance | 9 | 110503154 | 110503154 | Human | | name |
| 598222470 | CV3912635 | single nucleotide variant | NM_153366.4(SVEP1):c.2656G>A (p.Asp886Asn) | not specified [RCV005293801] | uncertain significance | 9 | 110472267 | 110472267 | Human | | name |
| 598222476 | CV3912636 | single nucleotide variant | NM_153366.4(SVEP1):c.1588C>T (p.Arg530Cys) | not specified [RCV005293802] | uncertain significance | 9 | 110499134 | 110499134 | Human | | name |
| 598222495 | CV3912640 | single nucleotide variant | NM_153366.4(SVEP1):c.2156A>G (p.His719Arg) | not specified [RCV005293805] | uncertain significance | 9 | 110482375 | 110482375 | Human | | name |
| 598263671 | CV3912650 | single nucleotide variant | NM_153366.4(SVEP1):c.1073A>G (p.Glu358Gly) | not specified [RCV005280576] | uncertain significance | 9 | 110513998 | 110513998 | Human | | name |
| 598222551 | CV3912654 | single nucleotide variant | NM_153366.4(SVEP1):c.2111A>G (p.Tyr704Cys) | not specified [RCV005293813] | uncertain significance | 9 | 110482420 | 110482420 | Human | | name |
| 598222577 | CV3912658 | single nucleotide variant | NM_153366.4(SVEP1):c.1087A>G (p.Arg363Gly) | not specified [RCV005293817] | uncertain significance | 9 | 110513984 | 110513984 | Human | | name |
| 598263683 | CV3912659 | single nucleotide variant | NM_153366.4(SVEP1):c.2644G>A (p.Asp882Asn) | not specified [RCV005280580] | uncertain significance | 9 | 110472279 | 110472279 | Human | | name |
| 598222601 | CV3912664 | single nucleotide variant | NM_153366.4(SVEP1):c.2081T>C (p.Leu694Pro) | not specified [RCV005293821] | uncertain significance | 9 | 110482450 | 110482450 | Human | | name |
| 598222628 | CV3912675 | single nucleotide variant | NM_153366.4(SVEP1):c.2852A>G (p.Asn951Ser) | not specified [RCV005293826] | uncertain significance | 9 | 110471510 | 110471510 | Human | | name |
| 156399003 | CV2194924 | single nucleotide variant | NM_153366.4(SVEP1):c.5305A>T (p.Ile1769Leu) | not specified [RCV004075451] | uncertain significance | 9 | 110431963 | 110431963 | Human | | name |
| 156324117 | CV2198562 | single nucleotide variant | NM_153366.4(SVEP1):c.8975A>T (p.Asn2992Ile) | not specified [RCV004075587] | uncertain significance | 9 | 110406625 | 110406625 | Human | | name |
| 156368434 | CV2199847 | single nucleotide variant | NM_153366.4(SVEP1):c.8705C>T (p.Thr2902Met) | not specified [RCV004074040] | likely benign | 9 | 110406895 | 110406895 | Human | | name |
| 156072728 | CV2201360 | single nucleotide variant | NM_153366.4(SVEP1):c.3523G>T (p.Val1175Leu) | not specified [RCV004077484] | uncertain significance | 9 | 110458524 | 110458524 | Human | | name |
| 156087182 | CV2205788 | single nucleotide variant | NM_153366.4(SVEP1):c.7984G>A (p.Glu2662Lys) | not specified [RCV004075833] | uncertain significance | 9 | 110407616 | 110407616 | Human | | name |
| 156087196 | CV2205789 | single nucleotide variant | NM_153366.4(SVEP1):c.9853A>G (p.Arg3285Gly) | not specified [RCV004075834] | likely benign | 9 | 110389557 | 110389557 | Human | | name |
| 156380199 | CV2207984 | single nucleotide variant | NM_153366.4(SVEP1):c.4813G>A (p.Val1605Met) | not specified [RCV004086688] | uncertain significance | 9 | 110435316 | 110435316 | Human | | name |
| 156379955 | CV2211687 | single nucleotide variant | NM_153366.4(SVEP1):c.4154A>G (p.Asn1385Ser) | not specified [RCV004084573] | uncertain significance | 9 | 110447007 | 110447007 | Human | | name |
| 156107844 | CV2214282 | single nucleotide variant | NM_153366.4(SVEP1):c.3983G>A (p.Gly1328Glu) | not specified [RCV004086273] | uncertain significance | 9 | 110450179 | 110450179 | Human | | name |
| 156045970 | CV2216048 | single nucleotide variant | NM_153366.4(SVEP1):c.5926G>A (p.Gly1976Arg) | not specified [RCV004097083] | uncertain significance | 9 | 110427640 | 110427640 | Human | | name |
| 156380694 | CV2218896 | single nucleotide variant | NM_153366.4(SVEP1):c.8040G>A (p.Met2680Ile) | not specified [RCV004085123] | uncertain significance | 9 | 110407560 | 110407560 | Human | | name |
| 156249260 | CV2222094 | single nucleotide variant | NM_153366.4(SVEP1):c.8542G>A (p.Glu2848Lys) | not specified [RCV004104857] | uncertain significance | 9 | 110407058 | 110407058 | Human | | name |
| 156221502 | CV2222551 | single nucleotide variant | NM_153366.4(SVEP1):c.9235A>G (p.Ser3079Gly) | not specified [RCV004099385] | likely benign | 9 | 110406365 | 110406365 | Human | | name |
| 156233856 | CV2227797 | single nucleotide variant | NM_153366.4(SVEP1):c.3880A>T (p.Thr1294Ser) | not specified [RCV004094176] | uncertain significance | 9 | 110451310 | 110451310 | Human | | name |
| 155926542 | CV2230639 | single nucleotide variant | NM_153366.4(SVEP1):c.7577G>A (p.Arg2526Gln) | not specified [RCV004097593] | uncertain significance | 9 | 110408023 | 110408023 | Human | | name |
| 156384912 | CV2231221 | single nucleotide variant | NM_153366.4(SVEP1):c.3466T>C (p.Ser1156Pro) | not specified [RCV004094420] | uncertain significance | 9 | 110458970 | 110458970 | Human | | name |
| 156198099 | CV2237383 | single nucleotide variant | NM_153366.4(SVEP1):c.6412T>C (p.Ser2138Pro) | not specified [RCV004104571] | uncertain significance | 9 | 110411299 | 110411299 | Human | | name |
| 156137366 | CV2239871 | single nucleotide variant | NM_153366.4(SVEP1):c.4802G>A (p.Ser1601Asn) | not specified [RCV004108381] | uncertain significance | 9 | 110435327 | 110435327 | Human | | name |
| 155948753 | CV2242551 | single nucleotide variant | NM_153366.4(SVEP1):c.7097C>A (p.Ser2366Tyr) | not specified [RCV004113619] | uncertain significance | 9 | 110408503 | 110408503 | Human | | name |
| 155913159 | CV2245764 | single nucleotide variant | NM_153366.4(SVEP1):c.4859A>G (p.Lys1620Arg) | not specified [RCV004111625] | uncertain significance | 9 | 110435270 | 110435270 | Human | | name |
| 156001450 | CV2257853 | single nucleotide variant | NM_153366.4(SVEP1):c.5870C>A (p.Ala1957Asp) | not specified [RCV004127896] | uncertain significance | 9 | 110427696 | 110427696 | Human | | name |
| 156002177 | CV2257932 | single nucleotide variant | NM_153366.4(SVEP1):c.5761C>T (p.Leu1921Phe) | not specified [RCV004129750] | uncertain significance | 9 | 110429189 | 110429189 | Human | | name |
| 156079653 | CV2259219 | single nucleotide variant | NM_153366.4(SVEP1):c.5900C>G (p.Pro1967Arg) | not specified [RCV004122245] | uncertain significance | 9 | 110427666 | 110427666 | Human | | name |
| 156032408 | CV2259616 | single nucleotide variant | NM_153366.4(SVEP1):c.5239G>A (p.Asp1747Asn) | not specified [RCV004116656] | uncertain significance | 9 | 110432029 | 110432029 | Human | | name |
| 156145175 | CV2265030 | single nucleotide variant | NM_153366.4(SVEP1):c.6524G>A (p.Gly2175Glu) | not specified [RCV004126188] | uncertain significance | 9 | 110411187 | 110411187 | Human | | name |
| 156154927 | CV2266109 | single nucleotide variant | NM_153366.4(SVEP1):c.6781C>A (p.Pro2261Thr) | not specified [RCV004128703] | uncertain significance | 9 | 110408819 | 110408819 | Human | | name |
| 156277428 | CV2277030 | single nucleotide variant | NM_153366.4(SVEP1):c.6532A>G (p.Ile2178Val) | not specified [RCV004140350] | uncertain significance | 9 | 110411179 | 110411179 | Human | | name |
| 156271798 | CV2280807 | single nucleotide variant | NM_153366.4(SVEP1):c.8755G>A (p.Glu2919Lys) | not specified [RCV004145068] | uncertain significance | 9 | 110406845 | 110406845 | Human | | name |
| 155963808 | CV2282776 | single nucleotide variant | NM_153366.4(SVEP1):c.5355A>C (p.Glu1785Asp) | not specified [RCV004141630] | uncertain significance | 9 | 110430449 | 110430449 | Human | | name |
| 155964281 | CV2282824 | single nucleotide variant | NM_153366.4(SVEP1):c.3349C>T (p.Arg1117Cys) | not specified [RCV004143485] | uncertain significance | 9 | 110459087 | 110459087 | Human | | name |
| 155990024 | CV2285197 | single nucleotide variant | NM_153366.4(SVEP1):c.4402C>G (p.Pro1468Ala) | not specified [RCV004145405] | uncertain significance | 9 | 110445898 | 110445898 | Human | | name |
| 156006391 | CV2299554 | single nucleotide variant | NM_153366.4(SVEP1):c.9718T>G (p.Ser3240Ala) | not provided [RCV003434622]|not specified [RCV004154890] | likely benign|uncertain significance | 9 | 110400958 | 110400958 | Human | | name |
| 155903254 | CV2301607 | single nucleotide variant | NM_153366.4(SVEP1):c.6647A>T (p.Glu2216Val) | not specified [RCV004162513] | uncertain significance | 9 | 110411064 | 110411064 | Human | | name |
| 156019193 | CV2301780 | single nucleotide variant | NM_153366.4(SVEP1):c.7093C>T (p.Pro2365Ser) | not specified [RCV004156585] | uncertain significance | 9 | 110408507 | 110408507 | Human | | name |
| 155909933 | CV2303489 | single nucleotide variant | NM_153366.4(SVEP1):c.6720T>G (p.Ser2240Arg) | not specified [RCV004161595] | uncertain significance | 9 | 110408880 | 110408880 | Human | | name |
| 155963481 | CV2308279 | single nucleotide variant | NM_153366.4(SVEP1):c.6878G>A (p.Gly2293Asp) | not specified [RCV004164771] | uncertain significance | 9 | 110408722 | 110408722 | Human | | name |
| 156289896 | CV2309761 | single nucleotide variant | NM_153366.4(SVEP1):c.5371G>C (p.Ala1791Pro) | not specified [RCV004160885] | uncertain significance | 9 | 110430433 | 110430433 | Human | | name |
| 156200622 | CV2313089 | single nucleotide variant | NM_153366.4(SVEP1):c.5171G>A (p.Gly1724Asp) | not specified [RCV004161362] | uncertain significance | 9 | 110432524 | 110432524 | Human | | name |
| 156281809 | CV2317335 | single nucleotide variant | NM_153366.4(SVEP1):c.6947C>T (p.Pro2316Leu) | not specified [RCV004178818] | uncertain significance | 9 | 110408653 | 110408653 | Human | | name |
| 156050372 | CV2319372 | single nucleotide variant | NM_153366.4(SVEP1):c.9517A>G (p.Arg3173Gly) | not specified [RCV004180192] | uncertain significance | 9 | 110404476 | 110404476 | Human | | name |
| 156174990 | CV2326983 | single nucleotide variant | NM_153366.4(SVEP1):c.6698C>T (p.Pro2233Leu) | not specified [RCV004176790] | uncertain significance | 9 | 110408902 | 110408902 | Human | | name |
| 156165044 | CV2330016 | single nucleotide variant | NM_153366.4(SVEP1):c.6536A>G (p.Lys2179Arg) | not specified [RCV004185509] | uncertain significance | 9 | 110411175 | 110411175 | Human | | name |
| 156180110 | CV2331436 | single nucleotide variant | NM_153366.4(SVEP1):c.4864G>A (p.Asp1622Asn) | not specified [RCV004184070] | uncertain significance | 9 | 110435265 | 110435265 | Human | | name |
| 156294254 | CV2336720 | single nucleotide variant | NM_153366.4(SVEP1):c.8948G>A (p.Gly2983Glu) | not specified [RCV004196960] | uncertain significance | 9 | 110406652 | 110406652 | Human | | name |
| 155983745 | CV2348094 | single nucleotide variant | NM_153366.4(SVEP1):c.3056G>A (p.Arg1019Gln) | not specified [RCV004197774] | uncertain significance | 9 | 110469044 | 110469044 | Human | | name |
| 155920605 | CV2350538 | single nucleotide variant | NM_153366.4(SVEP1):c.5924C>T (p.Thr1975Met) | not specified [RCV004204896] | uncertain significance | 9 | 110427642 | 110427642 | Human | | name |
| 156112533 | CV2353438 | single nucleotide variant | NM_153366.4(SVEP1):c.9836G>A (p.Arg3279His) | not specified [RCV004205894] | uncertain significance | 9 | 110389574 | 110389574 | Human | | name |
| 156199722 | CV2362891 | single nucleotide variant | NM_153366.4(SVEP1):c.6799C>A (p.Pro2267Thr) | not specified [RCV004208999] | uncertain significance | 9 | 110408801 | 110408801 | Human | | name |
| 156268459 | CV2372048 | single nucleotide variant | NM_153366.4(SVEP1):c.9947C>T (p.Thr3316Met) | not specified [RCV004221717] | uncertain significance | 9 | 110387398 | 110387398 | Human | | name |
| 156260011 | CV2381067 | single nucleotide variant | NM_153366.4(SVEP1):c.9935T>C (p.Ile3312Thr) | not specified [RCV004225103] | uncertain significance | 9 | 110387410 | 110387410 | Human | | name |
| 156146554 | CV2381792 | single nucleotide variant | NM_153366.4(SVEP1):c.3917C>G (p.Thr1306Arg) | not specified [RCV004232241] | uncertain significance | 9 | 110450245 | 110450245 | Human | | name |
| 156146583 | CV2381793 | single nucleotide variant | NM_153366.4(SVEP1):c.7208C>A (p.Thr2403Asn) | not specified [RCV004232242] | uncertain significance | 9 | 110408392 | 110408392 | Human | | name |
| 156042790 | CV2387882 | single nucleotide variant | NM_153366.4(SVEP1):c.3431C>T (p.Pro1144Leu) | not specified [RCV004236435] | uncertain significance | 9 | 110459005 | 110459005 | Human | | name |
| 155969002 | CV2391525 | single nucleotide variant | NM_153366.4(SVEP1):c.7287C>G (p.Ser2429Arg) | not specified [RCV004239910] | uncertain significance | 9 | 110408313 | 110408313 | Human | | name |
| 156089880 | CV2392128 | single nucleotide variant | NM_153366.4(SVEP1):c.3047A>T (p.Glu1016Val) | not specified [RCV004238023] | uncertain significance | 9 | 110469053 | 110469053 | Human | | name |
| 156094567 | CV2398849 | single nucleotide variant | NM_153366.4(SVEP1):c.6743A>G (p.Asn2248Ser) | not specified [RCV004245171] | uncertain significance | 9 | 110408857 | 110408857 | Human | | name |
| 329358587 | CV2425202 | single nucleotide variant | NM_153366.4(SVEP1):c.7915G>A (p.Asp2639Asn) | not specified [RCV004250879] | uncertain significance | 9 | 110407685 | 110407685 | Human | | name |
| 329367982 | CV2427659 | single nucleotide variant | NM_153366.4(SVEP1):c.6448C>G (p.Pro2150Ala) | not specified [RCV004250283] | uncertain significance | 9 | 110411263 | 110411263 | Human | | name |
| 329372832 | CV2428671 | single nucleotide variant | NM_153366.4(SVEP1):c.9035T>C (p.Ile3012Thr) | not specified [RCV004255468] | uncertain significance | 9 | 110406565 | 110406565 | Human | | name |
| 329356286 | CV2442569 | single nucleotide variant | NM_153366.4(SVEP1):c.9113T>G (p.Leu3038Arg) | not specified [RCV004266791] | uncertain significance | 9 | 110406487 | 110406487 | Human | | name |
| 329375082 | CV2444865 | single nucleotide variant | NM_153366.4(SVEP1):c.5747A>G (p.Tyr1916Cys) | not specified [RCV004259102] | uncertain significance | 9 | 110429203 | 110429203 | Human | | name |
| 329401184 | CV2446241 | single nucleotide variant | NM_153366.4(SVEP1):c.6602C>T (p.Pro2201Leu) | not specified [RCV004264634] | uncertain significance | 9 | 110411109 | 110411109 | Human | | name |
| 329391678 | CV2448871 | single nucleotide variant | NM_153366.4(SVEP1):c.6766C>T (p.Pro2256Ser) | not specified [RCV004261549] | uncertain significance | 9 | 110408834 | 110408834 | Human | | name |
| 329386861 | CV2452613 | single nucleotide variant | NM_153366.4(SVEP1):c.5140T>A (p.Tyr1714Asn) | not specified [RCV004275188] | uncertain significance | 9 | 110432555 | 110432555 | Human | | name |
| 329360835 | CV2463031 | single nucleotide variant | NM_153366.4(SVEP1):c.7610C>T (p.Thr2537Ile) | not specified [RCV004272849] | uncertain significance | 9 | 110407990 | 110407990 | Human | | name |
| 329362666 | CV2464097 | single nucleotide variant | NM_153366.4(SVEP1):c.8197A>G (p.Thr2733Ala) | not specified [RCV004273793] | uncertain significance | 9 | 110407403 | 110407403 | Human | | name |
| 329382581 | CV2465272 | single nucleotide variant | NM_153366.4(SVEP1):c.7949C>T (p.Pro2650Leu) | not specified [RCV004281072] | uncertain significance | 9 | 110407651 | 110407651 | Human | | name |
| 329399166 | CV2469972 | single nucleotide variant | NM_153366.4(SVEP1):c.8300C>T (p.Ser2767Phe) | not specified [RCV004285426] | uncertain significance | 9 | 110407300 | 110407300 | Human | | name |
| 401755723 | CV2682617 | single nucleotide variant | NM_153366.4(SVEP1):c.9920A>G (p.Asn3307Ser) | not specified [RCV004292667] | uncertain significance | 9 | 110387425 | 110387425 | Human | | name |
| 401769265 | CV2693556 | single nucleotide variant | NM_153366.4(SVEP1):c.6461A>G (p.Asn2154Ser) | not specified [RCV004297535] | uncertain significance | 9 | 110411250 | 110411250 | Human | | name |
| 401726576 | CV2695727 | single nucleotide variant | NM_153366.4(SVEP1):c.3719G>A (p.Cys1240Tyr) | not specified [RCV004299528] | uncertain significance | 9 | 110455658 | 110455658 | Human | | name |
| 401744075 | CV2696930 | single nucleotide variant | NM_153366.4(SVEP1):c.9754G>A (p.Val3252Met) | not specified [RCV004292930] | uncertain significance | 9 | 110400922 | 110400922 | Human | | name |
| 401748302 | CV2698344 | single nucleotide variant | NM_153366.4(SVEP1):c.3055C>T (p.Arg1019Trp) | not specified [RCV004304886] | uncertain significance | 9 | 110469045 | 110469045 | Human | | name |
| 401730144 | CV2700459 | single nucleotide variant | NM_153366.4(SVEP1):c.6319G>C (p.Val2107Leu) | not specified [RCV004311097] | uncertain significance | 9 | 110411392 | 110411392 | Human | | name |
| 401783224 | CV2703892 | single nucleotide variant | NM_153366.4(SVEP1):c.6359C>T (p.Thr2120Ile) | not specified [RCV004306750] | uncertain significance | 9 | 110411352 | 110411352 | Human | | name |
| 401778902 | CV2705867 | single nucleotide variant | NM_153366.4(SVEP1):c.6806C>T (p.Pro2269Leu) | not specified [RCV004320480] | uncertain significance | 9 | 110408794 | 110408794 | Human | | name |
| 401737671 | CV2718169 | single nucleotide variant | NM_153366.4(SVEP1):c.7200T>G (p.Phe2400Leu) | not specified [RCV004315872] | uncertain significance | 9 | 110408400 | 110408400 | Human | | name |
| 401760122 | CV2718722 | single nucleotide variant | NM_153366.4(SVEP1):c.9185C>T (p.Thr3062Ile) | not specified [RCV004328478] | uncertain significance | 9 | 110406415 | 110406415 | Human | | name |
| 401772437 | CV2719642 | single nucleotide variant | NM_153366.4(SVEP1):c.3520G>A (p.Val1174Met) | not specified [RCV004327305] | uncertain significance | 9 | 110458527 | 110458527 | Human | | name |
| 401758242 | CV2729611 | single nucleotide variant | NM_153366.4(SVEP1):c.3638G>A (p.Arg1213His) | not specified [RCV004331875] | uncertain significance | 9 | 110457291 | 110457291 | Human | | name |
| 401865332 | CV2754226 | single nucleotide variant | NM_153366.4(SVEP1):c.5595T>G (p.Phe1865Leu) | not specified [RCV004334414] | uncertain significance | 9 | 110429940 | 110429940 | Human | | name |
| 401870623 | CV2769252 | single nucleotide variant | NM_153366.4(SVEP1):c.7982G>T (p.Trp2661Leu) | not specified [RCV004357266] | uncertain significance | 9 | 110407618 | 110407618 | Human | | name |
| 401893982 | CV2770184 | single nucleotide variant | NM_153366.4(SVEP1):c.3569G>T (p.Ser1190Ile) | not specified [RCV004356078] | uncertain significance | 9 | 110458478 | 110458478 | Human | | name |
| 401878583 | CV2770684 | single nucleotide variant | NM_153366.4(SVEP1):c.4041T>A (p.Asp1347Glu) | not specified [RCV004349732] | uncertain significance | 9 | 110450121 | 110450121 | Human | | name |
| 401862355 | CV2775239 | single nucleotide variant | NM_153366.4(SVEP1):c.6205C>A (p.Pro2069Thr) | not specified [RCV004348366] | uncertain significance | 9 | 110411506 | 110411506 | Human | | name |
| 401866034 | CV2775387 | single nucleotide variant | NM_153366.4(SVEP1):c.7798G>C (p.Gly2600Arg) | not specified [RCV004348790] | uncertain significance | 9 | 110407802 | 110407802 | Human | | name |
| 401882321 | CV2781658 | single nucleotide variant | NM_153366.4(SVEP1):c.9211C>T (p.Pro3071Ser) | not specified [RCV004354857] | uncertain significance | 9 | 110406389 | 110406389 | Human | | name |
| 401896877 | CV2788898 | single nucleotide variant | NM_153366.4(SVEP1):c.5473A>G (p.Thr1825Ala) | not specified [RCV004362935] | uncertain significance | 9 | 110430331 | 110430331 | Human | | name |
| 401872828 | CV2793029 | single nucleotide variant | NM_153366.4(SVEP1):c.9409G>T (p.Ala3137Ser) | not specified [RCV004360362] | uncertain significance | 9 | 110406191 | 110406191 | Human | | name |
| 401882491 | CV2793515 | single nucleotide variant | NM_153366.4(SVEP1):c.6214G>A (p.Gly2072Ser) | not specified [RCV004364190] | uncertain significance | 9 | 110411497 | 110411497 | Human | | name |
| 401911098 | CV2826305 | single nucleotide variant | NM_153366.4(SVEP1):c.7591G>A (p.Glu2531Lys) | not provided [RCV003425747] | likely benign | 9 | 110408009 | 110408009 | Human | | name |
| 401911101 | CV2826310 | single nucleotide variant | NM_153366.4(SVEP1):c.4904G>A (p.Gly1635Glu) | not provided [RCV003425750] | likely benign | 9 | 110434491 | 110434491 | Human | | name |
| 401911102 | CV2826311 | single nucleotide variant | NM_153366.4(SVEP1):c.3773C>T (p.Pro1258Leu) | not provided [RCV003425751] | likely benign | 9 | 110455604 | 110455604 | Human | | name |
| 401944877 | CV2840705 | single nucleotide variant | NM_153366.4(SVEP1):c.4876A>G (p.Ile1626Val) | not provided [RCV003457564] | likely benign | 9 | 110435253 | 110435253 | Human | | name |
| 405263890 | CV3185250 | single nucleotide variant | NM_153366.4(SVEP1):c.7180C>T (p.Pro2394Ser) | not provided [RCV003885814]|not specified [RCV004369681] | likely benign|uncertain significance | 9 | 110408420 | 110408420 | Human | | name |
| 405707749 | CV3323882 | single nucleotide variant | NM_153366.4(SVEP1):c.3001A>C (p.Asn1001His) | not specified [RCV004461312] | uncertain significance | 9 | 110469099 | 110469099 | Human | | name |
| 405707758 | CV3323883 | single nucleotide variant | NM_153366.4(SVEP1):c.3002A>G (p.Asn1001Ser) | not specified [RCV004461313] | uncertain significance | 9 | 110469098 | 110469098 | Human | | name |
| 405707764 | CV3323884 | single nucleotide variant | NM_153366.4(SVEP1):c.3148T>G (p.Ser1050Ala) | not specified [RCV004461314] | uncertain significance | 9 | 110468952 | 110468952 | Human | | name |
| 405707771 | CV3323885 | single nucleotide variant | NM_153366.4(SVEP1):c.3263C>T (p.Ser1088Leu) | not specified [RCV004461315] | likely benign | 9 | 110465924 | 110465924 | Human | | name |
| 405707777 | CV3323886 | single nucleotide variant | NM_153366.4(SVEP1):c.3454G>A (p.Ala1152Thr) | not specified [RCV004461316] | likely benign | 9 | 110458982 | 110458982 | Human | | name |
| 405707800 | CV3323889 | single nucleotide variant | NM_153366.4(SVEP1):c.3760A>G (p.Ile1254Val) | not specified [RCV004461319] | uncertain significance | 9 | 110455617 | 110455617 | Human | | name |
| 405707807 | CV3323890 | single nucleotide variant | NM_153366.4(SVEP1):c.3875G>A (p.Arg1292His) | not specified [RCV004461320] | likely benign | 9 | 110451315 | 110451315 | Human | | name |
| 405707812 | CV3323891 | single nucleotide variant | NM_153366.4(SVEP1):c.3926A>G (p.Asn1309Ser) | not specified [RCV004461321] | uncertain significance | 9 | 110450236 | 110450236 | Human | | name |
| 405707819 | CV3323892 | single nucleotide variant | NM_153366.4(SVEP1):c.4075A>C (p.Thr1359Pro) | not specified [RCV004461322] | uncertain significance | 9 | 110450087 | 110450087 | Human | | name |
| 405707826 | CV3323893 | single nucleotide variant | NM_153366.4(SVEP1):c.4096A>T (p.Ser1366Cys) | not specified [RCV004461323] | uncertain significance | 9 | 110450066 | 110450066 | Human | | name |
| 405707840 | CV3323895 | single nucleotide variant | NM_153366.4(SVEP1):c.4511C>T (p.Ser1504Leu) | not specified [RCV004461325] | uncertain significance | 9 | 110443673 | 110443673 | Human | | name |
| 405707846 | CV3323896 | single nucleotide variant | NM_153366.4(SVEP1):c.4525A>G (p.Arg1509Gly) | not specified [RCV004461326] | uncertain significance | 9 | 110443659 | 110443659 | Human | | name |
| 405707860 | CV3323898 | single nucleotide variant | NM_153366.4(SVEP1):c.4576G>C (p.Val1526Leu) | not specified [RCV004461328] | uncertain significance | 9 | 110443608 | 110443608 | Human | | name |
| 405707867 | CV3323899 | single nucleotide variant | NM_153366.4(SVEP1):c.4710T>G (p.Phe1570Leu) | not specified [RCV004461329] | uncertain significance | 9 | 110436434 | 110436434 | Human | | name |
| 405707882 | CV3323901 | single nucleotide variant | NM_153366.4(SVEP1):c.5384C>T (p.Pro1795Leu) | not specified [RCV004461331] | uncertain significance | 9 | 110430420 | 110430420 | Human | | name |
| 405707887 | CV3323902 | single nucleotide variant | NM_153366.4(SVEP1):c.5411T>A (p.Ile1804Asn) | not specified [RCV004461332] | uncertain significance | 9 | 110430393 | 110430393 | Human | | name |
| 405707895 | CV3323903 | single nucleotide variant | NM_153366.4(SVEP1):c.5531C>A (p.Ala1844Asp) | not specified [RCV004461333] | uncertain significance | 9 | 110430004 | 110430004 | Human | | name |
| 405707901 | CV3323904 | single nucleotide variant | NM_153366.4(SVEP1):c.5573T>C (p.Ile1858Thr) | not specified [RCV004461334] | uncertain significance | 9 | 110429962 | 110429962 | Human | | name |
| 405707914 | CV3323906 | single nucleotide variant | NM_153366.4(SVEP1):c.6076A>G (p.Ile2026Val) | not specified [RCV004461336] | uncertain significance | 9 | 110411635 | 110411635 | Human | | name |
| 405707921 | CV3323907 | single nucleotide variant | NM_153366.4(SVEP1):c.6433C>T (p.Arg2145Trp) | not specified [RCV004461337] | uncertain significance | 9 | 110411278 | 110411278 | Human | | name |
| 405707931 | CV3323908 | single nucleotide variant | NM_153366.4(SVEP1):c.6496G>C (p.Ala2166Pro) | not specified [RCV004461338] | uncertain significance | 9 | 110411215 | 110411215 | Human | | name |
| 405707936 | CV3323909 | single nucleotide variant | NM_153366.4(SVEP1):c.6600C>G (p.His2200Gln) | not specified [RCV004461339] | uncertain significance | 9 | 110411111 | 110411111 | Human | | name |
| 405707944 | CV3323910 | single nucleotide variant | NM_153366.4(SVEP1):c.6815A>G (p.Asn2272Ser) | not specified [RCV004461340] | uncertain significance | 9 | 110408785 | 110408785 | Human | | name |
| 405707951 | CV3323911 | single nucleotide variant | NM_153366.4(SVEP1):c.7046G>T (p.Cys2349Phe) | not specified [RCV004461341] | uncertain significance | 9 | 110408554 | 110408554 | Human | | name |
| 405707956 | CV3323912 | single nucleotide variant | NM_153366.4(SVEP1):c.7130A>G (p.Lys2377Arg) | not specified [RCV004461342] | uncertain significance | 9 | 110408470 | 110408470 | Human | | name |
| 405707962 | CV3323913 | single nucleotide variant | NM_153366.4(SVEP1):c.7351A>C (p.Ile2451Leu) | not specified [RCV004461343] | uncertain significance | 9 | 110408249 | 110408249 | Human | | name |
| 405707965 | CV3323914 | single nucleotide variant | NM_153366.4(SVEP1):c.7558G>A (p.Val2520Ile) | not specified [RCV004461344] | likely benign | 9 | 110408042 | 110408042 | Human | | name |
| 405707974 | CV3323915 | single nucleotide variant | NM_153366.4(SVEP1):c.7649C>T (p.Ser2550Phe) | not specified [RCV004461345] | uncertain significance | 9 | 110407951 | 110407951 | Human | | name |
| 405707987 | CV3323917 | single nucleotide variant | NM_153366.4(SVEP1):c.7820C>T (p.Thr2607Ile) | not specified [RCV004461347] | uncertain significance | 9 | 110407780 | 110407780 | Human | | name |
| 405708007 | CV3323919 | single nucleotide variant | NM_153366.4(SVEP1):c.7996G>C (p.Glu2666Gln) | not specified [RCV004461349] | uncertain significance | 9 | 110407604 | 110407604 | Human | | name |
| 405708012 | CV3323920 | single nucleotide variant | NM_153366.4(SVEP1):c.8003C>T (p.Pro2668Leu) | not specified [RCV004461350] | uncertain significance | 9 | 110407597 | 110407597 | Human | | name |
| 405708028 | CV3323922 | single nucleotide variant | NM_153366.4(SVEP1):c.8313A>C (p.Glu2771Asp) | not specified [RCV004461352] | uncertain significance | 9 | 110407287 | 110407287 | Human | | name |
| 405708042 | CV3323924 | single nucleotide variant | NM_153366.4(SVEP1):c.8753A>G (p.His2918Arg) | not specified [RCV004461354] | uncertain significance | 9 | 110406847 | 110406847 | Human | | name |
| 405708057 | CV3323926 | single nucleotide variant | NM_153366.4(SVEP1):c.9058A>G (p.Thr3020Ala) | not specified [RCV004461356] | uncertain significance | 9 | 110406542 | 110406542 | Human | | name |
| 405708065 | CV3323927 | single nucleotide variant | NM_153366.4(SVEP1):c.9290A>G (p.Gln3097Arg) | not specified [RCV004461357] | uncertain significance | 9 | 110406310 | 110406310 | Human | | name |
| 405708071 | CV3323928 | single nucleotide variant | NM_153366.4(SVEP1):c.9458C>T (p.Thr3153Met) | not specified [RCV004461358] | likely benign | 9 | 110404535 | 110404535 | Human | | name |
| 405708080 | CV3323929 | single nucleotide variant | NM_153366.4(SVEP1):c.9671A>T (p.Asp3224Val) | not specified [RCV004461359] | uncertain significance | 9 | 110401005 | 110401005 | Human | | name |
| 405708093 | CV3323931 | single nucleotide variant | NM_153366.4(SVEP1):c.9835C>T (p.Arg3279Cys) | not specified [RCV004461361] | uncertain significance | 9 | 110389575 | 110389575 | Human | | name |
| 405708100 | CV3323932 | single nucleotide variant | NM_153366.4(SVEP1):c.9977A>T (p.Asn3326Ile) | not specified [RCV004461362] | uncertain significance | 9 | 110387368 | 110387368 | Human | | name |
| 405708106 | CV3323933 | single nucleotide variant | NM_153366.4(SVEP1):c.9988A>G (p.Ser3330Gly) | not specified [RCV004461363] | uncertain significance | 9 | 110387357 | 110387357 | Human | | name |
| 407505004 | CV3481997 | single nucleotide variant | NM_153366.4(SVEP1):c.5837C>T (p.Thr1946Met) | not specified [RCV004670737] | likely benign | 9 | 110427729 | 110427729 | Human | | name |
| 407505078 | CV3481999 | single nucleotide variant | NM_153366.4(SVEP1):c.3517A>G (p.Ser1173Gly) | not specified [RCV004670739] | uncertain significance | 9 | 110458530 | 110458530 | Human | | name |
| 407505081 | CV3482001 | single nucleotide variant | NM_153366.4(SVEP1):c.3620C>G (p.Thr1207Ser) | not specified [RCV004670740] | uncertain significance | 9 | 110457309 | 110457309 | Human | | name |
| 407530231 | CV3482002 | single nucleotide variant | NM_153366.4(SVEP1):c.5099T>C (p.Phe1700Ser) | not specified [RCV004681778] | uncertain significance | 9 | 110432596 | 110432596 | Human | | name |
| 407505084 | CV3482003 | single nucleotide variant | NM_153366.4(SVEP1):c.3620C>A (p.Thr1207Asn) | not specified [RCV004670741] | uncertain significance | 9 | 110457309 | 110457309 | Human | | name |
| 407505091 | CV3482005 | single nucleotide variant | NM_153366.4(SVEP1):c.9344C>T (p.Pro3115Leu) | not specified [RCV004670743] | uncertain significance | 9 | 110406256 | 110406256 | Human | | name |
| 407505097 | CV3482007 | single nucleotide variant | NM_153366.4(SVEP1):c.3620C>T (p.Thr1207Ile) | not specified [RCV004670745] | uncertain significance | 9 | 110457309 | 110457309 | Human | | name |
| 407530232 | CV3482008 | single nucleotide variant | NM_153366.4(SVEP1):c.8632A>T (p.Ser2878Cys) | not specified [RCV004681779] | uncertain significance | 9 | 110406968 | 110406968 | Human | | name |
| 407505105 | CV3482010 | single nucleotide variant | NM_153366.4(SVEP1):c.9937G>C (p.Glu3313Gln) | not specified [RCV004670747] | uncertain significance | 9 | 110387408 | 110387408 | Human | | name |
| 407505107 | CV3482011 | single nucleotide variant | NM_153366.4(SVEP1):c.7809T>A (p.Ser2603Arg) | not specified [RCV004670748] | uncertain significance | 9 | 110407791 | 110407791 | Human | | name |
| 407505117 | CV3482014 | single nucleotide variant | NM_153366.4(SVEP1):c.8555A>C (p.Gln2852Pro) | not specified [RCV004670751] | uncertain significance | 9 | 110407045 | 110407045 | Human | | name |
| 407530233 | CV3482015 | single nucleotide variant | NM_153366.4(SVEP1):c.6386G>A (p.Gly2129Asp) | not specified [RCV004681780] | uncertain significance | 9 | 110411325 | 110411325 | Human | | name |
| 407530235 | CV3482017 | single nucleotide variant | NM_153366.4(SVEP1):c.6745C>T (p.Arg2249Cys) | not specified [RCV004681782] | uncertain significance | 9 | 110408855 | 110408855 | Human | | name |
| 407505121 | CV3482018 | single nucleotide variant | NM_153366.4(SVEP1):c.9592A>G (p.Ser3198Gly) | not specified [RCV004670752] | uncertain significance | 9 | 110404401 | 110404401 | Human | | name |
| 407530236 | CV3482020 | single nucleotide variant | NM_153366.4(SVEP1):c.3638G>T (p.Arg1213Leu) | not specified [RCV004681783] | uncertain significance | 9 | 110457291 | 110457291 | Human | | name |
| 407530237 | CV3482021 | single nucleotide variant | NM_153366.4(SVEP1):c.6311C>G (p.Ala2104Gly) | not specified [RCV004681784] | uncertain significance | 9 | 110411400 | 110411400 | Human | | name |
| 407505127 | CV3482022 | single nucleotide variant | NM_153366.4(SVEP1):c.3236C>G (p.Pro1079Arg) | not specified [RCV004670754] | uncertain significance | 9 | 110465951 | 110465951 | Human | | name |
| 407505130 | CV3482023 | single nucleotide variant | NM_153366.4(SVEP1):c.9256A>G (p.Ile3086Val) | not specified [RCV004670755] | likely benign | 9 | 110406344 | 110406344 | Human | | name |
| 407530238 | CV3482024 | single nucleotide variant | NM_153366.4(SVEP1):c.5516T>C (p.Ile1839Thr) | not specified [RCV004681785] | uncertain significance | 9 | 110430288 | 110430288 | Human | | name |
| 597769782 | CV3608839 | single nucleotide variant | NM_153366.4(SVEP1):c.4073C>G (p.Ala1358Gly) | not specified [RCV004871321] | uncertain significance | 9 | 110450089 | 110450089 | Human | | name |
| 597769787 | CV3608840 | single nucleotide variant | NM_153366.4(SVEP1):c.8200A>G (p.Ser2734Gly) | not specified [RCV004871322] | uncertain significance | 9 | 110407400 | 110407400 | Human | | name |
| 597769792 | CV3608841 | single nucleotide variant | NM_153366.4(SVEP1):c.9145G>A (p.Asp3049Asn) | not specified [RCV004871323] | likely benign | 9 | 110406455 | 110406455 | Human | | name |
| 597769797 | CV3608842 | single nucleotide variant | NM_153366.4(SVEP1):c.5924C>A (p.Thr1975Lys) | not specified [RCV004871324] | uncertain significance | 9 | 110427642 | 110427642 | Human | | name |
| 597769801 | CV3608843 | single nucleotide variant | NM_153366.4(SVEP1):c.9551C>T (p.Pro3184Leu) | not specified [RCV004871325] | uncertain significance | 9 | 110404442 | 110404442 | Human | | name |
| 597769814 | CV3608847 | single nucleotide variant | NM_153366.4(SVEP1):c.5428G>A (p.Glu1810Lys) | not specified [RCV004871328] | uncertain significance | 9 | 110430376 | 110430376 | Human | | name |
| 597769819 | CV3608848 | single nucleotide variant | NM_153366.4(SVEP1):c.7973C>T (p.Ala2658Val) | not specified [RCV004871329] | uncertain significance | 9 | 110407627 | 110407627 | Human | | name |
| 597769830 | CV3608850 | single nucleotide variant | NM_153366.4(SVEP1):c.5552C>A (p.Ala1851Asp) | not specified [RCV004871331] | uncertain significance | 9 | 110429983 | 110429983 | Human | | name |
| 597769835 | CV3608851 | single nucleotide variant | NM_153366.4(SVEP1):c.5236G>A (p.Val1746Ile) | not specified [RCV004871332] | uncertain significance | 9 | 110432032 | 110432032 | Human | | name |
| 597769839 | CV3608852 | single nucleotide variant | NM_153366.4(SVEP1):c.6565A>G (p.Thr2189Ala) | not specified [RCV004871333] | uncertain significance | 9 | 110411146 | 110411146 | Human | | name |
| 597769844 | CV3608854 | single nucleotide variant | NM_153366.4(SVEP1):c.4090G>C (p.Ala1364Pro) | not specified [RCV004871334] | uncertain significance | 9 | 110450072 | 110450072 | Human | | name |
| 597769848 | CV3608855 | single nucleotide variant | NM_153366.4(SVEP1):c.6338T>C (p.Met2113Thr) | not specified [RCV004871335] | uncertain significance | 9 | 110411373 | 110411373 | Human | | name |
| 597769852 | CV3608856 | single nucleotide variant | NM_153366.4(SVEP1):c.8012A>G (p.His2671Arg) | not specified [RCV004871336] | uncertain significance | 9 | 110407588 | 110407588 | Human | | name |
| 597769866 | CV3608859 | single nucleotide variant | NM_153366.4(SVEP1):c.9565C>G (p.His3189Asp) | not specified [RCV004871339] | uncertain significance | 9 | 110404428 | 110404428 | Human | | name |
| 597794572 | CV3608860 | single nucleotide variant | NM_153366.4(SVEP1):c.5861C>A (p.Ala1954Glu) | not specified [RCV004877899] | uncertain significance | 9 | 110427705 | 110427705 | Human | | name |
| 597769871 | CV3608861 | single nucleotide variant | NM_153366.4(SVEP1):c.4964A>G (p.Asn1655Ser) | not specified [RCV004871340] | likely benign | 9 | 110434431 | 110434431 | Human | | name |
| 597769875 | CV3608862 | single nucleotide variant | NM_153366.4(SVEP1):c.3099G>C (p.Lys1033Asn) | not specified [RCV004871341] | uncertain significance | 9 | 110469001 | 110469001 | Human | | name |
| 597769886 | CV3608865 | single nucleotide variant | NM_153366.4(SVEP1):c.6192G>T (p.Gln2064His) | not specified [RCV004871343] | uncertain significance | 9 | 110411519 | 110411519 | Human | | name |
| 597769896 | CV3608867 | single nucleotide variant | NM_153366.4(SVEP1):c.3023A>G (p.Tyr1008Cys) | not specified [RCV004871345] | uncertain significance | 9 | 110469077 | 110469077 | Human | | name |
| 597769901 | CV3608868 | single nucleotide variant | NM_153366.4(SVEP1):c.3301G>T (p.Val1101Leu) | not specified [RCV004871346] | uncertain significance | 9 | 110465886 | 110465886 | Human | | name |
| 597794575 | CV3608870 | single nucleotide variant | NM_153366.4(SVEP1):c.4265A>C (p.Gln1422Pro) | not specified [RCV004877900] | uncertain significance | 9 | 110446035 | 110446035 | Human | | name |
| 597769916 | CV3608872 | single nucleotide variant | NM_153366.4(SVEP1):c.8429C>G (p.Thr2810Ser) | not specified [RCV004871349] | uncertain significance | 9 | 110407171 | 110407171 | Human | | name |
| 597769921 | CV3608873 | single nucleotide variant | NM_153366.4(SVEP1):c.4948C>A (p.Pro1650Thr) | not specified [RCV004871350] | uncertain significance | 9 | 110434447 | 110434447 | Human | | name |
| 597794578 | CV3608874 | single nucleotide variant | NM_153366.4(SVEP1):c.5881G>A (p.Val1961Ile) | not specified [RCV004877901] | uncertain significance | 9 | 110427685 | 110427685 | Human | | name |
| 597769926 | CV3608875 | single nucleotide variant | NM_153366.4(SVEP1):c.8905G>A (p.Gly2969Ser) | not specified [RCV004871351] | uncertain significance | 9 | 110406695 | 110406695 | Human | | name |
| 597769933 | CV3608876 | single nucleotide variant | NM_153366.4(SVEP1):c.5361A>G (p.Ile1787Met) | not specified [RCV004871352] | uncertain significance | 9 | 110430443 | 110430443 | Human | | name |
| 597769940 | CV3608877 | single nucleotide variant | NM_153366.4(SVEP1):c.9854G>C (p.Arg3285Thr) | not specified [RCV004871353] | uncertain significance | 9 | 110389556 | 110389556 | Human | | name |
| 597769945 | CV3608878 | single nucleotide variant | NM_153366.4(SVEP1):c.9197C>T (p.Ser3066Phe) | not specified [RCV004871354] | uncertain significance | 9 | 110406403 | 110406403 | Human | | name |
| 597769952 | CV3608879 | single nucleotide variant | NM_153366.4(SVEP1):c.7723G>A (p.Gly2575Ser) | not specified [RCV004871355] | uncertain significance | 9 | 110407877 | 110407877 | Human | | name |
| 597769958 | CV3608880 | single nucleotide variant | NM_153366.4(SVEP1):c.8204T>C (p.Met2735Thr) | not specified [RCV004871356] | uncertain significance | 9 | 110407396 | 110407396 | Human | | name |
| 597794581 | CV3608881 | single nucleotide variant | NM_153366.4(SVEP1):c.3119A>G (p.Tyr1040Cys) | not specified [RCV004877902] | uncertain significance | 9 | 110468981 | 110468981 | Human | | name |
| 597769963 | CV3608882 | single nucleotide variant | NM_153366.4(SVEP1):c.9187T>C (p.Ser3063Pro) | not specified [RCV004871357] | uncertain significance | 9 | 110406413 | 110406413 | Human | | name |
| 597769969 | CV3608883 | single nucleotide variant | NM_153366.4(SVEP1):c.8789C>T (p.Thr2930Ile) | not specified [RCV004871358] | uncertain significance | 9 | 110406811 | 110406811 | Human | | name |
| 597769974 | CV3608885 | single nucleotide variant | NM_153366.4(SVEP1):c.6845T>G (p.Val2282Gly) | not specified [RCV004871359] | uncertain significance | 9 | 110408755 | 110408755 | Human | | name |
| 597769979 | CV3608886 | single nucleotide variant | NM_153366.4(SVEP1):c.3637C>T (p.Arg1213Cys) | not specified [RCV004871360] | uncertain significance | 9 | 110457292 | 110457292 | Human | | name |
| 597769983 | CV3608887 | single nucleotide variant | NM_153366.4(SVEP1):c.5419G>A (p.Val1807Ile) | not specified [RCV004871361] | uncertain significance | 9 | 110430385 | 110430385 | Human | | name |
| 597769994 | CV3608889 | single nucleotide variant | NM_153366.4(SVEP1):c.5536T>C (p.Ser1846Pro) | not specified [RCV004871363] | uncertain significance | 9 | 110429999 | 110429999 | Human | | name |
| 597769999 | CV3608890 | single nucleotide variant | NM_153366.4(SVEP1):c.5359A>C (p.Ile1787Leu) | not specified [RCV004871364] | uncertain significance | 9 | 110430445 | 110430445 | Human | | name |
| 597770005 | CV3608891 | single nucleotide variant | NM_153366.4(SVEP1):c.6740C>A (p.Ala2247Asp) | not specified [RCV004871365] | uncertain significance | 9 | 110408860 | 110408860 | Human | | name |
| 597770021 | CV3608894 | single nucleotide variant | NM_153366.4(SVEP1):c.4649C>T (p.Ala1550Val) | not specified [RCV004871368] | uncertain significance | 9 | 110436495 | 110436495 | Human | | name |
| 597770026 | CV3608895 | single nucleotide variant | NM_153366.4(SVEP1):c.5716T>C (p.Ser1906Pro) | not specified [RCV004871369] | uncertain significance | 9 | 110429234 | 110429234 | Human | | name |
| 597770031 | CV3608896 | single nucleotide variant | NM_153366.4(SVEP1):c.9677C>A (p.Thr3226Asn) | not specified [RCV004871370] | uncertain significance | 9 | 110400999 | 110400999 | Human | | name |
| 598222446 | CV3912631 | single nucleotide variant | NM_153366.4(SVEP1):c.4712T>C (p.Val1571Ala) | not specified [RCV005293797] | uncertain significance | 9 | 110436432 | 110436432 | Human | | name |
| 598222452 | CV3912632 | single nucleotide variant | NM_153366.4(SVEP1):c.3860G>A (p.Gly1287Asp) | not specified [RCV005293798] | uncertain significance | 9 | 110451330 | 110451330 | Human | | name |
| 598222457 | CV3912633 | single nucleotide variant | NM_153366.4(SVEP1):c.5761C>A (p.Leu1921Ile) | not specified [RCV005293799] | uncertain significance | 9 | 110429189 | 110429189 | Human | | name |
| 598222463 | CV3912634 | single nucleotide variant | NM_153366.4(SVEP1):c.4585G>A (p.Asp1529Asn) | not specified [RCV005293800] | uncertain significance | 9 | 110443599 | 110443599 | Human | | name |
| 598222483 | CV3912637 | single nucleotide variant | NM_153366.4(SVEP1):c.8827C>G (p.Leu2943Val) | not specified [RCV005293803] | uncertain significance | 9 | 110406773 | 110406773 | Human | | name |
| 598222488 | CV3912638 | single nucleotide variant | NM_153366.4(SVEP1):c.5080C>T (p.Pro1694Ser) | not specified [RCV005293804] | uncertain significance | 9 | 110432615 | 110432615 | Human | | name |
| 598263661 | CV3912639 | single nucleotide variant | NM_153366.4(SVEP1):c.4426G>A (p.Gly1476Ser) | not specified [RCV005280573] | uncertain significance | 9 | 110445874 | 110445874 | Human | | name |
| 598222510 | CV3912642 | single nucleotide variant | NM_153366.4(SVEP1):c.6704A>G (p.Tyr2235Cys) | not specified [RCV005293807] | uncertain significance | 9 | 110408896 | 110408896 | Human | | name |
| 598222517 | CV3912643 | single nucleotide variant | NM_153366.4(SVEP1):c.3245G>A (p.Gly1082Asp) | not specified [RCV005293808] | uncertain significance | 9 | 110465942 | 110465942 | Human | | name |
| 598222523 | CV3912644 | single nucleotide variant | NM_153366.4(SVEP1):c.4251G>T (p.Arg1417Ser) | not specified [RCV005293809] | uncertain significance | 9 | 110446910 | 110446910 | Human | | name |
| 598263664 | CV3912646 | single nucleotide variant | NM_153366.4(SVEP1):c.4802G>T (p.Ser1601Ile) | not specified [RCV005280574] | uncertain significance | 9 | 110435327 | 110435327 | Human | | name |
| 598263667 | CV3912647 | single nucleotide variant | NM_153366.4(SVEP1):c.8202C>G (p.Ser2734Arg) | not specified [RCV005280575] | uncertain significance | 9 | 110407398 | 110407398 | Human | | name |
| 598222537 | CV3912648 | single nucleotide variant | NM_153366.4(SVEP1):c.3804A>C (p.Glu1268Asp) | not specified [RCV005293811] | uncertain significance | 9 | 110451386 | 110451386 | Human | | name |
| 598222545 | CV3912649 | single nucleotide variant | NM_153366.4(SVEP1):c.6343G>A (p.Gly2115Ser) | not specified [RCV005293812] | uncertain significance | 9 | 110411368 | 110411368 | Human | | name |
| 598263674 | CV3912651 | single nucleotide variant | NM_153366.4(SVEP1):c.7481A>G (p.Lys2494Arg) | not specified [RCV005280577] | uncertain significance | 9 | 110408119 | 110408119 | Human | | name |
| 598263680 | CV3912653 | single nucleotide variant | NM_153366.4(SVEP1):c.8233C>T (p.Pro2745Ser) | not specified [RCV005280579] | uncertain significance | 9 | 110407367 | 110407367 | Human | | name |
| 598222557 | CV3912655 | single nucleotide variant | NM_153366.4(SVEP1):c.4823G>T (p.Trp1608Leu) | not specified [RCV005293814] | uncertain significance | 9 | 110435306 | 110435306 | Human | | name |
| 598222563 | CV3912656 | single nucleotide variant | NM_153366.4(SVEP1):c.8306G>A (p.Arg2769His) | not specified [RCV005293815] | likely benign | 9 | 110407294 | 110407294 | Human | | name |
| 598222571 | CV3912657 | single nucleotide variant | NM_153366.4(SVEP1):c.4705T>G (p.Ser1569Ala) | not specified [RCV005293816] | uncertain significance | 9 | 110436439 | 110436439 | Human | | name |
| 598263687 | CV3912661 | single nucleotide variant | NM_153366.4(SVEP1):c.9894G>T (p.Arg3298Ser) | not specified [RCV005280581] | uncertain significance | 9 | 110387451 | 110387451 | Human | | name |
| 598222589 | CV3912662 | single nucleotide variant | NM_153366.4(SVEP1):c.3806A>T (p.Asn1269Ile) | not specified [RCV005293819] | uncertain significance | 9 | 110451384 | 110451384 | Human | | name |
| 598222594 | CV3912663 | single nucleotide variant | NM_153366.4(SVEP1):c.9893G>A (p.Arg3298Lys) | not specified [RCV005293820] | uncertain significance | 9 | 110387452 | 110387452 | Human | | name |
| 598263690 | CV3912665 | single nucleotide variant | NM_153366.4(SVEP1):c.7882A>G (p.Lys2628Glu) | not specified [RCV005280582] | uncertain significance | 9 | 110407718 | 110407718 | Human | | name |
| 598222611 | CV3912668 | single nucleotide variant | NM_153366.4(SVEP1):c.8860G>T (p.Asp2954Tyr) | not specified [RCV005293823] | uncertain significance | 9 | 110406740 | 110406740 | Human | | name |
| 598263696 | CV3912669 | single nucleotide variant | NM_153366.4(SVEP1):c.3457G>A (p.Gly1153Ser) | not specified [RCV005280584] | uncertain significance | 9 | 110458979 | 110458979 | Human | | name |
| 598263699 | CV3912670 | single nucleotide variant | NM_153366.4(SVEP1):c.8644G>A (p.Ala2882Thr) | not specified [RCV005280585] | likely benign | 9 | 110406956 | 110406956 | Human | | name |
| 598222617 | CV3912671 | single nucleotide variant | NM_153366.4(SVEP1):c.7586G>A (p.Arg2529Gln) | not specified [RCV005293824] | likely benign | 9 | 110408014 | 110408014 | Human | | name |
| 598222623 | CV3912672 | single nucleotide variant | NM_153366.4(SVEP1):c.7424A>G (p.Asn2475Ser) | not specified [RCV005293825] | uncertain significance | 9 | 110408176 | 110408176 | Human | | name |
| 598263706 | CV3912674 | single nucleotide variant | NM_153366.4(SVEP1):c.5869G>T (p.Ala1957Ser) | not specified [RCV005280587] | uncertain significance | 9 | 110427697 | 110427697 | Human | | name |
| 598222634 | CV3912676 | single nucleotide variant | NM_153366.4(SVEP1):c.7550G>A (p.Gly2517Glu) | not specified [RCV005293827] | uncertain significance | 9 | 110408050 | 110408050 | Human | | name |
| 8633185 | CV88398 | single nucleotide variant | NM_153366.3(SVEP1):c.9586G>A (p.Asp3196Asn) | Malignant melanoma [RCV000068490] | not provided | 9 | 110404407 | 110404407 | Human | | name |
| 8633186 | CV88399 | single nucleotide variant | NM_153366.3(SVEP1):c.8504C>T (p.Ser2835Leu) | Malignant melanoma [RCV000068491] | not provided | 9 | 110407096 | 110407096 | Human | | name |
| 156074109 | CV2201453 | single nucleotide variant | NM_153366.4(SVEP1):c.10378G>A (p.Gly3460Arg) | not specified [RCV004079606] | uncertain significance | 9 | 110379377 | 110379377 | Human | | name |
| 155927497 | CV2230797 | single nucleotide variant | NM_153366.4(SVEP1):c.10449A>C (p.Gln3483His) | not specified [RCV004092014] | uncertain significance | 9 | 110377326 | 110377326 | Human | | name |
| 156131292 | CV2235226 | single nucleotide variant | NM_153366.4(SVEP1):c.10181G>T (p.Gly3394Val) | not specified [RCV004107274] | uncertain significance | 9 | 110385954 | 110385954 | Human | | name |
| 155969616 | CV2309090 | single nucleotide variant | NM_153366.4(SVEP1):c.10225G>A (p.Ala3409Thr) | not specified [RCV004171451] | uncertain significance | 9 | 110385910 | 110385910 | Human | | name |
| 155969154 | CV2339391 | single nucleotide variant | NM_153366.4(SVEP1):c.10531G>A (p.Gly3511Arg) | not specified [RCV004191613] | uncertain significance | 9 | 110375437 | 110375437 | Human | | name |
| 155984232 | CV2367886 | single nucleotide variant | NM_153366.4(SVEP1):c.10124A>T (p.Tyr3375Phe) | not specified [RCV004222988] | uncertain significance | 9 | 110386011 | 110386011 | Human | | name |
| 401776877 | CV2721508 | single nucleotide variant | NM_153366.4(SVEP1):c.10039C>G (p.His3347Asp) | not specified [RCV004316024] | uncertain significance | 9 | 110387306 | 110387306 | Human | | name |
| 401899835 | CV2758922 | single nucleotide variant | NM_153366.4(SVEP1):c.10538G>A (p.Arg3513His) | not specified [RCV004339999] | uncertain significance | 9 | 110375430 | 110375430 | Human | | name |
| 401861391 | CV2759549 | single nucleotide variant | NM_153366.4(SVEP1):c.10370T>C (p.Leu3457Ser) | not specified [RCV004338530] | uncertain significance | 9 | 110379385 | 110379385 | Human | | name |
| 405707635 | CV3323865 | single nucleotide variant | NM_153366.4(SVEP1):c.10451G>A (p.Arg3484His) | not specified [RCV004461295] | uncertain significance | 9 | 110377324 | 110377324 | Human | | name |
| 405707642 | CV3323866 | single nucleotide variant | NM_153366.4(SVEP1):c.10627G>A (p.Gly3543Ser) | not specified [RCV004461296] | uncertain significance | 9 | 110369990 | 110369990 | Human | | name |
| 407505100 | CV3482009 | single nucleotide variant | NM_153366.4(SVEP1):c.10276A>G (p.Ile3426Val) | not specified [RCV004670746] | uncertain significance | 9 | 110379479 | 110379479 | Human | | name |
| 407505114 | CV3482013 | single nucleotide variant | NM_153366.4(SVEP1):c.10043C>T (p.Pro3348Leu) | not specified [RCV004670750] | uncertain significance | 9 | 110387302 | 110387302 | Human | | name |
| 597769805 | CV3608845 | single nucleotide variant | NM_153366.4(SVEP1):c.10595A>G (p.His3532Arg) | not specified [RCV004871326] | uncertain significance | 9 | 110375373 | 110375373 | Human | | name |
| 597769810 | CV3608846 | single nucleotide variant | NM_153366.4(SVEP1):c.10090C>T (p.Pro3364Ser) | not specified [RCV004871327] | uncertain significance | 9 | 110386045 | 110386045 | Human | | name |
| 597769824 | CV3608849 | single nucleotide variant | NM_153366.4(SVEP1):c.10489C>T (p.Arg3497Cys) | not specified [RCV004871330] | uncertain significance | 9 | 110377286 | 110377286 | Human | | name |
| 597769880 | CV3608864 | single nucleotide variant | NM_153366.4(SVEP1):c.10462T>G (p.Cys3488Gly) | not specified [RCV004871342] | uncertain significance | 9 | 110377313 | 110377313 | Human | | name |
| 597769891 | CV3608866 | single nucleotide variant | NM_153366.4(SVEP1):c.10576T>C (p.Trp3526Arg) | not specified [RCV004871344] | uncertain significance | 9 | 110375392 | 110375392 | Human | | name |
| 597769990 | CV3608888 | single nucleotide variant | NM_153366.4(SVEP1):c.10706C>T (p.Thr3569Ile) | not specified [RCV004871362] | uncertain significance | 9 | 110366549 | 110366549 | Human | | name |
| 597770009 | CV3608892 | single nucleotide variant | NM_153366.4(SVEP1):c.10637G>A (p.Cys3546Tyr) | not specified [RCV004871366] | uncertain significance | 9 | 110369980 | 110369980 | Human | | name |
| 598263677 | CV3912652 | single nucleotide variant | NM_153366.4(SVEP1):c.10100C>T (p.Ala3367Val) | not specified [RCV005280578] | uncertain significance | 9 | 110386035 | 110386035 | Human | | name |
| 598263703 | CV3912673 | single nucleotide variant | NM_153366.4(SVEP1):c.10212G>T (p.Trp3404Cys) | not specified [RCV005280586] | uncertain significance | 9 | 110385923 | 110385923 | Human | | name |
