| 401720820 | CV2673502 | single nucleotide variant | NM_030649.3(ACAP3):c.5C>T (p.Thr2Ile) | not specified [RCV004288470] | uncertain significance | 1 | 1307811 | 1307811 | Human | | name |
| 407473857 | CV3427855 | single nucleotide variant | NM_030649.3(ACAP3):c.79G>T (p.Val27Leu) | not specified [RCV004600468] | uncertain significance | 1 | 1304112 | 1304112 | Human | | name |
| 407473895 | CV3427865 | single nucleotide variant | NM_030649.3(ACAP3):c.61G>A (p.Glu21Lys) | not specified [RCV004600477] | uncertain significance | 1 | 1304130 | 1304130 | Human | | name |
| 597726571 | CV3624851 | single nucleotide variant | NM_030649.3(ACAP3):c.71C>T (p.Thr24Met) | not specified [RCV004888419] | uncertain significance | 1 | 1304120 | 1304120 | Human | | name |
| 155901442 | CV2345806 | single nucleotide variant | NM_030649.3(ACAP3):c.213C>A (p.Asp71Glu) | not specified [RCV004205730] | uncertain significance | 1 | 1303174 | 1303174 | Human | | name |
| 401872708 | CV2779977 | single nucleotide variant | NM_030649.3(ACAP3):c.127A>G (p.Met43Val) | not specified [RCV004353568] | uncertain significance | 1 | 1303260 | 1303260 | Human | | name |
| 401935177 | CV2805475 | single nucleotide variant | NM_030649.3(ACAP3):c.1257C>A (p.Gly419=) | not provided [RCV003412600] | likely benign | 1 | 1296505 | 1296505 | Human | | name |
| 405731898 | CV3294909 | single nucleotide variant | NM_030649.3(ACAP3):c.119G>A (p.Cys40Tyr) | not specified [RCV004429454] | uncertain significance | 1 | 1303268 | 1303268 | Human | | name |
| 597752940 | CV3627503 | single nucleotide variant | NM_030649.3(ACAP3):c.217G>A (p.Val73Ile) | not specified [RCV004892947] | uncertain significance | 1 | 1303170 | 1303170 | Human | | name |
| 597692762 | CV3627699 | single nucleotide variant | NM_030649.3(ACAP3):c.239G>A (p.Arg80Lys) | not specified [RCV004884791] | uncertain significance | 1 | 1302962 | 1302962 | Human | | name |
| 597725894 | CV3628012 | single nucleotide variant | NM_030649.3(ACAP3):c.187G>A (p.Asp63Asn) | not specified [RCV004888325] | uncertain significance | 1 | 1303200 | 1303200 | Human | | name |
| 597793571 | CV3631177 | single nucleotide variant | NM_030649.3(ACAP3):c.217G>C (p.Val73Leu) | not specified [RCV004877361] | uncertain significance | 1 | 1303170 | 1303170 | Human | | name |
| 156287568 | CV2229643 | single nucleotide variant | NM_030649.3(ACAP3):c.562G>A (p.Asp188Asn) | not specified [RCV004103457] | uncertain significance | 1 | 1300163 | 1300163 | Human | | name |
| 156001905 | CV2257904 | single nucleotide variant | NM_030649.3(ACAP3):c.463G>A (p.Gly155Arg) | not specified [RCV004129729] | uncertain significance | 1 | 1300568 | 1300568 | Human | | name |
| 156019698 | CV2272669 | single nucleotide variant | NM_030649.3(ACAP3):c.997G>A (p.Glu333Lys) | not specified [RCV004133544] | uncertain significance | 1 | 1298032 | 1298032 | Human | | name |
| 156083634 | CV2289611 | single nucleotide variant | NM_030649.3(ACAP3):c.674T>G (p.Leu225Arg) | not specified [RCV004148535] | uncertain significance | 1 | 1299895 | 1299895 | Human | | name |
| 155907078 | CV2302147 | single nucleotide variant | NM_030649.3(ACAP3):c.919G>A (p.Ala307Thr) | not specified [RCV004159161] | uncertain significance | 1 | 1298110 | 1298110 | Human | | name |
| 156296898 | CV2319208 | single nucleotide variant | NM_030649.3(ACAP3):c.758C>G (p.Ser253Cys) | not specified [RCV004178260] | uncertain significance | 1 | 1298672 | 1298672 | Human | | name |
| 156090262 | CV2375189 | single nucleotide variant | NM_030649.3(ACAP3):c.737G>A (p.Arg246Gln) | not specified [RCV004230229] | uncertain significance | 1 | 1299832 | 1299832 | Human | | name |
| 329359018 | CV2425437 | single nucleotide variant | NM_030649.3(ACAP3):c.844G>A (p.Ala282Thr) | not specified [RCV004251092] | uncertain significance | 1 | 1298586 | 1298586 | Human | | name |
| 401882403 | CV2793478 | single nucleotide variant | NM_030649.3(ACAP3):c.337G>A (p.Glu113Lys) | not specified [RCV004362563] | uncertain significance | 1 | 1301989 | 1301989 | Human | | name |
| 405732269 | CV3294957 | single nucleotide variant | NM_030649.3(ACAP3):c.527A>G (p.Asn176Ser) | not specified [RCV004429502] | uncertain significance | 1 | 1300198 | 1300198 | Human | | name |
| 405732273 | CV3294958 | single nucleotide variant | NM_030649.3(ACAP3):c.551T>A (p.Phe184Tyr) | not specified [RCV004429503] | uncertain significance | 1 | 1300174 | 1300174 | Human | | name |
| 405732401 | CV3294975 | single nucleotide variant | NM_030649.3(ACAP3):c.875C>T (p.Ser292Phe) | not specified [RCV004429520] | uncertain significance | 1 | 1298410 | 1298410 | Human | | name |
| 405732429 | CV3294979 | single nucleotide variant | NM_030649.3(ACAP3):c.902A>G (p.Gln301Arg) | not specified [RCV004429524] | uncertain significance | 1 | 1298383 | 1298383 | Human | | name |
| 407473974 | CV3423945 | single nucleotide variant | NM_030649.3(ACAP3):c.805G>T (p.Val269Leu) | not specified [RCV004600497] | uncertain significance | 1 | 1298625 | 1298625 | Human | | name |
| 407474054 | CV3423965 | single nucleotide variant | NM_030649.3(ACAP3):c.736C>T (p.Arg246Trp) | not specified [RCV004600517] | uncertain significance | 1 | 1299833 | 1299833 | Human | | name |
| 597694922 | CV3624539 | single nucleotide variant | NM_030649.3(ACAP3):c.619C>G (p.Leu207Val) | not specified [RCV004884993] | uncertain significance | 1 | 1300017 | 1300017 | Human | | name |
| 597794322 | CV3628112 | single nucleotide variant | NM_030649.3(ACAP3):c.431G>A (p.Arg144Lys) | not specified [RCV004877608] | uncertain significance | 1 | 1300600 | 1300600 | Human | | name |
| 597724443 | CV3630979 | single nucleotide variant | NM_030649.3(ACAP3):c.860A>G (p.Asn287Ser) | not specified [RCV004888170] | uncertain significance | 1 | 1298570 | 1298570 | Human | | name |
| 598267932 | CV3929981 | single nucleotide variant | NM_030649.3(ACAP3):c.682G>A (p.Asp228Asn) | not specified [RCV005302274] | uncertain significance | 1 | 1299887 | 1299887 | Human | | name |
| 598235872 | CV3937078 | single nucleotide variant | NM_030649.3(ACAP3):c.323A>G (p.Gln108Arg) | not specified [RCV005295919] | uncertain significance | 1 | 1302003 | 1302003 | Human | | name |
| 156398115 | CV2204260 | single nucleotide variant | NM_030649.3(ACAP3):c.1026G>C (p.Met342Ile) | not specified [RCV004079094] | uncertain significance | 1 | 1297924 | 1297924 | Human | | name |
| 155988967 | CV2234266 | single nucleotide variant | NM_030649.3(ACAP3):c.1609A>C (p.Lys537Gln) | not specified [RCV004106339] | uncertain significance | 1 | 1295832 | 1295832 | Human | | name |
| 156363739 | CV2262698 | single nucleotide variant | NM_030649.3(ACAP3):c.1576G>A (p.Ala526Thr) | not specified [RCV004130888] | uncertain significance | 1 | 1295865 | 1295865 | Human | | name |
| 156068748 | CV2289583 | single nucleotide variant | NM_030649.3(ACAP3):c.1139G>C (p.Arg380Pro) | not specified [RCV004154298] | uncertain significance | 1 | 1296623 | 1296623 | Human | | name |
| 156294838 | CV2293257 | single nucleotide variant | NM_030649.3(ACAP3):c.1084A>G (p.Ile362Val) | not specified [RCV004150758] | uncertain significance | 1 | 1297866 | 1297866 | Human | | name |
| 156179967 | CV2298416 | single nucleotide variant | NM_030649.3(ACAP3):c.2204G>A (p.Arg735Gln) | not specified [RCV004162089] | uncertain significance | 1 | 1294135 | 1294135 | Human | | name |
| 156102184 | CV2313542 | single nucleotide variant | NM_030649.3(ACAP3):c.1115G>A (p.Ser372Asn) | not specified [RCV004163837] | uncertain significance | 1 | 1297835 | 1297835 | Human | | name |
| 156281450 | CV2321870 | single nucleotide variant | NM_030649.3(ACAP3):c.1825G>A (p.Asp609Asn) | not specified [RCV004179846] | uncertain significance | 1 | 1294805 | 1294805 | Human | | name |
| 156289960 | CV2324861 | single nucleotide variant | NM_030649.3(ACAP3):c.1631C>T (p.Ser544Phe) | not specified [RCV004173087] | uncertain significance | 1 | 1295810 | 1295810 | Human | | name |
| 156171931 | CV2326745 | single nucleotide variant | NM_030649.3(ACAP3):c.2054C>T (p.Ala685Val) | not specified [RCV004176590] | uncertain significance | 1 | 1294487 | 1294487 | Human | | name |
| 156306890 | CV2335306 | single nucleotide variant | NM_030649.3(ACAP3):c.1138C>T (p.Arg380Cys) | not specified [RCV004186870] | uncertain significance | 1 | 1296624 | 1296624 | Human | | name |
| 156190376 | CV2339574 | single nucleotide variant | NM_030649.3(ACAP3):c.1555C>T (p.Arg519Trp) | not specified [RCV004194239] | uncertain significance | 1 | 1295886 | 1295886 | Human | | name |
| 156199967 | CV2362910 | single nucleotide variant | NM_030649.3(ACAP3):c.1807C>A (p.Pro603Thr) | not specified [RCV004209015] | uncertain significance | 1 | 1295453 | 1295453 | Human | | name |
| 155939066 | CV2376525 | single nucleotide variant | NM_030649.3(ACAP3):c.1876G>A (p.Gly626Ser) | not specified [RCV004220696] | uncertain significance | 1 | 1294754 | 1294754 | Human | | name |
| 155936889 | CV2379923 | single nucleotide variant | NM_030649.3(ACAP3):c.1157C>T (p.Thr386Met) | not specified [RCV004222070] | uncertain significance | 1 | 1296605 | 1296605 | Human | | name |
| 329390702 | CV2437168 | single nucleotide variant | NM_030649.3(ACAP3):c.1616T>C (p.Leu539Pro) | not specified [RCV004262971] | likely benign | 1 | 1295825 | 1295825 | Human | | name |
| 329382748 | CV2445466 | single nucleotide variant | NM_030649.3(ACAP3):c.1198G>A (p.Val400Met) | not specified [RCV004257526] | uncertain significance | 1 | 1296564 | 1296564 | Human | | name |
| 329382580 | CV2449186 | single nucleotide variant | NM_030649.3(ACAP3):c.1789G>A (p.Gly597Arg) | not specified [RCV004264243] | uncertain significance | 1 | 1295471 | 1295471 | Human | | name |
| 329402483 | CV2454696 | single nucleotide variant | NM_030649.3(ACAP3):c.1367G>A (p.Arg456Gln) | not specified [RCV004269935] | uncertain significance | 1 | 1296251 | 1296251 | Human | | name |
| 329360916 | CV2463105 | single nucleotide variant | NM_030649.3(ACAP3):c.1167C>G (p.Ile389Met) | not specified [RCV004274908] | uncertain significance | 1 | 1296595 | 1296595 | Human | | name |
| 329398313 | CV2465006 | single nucleotide variant | NM_030649.3(ACAP3):c.2411C>T (p.Pro804Leu) | not specified [RCV004284913] | uncertain significance | 1 | 1293658 | 1293658 | Human | | name |
| 329353262 | CV2469057 | single nucleotide variant | NM_030649.3(ACAP3):c.1271C>G (p.Pro424Arg) | not specified [RCV004274301] | uncertain significance | 1 | 1296491 | 1296491 | Human | | name |
| 401729941 | CV2683868 | single nucleotide variant | NM_030649.3(ACAP3):c.1280G>A (p.Arg427His) | not specified [RCV004284593] | uncertain significance | 1 | 1296482 | 1296482 | Human | | name |
| 401746905 | CV2698731 | single nucleotide variant | NM_030649.3(ACAP3):c.1279C>T (p.Arg427Cys) | not specified [RCV004301187] | uncertain significance | 1 | 1296483 | 1296483 | Human | | name |
| 401859598 | CV2771726 | single nucleotide variant | NM_030649.3(ACAP3):c.1193G>A (p.Arg398His) | not specified [RCV004350511] | uncertain significance | 1 | 1296569 | 1296569 | Human | | name |
| 401885902 | CV2774890 | single nucleotide variant | NM_030649.3(ACAP3):c.2457C>G (p.Phe819Leu) | not specified [RCV004343969] | uncertain significance | 1 | 1293612 | 1293612 | Human | | name |
| 401860695 | CV2776146 | single nucleotide variant | NM_030649.3(ACAP3):c.2329G>C (p.Val777Leu) | not specified [RCV004353236] | uncertain significance | 1 | 1293854 | 1293854 | Human | | name |
| 401872117 | CV2792984 | single nucleotide variant | NM_030649.3(ACAP3):c.1675G>A (p.Val559Ile) | not specified [RCV004360323] | uncertain significance | 1 | 1295766 | 1295766 | Human | | name |
| 405731751 | CV3294890 | single nucleotide variant | NM_030649.3(ACAP3):c.1107C>A (p.Ser369Arg) | not specified [RCV004429435] | uncertain significance | 1 | 1297843 | 1297843 | Human | | name |
| 405731869 | CV3294905 | single nucleotide variant | NM_030649.3(ACAP3):c.1183A>T (p.Thr395Ser) | not specified [RCV004429450] | likely benign | 1 | 1296579 | 1296579 | Human | | name |
| 405731957 | CV3294917 | single nucleotide variant | NM_030649.3(ACAP3):c.1366C>T (p.Arg456Trp) | not specified [RCV004429462] | uncertain significance | 1 | 1296252 | 1296252 | Human | | name |
| 405731984 | CV3294920 | single nucleotide variant | NM_030649.3(ACAP3):c.1466G>C (p.Gly489Ala) | not specified [RCV004429465] | uncertain significance | 1 | 1296051 | 1296051 | Human | | name |
| 405731998 | CV3294922 | single nucleotide variant | NM_030649.3(ACAP3):c.1504C>A (p.Gln502Lys) | not specified [RCV004429467] | uncertain significance | 1 | 1295937 | 1295937 | Human | | name |
| 405732034 | CV3294927 | single nucleotide variant | NM_030649.3(ACAP3):c.1655G>A (p.Arg552His) | not specified [RCV004429472] | uncertain significance | 1 | 1295786 | 1295786 | Human | | name |
| 405732081 | CV3294933 | single nucleotide variant | NM_030649.3(ACAP3):c.1970C>T (p.Ala657Val) | not specified [RCV004429478] | uncertain significance | 1 | 1294571 | 1294571 | Human | | name |
| 405732112 | CV3294937 | single nucleotide variant | NM_030649.3(ACAP3):c.2019C>G (p.His673Gln) | not specified [RCV004429482] | uncertain significance | 1 | 1294522 | 1294522 | Human | | name |
| 405732175 | CV3294945 | single nucleotide variant | NM_030649.3(ACAP3):c.2182G>A (p.Asp728Asn) | not specified [RCV004429490] | uncertain significance | 1 | 1294157 | 1294157 | Human | | name |
| 405732235 | CV3294953 | single nucleotide variant | NM_030649.3(ACAP3):c.2307G>C (p.Gln769His) | not specified [RCV004429498] | uncertain significance | 1 | 1293876 | 1293876 | Human | | name |
| 407473936 | CV3423930 | single nucleotide variant | NM_030649.3(ACAP3):c.1990C>T (p.Arg664Cys) | not specified [RCV004600486] | uncertain significance | 1 | 1294551 | 1294551 | Human | | name |
| 407474016 | CV3423956 | single nucleotide variant | NM_030649.3(ACAP3):c.1787C>T (p.Ala596Val) | not specified [RCV004600508] | uncertain significance | 1 | 1295473 | 1295473 | Human | | name |
| 407473816 | CV3427845 | single nucleotide variant | NM_030649.3(ACAP3):c.1988T>C (p.Val663Ala) | not specified [RCV004600458] | uncertain significance | 1 | 1294553 | 1294553 | Human | | name |
| 597693238 | CV3624338 | single nucleotide variant | NM_030649.3(ACAP3):c.2416C>A (p.Pro806Thr) | not specified [RCV004884861] | uncertain significance | 1 | 1293653 | 1293653 | Human | | name |
| 597752839 | CV3624441 | single nucleotide variant | NM_030649.3(ACAP3):c.2341A>G (p.Asn781Asp) | not specified [RCV004893055] | uncertain significance | 1 | 1293842 | 1293842 | Human | | name |
| 597753394 | CV3624639 | single nucleotide variant | NM_030649.3(ACAP3):c.1099C>T (p.Arg367Cys) | not specified [RCV004893109] | uncertain significance | 1 | 1297851 | 1297851 | Human | | name |
| 597800281 | CV3624752 | single nucleotide variant | NM_030649.3(ACAP3):c.1663C>T (p.Arg555Trp) | not specified [RCV004880159] | uncertain significance | 1 | 1295778 | 1295778 | Human | | name |
| 597692080 | CV3627596 | single nucleotide variant | NM_030649.3(ACAP3):c.1975G>A (p.Gly659Ser) | not specified [RCV004884727] | uncertain significance | 1 | 1294566 | 1294566 | Human | | name |
| 597725303 | CV3627807 | single nucleotide variant | NM_030649.3(ACAP3):c.2393G>T (p.Arg798Leu) | not specified [RCV004888254] | uncertain significance | 1 | 1293676 | 1293676 | Human | | name |
| 597793966 | CV3627915 | single nucleotide variant | NM_030649.3(ACAP3):c.2275G>A (p.Gly759Ser) | not specified [RCV004877497] | uncertain significance | 1 | 1293908 | 1293908 | Human | | name |
| 597753246 | CV3630795 | single nucleotide variant | NM_030649.3(ACAP3):c.1930G>A (p.Glu644Lys) | not specified [RCV004893140] | uncertain significance | 1 | 1294611 | 1294611 | Human | | name |
| 597724820 | CV3631079 | single nucleotide variant | NM_030649.3(ACAP3):c.1792G>A (p.Ala598Thr) | not specified [RCV004888203] | uncertain significance | 1 | 1295468 | 1295468 | Human | | name |
| 598268540 | CV3926306 | single nucleotide variant | NM_030649.3(ACAP3):c.2077G>A (p.Glu693Lys) | not specified [RCV005302400] | uncertain significance | 1 | 1294464 | 1294464 | Human | | name |
| 598234971 | CV3926410 | single nucleotide variant | NM_030649.3(ACAP3):c.1619G>A (p.Arg540Gln) | not specified [RCV005295786] | uncertain significance | 1 | 1295822 | 1295822 | Human | | name |
| 598235293 | CV3926509 | single nucleotide variant | NM_030649.3(ACAP3):c.1024A>G (p.Met342Val) | not specified [RCV005295829] | uncertain significance | 1 | 1297926 | 1297926 | Human | | name |
| 598275410 | CV3926606 | single nucleotide variant | NM_030649.3(ACAP3):c.1651C>T (p.Arg551Cys) | not specified [RCV005304544] | uncertain significance | 1 | 1295790 | 1295790 | Human | | name |
| 598267641 | CV3929879 | single nucleotide variant | NM_030649.3(ACAP3):c.1376C>T (p.Thr459Met) | not specified [RCV005302215] | uncertain significance | 1 | 1296242 | 1296242 | Human | | name |
| 598234297 | CV3930086 | single nucleotide variant | NM_030649.3(ACAP3):c.2048C>T (p.Ala683Val) | not specified [RCV005295694] | uncertain significance | 1 | 1294493 | 1294493 | Human | | name |
| 598236045 | CV3937149 | single nucleotide variant | NM_030649.3(ACAP3):c.1353C>G (p.His451Gln) | not specified [RCV005295951] | uncertain significance | 1 | 1296265 | 1296265 | Human | | name |
| 598192380 | CV3937229 | single nucleotide variant | NM_030649.3(ACAP3):c.1042G>C (p.Glu348Gln) | not specified [RCV005288513] | uncertain significance | 1 | 1297908 | 1297908 | Human | | name |
| 598182465 | CV3937283 | single nucleotide variant | NM_030649.3(ACAP3):c.2341A>C (p.Asn781His) | not specified [RCV005311240] | uncertain significance | 1 | 1293842 | 1293842 | Human | | name |
| 598275595 | CV3937303 | single nucleotide variant | NM_030649.3(ACAP3):c.1870G>A (p.Ala624Thr) | not specified [RCV005304729] | uncertain significance | 1 | 1294760 | 1294760 | Human | | name |
