| 156142769 | CV2200037 | single nucleotide variant | NM_144985.4(CDH24):c.1363+390G>A | not specified [RCV004074194] | uncertain significance | 14 | 23052083 | 23052083 | Human | | name |
| 405720607 | CV3296536 | single nucleotide variant | NM_144985.4(CDH24):c.1363+461C>T | not specified [RCV004428085] | likely benign | 14 | 23052012 | 23052012 | Human | | name |
| 597795444 | CV3641889 | single nucleotide variant | NM_144985.4(CDH24):c.1363+476G>T | not specified [RCV004903676] | uncertain significance | 14 | 23051997 | 23051997 | Human | | name |
| 598168968 | CV3947402 | single nucleotide variant | NM_144985.4(CDH24):c.1363+486C>T | not specified [RCV005308339] | uncertain significance | 14 | 23051987 | 23051987 | Human | | name |
| 156112058 | CV2217983 | single nucleotide variant | NM_144985.4(CDH24):c.94C>T (p.Arg32Trp) | not specified [RCV004086432] | uncertain significance | 14 | 23055640 | 23055640 | Human | | name |
| 156203725 | CV2300756 | single nucleotide variant | NM_144985.4(CDH24):c.59G>A (p.Arg20His) | not specified [RCV004155688] | uncertain significance | 14 | 23055675 | 23055675 | Human | | name |
| 401862693 | CV2762349 | single nucleotide variant | NM_144985.4(CDH24):c.98A>G (p.Glu33Gly) | not specified [RCV004335461] | likely benign | 14 | 23055636 | 23055636 | Human | | name |
| 405720706 | CV3296549 | single nucleotide variant | NM_144985.4(CDH24):c.95G>A (p.Arg32Gln) | not specified [RCV004428098] | uncertain significance | 14 | 23055639 | 23055639 | Human | | name |
| 407454980 | CV3422300 | single nucleotide variant | NM_144985.4(CDH24):c.77G>A (p.Arg26Gln) | not specified [RCV004610091] | uncertain significance | 14 | 23055657 | 23055657 | Human | | name |
| 597789133 | CV3641884 | single nucleotide variant | NM_144985.4(CDH24):c.92C>T (p.Ser31Phe) | not specified [RCV004901687] | uncertain significance | 14 | 23055642 | 23055642 | Human | | name |
| 155985903 | CV2368187 | single nucleotide variant | NM_144985.4(CDH24):c.233G>A (p.Arg78His) | not specified [RCV004216528] | uncertain significance | 14 | 23055322 | 23055322 | Human | | name |
| 155966669 | CV2396101 | single nucleotide variant | NM_144985.4(CDH24):c.253G>A (p.Gly85Arg) | not specified [RCV004237633] | uncertain significance | 14 | 23055302 | 23055302 | Human | | name |
| 401887557 | CV2772012 | single nucleotide variant | NM_144985.4(CDH24):c.128G>A (p.Arg43Gln) | not specified [RCV004344690] | uncertain significance | 14 | 23055606 | 23055606 | Human | | name |
| 405720650 | CV3296542 | single nucleotide variant | NM_144985.4(CDH24):c.221G>A (p.Arg74Gln) | not specified [RCV004428091] | uncertain significance | 14 | 23055334 | 23055334 | Human | | name |
| 407454968 | CV3422294 | single nucleotide variant | NM_144985.4(CDH24):c.271G>A (p.Val91Ile) | not specified [RCV004610085] | uncertain significance | 14 | 23055284 | 23055284 | Human | | name |
| 156271142 | CV2195217 | single nucleotide variant | NM_144985.4(CDH24):c.796T>G (p.Phe266Val) | not specified [RCV004080155] | uncertain significance | 14 | 23054317 | 23054317 | Human | | name |
| 156281799 | CV2348805 | single nucleotide variant | NM_144985.4(CDH24):c.902G>A (p.Gly301Glu) | not specified [RCV004203251] | uncertain significance | 14 | 23054211 | 23054211 | Human | | name |
| 156267136 | CV2371742 | single nucleotide variant | NM_144985.4(CDH24):c.925A>T (p.Ile309Phe) | not specified [RCV004219410] | uncertain significance | 14 | 23054188 | 23054188 | Human | | name |
| 155956572 | CV2387315 | single nucleotide variant | NM_144985.4(CDH24):c.994C>T (p.Arg332Cys) | not specified [RCV004238403] | uncertain significance | 14 | 23053728 | 23053728 | Human | | name |
| 329353886 | CV2439915 | single nucleotide variant | NM_144985.4(CDH24):c.356C>T (p.Ala119Val) | not specified [RCV004257950] | uncertain significance | 14 | 23055199 | 23055199 | Human | | name |
| 329357346 | CV2457504 | single nucleotide variant | NM_144985.4(CDH24):c.494T>G (p.Val165Gly) | not specified [RCV004267315] | uncertain significance | 14 | 23055061 | 23055061 | Human | | name |
| 401726955 | CV2691913 | single nucleotide variant | NM_144985.4(CDH24):c.845G>A (p.Arg282Gln) | not specified [RCV004299650] | uncertain significance | 14 | 23054268 | 23054268 | Human | | name |
| 401860495 | CV2758502 | single nucleotide variant | NM_144985.4(CDH24):c.800C>G (p.Ser267Cys) | not specified [RCV004335554] | uncertain significance | 14 | 23054313 | 23054313 | Human | | name |
| 401898100 | CV2780974 | single nucleotide variant | NM_144985.4(CDH24):c.650G>A (p.Arg217Gln) | not specified [RCV004354506] | uncertain significance | 14 | 23054640 | 23054640 | Human | | name |
| 401866711 | CV2782922 | single nucleotide variant | NM_144985.4(CDH24):c.734T>A (p.Val245Glu) | not specified [RCV004361721] | uncertain significance | 14 | 23054556 | 23054556 | Human | | name |
| 405720685 | CV3296546 | single nucleotide variant | NM_144985.4(CDH24):c.658C>A (p.Gln220Lys) | not specified [RCV004428095] | uncertain significance | 14 | 23054632 | 23054632 | Human | | name |
| 405720691 | CV3296547 | single nucleotide variant | NM_144985.4(CDH24):c.743C>T (p.Thr248Met) | not specified [RCV004428096] | uncertain significance | 14 | 23054547 | 23054547 | Human | | name |
| 405720698 | CV3296548 | single nucleotide variant | NM_144985.4(CDH24):c.890G>A (p.Ser297Asn) | not specified [RCV004428097] | uncertain significance | 14 | 23054223 | 23054223 | Human | | name |
| 407454970 | CV3422295 | single nucleotide variant | NM_144985.4(CDH24):c.947G>A (p.Arg316Gln) | not specified [RCV004610086] | uncertain significance | 14 | 23054166 | 23054166 | Human | | name |
| 597789122 | CV3641881 | single nucleotide variant | NM_144985.4(CDH24):c.386C>T (p.Pro129Leu) | not specified [RCV004901684] | uncertain significance | 14 | 23055169 | 23055169 | Human | | name |
| 597795438 | CV3641887 | single nucleotide variant | NM_144985.4(CDH24):c.307G>C (p.Val103Leu) | not specified [RCV004903674] | uncertain significance | 14 | 23055248 | 23055248 | Human | | name |
| 597795441 | CV3641888 | single nucleotide variant | NM_144985.4(CDH24):c.920T>G (p.Phe307Cys) | not specified [RCV004903675] | uncertain significance | 14 | 23054193 | 23054193 | Human | | name |
| 598229650 | CV3947394 | single nucleotide variant | NM_144985.4(CDH24):c.364G>A (p.Val122Met) | not specified [RCV005319263] | uncertain significance | 14 | 23055191 | 23055191 | Human | | name |
| 598168938 | CV3947396 | single nucleotide variant | NM_144985.4(CDH24):c.943G>A (p.Gly315Ser) | not specified [RCV005308334] | uncertain significance | 14 | 23054170 | 23054170 | Human | | name |
| 598168945 | CV3947397 | single nucleotide variant | NM_144985.4(CDH24):c.317G>A (p.Ser106Asn) | not specified [RCV005308335] | uncertain significance | 14 | 23055238 | 23055238 | Human | | name |
| 598168974 | CV3947403 | single nucleotide variant | NM_144985.4(CDH24):c.760G>A (p.Asp254Asn) | not specified [RCV005308340] | uncertain significance | 14 | 23054530 | 23054530 | Human | | name |
| 598168988 | CV3947406 | single nucleotide variant | NM_144985.4(CDH24):c.509T>A (p.Ile170Asn) | not specified [RCV005308342] | uncertain significance | 14 | 23054854 | 23054854 | Human | | name |
| 8635174 | CV90396 | single nucleotide variant | NM_022478.3(CDH24):c.473C>T (p.Thr158Ile) | Malignant melanoma [RCV000070494] | not provided | 14 | 23055082 | 23055082 | Human | | name |
| 155919747 | CV2202771 | single nucleotide variant | NM_144985.4(CDH24):c.2059C>T (p.Arg687Trp) | not specified [RCV004083010] | uncertain significance | 14 | 23048267 | 23048267 | Human | | name |
| 156107651 | CV2214246 | single nucleotide variant | NM_144985.4(CDH24):c.1274A>T (p.Gln425Leu) | not specified [RCV004086239] | uncertain significance | 14 | 23052562 | 23052562 | Human | | name |
| 156133633 | CV2216854 | single nucleotide variant | NM_144985.4(CDH24):c.2098G>A (p.Ala700Thr) | not specified [RCV004083280] | uncertain significance | 14 | 23048228 | 23048228 | Human | | name |
| 156223599 | CV2229561 | single nucleotide variant | NM_144985.4(CDH24):c.1847C>G (p.Ala616Gly) | not specified [RCV004103383] | uncertain significance | 14 | 23048479 | 23048479 | Human | | name |
| 156368465 | CV2267010 | single nucleotide variant | NM_144985.4(CDH24):c.2077C>G (p.Gln693Glu) | not specified [RCV004131650] | uncertain significance | 14 | 23048249 | 23048249 | Human | | name |
| 155991538 | CV2276602 | single nucleotide variant | NM_144985.4(CDH24):c.1643G>A (p.Arg548His) | not specified [RCV004146089] | uncertain significance | 14 | 23049230 | 23049230 | Human | | name |
| 155903610 | CV2282261 | single nucleotide variant | NM_144985.4(CDH24):c.1022C>T (p.Thr341Ile) | not specified [RCV004133101] | uncertain significance | 14 | 23053700 | 23053700 | Human | | name |
| 156191987 | CV2289385 | single nucleotide variant | NM_144985.4(CDH24):c.1874G>A (p.Arg625Gln) | not specified [RCV004152348] | uncertain significance | 14 | 23048452 | 23048452 | Human | | name |
| 156267827 | CV2305126 | single nucleotide variant | NM_144985.4(CDH24):c.1411G>A (p.Asp471Asn) | not specified [RCV004169000] | uncertain significance | 14 | 23049896 | 23049896 | Human | | name |
| 156159090 | CV2314585 | single nucleotide variant | NM_144985.4(CDH24):c.1177G>A (p.Val393Ile) | not specified [RCV004168668] | uncertain significance | 14 | 23053545 | 23053545 | Human | | name |
| 155977264 | CV2324981 | single nucleotide variant | NM_144985.4(CDH24):c.1667T>C (p.Ile556Thr) | not specified [RCV004175229] | uncertain significance | 14 | 23049206 | 23049206 | Human | | name |
| 156064227 | CV2340739 | single nucleotide variant | NM_144985.4(CDH24):c.2015C>T (p.Ala672Val) | not specified [RCV004188104] | uncertain significance | 14 | 23048311 | 23048311 | Human | | name |
| 156147428 | CV2358010 | single nucleotide variant | NM_144985.4(CDH24):c.2261G>A (p.Gly754Asp) | not specified [RCV004209785] | uncertain significance | 14 | 23048065 | 23048065 | Human | | name |
| 156383865 | CV2361712 | single nucleotide variant | NM_144985.4(CDH24):c.1085G>A (p.Arg362His) | not specified [RCV004223192] | uncertain significance | 14 | 23053637 | 23053637 | Human | | name |
| 156154537 | CV2374941 | single nucleotide variant | NM_144985.4(CDH24):c.1279G>A (p.Glu427Lys) | not specified [RCV004227962] | uncertain significance | 14 | 23052557 | 23052557 | Human | | name |
| 155905930 | CV2393832 | single nucleotide variant | NM_144985.4(CDH24):c.1501C>T (p.Arg501Trp) | not specified [RCV004233660] | uncertain significance | 14 | 23049723 | 23049723 | Human | | name |
| 329398813 | CV2471728 | single nucleotide variant | NM_144985.4(CDH24):c.1691C>T (p.Pro564Leu) | not specified [RCV004287005] | uncertain significance | 14 | 23049182 | 23049182 | Human | | name |
| 401720867 | CV2673518 | single nucleotide variant | NM_144985.4(CDH24):c.1694C>T (p.Ala565Val) | not specified [RCV004288485] | uncertain significance | 14 | 23049179 | 23049179 | Human | | name |
| 401780426 | CV2726069 | single nucleotide variant | NM_144985.4(CDH24):c.2152G>A (p.Gly718Ser) | not specified [RCV004324424] | likely benign | 14 | 23048174 | 23048174 | Human | | name |
| 401867244 | CV2759138 | single nucleotide variant | NM_144985.4(CDH24):c.1877G>T (p.Arg626Leu) | not specified [RCV004342436] | uncertain significance | 14 | 23048449 | 23048449 | Human | | name |
| 401892431 | CV2781939 | single nucleotide variant | NM_144985.4(CDH24):c.1277C>T (p.Pro426Leu) | not specified [RCV004357176] | uncertain significance | 14 | 23052559 | 23052559 | Human | | name |
| 405720579 | CV3296532 | single nucleotide variant | NM_144985.4(CDH24):c.1046A>G (p.Tyr349Cys) | not specified [RCV004428081] | uncertain significance | 14 | 23053676 | 23053676 | Human | | name |
| 405720585 | CV3296533 | single nucleotide variant | NM_144985.4(CDH24):c.1073T>A (p.Val358Glu) | not specified [RCV004428082] | uncertain significance | 14 | 23053649 | 23053649 | Human | | name |
| 405720596 | CV3296534 | single nucleotide variant | NM_144985.4(CDH24):c.1084C>T (p.Arg362Cys) | not specified [RCV004428083] | uncertain significance | 14 | 23053638 | 23053638 | Human | | name |
| 405720602 | CV3296535 | single nucleotide variant | NM_144985.4(CDH24):c.1324C>T (p.Arg442Cys) | not specified [RCV004428084] | uncertain significance | 14 | 23052512 | 23052512 | Human | | name |
| 405720614 | CV3296537 | single nucleotide variant | NM_144985.4(CDH24):c.1411G>C (p.Asp471His) | not specified [RCV004428086] | uncertain significance | 14 | 23049896 | 23049896 | Human | | name |
| 405720620 | CV3296538 | single nucleotide variant | NM_144985.4(CDH24):c.1628G>A (p.Arg543His) | not specified [RCV004428087] | uncertain significance | 14 | 23049245 | 23049245 | Human | | name |
| 405720628 | CV3296539 | single nucleotide variant | NM_144985.4(CDH24):c.1789G>A (p.Ala597Thr) | not specified [RCV004428088] | likely benign | 14 | 23049084 | 23049084 | Human | | name |
| 405720635 | CV3296540 | single nucleotide variant | NM_144985.4(CDH24):c.1807G>A (p.Ala603Thr) | not specified [RCV004428089] | uncertain significance | 14 | 23049066 | 23049066 | Human | | name |
| 405720642 | CV3296541 | single nucleotide variant | NM_144985.4(CDH24):c.2056C>T (p.Pro686Ser) | not specified [RCV004428090] | uncertain significance | 14 | 23048270 | 23048270 | Human | | name |
| 405720659 | CV3296543 | single nucleotide variant | NM_144985.4(CDH24):c.2272C>T (p.Pro758Ser) | not specified [RCV004428092] | uncertain significance | 14 | 23048054 | 23048054 | Human | | name |
| 405720667 | CV3296544 | single nucleotide variant | NM_144985.4(CDH24):c.2332C>T (p.Pro778Ser) | not specified [RCV004428093] | uncertain significance | 14 | 23047994 | 23047994 | Human | | name |
| 405720679 | CV3296545 | single nucleotide variant | NM_144985.4(CDH24):c.2341C>A (p.Pro781Thr) | not specified [RCV004428094] | uncertain significance | 14 | 23047985 | 23047985 | Human | | name |
| 407454972 | CV3422296 | single nucleotide variant | NM_144985.4(CDH24):c.1682G>T (p.Trp561Leu) | not specified [RCV004610087] | uncertain significance | 14 | 23049191 | 23049191 | Human | | name |
| 407454974 | CV3422297 | single nucleotide variant | NM_144985.4(CDH24):c.1747G>A (p.Gly583Ser) | not specified [RCV004610088] | uncertain significance | 14 | 23049126 | 23049126 | Human | | name |
| 407454975 | CV3422298 | single nucleotide variant | NM_144985.4(CDH24):c.1193C>T (p.Ala398Val) | not specified [RCV004610089] | uncertain significance | 14 | 23053529 | 23053529 | Human | | name |
| 407454977 | CV3422299 | single nucleotide variant | NM_144985.4(CDH24):c.1900G>A (p.Val634Ile) | not specified [RCV004610090] | uncertain significance | 14 | 23048426 | 23048426 | Human | | name |
| 407454982 | CV3422301 | single nucleotide variant | NM_144985.4(CDH24):c.2233T>G (p.Ser745Ala) | not specified [RCV004610092] | uncertain significance | 14 | 23048093 | 23048093 | Human | | name |
| 407454984 | CV3422302 | single nucleotide variant | NM_144985.4(CDH24):c.1382C>T (p.Ser461Leu) | not specified [RCV004610093] | uncertain significance | 14 | 23049925 | 23049925 | Human | | name |
| 407454986 | CV3422303 | single nucleotide variant | NM_144985.4(CDH24):c.1975G>A (p.Ala659Thr) | not specified [RCV004610094] | uncertain significance | 14 | 23048351 | 23048351 | Human | | name |
| 597789100 | CV3641875 | single nucleotide variant | NM_144985.4(CDH24):c.1592A>G (p.Asn531Ser) | not specified [RCV004901678] | uncertain significance | 14 | 23049632 | 23049632 | Human | | name |
| 597789106 | CV3641877 | single nucleotide variant | NM_144985.4(CDH24):c.1738C>G (p.Gln580Glu) | not specified [RCV004901680] | uncertain significance | 14 | 23049135 | 23049135 | Human | | name |
| 597789110 | CV3641878 | single nucleotide variant | NM_144985.4(CDH24):c.2194G>C (p.Gly732Arg) | not specified [RCV004901681] | uncertain significance | 14 | 23048132 | 23048132 | Human | | name |
| 597789114 | CV3641879 | single nucleotide variant | NM_144985.4(CDH24):c.1259G>A (p.Arg420His) | not specified [RCV004901682] | uncertain significance | 14 | 23052577 | 23052577 | Human | | name |
| 597789118 | CV3641880 | single nucleotide variant | NM_144985.4(CDH24):c.2291C>T (p.Pro764Leu) | not specified [RCV004901683] | uncertain significance | 14 | 23048035 | 23048035 | Human | | name |
| 597789124 | CV3641882 | single nucleotide variant | NM_144985.4(CDH24):c.1897A>T (p.Met633Leu) | not specified [RCV004901685] | uncertain significance | 14 | 23048429 | 23048429 | Human | | name |
| 597789615 | CV3641883 | single nucleotide variant | NM_144985.4(CDH24):c.1513A>G (p.Arg505Gly) | not specified [RCV004901686] | uncertain significance | 14 | 23049711 | 23049711 | Human | | name |
| 597789137 | CV3641885 | single nucleotide variant | NM_144985.4(CDH24):c.2017C>T (p.Pro673Ser) | not specified [RCV004901688] | uncertain significance | 14 | 23048309 | 23048309 | Human | | name |
| 598168933 | CV3947395 | single nucleotide variant | NM_144985.4(CDH24):c.1384C>T (p.Arg462Cys) | not specified [RCV005308333] | uncertain significance | 14 | 23049923 | 23049923 | Human | | name |
| 598168951 | CV3947398 | single nucleotide variant | NM_144985.4(CDH24):c.2211C>G (p.Cys737Trp) | not specified [RCV005308336] | uncertain significance | 14 | 23048115 | 23048115 | Human | | name |
| 598168957 | CV3947400 | single nucleotide variant | NM_144985.4(CDH24):c.2248G>C (p.Gly750Arg) | not specified [RCV005308337] | uncertain significance | 14 | 23048078 | 23048078 | Human | | name |
| 598168961 | CV3947401 | single nucleotide variant | NM_144985.4(CDH24):c.2112G>C (p.Gln704His) | not specified [RCV005308338] | uncertain significance | 14 | 23048214 | 23048214 | Human | | name |
| 598168980 | CV3947404 | single nucleotide variant | NM_144985.4(CDH24):c.1945G>C (p.Asp649His) | not specified [RCV005308341] | uncertain significance | 14 | 23048381 | 23048381 | Human | | name |
| 598229662 | CV3947405 | single nucleotide variant | NM_144985.4(CDH24):c.1093G>A (p.Val365Met) | not specified [RCV005319265] | uncertain significance | 14 | 23053629 | 23053629 | Human | | name |