| 401927460 | CV2812642 | single nucleotide variant | NM_022111.4(CLSPN):c.165G>A (p.Lys55=) | not provided [RCV003406334] | likely benign | 1 | 35764683 | 35764683 | Human | | name |
| 329390472 | CV2440319 | single nucleotide variant | NM_022111.4(CLSPN):c.79C>T (p.Pro27Ser) | not specified [RCV004262798] | uncertain significance | 1 | 35765272 | 35765272 | Human | | name |
| 401742386 | CV2673770 | single nucleotide variant | NM_022111.4(CLSPN):c.28C>A (p.His10Asn) | not specified [RCV004293157] | uncertain significance | 1 | 35765323 | 35765323 | Human | | name |
| 401927459 | CV2812641 | single nucleotide variant | NM_022111.4(CLSPN):c.906G>A (p.Leu302=) | not provided [RCV003406333] | likely benign | 1 | 35761194 | 35761194 | Human | | name |
| 407463239 | CV3429317 | single nucleotide variant | NM_022111.4(CLSPN):c.89G>C (p.Ser30Thr) | not specified [RCV004613171] | uncertain significance | 1 | 35765262 | 35765262 | Human | | name |
| 155989521 | CV2371948 | single nucleotide variant | NM_022111.4(CLSPN):c.181G>T (p.Val61Phe) | not specified [RCV004221629] | uncertain significance | 1 | 35764667 | 35764667 | Human | | name |
| 401730363 | CV2680280 | single nucleotide variant | NM_022111.4(CLSPN):c.158G>A (p.Ser53Asn) | not specified [RCV004286747] | uncertain significance | 1 | 35764690 | 35764690 | Human | | name |
| 405783336 | CV3305828 | single nucleotide variant | NM_022111.4(CLSPN):c.253G>A (p.Glu85Lys) | not specified [RCV004437340] | uncertain significance | 1 | 35764595 | 35764595 | Human | | name |
| 405783355 | CV3305831 | single nucleotide variant | NM_022111.4(CLSPN):c.268G>C (p.Glu90Gln) | not specified [RCV004437343] | uncertain significance | 1 | 35764580 | 35764580 | Human | | name |
| 597792171 | CV3656933 | single nucleotide variant | NM_022111.4(CLSPN):c.295A>G (p.Lys99Glu) | not specified [RCV004902541] | uncertain significance | 1 | 35764553 | 35764553 | Human | | name |
| 598244938 | CV3944825 | single nucleotide variant | NM_022111.4(CLSPN):c.113T>C (p.Ile38Thr) | not specified [RCV005322112] | uncertain significance | 1 | 35765238 | 35765238 | Human | | name |
| 598245093 | CV3944848 | single nucleotide variant | NM_022111.4(CLSPN):c.235A>C (p.Thr79Pro) | not specified [RCV005322135] | uncertain significance | 1 | 35764613 | 35764613 | Human | | name |
| 15169467 | CV732408 | single nucleotide variant | NM_022111.4(CLSPN):c.1014A>G (p.Lys338=) | not provided [RCV000905063] | benign | 1 | 35760907 | 35760907 | Human | | name |
| 156191091 | CV2206125 | single nucleotide variant | NM_022111.4(CLSPN):c.916T>C (p.Tyr306His) | not specified [RCV004078532] | uncertain significance | 1 | 35761184 | 35761184 | Human | | name |
| 156331579 | CV2220547 | single nucleotide variant | NM_022111.4(CLSPN):c.428A>G (p.Asp143Gly) | not specified [RCV004097752] | uncertain significance | 1 | 35764420 | 35764420 | Human | | name |
| 156170019 | CV2380548 | single nucleotide variant | NM_022111.4(CLSPN):c.314A>G (p.Lys105Arg) | not specified [RCV004224871] | uncertain significance | 1 | 35764534 | 35764534 | Human | | name |
| 405783361 | CV3305832 | single nucleotide variant | NM_022111.4(CLSPN):c.298A>G (p.Ile100Val) | not specified [RCV004437344] | likely benign | 1 | 35764550 | 35764550 | Human | | name |
| 405783384 | CV3305836 | single nucleotide variant | NM_022111.4(CLSPN):c.463A>G (p.Ile155Val) | not specified [RCV004437348] | uncertain significance | 1 | 35764385 | 35764385 | Human | | name |
| 405783390 | CV3305837 | single nucleotide variant | NM_022111.4(CLSPN):c.639C>G (p.Asp213Glu) | not specified [RCV004437349] | uncertain significance | 1 | 35763265 | 35763265 | Human | | name |
| 405783396 | CV3305838 | single nucleotide variant | NM_022111.4(CLSPN):c.830A>G (p.Lys277Arg) | not specified [RCV004437350] | uncertain significance | 1 | 35762063 | 35762063 | Human | | name |
| 407463206 | CV3429308 | single nucleotide variant | NM_022111.4(CLSPN):c.610G>A (p.Asp204Asn) | not specified [RCV004613162] | uncertain significance | 1 | 35763294 | 35763294 | Human | | name |
| 407463225 | CV3429313 | single nucleotide variant | NM_022111.4(CLSPN):c.803C>T (p.Ser268Leu) | not specified [RCV004613167] | uncertain significance | 1 | 35762423 | 35762423 | Human | | name |
| 597792125 | CV3656918 | single nucleotide variant | NM_022111.4(CLSPN):c.697T>G (p.Leu233Val) | not specified [RCV004902527] | uncertain significance | 1 | 35763207 | 35763207 | Human | | name |
| 597792128 | CV3656919 | single nucleotide variant | NM_022111.4(CLSPN):c.424A>G (p.Thr142Ala) | not specified [RCV004902528] | uncertain significance | 1 | 35764424 | 35764424 | Human | | name |
| 597792154 | CV3656928 | single nucleotide variant | NM_022111.4(CLSPN):c.539T>C (p.Met180Thr) | not specified [RCV004902536] | uncertain significance | 1 | 35764309 | 35764309 | Human | | name |
| 597792165 | CV3656931 | single nucleotide variant | NM_022111.4(CLSPN):c.725A>G (p.Asn242Ser) | not specified [RCV004902539] | uncertain significance | 1 | 35763179 | 35763179 | Human | | name |
| 598245021 | CV3944838 | single nucleotide variant | NM_022111.4(CLSPN):c.574A>C (p.Lys192Gln) | not specified [RCV005322125] | uncertain significance | 1 | 35764274 | 35764274 | Human | | name |
| 598245061 | CV3944844 | single nucleotide variant | NM_022111.4(CLSPN):c.676C>A (p.Pro226Thr) | not specified [RCV005322131] | uncertain significance | 1 | 35763228 | 35763228 | Human | | name |
| 598245070 | CV3944845 | single nucleotide variant | NM_022111.4(CLSPN):c.954C>A (p.Phe318Leu) | not specified [RCV005322132] | uncertain significance | 1 | 35761146 | 35761146 | Human | | name |
| 156048660 | CV2220203 | single nucleotide variant | NM_022111.4(CLSPN):c.2533G>A (p.Ala845Thr) | not specified [RCV004095662] | uncertain significance | 1 | 35748001 | 35748001 | Human | | name |
| 155979478 | CV2243805 | single nucleotide variant | NM_022111.4(CLSPN):c.2585G>A (p.Cys862Tyr) | not specified [RCV004114770] | uncertain significance | 1 | 35747949 | 35747949 | Human | | name |
| 156104605 | CV2260589 | single nucleotide variant | NM_022111.4(CLSPN):c.2146C>A (p.Pro716Thr) | not specified [RCV004123359] | uncertain significance | 1 | 35749694 | 35749694 | Human | | name |
| 156363800 | CV2262710 | single nucleotide variant | NM_022111.4(CLSPN):c.2778T>A (p.His926Gln) | not specified [RCV004130897] | uncertain significance | 1 | 35746842 | 35746842 | Human | | name |
| 156055914 | CV2269680 | single nucleotide variant | NM_022111.4(CLSPN):c.1543G>A (p.Asp515Asn) | not specified [RCV004126671] | uncertain significance | 1 | 35760378 | 35760378 | Human | | name |
| 155917851 | CV2275089 | single nucleotide variant | NM_022111.4(CLSPN):c.2357A>C (p.Tyr786Ser) | not specified [RCV004136900] | uncertain significance | 1 | 35748520 | 35748520 | Human | | name |
| 156284329 | CV2291898 | single nucleotide variant | NM_022111.4(CLSPN):c.2980G>A (p.Glu994Lys) | not specified [RCV004158419] | uncertain significance | 1 | 35743517 | 35743517 | Human | | name |
| 156055426 | CV2308782 | single nucleotide variant | NM_022111.4(CLSPN):c.2383C>T (p.Arg795Cys) | not specified [RCV004169096] | uncertain significance | 1 | 35748494 | 35748494 | Human | | name |
| 155975189 | CV2341515 | single nucleotide variant | NM_022111.4(CLSPN):c.1205T>A (p.Val402Glu) | not specified [RCV004188907] | uncertain significance | 1 | 35760716 | 35760716 | Human | | name |
| 155936377 | CV2380419 | single nucleotide variant | NM_022111.4(CLSPN):c.2960C>T (p.Thr987Ile) | not specified [RCV004218022] | uncertain significance | 1 | 35745457 | 35745457 | Human | | name |
| 156345383 | CV2382182 | single nucleotide variant | NM_022111.4(CLSPN):c.1526G>A (p.Arg509Gln) | not specified [RCV004228134] | uncertain significance | 1 | 35760395 | 35760395 | Human | | name |
| 156091657 | CV2389485 | single nucleotide variant | NM_022111.4(CLSPN):c.1164G>C (p.Gln388His) | not specified [RCV004243566] | uncertain significance | 1 | 35760757 | 35760757 | Human | | name |
| 329362213 | CV2466185 | single nucleotide variant | NM_022111.4(CLSPN):c.1081C>T (p.His361Tyr) | not specified [RCV004279831] | uncertain significance | 1 | 35760840 | 35760840 | Human | | name |
| 401736285 | CV2688750 | single nucleotide variant | NM_022111.4(CLSPN):c.1676A>T (p.Asp559Val) | not specified [RCV004303779] | uncertain significance | 1 | 35753840 | 35753840 | Human | | name |
| 401735588 | CV2692147 | single nucleotide variant | NM_022111.4(CLSPN):c.1654A>C (p.Asn552His) | not specified [RCV004301849] | uncertain significance | 1 | 35753862 | 35753862 | Human | | name |
| 401750765 | CV2712123 | single nucleotide variant | NM_022111.4(CLSPN):c.2747C>T (p.Thr916Ile) | not specified [RCV004311852] | uncertain significance | 1 | 35746873 | 35746873 | Human | | name |
| 401857692 | CV2756268 | single nucleotide variant | NM_022111.4(CLSPN):c.1090G>A (p.Gly364Ser) | not specified [RCV004338362] | uncertain significance | 1 | 35760831 | 35760831 | Human | | name |
| 401892071 | CV2775917 | single nucleotide variant | NM_022111.4(CLSPN):c.2387G>A (p.Gly796Glu) | not specified [RCV004344944] | uncertain significance | 1 | 35748490 | 35748490 | Human | | name |
| 401895423 | CV2786465 | single nucleotide variant | NM_022111.4(CLSPN):c.1348G>A (p.Ala450Thr) | not specified [RCV004362044] | uncertain significance | 1 | 35760573 | 35760573 | Human | | name |
| 401895231 | CV2789781 | single nucleotide variant | NM_022111.4(CLSPN):c.1678A>G (p.Met560Val) | not specified [RCV004361887] | likely benign | 1 | 35753838 | 35753838 | Human | | name |
| 401927534 | CV2812640 | single nucleotide variant | NM_022111.4(CLSPN):c.2674C>A (p.Pro892Thr) | not provided [RCV003406332] | likely benign | 1 | 35746946 | 35746946 | Human | 6 | name |
| 405783266 | CV3305816 | single nucleotide variant | NM_022111.4(CLSPN):c.1027C>T (p.His343Tyr) | not specified [RCV004437328] | uncertain significance | 1 | 35760894 | 35760894 | Human | | name |
| 405783272 | CV3305817 | single nucleotide variant | NM_022111.4(CLSPN):c.1133A>G (p.Asn378Ser) | not specified [RCV004437329] | uncertain significance | 1 | 35760788 | 35760788 | Human | | name |
| 405783277 | CV3305818 | single nucleotide variant | NM_022111.4(CLSPN):c.1136C>T (p.Ala379Val) | not specified [RCV004437330] | uncertain significance | 1 | 35760785 | 35760785 | Human | | name |
| 405783284 | CV3305819 | single nucleotide variant | NM_022111.4(CLSPN):c.1160C>T (p.Thr387Ile) | not specified [RCV004437331] | uncertain significance | 1 | 35760761 | 35760761 | Human | | name |
| 405783295 | CV3305821 | single nucleotide variant | NM_022111.4(CLSPN):c.1396G>A (p.Glu466Lys) | not specified [RCV004437333] | uncertain significance | 1 | 35760525 | 35760525 | Human | | name |
| 405783302 | CV3305822 | single nucleotide variant | NM_022111.4(CLSPN):c.1943A>G (p.Glu648Gly) | not specified [RCV004437334] | uncertain significance | 1 | 35751335 | 35751335 | Human | | name |
| 405783308 | CV3305823 | single nucleotide variant | NM_022111.4(CLSPN):c.2165A>G (p.Asp722Gly) | not specified [RCV004437335] | uncertain significance | 1 | 35749675 | 35749675 | Human | | name |
| 405783313 | CV3305824 | single nucleotide variant | NM_022111.4(CLSPN):c.2411G>A (p.Gly804Glu) | not specified [RCV004437336] | uncertain significance | 1 | 35748466 | 35748466 | Human | | name |
| 405783320 | CV3305825 | single nucleotide variant | NM_022111.4(CLSPN):c.2421A>T (p.Arg807Ser) | not specified [RCV004437337] | uncertain significance | 1 | 35748456 | 35748456 | Human | | name |
| 405783325 | CV3305826 | single nucleotide variant | NM_022111.4(CLSPN):c.2495C>T (p.Pro832Leu) | not specified [RCV004437338] | uncertain significance | 1 | 35748039 | 35748039 | Human | | name |
| 405783342 | CV3305829 | single nucleotide variant | NM_022111.4(CLSPN):c.2567C>G (p.Ala856Gly) | not specified [RCV004437341] | uncertain significance | 1 | 35747967 | 35747967 | Human | | name |
| 405783349 | CV3305830 | single nucleotide variant | NM_022111.4(CLSPN):c.2588T>C (p.Leu863Ser) | not specified [RCV004437342] | uncertain significance | 1 | 35747946 | 35747946 | Human | | name |
| 407463554 | CV3429309 | single nucleotide variant | NM_022111.4(CLSPN):c.1663G>A (p.Val555Ile) | not specified [RCV004613163] | likely benign | 1 | 35753853 | 35753853 | Human | | name |
| 407463214 | CV3429310 | single nucleotide variant | NM_022111.4(CLSPN):c.2059A>G (p.Ile687Val) | not specified [RCV004613164] | uncertain significance | 1 | 35749781 | 35749781 | Human | | name |
| 407463236 | CV3429316 | single nucleotide variant | NM_022111.4(CLSPN):c.1172C>T (p.Thr391Ile) | not specified [RCV004613170] | uncertain significance | 1 | 35760749 | 35760749 | Human | | name |
| 407463244 | CV3429318 | single nucleotide variant | NM_022111.4(CLSPN):c.2678G>A (p.Arg893Gln) | not specified [RCV004613172] | uncertain significance | 1 | 35746942 | 35746942 | Human | | name |
| 407463252 | CV3429320 | single nucleotide variant | NM_022111.4(CLSPN):c.2005G>A (p.Glu669Lys) | not specified [RCV004613174] | uncertain significance | 1 | 35751273 | 35751273 | Human | | name |
| 597792041 | CV3656916 | single nucleotide variant | NM_022111.4(CLSPN):c.1637G>A (p.Arg546Lys) | not specified [RCV004902525] | uncertain significance | 1 | 35753879 | 35753879 | Human | | name |
| 597792122 | CV3656917 | single nucleotide variant | NM_022111.4(CLSPN):c.2826C>A (p.Asn942Lys) | not specified [RCV004902526] | uncertain significance | 1 | 35746794 | 35746794 | Human | | name |
| 597792131 | CV3656921 | single nucleotide variant | NM_022111.4(CLSPN):c.1600C>T (p.Arg534Cys) | not specified [RCV004902529] | uncertain significance | 1 | 35753916 | 35753916 | Human | | name |
| 597792139 | CV3656923 | single nucleotide variant | NM_022111.4(CLSPN):c.1657G>A (p.Val553Met) | not specified [RCV004902531] | uncertain significance | 1 | 35753859 | 35753859 | Human | | name |
| 597792142 | CV3656924 | single nucleotide variant | NM_022111.4(CLSPN):c.2374C>A (p.Gln792Lys) | not specified [RCV004902532] | uncertain significance | 1 | 35748503 | 35748503 | Human | | name |
| 597792148 | CV3656926 | single nucleotide variant | NM_022111.4(CLSPN):c.1564C>T (p.Pro522Ser) | not specified [RCV004902534] | uncertain significance | 1 | 35760357 | 35760357 | Human | | name |
| 597792151 | CV3656927 | single nucleotide variant | NM_022111.4(CLSPN):c.1837C>T (p.Arg613Cys) | not specified [RCV004902535] | uncertain significance | 1 | 35751441 | 35751441 | Human | | name |
| 597792159 | CV3656929 | single nucleotide variant | NM_022111.4(CLSPN):c.1009T>A (p.Ser337Thr) | not specified [RCV004902537] | uncertain significance | 1 | 35760912 | 35760912 | Human | | name |
| 597792168 | CV3656932 | single nucleotide variant | NM_022111.4(CLSPN):c.1332G>T (p.Gln444His) | not specified [RCV004902540] | uncertain significance | 1 | 35760589 | 35760589 | Human | | name |
| 598244944 | CV3944826 | single nucleotide variant | NM_022111.4(CLSPN):c.1732G>A (p.Ala578Thr) | not specified [RCV005322113] | uncertain significance | 1 | 35753784 | 35753784 | Human | | name |
| 598244951 | CV3944827 | single nucleotide variant | NM_022111.4(CLSPN):c.1601G>A (p.Arg534His) | not specified [RCV005322114] | uncertain significance | 1 | 35753915 | 35753915 | Human | | name |
| 598244956 | CV3944828 | single nucleotide variant | NM_022111.4(CLSPN):c.2078A>C (p.Lys693Thr) | not specified [RCV005322115] | uncertain significance | 1 | 35749762 | 35749762 | Human | | name |
| 598244964 | CV3944829 | single nucleotide variant | NM_022111.4(CLSPN):c.2117T>C (p.Ile706Thr) | not specified [RCV005322116] | uncertain significance | 1 | 35749723 | 35749723 | Human | | name |
| 598244970 | CV3944830 | single nucleotide variant | NM_022111.4(CLSPN):c.1144G>A (p.Val382Ile) | not specified [RCV005322117] | uncertain significance | 1 | 35760777 | 35760777 | Human | | name |
| 598244994 | CV3944834 | single nucleotide variant | NM_022111.4(CLSPN):c.2779C>A (p.Leu927Ile) | not specified [RCV005322121] | uncertain significance | 1 | 35746841 | 35746841 | Human | | name |
| 598244999 | CV3944835 | single nucleotide variant | NM_022111.4(CLSPN):c.2528A>G (p.Tyr843Cys) | not specified [RCV005322122] | uncertain significance | 1 | 35748006 | 35748006 | Human | | name |
| 598245007 | CV3944836 | single nucleotide variant | NM_022111.4(CLSPN):c.2723T>G (p.Met908Arg) | not specified [RCV005322123] | uncertain significance | 1 | 35746897 | 35746897 | Human | | name |
| 598245014 | CV3944837 | single nucleotide variant | NM_022111.4(CLSPN):c.1847G>A (p.Arg616His) | not specified [RCV005322124] | uncertain significance | 1 | 35751431 | 35751431 | Human | | name |
| 598245028 | CV3944839 | single nucleotide variant | NM_022111.4(CLSPN):c.1951G>A (p.Glu651Lys) | not specified [RCV005322126] | uncertain significance | 1 | 35751327 | 35751327 | Human | | name |
| 598245047 | CV3944842 | single nucleotide variant | NM_022111.4(CLSPN):c.1685C>A (p.Thr562Asn) | not specified [RCV005322129] | uncertain significance | 1 | 35753831 | 35753831 | Human | | name |
| 598245054 | CV3944843 | single nucleotide variant | NM_022111.4(CLSPN):c.2830T>A (p.Cys944Ser) | not specified [RCV005322130] | uncertain significance | 1 | 35746790 | 35746790 | Human | | name |
| 598245086 | CV3944847 | single nucleotide variant | NM_022111.4(CLSPN):c.1627G>C (p.Ala543Pro) | not specified [RCV005322134] | uncertain significance | 1 | 35753889 | 35753889 | Human | | name |
| 155795112 | CV1858925 | single nucleotide variant | NM_022111.4(CLSPN):c.3585A>T (p.Glu1195Asp) | Myoepithelial tumor [RCV002463890] | uncertain significance | 1 | 35738071 | 35738071 | Human | 1 | name |
| 155914697 | CV2264619 | single nucleotide variant | NM_022111.4(CLSPN):c.3683T>C (p.Ile1228Thr) | not specified [RCV004132625] | uncertain significance | 1 | 35737403 | 35737403 | Human | | name |
| 156057078 | CV2266667 | single nucleotide variant | NM_022111.4(CLSPN):c.3095A>T (p.Asp1032Val) | not specified [RCV004131201] | uncertain significance | 1 | 35743189 | 35743189 | Human | | name |
| 156069766 | CV2316820 | single nucleotide variant | NM_022111.4(CLSPN):c.3556A>G (p.Met1186Val) | not specified [RCV004172309] | uncertain significance | 1 | 35738457 | 35738457 | Human | | name |
| 156230363 | CV2348675 | single nucleotide variant | NM_022111.4(CLSPN):c.3202G>A (p.Glu1068Lys) | not specified [RCV004201091] | uncertain significance | 1 | 35739471 | 35739471 | Human | | name |
| 329356517 | CV2460380 | single nucleotide variant | NM_022111.4(CLSPN):c.3619A>G (p.Met1207Val) | not specified [RCV004268696] | uncertain significance | 1 | 35738037 | 35738037 | Human | | name |
| 401772281 | CV2687473 | single nucleotide variant | NM_022111.4(CLSPN):c.3032A>G (p.Asp1011Gly) | not specified [RCV004300714] | uncertain significance | 1 | 35743465 | 35743465 | Human | | name |
| 401731139 | CV2707736 | single nucleotide variant | NM_022111.4(CLSPN):c.3728G>C (p.Arg1243Thr) | not specified [RCV004306987] | uncertain significance | 1 | 35737358 | 35737358 | Human | | name |
| 401879537 | CV2755189 | single nucleotide variant | NM_022111.4(CLSPN):c.3227T>C (p.Ile1076Thr) | not specified [RCV004337381] | uncertain significance | 1 | 35739446 | 35739446 | Human | | name |
| 401861381 | CV2779686 | single nucleotide variant | NM_022111.4(CLSPN):c.3915G>C (p.Lys1305Asn) | not specified [RCV004351378] | uncertain significance | 1 | 35736601 | 35736601 | Human | | name |
| 405783367 | CV3305833 | single nucleotide variant | NM_022111.4(CLSPN):c.3070C>G (p.Leu1024Val) | not specified [RCV004437345] | uncertain significance | 1 | 35743214 | 35743214 | Human | | name |
| 405783378 | CV3305835 | single nucleotide variant | NM_022111.4(CLSPN):c.3992G>A (p.Arg1331Gln) | not specified [RCV004437347] | likely benign | 1 | 35736524 | 35736524 | Human | | name |
| 407463218 | CV3429311 | single nucleotide variant | NM_022111.4(CLSPN):c.3687G>C (p.Gln1229His) | not specified [RCV004613165] | uncertain significance | 1 | 35737399 | 35737399 | Human | | name |
| 407463222 | CV3429312 | single nucleotide variant | NM_022111.4(CLSPN):c.3208G>A (p.Glu1070Lys) | not specified [RCV004613166] | uncertain significance | 1 | 35739465 | 35739465 | Human | | name |
| 407463232 | CV3429315 | single nucleotide variant | NM_022111.4(CLSPN):c.3717T>G (p.Phe1239Leu) | not specified [RCV004613169] | uncertain significance | 1 | 35737369 | 35737369 | Human | | name |
| 407463249 | CV3429319 | single nucleotide variant | NM_022111.4(CLSPN):c.3247G>A (p.Val1083Ile) | not specified [RCV004613173] | uncertain significance | 1 | 35739426 | 35739426 | Human | | name |
| 597792136 | CV3656922 | single nucleotide variant | NM_022111.4(CLSPN):c.3830C>T (p.Pro1277Leu) | not specified [RCV004902530] | uncertain significance | 1 | 35736993 | 35736993 | Human | | name |
| 597792145 | CV3656925 | single nucleotide variant | NM_022111.4(CLSPN):c.3445A>G (p.Met1149Val) | not specified [RCV004902533] | uncertain significance | 1 | 35738568 | 35738568 | Human | | name |
| 597792162 | CV3656930 | single nucleotide variant | NM_022111.4(CLSPN):c.3335G>A (p.Arg1112Gln) | not specified [RCV004902538] | uncertain significance | 1 | 35739231 | 35739231 | Human | | name |
| 598244977 | CV3944831 | single nucleotide variant | NM_022111.4(CLSPN):c.3833G>A (p.Arg1278Gln) | not specified [RCV005322118] | uncertain significance | 1 | 35736990 | 35736990 | Human | | name |
| 598244983 | CV3944832 | single nucleotide variant | NM_022111.4(CLSPN):c.3676A>G (p.Met1226Val) | not specified [RCV005322119] | likely benign | 1 | 35737410 | 35737410 | Human | | name |
| 598245035 | CV3944840 | single nucleotide variant | NM_022111.4(CLSPN):c.3949C>T (p.Pro1317Ser) | not specified [RCV005322127] | uncertain significance | 1 | 35736567 | 35736567 | Human | | name |
| 598245078 | CV3944846 | single nucleotide variant | NM_022111.4(CLSPN):c.3704T>C (p.Leu1235Pro) | not specified [RCV005322133] | uncertain significance | 1 | 35737382 | 35737382 | Human | | name |
| 8624990 | CV80109 | single nucleotide variant | NM_001190481.1(CLSPN):c.2238C>T (p.Ser746=) | Malignant melanoma [RCV000060185] | not provided | 1 | 35748447 | 35748447 | Human | | name |
| 8629518 | CV84665 | single nucleotide variant | NM_001190481.1(CLSPN):c.1391C>T (p.Pro464Leu) | Malignant melanoma [RCV000064747] | not provided | 1 | 35760530 | 35760530 | Human | | name |
