| 155696512 | CV1800742 | single nucleotide variant | NM_001868.4(CPA1):c.-5G>C | Hereditary pancreatitis [RCV002358000] | uncertain significance | 7 | 130380516 | 130380516 | Human | 1 | name |
| 155747739 | CV1849743 | single nucleotide variant | NM_001868.4(CPA1):c.-1C>G | Hereditary pancreatitis [RCV002417121] | uncertain significance | 7 | 130380520 | 130380520 | Human | 1 | name |
| 150535060 | CV1306797 | single nucleotide variant | NM_001868.4(CPA1):c.*97A>C | not provided [RCV001757795] | likely benign | 7 | 130388108 | 130388108 | Human | | name |
| 153303610 | CV1690377 | single nucleotide variant | NM_001868.4(CPA1):c.*16C>A | not provided [RCV002269420] | likely benign | 7 | 130388027 | 130388027 | Human | | name |
| 127329053 | CV1138521 | single nucleotide variant | NM_001868.4(CPA1):c.65+3A>G | Hereditary pancreatitis [RCV002368494]|not provided [RCV001487203] | likely benign|uncertain significance | 7 | 130380588 | 130380588 | Human | 1 | name |
| 151812087 | CV1510362 | single nucleotide variant | NM_001868.4(CPA1):c.65+4G>A | not provided [RCV001918712] | uncertain significance | 7 | 130380589 | 130380589 | Human | | name |
| 155667134 | CV1812080 | single nucleotide variant | NM_001868.4(CPA1):c.66-3C>T | Hereditary pancreatitis [RCV002366785] | uncertain significance | 7 | 130381095 | 130381095 | Human | 1 | name |
| 156238670 | CV1882296 | deletion | NM_001868.4(CPA1):c.66-3del | not provided [RCV003085660] | likely benign | 7 | 130381093 | 130381093 | Human | | name |
| 405049847 | CV3025456 | duplication | NM_001868.4(CPA1):c.65+1dup | not provided [RCV003696902] | uncertain significance | 7 | 130380582 | 130380583 | Human | | name |
| 25325095 | CV815376 | deletion | NM_001868.4(CPA1):c.65+3del | Hereditary pancreatitis [RCV002354953]|not provided [RCV001419046] | likely benign|uncertain significance | 7 | 130380588 | 130380588 | Human | 1 | name |
| 126752760 | CV1007247 | single nucleotide variant | NM_001868.4(CPA1):c.483+4A>G | not provided [RCV001316372] | uncertain significance | 7 | 130382213 | 130382213 | Human | | name |
| 126761239 | CV1027786 | single nucleotide variant | NM_001868.4(CPA1):c.696+5C>T | Hereditary pancreatitis [RCV002259106]|not provided [RCV001340634] | uncertain significance | 7 | 130383799 | 130383799 | Human | 1 | name |
| 127277062 | CV1074436 | single nucleotide variant | NM_001868.4(CPA1):c.381+9G>A | not provided [RCV001407536] | likely benign | 7 | 130381872 | 130381872 | Human | | name |
| 127264434 | CV1074438 | single nucleotide variant | NM_001868.4(CPA1):c.585+7C>T | not provided [RCV001403280] | likely benign | 7 | 130383499 | 130383499 | Human | | name |
| 127297689 | CV1138522 | single nucleotide variant | NM_001868.4(CPA1):c.148-4C>T | Hereditary pancreatitis [RCV002388534]|not provided [RCV001497827] | likely benign|uncertain significance | 7 | 130381626 | 130381626 | Human | 1 | name |
| 127320899 | CV1138523 | single nucleotide variant | NM_001868.4(CPA1):c.585+8C>T | not provided [RCV001484379] | likely benign | 7 | 130383500 | 130383500 | Human | | name |
| 150496754 | CV1271608 | single nucleotide variant | NM_001868.4(CPA1):c.66-90G>A | not provided [RCV001688909] | benign | 7 | 130381008 | 130381008 | Human | | name |
| 151863972 | CV1374536 | single nucleotide variant | NM_001868.4(CPA1):c.147+4A>C | Hereditary pancreatitis [RCV002388772]|not provided [RCV001884307] | uncertain significance | 7 | 130381183 | 130381183 | Human | 1 | name |
| 151775968 | CV1440261 | single nucleotide variant | NM_001868.4(CPA1):c.787+1G>A | Hereditary pancreatitis [RCV004040570]|not provided [RCV001874904] | likely benign|uncertain significance | 7 | 130384627 | 130384627 | Human | 1 | name |
| 151802003 | CV1442353 | single nucleotide variant | NM_001868.4(CPA1):c.586-2A>G | Hereditary pancreatitis [RCV002352741]|not provided [RCV002011660] | uncertain significance | 7 | 130383682 | 130383682 | Human | 1 | name |
| 152124333 | CV1527656 | single nucleotide variant | NM_001868.4(CPA1):c.65+14G>A | not provided [RCV002082000] | likely benign | 7 | 130380599 | 130380599 | Human | | name |
| 152163152 | CV1561207 | single nucleotide variant | NM_001868.4(CPA1):c.788-6C>G | not provided [RCV002104183] | benign | 7 | 130385140 | 130385140 | Human | | name |
| 152137931 | CV1563459 | single nucleotide variant | NM_001868.4(CPA1):c.66-11A>T | Hereditary pancreatitis [RCV002256902]|not provided [RCV002200197] | likely benign|uncertain significance | 7 | 130381087 | 130381087 | Human | 1 | name |
| 152135726 | CV1595024 | single nucleotide variant | NM_001868.4(CPA1):c.788-5C>A | Hereditary pancreatitis [RCV002407364]|not provided [RCV002199914] | likely benign|uncertain significance | 7 | 130385141 | 130385141 | Human | 1 | name |
| 152056889 | CV1656463 | single nucleotide variant | NM_001868.4(CPA1):c.988-7T>C | not provided [RCV002109654] | likely benign | 7 | 130385832 | 130385832 | Human | | name |
| 153002495 | CV1685091 | single nucleotide variant | NM_001868.4(CPA1):c.696+6G>A | Hereditary pancreatitis [RCV002259241] | likely benign | 7 | 130383800 | 130383800 | Human | 1 | name |
| 155680091 | CV1807127 | single nucleotide variant | NM_001868.4(CPA1):c.586-1G>T | Hereditary pancreatitis [RCV002353416] | uncertain significance | 7 | 130383683 | 130383683 | Human | 1 | name |
| 155742197 | CV1816585 | single nucleotide variant | NM_001868.4(CPA1):c.787+2T>A | Hereditary pancreatitis [RCV002412283] | uncertain significance | 7 | 130384628 | 130384628 | Human | 1 | name |
| 155675107 | CV1828898 | single nucleotide variant | NM_001868.4(CPA1):c.988-3C>T | Hereditary pancreatitis [RCV002387397] | uncertain significance | 7 | 130385836 | 130385836 | Human | 1 | name |
| 156163494 | CV1903215 | single nucleotide variant | NM_001868.4(CPA1):c.696+4C>G | not provided [RCV003082989] | uncertain significance | 7 | 130383798 | 130383798 | Human | | name |
| 155958292 | CV1903875 | single nucleotide variant | NM_001868.4(CPA1):c.586-8C>T | not provided [RCV003095707] | likely benign | 7 | 130383676 | 130383676 | Human | | name |
| 156446986 | CV1948680 | single nucleotide variant | NM_001868.4(CPA1):c.148-6C>G | not provided [RCV003118510] | uncertain significance | 7 | 130381624 | 130381624 | Human | | name |
| 156385901 | CV1971993 | single nucleotide variant | NM_001868.4(CPA1):c.483+5C>T | not provided [RCV002604292] | uncertain significance | 7 | 130382214 | 130382214 | Human | | name |
| 156395140 | CV2016012 | single nucleotide variant | NM_001868.4(CPA1):c.697-9C>T | not provided [RCV002725475] | likely benign | 7 | 130384527 | 130384527 | Human | | name |
| 11542908 | CV252618 | single nucleotide variant | NM_001868.4(CPA1):c.788-5C>G | Hereditary pancreatitis [RCV002256184]|not provided [RCV001312152]|not specified [RCV000241762] | benign|likely benign | 7 | 130385141 | 130385141 | Human | 1 | name |
| 401765390 | CV2733679 | single nucleotide variant | NM_001868.4(CPA1):c.382-4T>A | Hereditary pancreatitis [RCV003301383] | likely benign | 7 | 130382104 | 130382104 | Human | 1 | name |
| 405202921 | CV3036368 | single nucleotide variant | NM_001868.4(CPA1):c.586-6C>A | not provided [RCV003707635] | uncertain significance | 7 | 130383678 | 130383678 | Human | | name |
| 405177994 | CV3049573 | duplication | NM_001868.4(CPA1):c.381+7dup | not provided [RCV003728451] | likely benign | 7 | 130381867 | 130381868 | Human | | name |
| 402500182 | CV3170492 | single nucleotide variant | NM_001868.4(CPA1):c.586-3C>G | not provided [RCV003877864] | uncertain significance | 7 | 130383681 | 130383681 | Human | | name |
| 405259672 | CV3186372 | single nucleotide variant | NM_001868.4(CPA1):c.147+5G>C | not provided [RCV003884131] | likely benign | 7 | 130381184 | 130381184 | Human | | name |
| 407456878 | CV3419509 | single nucleotide variant | NM_001868.4(CPA1):c.988-2A>G | Hereditary pancreatitis [RCV004610903] | likely benign | 7 | 130385837 | 130385837 | Human | 1 | name |
| 597630374 | CV3654356 | single nucleotide variant | NM_001868.4(CPA1):c.788-4A>C | Hereditary pancreatitis [RCV004822633] | likely benign | 7 | 130385142 | 130385142 | Human | 1 | name |
| 597630380 | CV3654360 | single nucleotide variant | NM_001868.4(CPA1):c.788-5C>T | Hereditary pancreatitis [RCV004822636] | uncertain significance | 7 | 130385141 | 130385141 | Human | 1 | name |
| 597630406 | CV3654372 | single nucleotide variant | NM_001868.4(CPA1):c.788-3C>G | Hereditary pancreatitis [RCV004822648] | uncertain significance | 7 | 130385143 | 130385143 | Human | 1 | name |
| 597970460 | CV3832488 | single nucleotide variant | NM_001868.4(CPA1):c.586-8C>A | not provided [RCV005166567] | likely benign | 7 | 130383676 | 130383676 | Human | | name |
| 598235051 | CV3945107 | single nucleotide variant | NM_001868.4(CPA1):c.381+2T>C | Hereditary pancreatitis [RCV005320174] | uncertain significance | 7 | 130381865 | 130381865 | Human | 1 | name |
| 15194414 | CV730466 | single nucleotide variant | NM_001868.4(CPA1):c.585+9G>A | not provided [RCV000889218] | likely benign | 7 | 130383501 | 130383501 | Human | | name |
| 15131941 | CV759514 | single nucleotide variant | NM_001868.4(CPA1):c.381+7G>C | not provided [RCV000920251] | likely benign | 7 | 130381870 | 130381870 | Human | | name |
| 25324213 | CV815377 | single nucleotide variant | NM_001868.4(CPA1):c.586-3C>A | Hereditary pancreatitis [RCV002337077]|not provided [RCV002067676] | benign|likely benign | 7 | 130383681 | 130383681 | Human | 1 | name |
| 150447808 | CV1216169 | single nucleotide variant | NM_001868.4(CPA1):c.65+143A>G | not provided [RCV001611467] | benign | 7 | 130380728 | 130380728 | Human | | name |
| 150430361 | CV1230841 | single nucleotide variant | NM_001868.4(CPA1):c.381+57T>C | not provided [RCV001641390] | benign | 7 | 130381920 | 130381920 | Human | | name |
| 150501399 | CV1238387 | duplication | NM_001868.4(CPA1):c.697-63dup | not provided [RCV001656817] | benign | 7 | 130384467 | 130384468 | Human | | name |
| 150487097 | CV1262683 | deletion | NM_001868.4(CPA1):c.696+27del | not provided [RCV001687080] | benign | 7 | 130383817 | 130383817 | Human | | name |
| 150496207 | CV1272824 | single nucleotide variant | NM_001868.4(CPA1):c.484-53A>G | not provided [RCV001688747] | benign | 7 | 130383338 | 130383338 | Human | | name |
| 150536161 | CV1309157 | single nucleotide variant | NM_001868.4(CPA1):c.65+174C>T | not provided [RCV001759364] | likely benign | 7 | 130380759 | 130380759 | Human | | name |
| 151759780 | CV1343124 | single nucleotide variant | NM_001868.4(CPA1):c.987+12C>A | not provided [RCV002024225] | likely benign | 7 | 130385357 | 130385357 | Human | | name |
| 151816511 | CV1344573 | single nucleotide variant | NM_001868.4(CPA1):c.484-20C>G | not provided [RCV001919137] | likely benign|uncertain significance | 7 | 130383371 | 130383371 | Human | | name |
| 152077657 | CV1531356 | single nucleotide variant | NM_001868.4(CPA1):c.696+14C>A | not provided [RCV002210809] | likely benign | 7 | 130383808 | 130383808 | Human | | name |
| 152069718 | CV1535466 | single nucleotide variant | NM_001868.4(CPA1):c.484-18C>A | not provided [RCV002091418] | likely benign | 7 | 130383373 | 130383373 | Human | | name |
| 152109215 | CV1556483 | single nucleotide variant | NM_001868.4(CPA1):c.484-20C>A | not provided [RCV002096615] | likely benign | 7 | 130383371 | 130383371 | Human | | name |
| 152089366 | CV1580648 | single nucleotide variant | NM_001868.4(CPA1):c.586-20C>T | not provided [RCV002093955] | likely benign | 7 | 130383664 | 130383664 | Human | | name |
| 152037493 | CV1596288 | single nucleotide variant | NM_001868.4(CPA1):c.586-15C>G | not provided [RCV002125584] | benign | 7 | 130383669 | 130383669 | Human | | name |
| 152082845 | CV1623630 | deletion | NM_001868.4(CPA1):c.148-11del | not provided [RCV002149540] | benign | 7 | 130381619 | 130381619 | Human | | name |
| 152155842 | CV1629613 | single nucleotide variant | NM_001868.4(CPA1):c.381+18G>A | not provided [RCV002202634] | likely benign | 7 | 130381881 | 130381881 | Human | | name |
| 156446273 | CV1951309 | single nucleotide variant | NM_001868.4(CPA1):c.697-20G>C | not provided [RCV003117244] | likely benign | 7 | 130384516 | 130384516 | Human | | name |
| 155937725 | CV2125832 | single nucleotide variant | NM_001868.4(CPA1):c.1073-6C>A | not provided [RCV002971068] | likely benign|uncertain significance | 7 | 130387818 | 130387818 | Human | | name |
| 405136316 | CV2906896 | single nucleotide variant | NM_001868.4(CPA1):c.788-11T>C | not provided [RCV003560431] | likely benign | 7 | 130385135 | 130385135 | Human | | name |
| 405208719 | CV2909386 | single nucleotide variant | NM_001868.4(CPA1):c.1073-1G>A | not provided [RCV003566851] | uncertain significance | 7 | 130387823 | 130387823 | Human | | name |
| 405222840 | CV2976290 | single nucleotide variant | NM_001868.4(CPA1):c.788-10C>A | not provided [RCV003680890] | likely benign | 7 | 130385136 | 130385136 | Human | | name |
| 405225612 | CV3058221 | single nucleotide variant | NM_001868.4(CPA1):c.987+16G>A | not provided [RCV003733850] | likely benign | 7 | 130385361 | 130385361 | Human | | name |
| 405224768 | CV3058229 | single nucleotide variant | NM_001868.4(CPA1):c.787+20G>C | not provided [RCV003733854] | likely benign | 7 | 130384646 | 130384646 | Human | | name |
| 405223374 | CV3061283 | single nucleotide variant | NM_001868.4(CPA1):c.148-18G>T | not provided [RCV003733655] | uncertain significance | 7 | 130381612 | 130381612 | Human | | name |
| 405223561 | CV3061348 | single nucleotide variant | NM_001868.4(CPA1):c.148-18G>A | not provided [RCV003733683] | uncertain significance | 7 | 130381612 | 130381612 | Human | | name |
| 405224539 | CV3061474 | single nucleotide variant | NM_001868.4(CPA1):c.987+14T>C | not provided [RCV003733731] | likely benign | 7 | 130385359 | 130385359 | Human | | name |
| 405226811 | CV3068387 | single nucleotide variant | NM_001868.4(CPA1):c.381+20C>T | not provided [RCV003733989] | likely benign | 7 | 130381883 | 130381883 | Human | | name |
| 405086657 | CV3137690 | single nucleotide variant | NM_001868.4(CPA1):c.585+10G>T | not provided [RCV003834399] | likely benign | 7 | 130383502 | 130383502 | Human | | name |
| 405234681 | CV3155568 | single nucleotide variant | NM_001868.4(CPA1):c.381+11C>T | not provided [RCV003853546] | likely benign | 7 | 130381874 | 130381874 | Human | | name |
| 597936793 | CV3774575 | single nucleotide variant | NM_001868.4(CPA1):c.988-14G>C | not provided [RCV005117608] | likely benign | 7 | 130385825 | 130385825 | Human | | name |
| 597948983 | CV3848794 | single nucleotide variant | NM_001868.4(CPA1):c.987+15C>T | not provided [RCV005189731] | likely benign | 7 | 130385360 | 130385360 | Human | | name |
| 597957651 | CV3848912 | single nucleotide variant | NM_001868.4(CPA1):c.787+17C>G | not provided [RCV005191913] | likely benign | 7 | 130384643 | 130384643 | Human | | name |
| 597949398 | CV3852553 | single nucleotide variant | NM_001868.4(CPA1):c.148-11G>C | not provided [RCV005189631] | likely benign | 7 | 130381619 | 130381619 | Human | | name |
| 597869034 | CV3858328 | single nucleotide variant | NM_001868.4(CPA1):c.1073-1G>T | not provided [RCV005197071] | uncertain significance | 7 | 130387823 | 130387823 | Human | | name |
| 25329172 | CV815378 | single nucleotide variant | NM_001868.4(CPA1):c.1072+1G>T | Hereditary pancreatitis [RCV002320219] | uncertain significance | 7 | 130385924 | 130385924 | Human | 1 | name |
| 26919955 | CV852066 | single nucleotide variant | NM_001868.4(CPA1):c.988-10T>A | not provided [RCV001046727] | likely benign|uncertain significance | 7 | 130385829 | 130385829 | Human | | name |
| 127266241 | CV1096075 | single nucleotide variant | NM_001868.4(CPA1):c.1072+10C>T | not provided [RCV001429349] | likely benign | 7 | 130385933 | 130385933 | Human | | name |
| 150333498 | CV1169222 | single nucleotide variant | NM_001868.4(CPA1):c.148-140C>T | not provided [RCV001537366] | benign | 7 | 130381490 | 130381490 | Human | | name |
| 150499143 | CV1224539 | single nucleotide variant | NM_001868.4(CPA1):c.1073-32A>G | not provided [RCV001620370] | benign | 7 | 130387792 | 130387792 | Human | | name |
| 150458575 | CV1235950 | single nucleotide variant | NM_001868.4(CPA1):c.697-260C>G | not provided [RCV001648920] | benign | 7 | 130384276 | 130384276 | Human | | name |
| 150446641 | CV1261393 | single nucleotide variant | NM_001868.4(CPA1):c.787+234G>C | not provided [RCV001680067] | benign | 7 | 130384860 | 130384860 | Human | | name |
| 150445005 | CV1269365 | single nucleotide variant | NM_001868.4(CPA1):c.987+182G>C | not provided [RCV001691052] | benign | 7 | 130385527 | 130385527 | Human | 1 | name |
| 150445005 | CV1269365 | single nucleotide variant | NM_001868.4(CPA1):c.987+182G>C | not provided [RCV001691052] | benign | 7 | 130385527 | 130385528 | Human | 1 | name |
| 152061974 | CV1594875 | single nucleotide variant | NM_001868.4(CPA1):c.1072+18C>T | not provided [RCV002190632] | likely benign | 7 | 130385941 | 130385941 | Human | | name |
| 152157041 | CV1629792 | single nucleotide variant | NM_001868.4(CPA1):c.1073-11T>C | not provided [RCV002202775] | likely benign | 7 | 130387813 | 130387813 | Human | | name |
| 152120805 | CV1662069 | single nucleotide variant | NM_001868.4(CPA1):c.1072+16G>C | not provided [RCV002117826] | benign|likely benign | 7 | 130385939 | 130385939 | Human | | name |
| 153001884 | CV1685089 | single nucleotide variant | NM_001868.4(CPA1):c.1073-10C>T | Hereditary pancreatitis [RCV002257295] | uncertain significance | 7 | 130387814 | 130387814 | Human | 1 | name |
| 405225123 | CV3058202 | single nucleotide variant | NM_001868.4(CPA1):c.1072+11G>A | not provided [RCV003733846] | likely benign | 7 | 130385934 | 130385934 | Human | | name |
| 150484854 | CV1250109 | single nucleotide variant | NM_001868.4(CPA1):c.1072+131A>G | not provided [RCV001673722] | benign | 7 | 130386054 | 130386054 | Human | 2 | name |
| 150484854 | CV1250109 | single nucleotide variant | NM_001868.4(CPA1):c.1072+131A>G | not provided [RCV001673722] | benign | 7 | 130386054 | 130386055 | Human | 2 | name |
| 150461013 | CV1264254 | single nucleotide variant | NM_001868.4(CPA1):c.1072+289G>C | not provided [RCV001682171] | benign | 7 | 130386212 | 130386212 | Human | | name |
| 155731288 | CV1825928 | single nucleotide variant | NM_001868.4(CPA1):c.9G>A (p.Gly3=) | Hereditary pancreatitis [RCV002383145] | likely benign | 7 | 130380529 | 130380529 | Human | 1 | name |
| 155731351 | CV1825941 | single nucleotide variant | NM_001868.4(CPA1):c.9G>T (p.Gly3=) | Hereditary pancreatitis [RCV002383158]|not provided [RCV003718581] | likely benign | 7 | 130380529 | 130380529 | Human | 1 | name |
| 155719504 | CV1837378 | single nucleotide variant | NM_001868.4(CPA1):c.15G>A (p.Leu5=) | Hereditary pancreatitis [RCV002398665]|not provided [RCV005097626] | likely benign|uncertain significance | 7 | 130380535 | 130380535 | Human | 1 | name |
| 155747714 | CV1849722 | single nucleotide variant | NM_001868.4(CPA1):c.19T>C (p.Leu7=) | Hereditary pancreatitis [RCV002417100] | likely benign | 7 | 130380539 | 130380539 | Human | 1 | name |
| 405167770 | CV2950950 | single nucleotide variant | NM_001868.4(CPA1):c.12G>A (p.Leu4=) | not provided [RCV003675170] | likely benign | 7 | 130380532 | 130380532 | Human | | name |
| 597630488 | CV3650906 | single nucleotide variant | NM_001868.4(CPA1):c.27C>G (p.Val9=) | Hereditary pancreatitis [RCV004822685] | likely benign | 7 | 130380547 | 130380547 | Human | 1 | name |
| 150514238 | CV1228123 | duplication | NM_001868.4(CPA1):c.697-64_697-63dup | not provided [RCV001638401] | benign | 7 | 130384467 | 130384468 | Human | | name |
| 151852900 | CV1376173 | single nucleotide variant | NM_001868.4(CPA1):c.93C>T (p.Ala31=) | Hereditary pancreatitis [RCV002370686]|not provided [RCV001996189] | likely benign | 7 | 130381125 | 130381125 | Human | 1 | name |
| 152142365 | CV1526660 | single nucleotide variant | NM_001868.4(CPA1):c.93C>G (p.Ala31=) | Hereditary pancreatitis [RCV002372965]|not provided [RCV002084331] | likely benign | 7 | 130381125 | 130381125 | Human | 1 | name |
| 152164512 | CV1557652 | single nucleotide variant | NM_001868.4(CPA1):c.75G>C (p.Val25=) | Hereditary pancreatitis [RCV002391265]|not provided [RCV002141536] | likely benign | 7 | 130381107 | 130381107 | Human | 1 | name |
| 152099522 | CV1595589 | single nucleotide variant | NM_001868.4(CPA1):c.36G>A (p.Gly12=) | Hereditary pancreatitis [RCV002352953]|not provided [RCV002213815] | likely benign | 7 | 130380556 | 130380556 | Human | 1 | name |
| 152098654 | CV1611758 | deletion | NM_001868.4(CPA1):c.148-13_148-12del | not provided [RCV002172806] | likely benign | 7 | 130381617 | 130381618 | Human | | name |
| 155716114 | CV1785096 | single nucleotide variant | NM_001868.4(CPA1):c.30G>A (p.Leu10=) | Hereditary pancreatitis [RCV002325956] | likely benign | 7 | 130380550 | 130380550 | Human | 1 | name |
| 155716142 | CV1785104 | single nucleotide variant | NM_001868.4(CPA1):c.30G>C (p.Leu10=) | Hereditary pancreatitis [RCV002325964] | likely benign | 7 | 130380550 | 130380550 | Human | 1 | name |
| 155702337 | CV1788433 | single nucleotide variant | NM_001868.4(CPA1):c.31T>C (p.Leu11=) | Hereditary pancreatitis [RCV002322966]|not provided [RCV003099286] | likely benign | 7 | 130380551 | 130380551 | Human | 1 | name |
| 155735050 | CV1797886 | single nucleotide variant | NM_001868.4(CPA1):c.42C>A (p.Val14=) | Hereditary pancreatitis [RCV002330292] | likely benign | 7 | 130380562 | 130380562 | Human | 1 | name |
| 155738415 | CV1797894 | single nucleotide variant | NM_001868.4(CPA1):c.42C>T (p.Val14=) | Hereditary pancreatitis [RCV002331862] | likely benign | 7 | 130380562 | 130380562 | Human | 1 | name |
| 155704293 | CV1810663 | single nucleotide variant | NM_001868.4(CPA1):c.57C>T (p.Asp19=) | Hereditary pancreatitis [RCV002359852] | likely benign | 7 | 130380577 | 130380577 | Human | 1 | name |
| 155705559 | CV1811244 | single nucleotide variant | NM_001868.4(CPA1):c.60T>C (p.Phe20=) | Hereditary pancreatitis [RCV002360171] | likely benign | 7 | 130380580 | 130380580 | Human | 1 | name |
| 155699069 | CV1813336 | single nucleotide variant | NM_001868.4(CPA1):c.75G>A (p.Val25=) | Hereditary pancreatitis [RCV002394235] | likely benign | 7 | 130381107 | 130381107 | Human | 1 | name |
| 155665620 | CV1813874 | single nucleotide variant | NM_001868.4(CPA1):c.79C>A (p.Arg27=) | Hereditary pancreatitis [RCV002419140] | likely benign | 7 | 130381111 | 130381111 | Human | 1 | name |
| 155702476 | CV1825344 | single nucleotide variant | NM_001868.4(CPA1):c.96T>C (p.Asp32=) | Hereditary pancreatitis [RCV002376666] | likely benign | 7 | 130381128 | 130381128 | Human | 1 | name |
| 329364212 | CV2425548 | single nucleotide variant | NM_001868.4(CPA1):c.84C>A (p.Ile28=) | Hereditary pancreatitis [RCV003181580] | likely benign | 7 | 130381116 | 130381116 | Human | 1 | name |
| 401885439 | CV2783296 | single nucleotide variant | NM_001868.4(CPA1):c.8G>T (p.Gly3Val) | Hereditary pancreatitis [RCV003386798] | uncertain significance | 7 | 130380528 | 130380528 | Human | 1 | name |
| 401868442 | CV2787430 | single nucleotide variant | NM_001868.4(CPA1):c.63G>A (p.Val21=) | Hereditary pancreatitis [RCV003380206] | likely benign | 7 | 130380583 | 130380583 | Human | 1 | name |
| 405137449 | CV2907186 | single nucleotide variant | NM_001868.4(CPA1):c.3G>T (p.Met1Ile) | not provided [RCV003560564] | uncertain significance | 7 | 130380523 | 130380523 | Human | | name |
| 405655653 | CV3380138 | single nucleotide variant | NM_001868.4(CPA1):c.51G>A (p.Lys17=) | Hereditary pancreatitis [RCV004511150] | likely benign | 7 | 130380571 | 130380571 | Human | 1 | name |
| 405655683 | CV3380157 | single nucleotide variant | NM_001868.4(CPA1):c.69T>C (p.His23=) | Hereditary pancreatitis [RCV004511169] | likely benign | 7 | 130381101 | 130381101 | Human | 1 | name |
| 405655690 | CV3380161 | single nucleotide variant | NM_001868.4(CPA1):c.84C>T (p.Ile28=) | Hereditary pancreatitis [RCV004511173] | likely benign | 7 | 130381116 | 130381116 | Human | 1 | name |
| 405655704 | CV3380170 | single nucleotide variant | NM_001868.4(CPA1):c.99G>A (p.Glu33=) | Hereditary pancreatitis [RCV004511182] | likely benign | 7 | 130381131 | 130381131 | Human | 1 | name |
| 407456886 | CV3419512 | single nucleotide variant | NM_001868.4(CPA1):c.5G>C (p.Arg2Pro) | Hereditary pancreatitis [RCV004610906] | uncertain significance | 7 | 130380525 | 130380525 | Human | 1 | name |
| 597630481 | CV3650903 | single nucleotide variant | NM_001868.4(CPA1):c.63G>C (p.Val21=) | Hereditary pancreatitis [RCV004822682] | likely benign | 7 | 130380583 | 130380583 | Human | 1 | name |
| 597630367 | CV3654353 | single nucleotide variant | NM_001868.4(CPA1):c.45T>C (p.Phe15=) | Hereditary pancreatitis [RCV004822630] | likely benign | 7 | 130380565 | 130380565 | Human | 1 | name |
| 598235047 | CV3945106 | single nucleotide variant | NM_001868.4(CPA1):c.54G>A (p.Glu18=) | Hereditary pancreatitis [RCV005320172] | likely benign | 7 | 130380574 | 130380574 | Human | 1 | name |
| 25329589 | CV808946 | single nucleotide variant | NM_001868.4(CPA1):c.2T>C (p.Met1Thr) | Hereditary pancreatitis [RCV002346217]|not provided [RCV002549469] | likely benign|uncertain significance | 7 | 130380522 | 130380522 | Human | 1 | name |
| 25324410 | CV808947 | single nucleotide variant | NM_001868.4(CPA1):c.5G>A (p.Arg2Gln) | CPA1-related disorder [RCV003918646]|Hereditary pancreatitis [RCV002346226]|not provided [RCV001475985] | benign|likely benign | 7 | 130380525 | 130380525 | Human | 1 | name , trait , alternate_id |
| 126743901 | CV992097 | single nucleotide variant | NM_001868.4(CPA1):c.4C>T (p.Arg2Trp) | Hereditary pancreatitis [RCV002339720]|not provided [RCV001296259] | uncertain significance | 7 | 130380524 | 130380524 | Human | 1 | name |
| 127249459 | CV1074435 | single nucleotide variant | NM_001868.4(CPA1):c.273G>A (p.Glu91=) | Hereditary pancreatitis [RCV002438916]|not provided [RCV001399603] | likely benign | 7 | 130381755 | 130381755 | Human | 1 | name |
| 127248433 | CV1096072 | single nucleotide variant | NM_001868.4(CPA1):c.201G>T (p.Val67=) | Hereditary pancreatitis [RCV002420953]|not provided [RCV001424927] | likely benign|uncertain significance | 7 | 130381683 | 130381683 | Human | 1 | name |
| 127316401 | CV1117592 | single nucleotide variant | NM_001868.4(CPA1):c.276C>T (p.Asp92=) | Hereditary pancreatitis [RCV002439103]|not provided [RCV001465530] | likely benign | 7 | 130381758 | 130381758 | Human | 1 | name |
| 151893327 | CV1338109 | single nucleotide variant | NM_001868.4(CPA1):c.23G>T (p.Ser8Ile) | Hereditary pancreatitis [RCV002449500]|not provided [RCV001944924] | uncertain significance | 7 | 130380543 | 130380543 | Human | 1 | name |
| 152051335 | CV1527952 | single nucleotide variant | NM_001868.4(CPA1):c.222G>T (p.Ala74=) | Hereditary pancreatitis [RCV002416464]|not provided [RCV002089197] | likely benign | 7 | 130381704 | 130381704 | Human | 1 | name |
| 152165617 | CV1543822 | single nucleotide variant | NM_001868.4(CPA1):c.291G>A (p.Leu97=) | Hereditary pancreatitis [RCV002434554]|not provided [RCV002124051] | likely benign | 7 | 130381773 | 130381773 | Human | 1 | name |
| 152145486 | CV1553787 | single nucleotide variant | NM_001868.4(CPA1):c.204C>T (p.Pro68=) | Hereditary pancreatitis [RCV002416493]|not provided [RCV002138746] | likely benign | 7 | 130381686 | 130381686 | Human | 1 | name |
| 152154526 | CV1560799 | single nucleotide variant | NM_001868.4(CPA1):c.160C>A (p.Arg54=) | Hereditary pancreatitis [RCV002391229]|not provided [RCV002102742] | likely benign | 7 | 130381642 | 130381642 | Human | 1 | name |
| 152092173 | CV1602979 | single nucleotide variant | NM_001868.4(CPA1):c.165G>A (p.Gly55=) | Hereditary pancreatitis [RCV002391356]|not provided [RCV002194440] | likely benign | 7 | 130381647 | 130381647 | Human | 1 | name |
| 152032832 | CV1643191 | single nucleotide variant | NM_001868.4(CPA1):c.141C>T (p.His47=) | Hereditary pancreatitis [RCV002391186]|not provided [RCV002205055] | likely benign | 7 | 130381173 | 130381173 | Human | 1 | name |
| 155681248 | CV1812813 | single nucleotide variant | NM_001868.4(CPA1):c.123G>A (p.Glu41=) | Hereditary pancreatitis [RCV002371126] | likely benign | 7 | 130381155 | 130381155 | Human | 1 | name |
| 155665833 | CV1823552 | duplication | NM_001868.4(CPA1):c.8_9dup (p.Leu4fs) | Hereditary pancreatitis [RCV002419183]|not provided [RCV003776471] | likely benign|uncertain significance | 7 | 130380524 | 130380525 | Human | 1 | name |
| 155704496 | CV1827961 | single nucleotide variant | NM_001868.4(CPA1):c.165G>T (p.Gly55=) | Hereditary pancreatitis [RCV002395089] | likely benign | 7 | 130381647 | 130381647 | Human | 1 | name |
| 155700457 | CV1836745 | single nucleotide variant | NM_001868.4(CPA1):c.144G>A (p.Leu48=) | Hereditary pancreatitis [RCV002394558] | likely benign | 7 | 130381176 | 130381176 | Human | 1 | name |
| 155700491 | CV1836753 | single nucleotide variant | NM_001868.4(CPA1):c.144G>C (p.Leu48=) | Hereditary pancreatitis [RCV002394566] | likely benign | 7 | 130381176 | 130381176 | Human | 1 | name |
| 155746185 | CV1838993 | single nucleotide variant | NM_001868.4(CPA1):c.186C>T (p.Pro62=) | Hereditary pancreatitis [RCV002415064] | likely benign | 7 | 130381668 | 130381668 | Human | 1 | name |
| 155743352 | CV1839377 | single nucleotide variant | NM_001868.4(CPA1):c.183C>G (p.Ser61=) | Hereditary pancreatitis [RCV002412796] | likely benign | 7 | 130381665 | 130381665 | Human | 1 | name |
| 155713960 | CV1841761 | single nucleotide variant | NM_001868.4(CPA1):c.249C>T (p.Gly83=) | Hereditary pancreatitis [RCV002431041] | likely benign | 7 | 130381731 | 130381731 | Human | 1 | name |
| 155693576 | CV1842201 | single nucleotide variant | NM_001868.4(CPA1):c.261G>A (p.Glu87=) | Hereditary pancreatitis [RCV002426390] | likely benign | 7 | 130381743 | 130381743 | Human | 1 | name |
| 155709541 | CV1843915 | single nucleotide variant | NM_001868.4(CPA1):c.213C>T (p.Ser71=) | Hereditary pancreatitis [RCV002430510] | likely benign | 7 | 130381695 | 130381695 | Human | 1 | name |
| 155717202 | CV1844875 | single nucleotide variant | NM_001868.4(CPA1):c.235C>T (p.Leu79=) | Hereditary pancreatitis [RCV002448515] | likely benign | 7 | 130381717 | 130381717 | Human | 1 | name |
| 155711698 | CV1845181 | single nucleotide variant | NM_001868.4(CPA1):c.246C>T (p.His82=) | Hereditary pancreatitis [RCV002430775] | likely benign | 7 | 130381728 | 130381728 | Human | 1 | name |
| 155699379 | CV1847524 | single nucleotide variant | NM_001868.4(CPA1):c.222G>A (p.Ala74=) | Hereditary pancreatitis [RCV002428227] | likely benign | 7 | 130381704 | 130381704 | Human | 1 | name |
| 155694530 | CV1848114 | single nucleotide variant | NM_001868.4(CPA1):c.243C>T (p.Ser81=) | Hereditary pancreatitis [RCV002460002] | likely benign | 7 | 130381725 | 130381725 | Human | 1 | name |
| 155674951 | CV1855857 | single nucleotide variant | NM_001868.4(CPA1):c.288G>C (p.Leu96=) | Hereditary pancreatitis [RCV002437908] | likely benign | 7 | 130381770 | 130381770 | Human | 1 | name |
| 156227638 | CV2176538 | single nucleotide variant | NM_001868.4(CPA1):c.204C>G (p.Pro68=) | not provided [RCV003059183] | likely benign | 7 | 130381686 | 130381686 | Human | | name |
| 329364205 | CV2425540 | single nucleotide variant | NM_001868.4(CPA1):c.17T>C (p.Val6Ala) | Hereditary pancreatitis [RCV003181573] | uncertain significance | 7 | 130380537 | 130380537 | Human | 1 | name |
| 329364215 | CV2425551 | single nucleotide variant | NM_001868.4(CPA1):c.196C>A (p.Arg66=) | Hereditary pancreatitis [RCV003181582] | likely benign | 7 | 130381678 | 130381678 | Human | 1 | name |
| 329389912 | CV2465595 | single nucleotide variant | NM_001868.4(CPA1):c.297G>A (p.Glu99=) | Hereditary pancreatitis [RCV003216500]|not provided [RCV005061115] | likely benign | 7 | 130381779 | 130381779 | Human | 1 | name |
| 329389904 | CV2465602 | single nucleotide variant | NM_001868.4(CPA1):c.14T>C (p.Leu5Pro) | Hereditary pancreatitis [RCV003216507] | uncertain significance | 7 | 130380534 | 130380534 | Human | 1 | name |
| 11543296 | CV252615 | single nucleotide variant | NM_001868.4(CPA1):c.165G>C (p.Gly55=) | Hereditary pancreatitis [RCV002318975]|not provided [RCV001511899]|not specified [RCV000242274] | benign | 7 | 130381647 | 130381647 | Human | 3 | name |
| 401775062 | CV2723968 | single nucleotide variant | NM_001868.4(CPA1):c.285G>A (p.Ser95=) | Hereditary pancreatitis [RCV003305488] | likely benign | 7 | 130381767 | 130381767 | Human | 1 | name |
| 401885646 | CV2783259 | single nucleotide variant | NM_001868.4(CPA1):c.120G>A (p.Lys40=) | Hereditary pancreatitis [RCV003386761] | likely benign | 7 | 130381152 | 130381152 | Human | 1 | name |
| 401884966 | CV2786633 | single nucleotide variant | NM_001868.4(CPA1):c.102C>T (p.Ala34=) | Hereditary pancreatitis [RCV003386627] | likely benign | 7 | 130381134 | 130381134 | Human | 1 | name |
| 401885096 | CV2786673 | single nucleotide variant | NM_001868.4(CPA1):c.216C>A (p.Ile72=) | Hereditary pancreatitis [RCV003386667] | likely benign | 7 | 130381698 | 130381698 | Human | 1 | name |
| 405655636 | CV3380127 | single nucleotide variant | NM_001868.4(CPA1):c.294C>T (p.Asp98=) | Hereditary pancreatitis [RCV004511139] | likely benign | 7 | 130381776 | 130381776 | Human | 1 | name |
| 405655605 | CV3383119 | single nucleotide variant | NM_001868.4(CPA1):c.10T>A (p.Leu4Met) | Hereditary pancreatitis [RCV004511120] | uncertain significance | 7 | 130380530 | 130380530 | Human | 1 | name |
| 405655628 | CV3383133 | single nucleotide variant | NM_001868.4(CPA1):c.126G>A (p.Leu42=) | Hereditary pancreatitis [RCV004511134] | likely benign | 7 | 130381158 | 130381158 | Human | 1 | name |
| 405655630 | CV3383134 | single nucleotide variant | NM_001868.4(CPA1):c.156C>T (p.Phe52=) | Hereditary pancreatitis [RCV004511135] | likely benign | 7 | 130381638 | 130381638 | Human | 1 | name |
| 407456889 | CV3419514 | single nucleotide variant | NM_001868.4(CPA1):c.279G>A (p.Val93=) | Hereditary pancreatitis [RCV004610908] | likely benign | 7 | 130381761 | 130381761 | Human | 1 | name |
| 407456895 | CV3419518 | single nucleotide variant | NM_001868.4(CPA1):c.270C>T (p.Ile90=) | Hereditary pancreatitis [RCV004610912] | likely benign | 7 | 130381752 | 130381752 | Human | 1 | name |
| 597630490 | CV3650907 | single nucleotide variant | NM_001868.4(CPA1):c.243C>G (p.Ser81=) | Hereditary pancreatitis [RCV004822686] | likely benign | 7 | 130381725 | 130381725 | Human | 1 | name |
| 597630399 | CV3654369 | single nucleotide variant | NM_001868.4(CPA1):c.148C>T (p.Leu50=) | Hereditary pancreatitis [RCV004822645] | likely benign | 7 | 130381630 | 130381630 | Human | 1 | name |
| 597630409 | CV3654373 | single nucleotide variant | NM_001868.4(CPA1):c.282G>A (p.Gln94=) | Hereditary pancreatitis [RCV004822649] | likely benign | 7 | 130381764 | 130381764 | Human | 1 | name |
| 597630427 | CV3654382 | single nucleotide variant | NM_001868.4(CPA1):c.171C>T (p.Ala57=) | Hereditary pancreatitis [RCV004822657] | likely benign | 7 | 130381653 | 130381653 | Human | 1 | name |
| 597630429 | CV3654383 | single nucleotide variant | NM_001868.4(CPA1):c.16G>C (p.Val6Leu) | Hereditary pancreatitis [RCV004822658] | uncertain significance | 7 | 130380536 | 130380536 | Human | 1 | name |
| 598235057 | CV3945109 | single nucleotide variant | NM_001868.4(CPA1):c.11T>G (p.Leu4Trp) | Hereditary pancreatitis [RCV005320176] | uncertain significance | 7 | 130380531 | 130380531 | Human | 1 | name |
| 598235109 | CV3945124 | single nucleotide variant | NM_001868.4(CPA1):c.288G>A (p.Leu96=) | Hereditary pancreatitis [RCV005320191] | likely benign | 7 | 130381770 | 130381770 | Human | 1 | name |
| 598235127 | CV3945128 | single nucleotide variant | NM_001868.4(CPA1):c.195C>T (p.Val65=) | Hereditary pancreatitis [RCV005320195] | likely benign | 7 | 130381677 | 130381677 | Human | 1 | name |
| 126748221 | CV1027785 | single nucleotide variant | NM_001868.4(CPA1):c.696G>A (p.Thr232=) | Hereditary pancreatitis [RCV002377496]|not provided [RCV001351821] | uncertain significance | 7 | 130383794 | 130383794 | Human | 1 | name |
| 126922771 | CV1044695 | single nucleotide variant | NM_001868.4(CPA1):c.86C>G (p.Ser29Cys) | Hereditary pancreatitis [RCV002447470]|not provided [RCV001365061] | uncertain significance | 7 | 130381118 | 130381118 | Human | 1 | name |
| 127268345 | CV1074439 | single nucleotide variant | NM_001868.4(CPA1):c.828C>T (p.His276=) | Hereditary pancreatitis [RCV002432114]|not provided [RCV001404365] | likely benign | 7 | 130385186 | 130385186 | Human | 1 | name |
| 127236633 | CV1096073 | single nucleotide variant | NM_001868.4(CPA1):c.582G>A (p.Lys194=) | Hereditary pancreatitis [RCV002358971]|not provided [RCV001433382] | likely benign | 7 | 130383489 | 130383489 | Human | 1 | name |
| 127278514 | CV1096074 | single nucleotide variant | NM_001868.4(CPA1):c.606G>A (p.Gln202=) | not provided [RCV001445118] | likely benign | 7 | 130383704 | 130383704 | Human | | name |
| 127328986 | CV1117593 | single nucleotide variant | NM_001868.4(CPA1):c.522C>T (p.Ile174=) | Hereditary pancreatitis [RCV002342057]|not provided [RCV001469919] | likely benign | 7 | 130383429 | 130383429 | Human | 1 | name |
| 127292659 | CV1117594 | single nucleotide variant | NM_001868.4(CPA1):c.792C>G (p.Ser264=) | Hereditary pancreatitis [RCV002421020]|not provided [RCV001451803] | likely benign | 7 | 130385150 | 130385150 | Human | 1 | name |
| 127291621 | CV1117595 | single nucleotide variant | NM_001868.4(CPA1):c.834G>A (p.Lys278=) | Hereditary pancreatitis [RCV002439139]|not provided [RCV001476134] | likely benign | 7 | 130385192 | 130385192 | Human | 1 | name |
| 127291787 | CV1117596 | single nucleotide variant | NM_001868.4(CPA1):c.861G>A (p.Lys287=) | Hereditary pancreatitis [RCV002449263]|not provided [RCV001476168] | likely benign | 7 | 130385219 | 130385219 | Human | 1 | name |
| 127320085 | CV1138524 | single nucleotide variant | NM_001868.4(CPA1):c.657C>T (p.Ile219=) | Hereditary pancreatitis [RCV002377881]|not provided [RCV001504292] | likely benign | 7 | 130383755 | 130383755 | Human | 1 | name |
| 127302970 | CV1138525 | single nucleotide variant | NM_001868.4(CPA1):c.825C>T (p.Tyr275=) | CPA1-related disorder [RCV003980405]|Hereditary pancreatitis [RCV002432342]|not provided [RCV001479108] | likely benign | 7 | 130385183 | 130385183 | Human | 1 | name , trait , alternate_id |
| 151736012 | CV1351268 | single nucleotide variant | NM_001868.4(CPA1):c.80G>A (p.Arg27Gln) | Hereditary pancreatitis [RCV002423129]|not provided [RCV002021822] | uncertain significance | 7 | 130381112 | 130381112 | Human | 1 | name |
| 151866017 | CV1354645 | single nucleotide variant | NM_001868.4(CPA1):c.71A>T (p.Gln24Leu) | not provided [RCV001924612] | uncertain significance | 7 | 130381103 | 130381103 | Human | | name |
| 151886020 | CV1367201 | single nucleotide variant | NM_001868.4(CPA1):c.52G>A (p.Glu18Lys) | not provided [RCV002000603] | uncertain significance | 7 | 130380572 | 130380572 | Human | | name |
| 151843935 | CV1457698 | single nucleotide variant | NM_001868.4(CPA1):c.40G>C (p.Val14Leu) | Hereditary pancreatitis [RCV002324351]|not provided [RCV001936456] | likely benign|uncertain significance | 7 | 130380560 | 130380560 | Human | 1 | name |
| 151716982 | CV1465069 | single nucleotide variant | NM_001868.4(CPA1):c.55G>T (p.Asp19Tyr) | not provided [RCV002003073] | uncertain significance | 7 | 130380575 | 130380575 | Human | | name |
| 152042097 | CV1553684 | single nucleotide variant | NM_001868.4(CPA1):c.894C>T (p.Asn298=) | Hereditary pancreatitis [RCV002372888]|not provided [RCV002088096] | likely benign | 7 | 130385252 | 130385252 | Human | 1 | name |
| 152128004 | CV1554308 | single nucleotide variant | NM_001868.4(CPA1):c.774C>T (p.Asp258=) | Hereditary pancreatitis [RCV002255733]|not provided [RCV002176421] | likely benign | 7 | 130384613 | 130384613 | Human | 1 | name |
| 152046881 | CV1561516 | single nucleotide variant | NM_001868.4(CPA1):c.546G>A (p.Glu182=) | Hereditary pancreatitis [RCV002346479]|not provided [RCV002108444] | likely benign | 7 | 130383453 | 130383453 | Human | 1 | name |
| 152116243 | CV1566843 | single nucleotide variant | NM_001868.4(CPA1):c.759C>G (p.Pro253=) | Hereditary pancreatitis [RCV002391226]|not provided [RCV002097527] | likely benign | 7 | 130384598 | 130384598 | Human | 1 | name |
| 152170421 | CV1567614 | single nucleotide variant | NM_001868.4(CPA1):c.633C>T (p.Asp211=) | Hereditary pancreatitis [RCV002363631]|not provided [RCV002183144] | likely benign | 7 | 130383731 | 130383731 | Human | 1 | name |
| 152167531 | CV1577467 | single nucleotide variant | NM_001868.4(CPA1):c.345C>T (p.Asp115=) | Hereditary pancreatitis [RCV002454392]|not provided [RCV002204728] | likely benign | 7 | 130381827 | 130381827 | Human | 1 | name |
| 152168856 | CV1613966 | single nucleotide variant | NM_001868.4(CPA1):c.762C>T (p.Asn254=) | Hereditary pancreatitis [RCV002391335]|not provided [RCV002161256] | likely benign | 7 | 130384601 | 130384601 | Human | 1 | name |
| 152139873 | CV1628678 | single nucleotide variant | NM_001868.4(CPA1):c.792C>T (p.Ser264=) | Hereditary pancreatitis [RCV002416417]|not provided [RCV002100625] | likely benign | 7 | 130385150 | 130385150 | Human | 1 | name |
| 155715932 | CV1785048 | single nucleotide variant | NM_001868.4(CPA1):c.309G>A (p.Gln103=) | Hereditary pancreatitis [RCV002325908] | likely benign | 7 | 130381791 | 130381791 | Human | 1 | name |
| 155732255 | CV1785696 | single nucleotide variant | NM_001868.4(CPA1):c.336C>T (p.Arg112=) | Hereditary pancreatitis [RCV002451716] | likely benign | 7 | 130381818 | 130381818 | Human | 1 | name |
| 155664567 | CV1786960 | single nucleotide variant | NM_001868.4(CPA1):c.387T>C (p.Tyr129=) | Hereditary pancreatitis [RCV002366308] | likely benign | 7 | 130382113 | 130382113 | Human | 1 | name |
| 155704350 | CV1787578 | single nucleotide variant | NM_001868.4(CPA1):c.408G>A (p.Val136=) | Hereditary pancreatitis [RCV002323205] | likely benign | 7 | 130382134 | 130382134 | Human | 1 | name |
| 155701296 | CV1788265 | single nucleotide variant | NM_001868.4(CPA1):c.318C>G (p.Ala106=) | Hereditary pancreatitis [RCV002322833] | likely benign | 7 | 130381800 | 130381800 | Human | 1 | name |
| 155688595 | CV1788959 | single nucleotide variant | NM_001868.4(CPA1):c.348T>A (p.Thr116=) | Hereditary pancreatitis [RCV002459013] | likely benign | 7 | 130381830 | 130381830 | Human | 1 | name |
| 155664169 | CV1789783 | single nucleotide variant | NM_001868.4(CPA1):c.369C>T (p.His123=) | Hereditary pancreatitis [RCV002348875] | likely benign | 7 | 130381851 | 130381851 | Human | 1 | name |
| 155696231 | CV1790658 | single nucleotide variant | NM_001868.4(CPA1):c.405G>A (p.Leu135=) | Hereditary pancreatitis [RCV002321378] | likely benign | 7 | 130382131 | 130382131 | Human | 1 | name |
| 155721166 | CV1793386 | single nucleotide variant | NM_001868.4(CPA1):c.37G>A (p.Ala13Thr) | Hereditary pancreatitis [RCV002363957] | uncertain significance | 7 | 130380557 | 130380557 | Human | 1 | name |
| 155739902 | CV1794441 | single nucleotide variant | NM_001868.4(CPA1):c.435G>A (p.Lys145=) | Hereditary pancreatitis [RCV002332332] | likely benign | 7 | 130382161 | 130382161 | Human | 1 | name |
| 155710710 | CV1795078 | single nucleotide variant | NM_001868.4(CPA1):c.324G>C (p.Arg108=) | Hereditary pancreatitis [RCV002324879] | likely benign | 7 | 130381806 | 130381806 | Human | 1 | name |
| 155704346 | CV1795382 | single nucleotide variant | NM_001868.4(CPA1):c.327C>T (p.Ser109=) | Hereditary pancreatitis [RCV002445740] | likely benign | 7 | 130381809 | 130381809 | Human | 1 | name |
| 155664532 | CV1795424 | single nucleotide variant | NM_001868.4(CPA1):c.33G>T (p.Leu11Phe) | Hereditary pancreatitis [RCV002452059] | uncertain significance | 7 | 130380553 | 130380553 | Human | 1 | name |
| 155717521 | CV1795713 | single nucleotide variant | NM_001868.4(CPA1):c.342C>G (p.Thr114=) | Hereditary pancreatitis [RCV002337448]|not provided [RCV003718485] | likely benign | 7 | 130381824 | 130381824 | Human | 1 | name |
| 155682215 | CV1795719 | single nucleotide variant | NM_001868.4(CPA1):c.342C>T (p.Thr114=) | Hereditary pancreatitis [RCV002457008] | likely benign | 7 | 130381824 | 130381824 | Human | 1 | name |
| 155675777 | CV1795949 | single nucleotide variant | NM_001868.4(CPA1):c.357C>T (p.Tyr119=) | Hereditary pancreatitis [RCV002455074]|not provided [RCV003102397] | likely benign | 7 | 130381839 | 130381839 | Human | 1 | name |
| 155705594 | CV1797230 | single nucleotide variant | NM_001868.4(CPA1):c.411G>A (p.Ala137=) | Hereditary pancreatitis [RCV002323484]|not provided [RCV003560958] | likely benign | 7 | 130382137 | 130382137 | Human | 1 | name |
| 155735004 | CV1797866 | single nucleotide variant | NM_001868.4(CPA1):c.429C>T (p.Val143=) | Hereditary pancreatitis [RCV002330272] | likely benign | 7 | 130382155 | 130382155 | Human | 1 | name |
| 155735970 | CV1798450 | single nucleotide variant | NM_001868.4(CPA1):c.465T>C (p.Arg155=) | Hereditary pancreatitis [RCV002330486] | likely benign | 7 | 130382191 | 130382191 | Human | 1 | name |
| 155736275 | CV1798652 | single nucleotide variant | NM_001868.4(CPA1):c.468C>T (p.Pro156=) | Hereditary pancreatitis [RCV002330555] | likely benign | 7 | 130382194 | 130382194 | Human | 1 | name |
| 155734720 | CV1799084 | single nucleotide variant | NM_001868.4(CPA1):c.492G>C (p.Thr164=) | Hereditary pancreatitis [RCV002340760] | likely benign | 7 | 130383399 | 130383399 | Human | 1 | name |
| 155739582 | CV1799089 | single nucleotide variant | NM_001868.4(CPA1):c.492G>T (p.Thr164=) | Hereditary pancreatitis [RCV002342624] | likely benign | 7 | 130383399 | 130383399 | Human | 1 | name |
| 155668105 | CV1799843 | single nucleotide variant | NM_001868.4(CPA1):c.543G>A (p.Arg181=) | Hereditary pancreatitis [RCV002349597] | likely benign | 7 | 130383450 | 130383450 | Human | 1 | name |
| 155746576 | CV1800233 | single nucleotide variant | NM_001868.4(CPA1):c.570C>G (p.Val190=) | Hereditary pancreatitis [RCV002347604] | likely benign | 7 | 130383477 | 130383477 | Human | 1 | name |
| 155672442 | CV1801030 | single nucleotide variant | NM_001868.4(CPA1):c.627T>C (p.Ile209=) | Hereditary pancreatitis [RCV002368690] | likely benign | 7 | 130383725 | 130383725 | Human | 1 | name |
| 155673029 | CV1801212 | single nucleotide variant | NM_001868.4(CPA1):c.630C>G (p.Leu210=) | Hereditary pancreatitis [RCV002368828] | likely benign | 7 | 130383728 | 130383728 | Human | 1 | name |
| 155739353 | CV1801671 | single nucleotide variant | NM_001868.4(CPA1):c.462G>T (p.Gly154=) | Hereditary pancreatitis [RCV002342562] | likely benign | 7 | 130382188 | 130382188 | Human | 1 | name |
| 155740117 | CV1802245 | single nucleotide variant | NM_001868.4(CPA1):c.489C>T (p.Ser163=) | Hereditary pancreatitis [RCV002332395]|not provided [RCV003102649] | likely benign | 7 | 130383396 | 130383396 | Human | 1 | name |
| 155722526 | CV1802646 | single nucleotide variant | NM_001868.4(CPA1):c.513C>T (p.Ala171=) | Hereditary pancreatitis [RCV002338195]|not provided [RCV003776040] | likely benign | 7 | 130383420 | 130383420 | Human | 1 | name |
| 155666896 | CV1803106 | single nucleotide variant | NM_001868.4(CPA1):c.540C>T (p.Ser180=) | Hereditary pancreatitis [RCV002349407] | likely benign | 7 | 130383447 | 130383447 | Human | 1 | name |
| 155744107 | CV1803319 | single nucleotide variant | NM_001868.4(CPA1):c.564T>C (p.Ser188=) | Hereditary pancreatitis [RCV002345195] | likely benign | 7 | 130383471 | 130383471 | Human | 1 | name |
| 155746196 | CV1803466 | single nucleotide variant | NM_001868.4(CPA1):c.567G>A (p.Gly189=) | Hereditary pancreatitis [RCV002347415] | likely benign | 7 | 130383474 | 130383474 | Human | 1 | name |
| 155687559 | CV1803656 | single nucleotide variant | NM_001868.4(CPA1):c.591T>C (p.Thr197=) | Hereditary pancreatitis [RCV002355810] | likely benign | 7 | 130383689 | 130383689 | Human | 1 | name |
| 155689282 | CV1803968 | single nucleotide variant | NM_001868.4(CPA1):c.597C>T (p.Asp199=) | Hereditary pancreatitis [RCV002356122] | likely benign | 7 | 130383695 | 130383695 | Human | 1 | name |
| 155713872 | CV1804424 | single nucleotide variant | NM_001868.4(CPA1):c.649C>T (p.Leu217=) | Hereditary pancreatitis [RCV002362021]|not provided [RCV003574931] | likely benign | 7 | 130383747 | 130383747 | Human | 1 | name |
| 155722599 | CV1804452 | single nucleotide variant | NM_001868.4(CPA1):c.64G>A (p.Gly22Arg) | Hereditary pancreatitis [RCV002364130] | uncertain significance | 7 | 130380584 | 130380584 | Human | 1 | name |
| 155725608 | CV1804834 | single nucleotide variant | NM_001868.4(CPA1):c.657C>A (p.Ile219=) | Hereditary pancreatitis [RCV002364487] | likely benign | 7 | 130383755 | 130383755 | Human | 1 | name |
| 155738089 | CV1805004 | single nucleotide variant | NM_001868.4(CPA1):c.456T>C (p.Tyr152=) | Hereditary pancreatitis [RCV002342127] | likely benign | 7 | 130382182 | 130382182 | Human | 1 | name |
| 155738579 | CV1805194 | single nucleotide variant | NM_001868.4(CPA1):c.459A>G (p.Glu153=) | Hereditary pancreatitis [RCV002342318] | likely benign | 7 | 130382185 | 130382185 | Human | 1 | name |
| 155720548 | CV1805405 | single nucleotide variant | NM_001868.4(CPA1):c.480G>A (p.Leu160=) | Hereditary pancreatitis [RCV002337942] | likely benign | 7 | 130382206 | 130382206 | Human | 1 | name |
| 155737182 | CV1805418 | single nucleotide variant | NM_001868.4(CPA1):c.480G>T (p.Leu160=) | Hereditary pancreatitis [RCV002330739] | likely benign | 7 | 130382206 | 130382206 | Human | 1 | name |
| 155742695 | CV1806167 | single nucleotide variant | NM_001868.4(CPA1):c.528G>A (p.Thr176=) | Hereditary pancreatitis [RCV002344509]|not provided [RCV003096679] | likely benign | 7 | 130383435 | 130383435 | Human | 1 | name |
| 155743078 | CV1806349 | single nucleotide variant | NM_001868.4(CPA1):c.531C>A (p.Gly177=) | Hereditary pancreatitis [RCV002344693]|not provided [RCV003718518] | likely benign | 7 | 130383438 | 130383438 | Human | 1 | name |
| 155743082 | CV1806352 | single nucleotide variant | NM_001868.4(CPA1):c.531C>T (p.Gly177=) | Hereditary pancreatitis [RCV002344696]|not provided [RCV003730098] | likely benign|uncertain significance | 7 | 130383438 | 130383438 | Human | 1 | name |
| 155676456 | CV1806526 | single nucleotide variant | NM_001868.4(CPA1):c.555C>G (p.Thr185=) | Hereditary pancreatitis [RCV002351968]|not provided [RCV003730104] | likely benign | 7 | 130383462 | 130383462 | Human | 1 | name |
| 155681193 | CV1807636 | single nucleotide variant | NM_001868.4(CPA1):c.615T>G (p.Ala205=) | Hereditary pancreatitis [RCV002353662] | likely benign | 7 | 130383713 | 130383713 | Human | 1 | name |
| 155690044 | CV1808191 | single nucleotide variant | NM_001868.4(CPA1):c.648C>T (p.Phe216=) | Hereditary pancreatitis [RCV002356237]|not provided [RCV005096947] | likely benign | 7 | 130383746 | 130383746 | Human | 1 | name |
| 155731822 | CV1808705 | single nucleotide variant | NM_001868.4(CPA1):c.453C>T (p.Thr151=) | Hereditary pancreatitis [RCV002340089] | likely benign | 7 | 130382179 | 130382179 | Human | 1 | name |
| 155739998 | CV1809177 | single nucleotide variant | NM_001868.4(CPA1):c.495G>A (p.Gly165=) | Hereditary pancreatitis [RCV002342787] | likely benign | 7 | 130383402 | 130383402 | Human | 1 | name |
| 155675561 | CV1810312 | single nucleotide variant | NM_001868.4(CPA1):c.552C>T (p.Val184=) | Hereditary pancreatitis [RCV002351813] | likely benign | 7 | 130383459 | 130383459 | Human | 1 | name |
| 155683629 | CV1811496 | single nucleotide variant | NM_001868.4(CPA1):c.637T>C (p.Leu213=) | Hereditary pancreatitis [RCV002354068] | likely benign | 7 | 130383735 | 130383735 | Human | 1 | name |
| 155726159 | CV1811869 | single nucleotide variant | NM_001868.4(CPA1):c.65G>C (p.Gly22Ala) | Hereditary pancreatitis [RCV002364564] | uncertain significance | 7 | 130380585 | 130380585 | Human | 1 | name |
| 155726250 | CV1811912 | single nucleotide variant | NM_001868.4(CPA1):c.660C>T (p.Val220=) | Hereditary pancreatitis [RCV002364582] | likely benign | 7 | 130383758 | 130383758 | Human | 1 | name |
| 155707135 | CV1812280 | single nucleotide variant | NM_001868.4(CPA1):c.690C>T (p.His230=) | Hereditary pancreatitis [RCV002378079] | likely benign | 7 | 130383788 | 130383788 | Human | 1 | name |
| 155698899 | CV1813289 | single nucleotide variant | NM_001868.4(CPA1):c.759C>A (p.Pro253=) | Hereditary pancreatitis [RCV002394188] | likely benign | 7 | 130384598 | 130384598 | Human | 1 | name |
| 155742411 | CV1813692 | single nucleotide variant | NM_001868.4(CPA1):c.795A>G (p.Gly265=) | Hereditary pancreatitis [RCV002412381] | likely benign | 7 | 130385153 | 130385153 | Human | 1 | name |
| 155665262 | CV1813800 | single nucleotide variant | NM_001868.4(CPA1):c.798C>T (p.Ala266=) | Hereditary pancreatitis [RCV002419071] | likely benign | 7 | 130385156 | 130385156 | Human | 1 | name |
| 155690139 | CV1814622 | single nucleotide variant | NM_001868.4(CPA1):c.882G>A (p.Lys294=) | Hereditary pancreatitis [RCV002373768] | likely benign | 7 | 130385240 | 130385240 | Human | 1 | name |
| 155683685 | CV1815061 | single nucleotide variant | NM_001868.4(CPA1):c.92C>T (p.Ala31Val) | Hereditary pancreatitis [RCV002371525] | uncertain significance | 7 | 130381124 | 130381124 | Human | 1 | name |
| 155677565 | CV1815106 | single nucleotide variant | NM_001868.4(CPA1):c.681C>T (p.Ala227=) | Hereditary pancreatitis [RCV002369579] | likely benign | 7 | 130383779 | 130383779 | Human | 1 | name |
| 155706827 | CV1815423 | single nucleotide variant | NM_001868.4(CPA1):c.687G>A (p.Thr229=) | Hereditary pancreatitis [RCV002378016]|not provided [RCV003730126] | likely benign | 7 | 130383785 | 130383785 | Human | 1 | name |
| 155706838 | CV1815432 | single nucleotide variant | NM_001868.4(CPA1):c.687G>T (p.Thr229=) | Hereditary pancreatitis [RCV002378019] | likely benign | 7 | 130383785 | 130383785 | Human | 1 | name |
| 155679542 | CV1815730 | single nucleotide variant | NM_001868.4(CPA1):c.717T>A (p.Thr239=) | Hereditary pancreatitis [RCV002370726] | likely benign | 7 | 130384556 | 130384556 | Human | 1 | name |
| 155696737 | CV1816157 | single nucleotide variant | NM_001868.4(CPA1):c.750C>T (p.Gly250=) | Hereditary pancreatitis [RCV002393750]|not provided [RCV003718552] | likely benign | 7 | 130384589 | 130384589 | Human | 1 | name |
| 155742160 | CV1816572 | single nucleotide variant | NM_001868.4(CPA1):c.786G>A (p.Gly262=) | Hereditary pancreatitis [RCV002412270] | likely benign | 7 | 130384625 | 130384625 | Human | 1 | name |
| 155747168 | CV1816707 | single nucleotide variant | NM_001868.4(CPA1):c.789G>A (p.Leu263=) | Hereditary pancreatitis [RCV002416620] | likely benign | 7 | 130385147 | 130385147 | Human | 1 | name |
| 155721556 | CV1817290 | single nucleotide variant | NM_001868.4(CPA1):c.864C>T (p.Ser288=) | Hereditary pancreatitis [RCV002449633] | likely benign | 7 | 130385222 | 130385222 | Human | 1 | name |
| 155722218 | CV1817509 | single nucleotide variant | NM_001868.4(CPA1):c.870A>G (p.Val290=) | Hereditary pancreatitis [RCV002449723] | likely benign | 7 | 130385228 | 130385228 | Human | 1 | name |
| 155712289 | CV1817944 | single nucleotide variant | NM_001868.4(CPA1):c.915C>T (p.Ile305=) | Hereditary pancreatitis [RCV002378823] | likely benign | 7 | 130385273 | 130385273 | Human | 1 | name |
| 155712957 | CV1818053 | single nucleotide variant | NM_001868.4(CPA1):c.918C>T (p.His306=) | Hereditary pancreatitis [RCV002378913]|not provided [RCV003738230] | likely benign | 7 | 130385276 | 130385276 | Human | 1 | name |
| 155701994 | CV1818486 | single nucleotide variant | NM_001868.4(CPA1):c.969C>G (p.Val323=) | Hereditary pancreatitis [RCV002376605] | likely benign | 7 | 130385327 | 130385327 | Human | 1 | name |
| 155718327 | CV1819351 | single nucleotide variant | NM_001868.4(CPA1):c.738C>T (p.Ser246=) | Hereditary pancreatitis [RCV002380436]|not provided [RCV005097106] | likely benign | 7 | 130384577 | 130384577 | Human | 1 | name |
| 155737729 | CV1820122 | single nucleotide variant | NM_001868.4(CPA1):c.77T>G (p.Leu26Arg) | Hereditary pancreatitis [RCV002409913] | uncertain significance | 7 | 130381109 | 130381109 | Human | 1 | name |
| 155713736 | CV1820617 | single nucleotide variant | NM_001868.4(CPA1):c.852G>A (p.Val284=) | Hereditary pancreatitis [RCV002447799] | likely benign | 7 | 130385210 | 130385210 | Human | 1 | name |
| 155744771 | CV1820627 | single nucleotide variant | NM_001868.4(CPA1):c.852G>T (p.Val284=) | Hereditary pancreatitis [RCV002414435] | likely benign | 7 | 130385210 | 130385210 | Human | 1 | name |
| 155700583 | CV1821103 | single nucleotide variant | NM_001868.4(CPA1):c.900G>A (p.Lys300=) | Hereditary pancreatitis [RCV002376385] | likely benign | 7 | 130385258 | 130385258 | Human | 1 | name |
| 155710071 | CV1821294 | single nucleotide variant | NM_001868.4(CPA1):c.906C>T (p.Phe302=) | Hereditary pancreatitis [RCV002378543] | likely benign | 7 | 130385264 | 130385264 | Human | 1 | name |
| 155692003 | CV1821514 | single nucleotide variant | NM_001868.4(CPA1):c.94G>A (p.Asp32Asn) | Hereditary pancreatitis [RCV002374133]|not provided [RCV003718573] | uncertain significance | 7 | 130381126 | 130381126 | Human | 1 | name |
| 155729015 | CV1823438 | single nucleotide variant | NM_001868.4(CPA1):c.76C>G (p.Leu26Val) | Hereditary pancreatitis [RCV002400578] | uncertain significance | 7 | 130381108 | 130381108 | Human | 1 | name |
| 155704965 | CV1824001 | single nucleotide variant | NM_001868.4(CPA1):c.840C>G (p.Ala280=) | Hereditary pancreatitis [RCV002445855] | likely benign | 7 | 130385198 | 130385198 | Human | 1 | name |
| 155711959 | CV1824210 | single nucleotide variant | NM_001868.4(CPA1):c.846C>T (p.Ser282=) | Hereditary pancreatitis [RCV002447581] | likely benign | 7 | 130385204 | 130385204 | Human | 1 | name |
| 155698611 | CV1824400 | single nucleotide variant | NM_001868.4(CPA1):c.885C>T (p.Asp295=) | Hereditary pancreatitis [RCV002375943] | likely benign | 7 | 130385243 | 130385243 | Human | 1 | name |
| 155699314 | CV1824605 | single nucleotide variant | NM_001868.4(CPA1):c.891G>A (p.Gly297=) | Hereditary pancreatitis [RCV002376120] | likely benign | 7 | 130385249 | 130385249 | Human | 1 | name |
| 155684372 | CV1824862 | single nucleotide variant | NM_001868.4(CPA1):c.933C>T (p.Leu311=) | Hereditary pancreatitis [RCV002371660] | likely benign | 7 | 130385291 | 130385291 | Human | 1 | name |
| 155684583 | CV1824938 | single nucleotide variant | NM_001868.4(CPA1):c.936C>A (p.Leu312=) | Hereditary pancreatitis [RCV002371716] | likely benign | 7 | 130385294 | 130385294 | Human | 1 | name |
| 155683962 | CV1825257 | single nucleotide variant | NM_001868.4(CPA1):c.930G>A (p.Gln310=) | Hereditary pancreatitis [RCV002371569] | likely benign | 7 | 130385288 | 130385288 | Human | 1 | name |
| 155730827 | CV1825852 | single nucleotide variant | NM_001868.4(CPA1):c.999C>T (p.Ser333=) | Hereditary pancreatitis [RCV002383069] | likely benign | 7 | 130385850 | 130385850 | Human | 1 | name |
| 155690703 | CV1826880 | deletion | NM_001868.4(CPA1):c.142del (p.Leu48fs) | Hereditary pancreatitis [RCV002392030] | likely benign | 7 | 130381173 | 130381173 | Human | 1 | name |
| 156323988 | CV2072180 | single nucleotide variant | NM_001868.4(CPA1):c.921C>T (p.Ser307=) | not provided [RCV002834892] | likely benign | 7 | 130385279 | 130385279 | Human | | name |
| 156260946 | CV2381262 | single nucleotide variant | NM_001868.4(CPA1):c.49A>C (p.Lys17Gln) | Hereditary pancreatitis [RCV004227325] | uncertain significance | 7 | 130380569 | 130380569 | Human | 1 | name |
| 329364199 | CV2425534 | single nucleotide variant | NM_001868.4(CPA1):c.816G>C (p.Ser272=) | Hereditary pancreatitis [RCV003181568] | likely benign | 7 | 130385174 | 130385174 | Human | 1 | name |
| 329363464 | CV2425536 | single nucleotide variant | NM_001868.4(CPA1):c.411G>C (p.Ala137=) | Hereditary pancreatitis [RCV003168237] | likely benign | 7 | 130382137 | 130382137 | Human | 1 | name |
| 329363467 | CV2425541 | single nucleotide variant | NM_001868.4(CPA1):c.420G>C (p.Pro140=) | Hereditary pancreatitis [RCV003168238] | likely benign | 7 | 130382146 | 130382146 | Human | 1 | name |
| 329364210 | CV2425546 | single nucleotide variant | NM_001868.4(CPA1):c.342C>A (p.Thr114=) | Hereditary pancreatitis [RCV003181578] | likely benign | 7 | 130381824 | 130381824 | Human | 1 | name |
| 329363468 | CV2425549 | single nucleotide variant | NM_001868.4(CPA1):c.612A>C (p.Ala204=) | Hereditary pancreatitis [RCV003168239] | likely benign | 7 | 130383710 | 130383710 | Human | 1 | name |
| 329363470 | CV2425556 | single nucleotide variant | NM_001868.4(CPA1):c.756C>T (p.Asp252=) | Hereditary pancreatitis [RCV003168241] | likely benign | 7 | 130384595 | 130384595 | Human | 1 | name |
| 329389925 | CV2465585 | single nucleotide variant | NM_001868.4(CPA1):c.420G>A (p.Pro140=) | Hereditary pancreatitis [RCV003216490]|not provided [RCV003730475] | likely benign | 7 | 130382146 | 130382146 | Human | 1 | name |
| 11545214 | CV252616 | single nucleotide variant | NM_001868.4(CPA1):c.474C>T (p.Tyr158=) | Hereditary pancreatitis [RCV002318976]|not provided [RCV001515482]|not specified [RCV000244832] | benign | 7 | 130382200 | 130382200 | Human | 1 | name |
| 11548966 | CV252617 | single nucleotide variant | NM_001868.4(CPA1):c.600C>T (p.Tyr200=) | Hereditary pancreatitis [RCV002347957]|not provided [RCV001515483]|not specified [RCV000249795] | benign | 7 | 130383698 | 130383698 | Human | 1 | name |
| 401775058 | CV2723966 | single nucleotide variant | NM_001868.4(CPA1):c.471T>C (p.Ile157=) | Hereditary pancreatitis [RCV003305486] | likely benign | 7 | 130382197 | 130382197 | Human | 1 | name |
| 401765397 | CV2733685 | single nucleotide variant | NM_001868.4(CPA1):c.423C>T (p.His141=) | Hereditary pancreatitis [RCV003301389] | likely benign | 7 | 130382149 | 130382149 | Human | 1 | name |
| 401765401 | CV2733688 | single nucleotide variant | NM_001868.4(CPA1):c.741C>A (p.Leu247=) | Hereditary pancreatitis [RCV003301392] | likely benign | 7 | 130384580 | 130384580 | Human | 1 | name |
| 401765403 | CV2733690 | single nucleotide variant | NM_001868.4(CPA1):c.933C>A (p.Leu311=) | Hereditary pancreatitis [RCV003301394] | likely benign | 7 | 130385291 | 130385291 | Human | 1 | name |
| 401885200 | CV2786705 | single nucleotide variant | NM_001868.4(CPA1):c.948T>C (p.Tyr316=) | Hereditary pancreatitis [RCV003386699]|not provided [RCV005104177] | likely benign | 7 | 130385306 | 130385306 | Human | 1 | name |
| 405193550 | CV2984895 | single nucleotide variant | NM_001868.4(CPA1):c.420G>T (p.Pro140=) | Hereditary pancreatitis [RCV004823179]|not provided [RCV003706540] | likely benign | 7 | 130382146 | 130382146 | Human | 1 | name |
| 405215080 | CV2985163 | single nucleotide variant | NM_001868.4(CPA1):c.522C>A (p.Ile174=) | not provided [RCV003709087] | likely benign | 7 | 130383429 | 130383429 | Human | | name |
| 402514911 | CV2991517 | single nucleotide variant | NM_001868.4(CPA1):c.402G>A (p.Leu134=) | not provided [RCV003689773] | likely benign | 7 | 130382128 | 130382128 | Human | | name |
| 405127983 | CV3167029 | single nucleotide variant | NM_001868.4(CPA1):c.315C>T (p.Phe105=) | not provided [RCV003854284] | likely benign | 7 | 130381797 | 130381797 | Human | | name |
| 405655638 | CV3380128 | single nucleotide variant | NM_001868.4(CPA1):c.300G>A (p.Glu100=) | Hereditary pancreatitis [RCV004511140]|not provided [RCV005065180] | likely benign | 7 | 130381782 | 130381782 | Human | 1 | name |
| 405655647 | CV3380134 | single nucleotide variant | NM_001868.4(CPA1):c.447C>T (p.Gly149=) | Hereditary pancreatitis [RCV004511146] | likely benign | 7 | 130382173 | 130382173 | Human | 1 | name |
| 405655656 | CV3380140 | single nucleotide variant | NM_001868.4(CPA1):c.537T>C (p.His179=) | Hereditary pancreatitis [RCV004511152] | likely benign | 7 | 130383444 | 130383444 | Human | 1 | name |
| 405655658 | CV3380141 | single nucleotide variant | NM_001868.4(CPA1):c.54G>C (p.Glu18Asp) | Hereditary pancreatitis [RCV004511153] | uncertain significance | 7 | 130380574 | 130380574 | Human | 1 | name |
| 405655667 | CV3380147 | single nucleotide variant | NM_001868.4(CPA1):c.61G>C (p.Val21Leu) | Hereditary pancreatitis [RCV004511159] | uncertain significance | 7 | 130380581 | 130380581 | Human | 1 | name |
| 405655677 | CV3380153 | single nucleotide variant | NM_001868.4(CPA1):c.64G>C (p.Gly22Arg) | Hereditary pancreatitis [RCV004511165] | uncertain significance | 7 | 130380584 | 130380584 | Human | 1 | name |
| 405655698 | CV3380166 | single nucleotide variant | NM_001868.4(CPA1):c.95A>G (p.Asp32Gly) | Hereditary pancreatitis [RCV004511178] | likely benign | 7 | 130381127 | 130381127 | Human | 1 | name |
| 405655700 | CV3380167 | single nucleotide variant | NM_001868.4(CPA1):c.972T>C (p.Pro324=) | Hereditary pancreatitis [RCV004511179] | likely benign | 7 | 130385330 | 130385330 | Human | 1 | name |
| 405655701 | CV3380168 | single nucleotide variant | NM_001868.4(CPA1):c.985C>T (p.Leu329=) | Hereditary pancreatitis [RCV004511180] | likely benign | 7 | 130385343 | 130385343 | Human | 1 | name |
| 407456893 | CV3419516 | single nucleotide variant | NM_001868.4(CPA1):c.348T>C (p.Thr116=) | Hereditary pancreatitis [RCV004610910] | likely benign | 7 | 130381830 | 130381830 | Human | 1 | name |
| 407456894 | CV3419517 | single nucleotide variant | NM_001868.4(CPA1):c.903C>G (p.Ala301=) | Hereditary pancreatitis [RCV004610911] | likely benign | 7 | 130385261 | 130385261 | Human | 1 | name |
| 407456898 | CV3419520 | single nucleotide variant | NM_001868.4(CPA1):c.318C>T (p.Ala106=) | Hereditary pancreatitis [RCV004610914] | likely benign | 7 | 130381800 | 130381800 | Human | 1 | name |
| 407456905 | CV3419523 | single nucleotide variant | NM_001868.4(CPA1):c.414G>A (p.Glu138=) | Hereditary pancreatitis [RCV004610917] | likely benign | 7 | 130382140 | 130382140 | Human | 1 | name |
| 407456924 | CV3419535 | single nucleotide variant | NM_001868.4(CPA1):c.654G>A (p.Glu218=) | Hereditary pancreatitis [RCV004610929] | likely benign | 7 | 130383752 | 130383752 | Human | 1 | name |
| 407456925 | CV3419536 | single nucleotide variant | NM_001868.4(CPA1):c.528G>T (p.Thr176=) | Hereditary pancreatitis [RCV004610930] | likely benign | 7 | 130383435 | 130383435 | Human | 1 | name |
| 407456928 | CV3419538 | single nucleotide variant | NM_001868.4(CPA1):c.837T>C (p.Phe279=) | Hereditary pancreatitis [RCV004610932] | likely benign | 7 | 130385195 | 130385195 | Human | 1 | name |
| 597630412 | CV3654375 | single nucleotide variant | NM_001868.4(CPA1):c.555C>T (p.Thr185=) | Hereditary pancreatitis [RCV004822650] | likely benign | 7 | 130383462 | 130383462 | Human | 1 | name |
| 597630441 | CV3654389 | single nucleotide variant | NM_001868.4(CPA1):c.807C>T (p.Asn269=) | Hereditary pancreatitis [RCV004822663] | likely benign | 7 | 130385165 | 130385165 | Human | 1 | name |
| 597630459 | CV3654399 | single nucleotide variant | NM_001868.4(CPA1):c.373C>T (p.Leu125=) | Hereditary pancreatitis [RCV004822672] | likely benign | 7 | 130381855 | 130381855 | Human | 1 | name |
| 597854220 | CV3821640 | single nucleotide variant | NM_001868.4(CPA1):c.618C>T (p.Phe206=) | not provided [RCV005174118] | likely benign | 7 | 130383716 | 130383716 | Human | | name |
| 597937965 | CV3852717 | single nucleotide variant | NM_001868.4(CPA1):c.669T>C (p.Pro223=) | not provided [RCV005187116] | likely benign | 7 | 130383767 | 130383767 | Human | | name |
| 598235092 | CV3945118 | single nucleotide variant | NM_001868.4(CPA1):c.92C>A (p.Ala31Asp) | Hereditary pancreatitis [RCV005320185] | uncertain significance | 7 | 130381124 | 130381124 | Human | 1 | name |
| 598235100 | CV3945121 | single nucleotide variant | NM_001868.4(CPA1):c.717T>G (p.Thr239=) | Hereditary pancreatitis [RCV005320188] | likely benign | 7 | 130384556 | 130384556 | Human | 1 | name |
| 598235120 | CV3945126 | single nucleotide variant | NM_001868.4(CPA1):c.57C>G (p.Asp19Glu) | Hereditary pancreatitis [RCV005320193] | likely benign | 7 | 130380577 | 130380577 | Human | 1 | name |
| 15186355 | CV699851 | single nucleotide variant | NM_001868.4(CPA1):c.867T>C (p.Ile289=) | CPA1-related disorder [RCV004758103]|Hereditary pancreatitis [RCV002255596]|not provided [RCV000953258] | benign|likely benign | 7 | 130385225 | 130385225 | Human | 1 | name , trait , alternate_id |
| 15184658 | CV710770 | single nucleotide variant | NM_001868.4(CPA1):c.321C>T (p.Phe107=) | CPA1-related disorder [RCV003962927]|Hereditary pancreatitis [RCV002409288]|not provided [RCV000975167] | benign | 7 | 130381803 | 130381803 | Human | 1 | name , trait , alternate_id |
| 15191542 | CV735957 | single nucleotide variant | NM_001868.4(CPA1):c.79C>T (p.Arg27Ter) | Hereditary pancreatitis [RCV002255574]|not provided [RCV000910277] | likely benign | 7 | 130381111 | 130381111 | Human | 1 | name |
| 15148065 | CV750424 | single nucleotide variant | NM_001868.4(CPA1):c.621C>T (p.Thr207=) | CPA1-related disorder [RCV003923298]|Hereditary pancreatitis [RCV002256602]|not provided [RCV000923027] | benign|likely benign | 7 | 130383719 | 130383719 | Human | 1 | name , trait , alternate_id |
| 15193923 | CV750425 | single nucleotide variant | NM_001868.4(CPA1):c.726C>T (p.His242=) | Hereditary pancreatitis [RCV002382068]|not provided [RCV000910977] | likely benign | 7 | 130384565 | 130384565 | Human | 1 | name |
| 15148070 | CV750426 | single nucleotide variant | NM_001868.4(CPA1):c.816G>A (p.Ser272=) | CPA1-related disorder [RCV003913105]|Hereditary pancreatitis [RCV002256603]|not provided [RCV000923028] | benign|likely benign | 7 | 130385174 | 130385174 | Human | 1 | name , trait , alternate_id |
| 15191134 | CV766115 | single nucleotide variant | NM_001868.4(CPA1):c.492G>A (p.Thr164=) | CPA1-related disorder [RCV003925804]|Hereditary pancreatitis [RCV002319130]|not provided [RCV000932716] | likely benign | 7 | 130383399 | 130383399 | Human | 1 | name , trait , alternate_id |
| 25318317 | CV808953 | single nucleotide variant | NM_001868.4(CPA1):c.405G>C (p.Leu135=) | Hereditary pancreatitis [RCV002319310]|not provided [RCV001424455] | likely benign | 7 | 130382131 | 130382131 | Human | 1 | name |
| 25321986 | CV808955 | single nucleotide variant | NM_001868.4(CPA1):c.486C>T (p.Phe162=) | Hereditary pancreatitis [RCV002319376]|not provided [RCV001519647] | benign|likely benign | 7 | 130383393 | 130383393 | Human | 1 | name |
| 25324803 | CV808960 | single nucleotide variant | NM_001868.4(CPA1):c.630C>T (p.Leu210=) | Hereditary pancreatitis [RCV002354937]|not provided [RCV001428447] | likely benign | 7 | 130383728 | 130383728 | Human | 1 | name |
| 25326811 | CV808963 | single nucleotide variant | NM_001868.4(CPA1):c.787T>C (p.Leu263=) | Hereditary pancreatitis [RCV002434413]|not provided [RCV001343037] | likely benign|uncertain significance | 7 | 130384626 | 130384626 | Human | 1 | name |
| 25329524 | CV808966 | single nucleotide variant | NM_001868.4(CPA1):c.846C>A (p.Ser282=) | Hereditary pancreatitis [RCV002346215] | likely benign | 7 | 130385204 | 130385204 | Human | 1 | name |
| 26900678 | CV833137 | single nucleotide variant | NM_001868.4(CPA1):c.330G>T (p.Arg110=) | Hereditary pancreatitis [RCV002320341]|not provided [RCV001067977] | likely benign|uncertain significance | 7 | 130381812 | 130381812 | Human | 1 | name |
| 38495864 | CV955056 | single nucleotide variant | NM_001868.4(CPA1):c.41T>C (p.Val14Ala) | Hereditary pancreatitis [RCV002327585]|not provided [RCV001242201] | likely benign|uncertain significance | 7 | 130380561 | 130380561 | Human | 1 | name |
| 126746052 | CV992098 | single nucleotide variant | NM_001868.4(CPA1):c.92C>G (p.Ala31Gly) | not provided [RCV001296526] | uncertain significance | 7 | 130381124 | 130381124 | Human | | name |
| 126771592 | CV1007246 | single nucleotide variant | NM_001868.4(CPA1):c.226A>G (p.Lys76Glu) | Hereditary pancreatitis [RCV002447367]|not provided [RCV001323251] | uncertain significance | 7 | 130381708 | 130381708 | Human | 1 | name |
| 126731313 | CV1027780 | single nucleotide variant | NM_001868.4(CPA1):c.221C>T (p.Ala74Val) | Hereditary pancreatitis [RCV002431988]|not provided [RCV001349405] | uncertain significance | 7 | 130381703 | 130381703 | Human | 1 | name |
| 126768944 | CV1027787 | single nucleotide variant | NM_001868.4(CPA1):c.1071T>A (p.Ile357=) | Hereditary pancreatitis [RCV003169654]|not provided [RCV001343646] | likely benign|uncertain significance | 7 | 130385922 | 130385922 | Human | 1 | name |
| 126908103 | CV1044696 | single nucleotide variant | NM_001868.4(CPA1):c.284C>T (p.Ser95Leu) | Hereditary pancreatitis [RCV002438856]|not provided [RCV001367593] | uncertain significance | 7 | 130381766 | 130381766 | Human | 1 | name |
| 127276237 | CV1096076 | single nucleotide variant | NM_001868.4(CPA1):c.1137C>T (p.Phe379=) | Hereditary pancreatitis [RCV002322469]|not provided [RCV001443725] | likely benign | 7 | 130387888 | 130387888 | Human | 1 | name |
| 127298608 | CV1117597 | single nucleotide variant | NM_001868.4(CPA1):c.1032C>T (p.Tyr344=) | Hereditary pancreatitis [RCV002396084]|not provided [RCV001460599] | likely benign | 7 | 130385883 | 130385883 | Human | 1 | name |
| 151713887 | CV1379585 | single nucleotide variant | NM_001868.4(CPA1):c.197G>A (p.Arg66Gln) | Hereditary pancreatitis [RCV002423076]|not provided [RCV001964837] | uncertain significance | 7 | 130381679 | 130381679 | Human | 1 | name |
| 151846163 | CV1395246 | single nucleotide variant | NM_001868.4(CPA1):c.203C>A (p.Pro68His) | not provided [RCV001995362] | uncertain significance | 7 | 130381685 | 130381685 | Human | | name |
| 151875981 | CV1406077 | single nucleotide variant | NM_001868.4(CPA1):c.295G>A (p.Glu99Lys) | Hereditary pancreatitis [RCV002441069]|not provided [RCV001981907] | uncertain significance | 7 | 130381777 | 130381777 | Human | 1 | name |
| 151768852 | CV1409609 | deletion | NM_001868.4(CPA1):c.401del (p.Leu134fs) | Hereditary pancreatitis [RCV002370461]|not provided [RCV001896133] | uncertain significance | 7 | 130382127 | 130382127 | Human | 1 | name |
| 151814297 | CV1460575 | single nucleotide variant | NM_001868.4(CPA1):c.218A>G (p.Gln73Arg) | Hereditary pancreatitis [RCV002425123]|not provided [RCV001878583] | uncertain significance | 7 | 130381700 | 130381700 | Human | 1 | name |
| 151827733 | CV1479846 | single nucleotide variant | NM_001868.4(CPA1):c.114G>C (p.Lys38Asn) | Hereditary pancreatitis [RCV002458769]|not provided [RCV001901498] | uncertain significance | 7 | 130381146 | 130381146 | Human | 1 | name |
| 151886766 | CV1514055 | single nucleotide variant | NM_001868.4(CPA1):c.208C>T (p.Pro70Ser) | Hereditary pancreatitis [RCV004042989]|not provided [RCV001962832] | uncertain significance | 7 | 130381690 | 130381690 | Human | 1 | name |
| 152164460 | CV1560701 | single nucleotide variant | NM_001868.4(CPA1):c.1089C>T (p.Ser363=) | Hereditary pancreatitis [RCV002443194]|not provided [RCV002160253] | likely benign | 7 | 130387840 | 130387840 | Human | 1 | name |
| 152105968 | CV1614797 | single nucleotide variant | NM_001868.4(CPA1):c.1107C>T (p.Tyr369=) | not provided [RCV002079614] | likely benign | 7 | 130387858 | 130387858 | Human | | name |
| 152146253 | CV1649505 | single nucleotide variant | NM_001868.4(CPA1):c.1173G>A (p.Leu391=) | not provided [RCV002121085] | likely benign | 7 | 130387924 | 130387924 | Human | | name |
| 152056879 | CV1656462 | single nucleotide variant | NM_001868.4(CPA1):c.1218G>A (p.Ala406=) | Hereditary pancreatitis [RCV002363608]|not provided [RCV002109653] | likely benign | 7 | 130387969 | 130387969 | Human | 1 | name |
| 155744868 | CV1771518 | single nucleotide variant | NM_001868.4(CPA1):c.211A>T (p.Ser71Cys) | not provided [RCV002303299] | uncertain significance | 7 | 130381693 | 130381693 | Human | | name |
| 155703249 | CV1785584 | single nucleotide variant | NM_001868.4(CPA1):c.1134C>T (p.Thr378=) | Hereditary pancreatitis [RCV002445597] | likely benign | 7 | 130387885 | 130387885 | Human | 1 | name |
| 155704223 | CV1787556 | single nucleotide variant | NM_001868.4(CPA1):c.1164C>A (p.Gly388=) | Hereditary pancreatitis [RCV002323183] | likely benign | 7 | 130387915 | 130387915 | Human | 1 | name |
| 155700148 | CV1791855 | single nucleotide variant | NM_001868.4(CPA1):c.1131C>T (p.Phe377=) | Hereditary pancreatitis [RCV002322658] | likely benign | 7 | 130387882 | 130387882 | Human | 1 | name |
| 155665363 | CV1792875 | single nucleotide variant | NM_001868.4(CPA1):c.1149C>T (p.Asp383=) | Hereditary pancreatitis [RCV002452237] | likely benign | 7 | 130387900 | 130387900 | Human | 1 | name |
| 155697342 | CV1794051 | single nucleotide variant | NM_001868.4(CPA1):c.1161T>C (p.Tyr387=) | Hereditary pancreatitis [RCV002375712] | likely benign | 7 | 130387912 | 130387912 | Human | 1 | name |
| 155664605 | CV1795441 | single nucleotide variant | NM_001868.4(CPA1):c.1011G>A (p.Val337=) | Hereditary pancreatitis [RCV002452076] | likely benign | 7 | 130385862 | 130385862 | Human | 1 | name |
| 155665880 | CV1796279 | single nucleotide variant | NM_001868.4(CPA1):c.1152T>A (p.Thr384=) | Hereditary pancreatitis [RCV002349246] | likely benign | 7 | 130387903 | 130387903 | Human | 1 | name |
| 155720039 | CV1796284 | single nucleotide variant | NM_001868.4(CPA1):c.1152T>C (p.Thr384=) | Hereditary pancreatitis [RCV002363788] | likely benign | 7 | 130387903 | 130387903 | Human | 1 | name |
| 155687228 | CV1796874 | single nucleotide variant | NM_001868.4(CPA1):c.115G>A (p.Val39Met) | Hereditary pancreatitis [RCV002373278] | uncertain significance | 7 | 130381147 | 130381147 | Human | 1 | name |
| 155735007 | CV1797868 | single nucleotide variant | NM_001868.4(CPA1):c.1170G>A (p.Leu390=) | Hereditary pancreatitis [RCV002330274] | likely benign | 7 | 130387921 | 130387921 | Human | 1 | name |
| 155738454 | CV1797910 | single nucleotide variant | NM_001868.4(CPA1):c.1170G>C (p.Leu390=) | Hereditary pancreatitis [RCV002331878] | likely benign | 7 | 130387921 | 130387921 | Human | 1 | name |
| 155707687 | CV1798703 | single nucleotide variant | NM_001868.4(CPA1):c.1182C>T (p.Ser394=) | Hereditary pancreatitis [RCV002335274] | likely benign | 7 | 130387933 | 130387933 | Human | 1 | name |
| 155672877 | CV1801176 | single nucleotide variant | NM_001868.4(CPA1):c.121G>A (p.Glu41Lys) | Hereditary pancreatitis [RCV002368800] | uncertain significance | 7 | 130381153 | 130381153 | Human | 1 | name |
| 155713914 | CV1804435 | single nucleotide variant | NM_001868.4(CPA1):c.1224G>A (p.Leu408=) | Hereditary pancreatitis [RCV002362027] | likely benign | 7 | 130387975 | 130387975 | Human | 1 | name |
| 155734907 | CV1809687 | single nucleotide variant | NM_001868.4(CPA1):c.1197A>G (p.Thr399=) | Hereditary pancreatitis [RCV002340835] | likely benign | 7 | 130387948 | 130387948 | Human | 1 | name |
| 155667675 | CV1812163 | single nucleotide variant | NM_001868.4(CPA1):c.101C>G (p.Ala34Gly) | Hereditary pancreatitis [RCV002366869] | uncertain significance | 7 | 130381133 | 130381133 | Human | 1 | name |
| 155742415 | CV1813704 | single nucleotide variant | NM_001868.4(CPA1):c.1254C>A (p.Pro418=) | Hereditary pancreatitis [RCV002412384] | likely benign | 7 | 130388005 | 130388005 | Human | 1 | name |
| 155697572 | CV1816332 | single nucleotide variant | NM_001868.4(CPA1):c.1245G>C (p.Leu415=) | Hereditary pancreatitis [RCV002393925] | likely benign | 7 | 130387996 | 130387996 | Human | 1 | name |
| 155741501 | CV1816413 | single nucleotide variant | NM_001868.4(CPA1):c.1251C>T (p.His417=) | Hereditary pancreatitis [RCV002412110] | likely benign | 7 | 130388002 | 130388002 | Human | 1 | name |
| 155729729 | CV1819757 | single nucleotide variant | NM_001868.4(CPA1):c.124C>G (p.Leu42Val) | Hereditary pancreatitis [RCV002400705] | uncertain significance | 7 | 130381156 | 130381156 | Human | 1 | name |
| 155669155 | CV1821804 | single nucleotide variant | NM_001868.4(CPA1):c.130G>A (p.Asp44Asn) | Hereditary pancreatitis [RCV002385410]|not provided [RCV003718583] | likely benign|uncertain significance | 7 | 130381162 | 130381162 | Human | 1 | name |
| 155718078 | CV1823105 | single nucleotide variant | NM_001868.4(CPA1):c.1242C>T (p.Thr414=) | Hereditary pancreatitis [RCV002380385] | likely benign | 7 | 130387993 | 130387993 | Human | 1 | name |
| 155688997 | CV1826625 | single nucleotide variant | NM_001868.4(CPA1):c.141C>A (p.His47Gln) | Hereditary pancreatitis [RCV002391775] | uncertain significance | 7 | 130381173 | 130381173 | Human | 1 | name |
| 155690090 | CV1826783 | single nucleotide variant | NM_001868.4(CPA1):c.1035G>A (p.Gly345=) | Hereditary pancreatitis [RCV002391933] | likely benign | 7 | 130385886 | 130385886 | Human | 1 | name |
| 155690585 | CV1826859 | single nucleotide variant | NM_001868.4(CPA1):c.1035G>C (p.Gly345=) | Hereditary pancreatitis [RCV002392009] | likely benign | 7 | 130385886 | 130385886 | Human | 1 | name |
| 155691954 | CV1827380 | single nucleotide variant | NM_001868.4(CPA1):c.1041G>A (p.Lys347=) | Hereditary pancreatitis [RCV002392276] | likely benign | 7 | 130385892 | 130385892 | Human | 1 | name |
| 155694060 | CV1827534 | single nucleotide variant | NM_001868.4(CPA1):c.1047C>T (p.Asn349=) | Hereditary pancreatitis [RCV002392658] | likely benign | 7 | 130385898 | 130385898 | Human | 1 | name |
| 155718064 | CV1827689 | single nucleotide variant | NM_001868.4(CPA1):c.158G>C (p.Trp53Ser) | Hereditary pancreatitis [RCV002398406] | uncertain significance | 7 | 130381640 | 130381640 | Human | 1 | name |
| 155730075 | CV1828370 | single nucleotide variant | NM_001868.4(CPA1):c.173A>T (p.His58Leu) | Hereditary pancreatitis [RCV002407476] | uncertain significance | 7 | 130381655 | 130381655 | Human | 1 | name |
| 155710365 | CV1830991 | single nucleotide variant | NM_001868.4(CPA1):c.1050T>C (p.Tyr350=) | Hereditary pancreatitis [RCV002403591]|not provided [RCV003720589] | likely benign | 7 | 130385901 | 130385901 | Human | 1 | name |
| 155680638 | CV1832923 | single nucleotide variant | NM_001868.4(CPA1):c.139C>T (p.His47Tyr) | Hereditary pancreatitis [RCV002389204] | uncertain significance | 7 | 130381171 | 130381171 | Human | 1 | name |
| 155711628 | CV1833213 | single nucleotide variant | NM_001868.4(CPA1):c.146A>G (p.Gln49Arg) | Hereditary pancreatitis [RCV002396893] | uncertain significance | 7 | 130381178 | 130381178 | Human | 1 | name |
| 155731746 | CV1833854 | single nucleotide variant | NM_001868.4(CPA1):c.161G>A (p.Arg54Gln) | Hereditary pancreatitis [RCV002401046] | likely benign|uncertain significance | 7 | 130381643 | 130381643 | Human | 1 | name |
| 155732010 | CV1835038 | single nucleotide variant | NM_001868.4(CPA1):c.179G>A (p.Gly60Asp) | Hereditary pancreatitis [RCV002407852] | uncertain significance | 7 | 130381661 | 130381661 | Human | 1 | name |
| 155733596 | CV1836154 | single nucleotide variant | NM_001868.4(CPA1):c.136G>A (p.Glu46Lys) | Hereditary pancreatitis [RCV002383673] | uncertain significance | 7 | 130381168 | 130381168 | Human | 1 | name |
| 155738979 | CV1839182 | single nucleotide variant | NM_001868.4(CPA1):c.182C>A (p.Ser61Tyr) | Hereditary pancreatitis [RCV002410506] | uncertain significance | 7 | 130381664 | 130381664 | Human | 1 | name |
| 155738992 | CV1839187 | single nucleotide variant | NM_001868.4(CPA1):c.182C>T (p.Ser61Phe) | Hereditary pancreatitis [RCV002410511] | uncertain significance | 7 | 130381664 | 130381664 | Human | 1 | name |
| 155682983 | CV1839880 | single nucleotide variant | NM_001868.4(CPA1):c.197G>C (p.Arg66Pro) | Hereditary pancreatitis [RCV002423656] | uncertain significance | 7 | 130381679 | 130381679 | Human | 1 | name |
| 155692082 | CV1841448 | single nucleotide variant | NM_001868.4(CPA1):c.238G>A (p.Glu80Lys) | Hereditary pancreatitis [RCV002459561] | uncertain significance | 7 | 130381720 | 130381720 | Human | 1 | name |
| 155723003 | CV1842031 | single nucleotide variant | NM_001868.4(CPA1):c.1008T>A (p.Ala336=) | Hereditary pancreatitis [RCV002432969] | likely benign | 7 | 130385859 | 130385859 | Human | 1 | name |
| 155701634 | CV1842450 | single nucleotide variant | NM_001868.4(CPA1):c.263C>T (p.Thr88Ile) | Hereditary pancreatitis [RCV002428627] | likely benign | 7 | 130381745 | 130381745 | Human | 1 | name |
| 155744195 | CV1842983 | single nucleotide variant | NM_001868.4(CPA1):c.193G>T (p.Val65Phe) | Hereditary pancreatitis [RCV002413165] | uncertain significance | 7 | 130381675 | 130381675 | Human | 1 | name |
| 155676845 | CV1843730 | single nucleotide variant | NM_001868.4(CPA1):c.1077A>G (p.Gln359=) | Hereditary pancreatitis [RCV002421834] | uncertain significance | 7 | 130387828 | 130387828 | Human | 1 | name |
| 155711667 | CV1845175 | single nucleotide variant | NM_001868.4(CPA1):c.246C>A (p.His82Gln) | Hereditary pancreatitis [RCV002430772] | uncertain significance | 7 | 130381728 | 130381728 | Human | 1 | name |
| 155696610 | CV1845333 | single nucleotide variant | NM_001868.4(CPA1):c.247G>C (p.Gly83Arg) | Hereditary pancreatitis [RCV002443946]|not provided [RCV003101868] | uncertain significance | 7 | 130381729 | 130381729 | Human | 1 | name |
| 155668335 | CV1846583 | single nucleotide variant | NM_001868.4(CPA1):c.1074T>C (p.Tyr358=) | Hereditary pancreatitis [RCV002419552] | likely benign | 7 | 130387825 | 130387825 | Human | 1 | name |
| 155698716 | CV1847343 | single nucleotide variant | NM_001868.4(CPA1):c.221C>G (p.Ala74Gly) | Hereditary pancreatitis [RCV002428057] | uncertain significance | 7 | 130381703 | 130381703 | Human | 1 | name |
| 155669051 | CV1848859 | single nucleotide variant | NM_001868.4(CPA1):c.257A>G (p.Tyr86Cys) | Hereditary pancreatitis [RCV002452823]|not provided [RCV003730222] | uncertain significance | 7 | 130381739 | 130381739 | Human | 1 | name |
| 155672213 | CV1849247 | single nucleotide variant | NM_001868.4(CPA1):c.270C>G (p.Ile90Met) | Hereditary pancreatitis [RCV002437437]|not provided [RCV003720637] | uncertain significance | 7 | 130381752 | 130381752 | Human | 1 | name |
| 155684827 | CV1850754 | single nucleotide variant | NM_001868.4(CPA1):c.228G>C (p.Lys76Asn) | Hereditary pancreatitis [RCV002457468] | uncertain significance | 7 | 130381710 | 130381710 | Human | 1 | name |
| 155678769 | CV1851883 | single nucleotide variant | NM_001868.4(CPA1):c.1008T>G (p.Ala336=) | Hereditary pancreatitis [RCV002455788] | likely benign | 7 | 130385859 | 130385859 | Human | 1 | name |
| 155680587 | CV1853265 | single nucleotide variant | NM_001868.4(CPA1):c.277G>A (p.Val93Met) | Hereditary pancreatitis [RCV002439716]|not provided [RCV003102208] | uncertain significance | 7 | 130381759 | 130381759 | Human | 1 | name |
| 155680611 | CV1853271 | single nucleotide variant | NM_001868.4(CPA1):c.277G>T (p.Val93Leu) | Hereditary pancreatitis [RCV002439722] | uncertain significance | 7 | 130381759 | 130381759 | Human | 1 | name |
| 155683236 | CV1853514 | single nucleotide variant | NM_001868.4(CPA1):c.293A>T (p.Asp98Val) | Hereditary pancreatitis [RCV002440145] | uncertain significance | 7 | 130381775 | 130381775 | Human | 1 | name |
| 155687448 | CV1853634 | single nucleotide variant | NM_001868.4(CPA1):c.294C>G (p.Asp98Glu) | Hereditary pancreatitis [RCV002441829] | uncertain significance | 7 | 130381776 | 130381776 | Human | 1 | name |
| 155681107 | CV1854491 | single nucleotide variant | NM_001868.4(CPA1):c.290T>C (p.Leu97Pro) | Hereditary pancreatitis [RCV002439823] | uncertain significance | 7 | 130381772 | 130381772 | Human | 1 | name |
| 155681123 | CV1854493 | single nucleotide variant | NM_001868.4(CPA1):c.290T>G (p.Leu97Arg) | Hereditary pancreatitis [RCV002439825] | uncertain significance | 7 | 130381772 | 130381772 | Human | 1 | name |
| 155698536 | CV1855082 | deletion | NM_001868.4(CPA1):c.306del (p.Glu102fs) | Hereditary pancreatitis [RCV002444321]|not provided [RCV003546853] | likely benign|uncertain significance | 7 | 130381788 | 130381788 | Human | 1 | name |
| 155668597 | CV1856167 | single nucleotide variant | NM_001868.4(CPA1):c.1125C>T (p.Tyr375=) | Hereditary pancreatitis [RCV002435869]|not provided [RCV003775444] | likely benign | 7 | 130387876 | 130387876 | Human | 1 | name |
| 155689766 | CV1856528 | single nucleotide variant | NM_001868.4(CPA1):c.297G>C (p.Glu99Asp) | Hereditary pancreatitis [RCV002442202] | uncertain significance | 7 | 130381779 | 130381779 | Human | 1 | name |
| 155955127 | CV1907097 | single nucleotide variant | NM_001868.4(CPA1):c.196C>T (p.Arg66Ter) | Hereditary pancreatitis [RCV004614357]|not provided [RCV003095541] | likely benign|uncertain significance | 7 | 130381678 | 130381678 | Human | 1 | name |
| 156370742 | CV1920206 | single nucleotide variant | NM_001868.4(CPA1):c.179G>C (p.Gly60Ala) | Hereditary pancreatitis [RCV003294537]|not provided [RCV002603154] | uncertain significance | 7 | 130381661 | 130381661 | Human | 1 | name |
| 156119698 | CV1982685 | single nucleotide variant | NM_001868.4(CPA1):c.179G>T (p.Gly60Val) | Hereditary pancreatitis [RCV004823048]|not provided [RCV002622896] | uncertain significance | 7 | 130381661 | 130381661 | Human | 1 | name |
| 156225382 | CV2005982 | single nucleotide variant | NM_001868.4(CPA1):c.267G>A (p.Met89Ile) | not provided [RCV002667381] | uncertain significance | 7 | 130381749 | 130381749 | Human | | name |
| 156358069 | CV2006757 | single nucleotide variant | NM_001868.4(CPA1):c.157T>G (p.Trp53Gly) | not provided [RCV002676060] | uncertain significance | 7 | 130381639 | 130381639 | Human | | name |
| 156116591 | CV2017004 | single nucleotide variant | NM_001868.4(CPA1):c.241T>C (p.Ser81Pro) | not provided [RCV002740038] | uncertain significance | 7 | 130381723 | 130381723 | Human | | name |
| 156006967 | CV2042003 | single nucleotide variant | NM_001868.4(CPA1):c.209C>T (p.Pro70Leu) | Hereditary pancreatitis [RCV003167724]|not provided [RCV002756479] | uncertain significance | 7 | 130381691 | 130381691 | Human | 1 | name |
| 155999512 | CV2045462 | single nucleotide variant | NM_001868.4(CPA1):c.143T>C (p.Leu48Pro) | Hereditary pancreatitis [RCV005321232]|not provided [RCV002756130] | uncertain significance | 7 | 130381175 | 130381175 | Human | 1 | name |
| 329364202 | CV2425537 | single nucleotide variant | NM_001868.4(CPA1):c.1254C>T (p.Pro418=) | Hereditary pancreatitis [RCV003181570] | likely benign | 7 | 130388005 | 130388005 | Human | 1 | name |
| 329364204 | CV2425539 | single nucleotide variant | NM_001868.4(CPA1):c.1215G>A (p.Leu405=) | Hereditary pancreatitis [RCV003181572] | likely benign | 7 | 130387966 | 130387966 | Human | 1 | name |
| 329364208 | CV2425544 | single nucleotide variant | NM_001868.4(CPA1):c.176C>G (p.Pro59Arg) | Hereditary pancreatitis [RCV003181576] | uncertain significance | 7 | 130381658 | 130381658 | Human | 1 | name |
| 329389928 | CV2465583 | single nucleotide variant | NM_001868.4(CPA1):c.149T>G (p.Leu50Arg) | Hereditary pancreatitis [RCV003216488] | uncertain significance | 7 | 130381631 | 130381631 | Human | 1 | name |
| 329389918 | CV2465591 | single nucleotide variant | NM_001868.4(CPA1):c.178G>A (p.Gly60Ser) | Hereditary pancreatitis [RCV003216496] | uncertain significance | 7 | 130381660 | 130381660 | Human | 1 | name |
| 329389916 | CV2465592 | single nucleotide variant | NM_001868.4(CPA1):c.143T>G (p.Leu48Arg) | Hereditary pancreatitis [RCV003216497] | uncertain significance | 7 | 130381175 | 130381175 | Human | 1 | name |
| 329389913 | CV2465594 | single nucleotide variant | NM_001868.4(CPA1):c.1158C>T (p.Arg386=) | Hereditary pancreatitis [RCV003216499] | likely benign | 7 | 130387909 | 130387909 | Human | 1 | name |
| 329389911 | CV2465596 | single nucleotide variant | NM_001868.4(CPA1):c.164G>A (p.Gly55Glu) | Hereditary pancreatitis [RCV003216501]|not provided [RCV005101369] | uncertain significance | 7 | 130381646 | 130381646 | Human | 1 | name |
| 401775072 | CV2723974 | single nucleotide variant | NM_001868.4(CPA1):c.1164C>T (p.Gly388=) | Hereditary pancreatitis [RCV003305494] | likely benign | 7 | 130387915 | 130387915 | Human | 1 | name |
| 401765391 | CV2733680 | single nucleotide variant | NM_001868.4(CPA1):c.1236G>A (p.Glu412=) | Hereditary pancreatitis [RCV003301384] | likely benign | 7 | 130387987 | 130387987 | Human | 1 | name |
| 401765398 | CV2733686 | single nucleotide variant | NM_001868.4(CPA1):c.265A>G (p.Met89Val) | Hereditary pancreatitis [RCV003301390] | uncertain significance | 7 | 130381747 | 130381747 | Human | 1 | name |
| 401885235 | CV2786716 | single nucleotide variant | NM_001868.4(CPA1):c.163G>T (p.Gly55Trp) | Hereditary pancreatitis [RCV003386710]|not provided [RCV003720872] | uncertain significance | 7 | 130381645 | 130381645 | Human | 1 | name |
| 401868440 | CV2787428 | single nucleotide variant | NM_001868.4(CPA1):c.1017C>G (p.Ala339=) | Hereditary pancreatitis [RCV003380204] | likely benign | 7 | 130385868 | 130385868 | Human | 1 | name |
| 405073349 | CV2941240 | single nucleotide variant | NM_001868.4(CPA1):c.149T>C (p.Leu50Pro) | not provided [RCV003664117] | uncertain significance | 7 | 130381631 | 130381631 | Human | | name |
| 405187745 | CV2964107 | single nucleotide variant | NM_001868.4(CPA1):c.1023C>T (p.Ala341=) | Hereditary pancreatitis [RCV005323514]|not provided [RCV003676834] | likely benign | 7 | 130385874 | 130385874 | Human | 1 | name |
| 405082398 | CV3046840 | single nucleotide variant | NM_001868.4(CPA1):c.160C>T (p.Arg54Trp) | Hereditary pancreatitis [RCV004823188]|not provided [RCV003717234] | likely benign|uncertain significance | 7 | 130381642 | 130381642 | Human | 1 | name |
| 405685814 | CV3235789 | single nucleotide variant | NM_001868.4(CPA1):c.116T>C (p.Val39Ala) | Hereditary pancreatitis [RCV004372303] | uncertain significance | 7 | 130381148 | 130381148 | Human | 1 | name |
| 405655631 | CV3380124 | single nucleotide variant | NM_001868.4(CPA1):c.212G>A (p.Ser71Asn) | Hereditary pancreatitis [RCV004511136] | uncertain significance | 7 | 130381694 | 130381694 | Human | 1 | name |
| 405655633 | CV3380125 | single nucleotide variant | NM_001868.4(CPA1):c.236T>C (p.Leu79Pro) | Hereditary pancreatitis [RCV004511137] | uncertain significance | 7 | 130381718 | 130381718 | Human | 1 | name |
| 405655635 | CV3380126 | single nucleotide variant | NM_001868.4(CPA1):c.247G>A (p.Gly83Ser) | Hereditary pancreatitis [RCV004511138] | uncertain significance | 7 | 130381729 | 130381729 | Human | 1 | name |
| 405655608 | CV3383121 | single nucleotide variant | NM_001868.4(CPA1):c.1134C>A (p.Thr378=) | Hereditary pancreatitis [RCV004511122] | likely benign | 7 | 130387885 | 130387885 | Human | 1 | name |
| 405655909 | CV3383122 | single nucleotide variant | NM_001868.4(CPA1):c.1134C>G (p.Thr378=) | Hereditary pancreatitis [RCV004511123] | likely benign | 7 | 130387885 | 130387885 | Human | 1 | name |
| 405655614 | CV3383124 | single nucleotide variant | NM_001868.4(CPA1):c.1143C>G (p.Leu381=) | Hereditary pancreatitis [RCV004511125]|not provided [RCV005104854] | likely benign | 7 | 130387894 | 130387894 | Human | 1 | name |
| 405655617 | CV3383126 | single nucleotide variant | NM_001868.4(CPA1):c.1158C>A (p.Arg386=) | Hereditary pancreatitis [RCV004511127] | likely benign | 7 | 130387909 | 130387909 | Human | 1 | name |
| 405655619 | CV3383127 | single nucleotide variant | NM_001868.4(CPA1):c.1179C>A (p.Ala393=) | Hereditary pancreatitis [RCV004511128] | likely benign | 7 | 130387930 | 130387930 | Human | 1 | name |
| 405655620 | CV3383128 | single nucleotide variant | NM_001868.4(CPA1):c.1209G>T (p.Thr403=) | Hereditary pancreatitis [RCV004511129] | likely benign | 7 | 130387960 | 130387960 | Human | 1 | name |
| 407456881 | CV3419510 | single nucleotide variant | NM_001868.4(CPA1):c.134T>C (p.Leu45Pro) | Hereditary pancreatitis [RCV004610904] | uncertain significance | 7 | 130381166 | 130381166 | Human | 1 | name |
| 407456891 | CV3419515 | single nucleotide variant | NM_001868.4(CPA1):c.131A>T (p.Asp44Val) | Hereditary pancreatitis [RCV004610909] | uncertain significance | 7 | 130381163 | 130381163 | Human | 1 | name |
| 407456902 | CV3419522 | single nucleotide variant | NM_001868.4(CPA1):c.272A>G (p.Glu91Gly) | Hereditary pancreatitis [RCV004610916] | uncertain significance | 7 | 130381754 | 130381754 | Human | 1 | name |
| 407456906 | CV3419524 | single nucleotide variant | NM_001868.4(CPA1):c.184C>G (p.Pro62Ala) | Hereditary pancreatitis [RCV004610918] | uncertain significance | 7 | 130381666 | 130381666 | Human | 1 | name |
| 407456908 | CV3419525 | single nucleotide variant | NM_001868.4(CPA1):c.125T>G (p.Leu42Arg) | Hereditary pancreatitis [RCV004610919] | uncertain significance | 7 | 130381157 | 130381157 | Human | 1 | name |
| 407456914 | CV3419529 | deletion | NM_001868.4(CPA1):c.986del (p.Leu329fs) | Hereditary pancreatitis [RCV004610923] | likely benign | 7 | 130385344 | 130385344 | Human | 1 | name |
| 407456933 | CV3419541 | single nucleotide variant | NM_001868.4(CPA1):c.1191C>T (p.Ile397=) | Hereditary pancreatitis [RCV004610935] | likely benign | 7 | 130387942 | 130387942 | Human | 1 | name |
| 597630477 | CV3650901 | single nucleotide variant | NM_001868.4(CPA1):c.1152T>G (p.Thr384=) | Hereditary pancreatitis [RCV004822680] | likely benign | 7 | 130387903 | 130387903 | Human | 1 | name |
| 597630500 | CV3650911 | single nucleotide variant | NM_001868.4(CPA1):c.228G>T (p.Lys76Asn) | Hereditary pancreatitis [RCV004822690] | uncertain significance | 7 | 130381710 | 130381710 | Human | 1 | name |
| 597630377 | CV3654357 | deletion | NM_001868.4(CPA1):c.530del (p.Gly177fs) | Hereditary pancreatitis [RCV004822634] | likely benign | 7 | 130383435 | 130383435 | Human | 1 | name |
| 597630393 | CV3654366 | single nucleotide variant | NM_001868.4(CPA1):c.199G>A (p.Val67Met) | Hereditary pancreatitis [RCV004822642] | uncertain significance | 7 | 130381681 | 130381681 | Human | 1 | name |
| 597630414 | CV3654376 | single nucleotide variant | NM_001868.4(CPA1):c.127G>C (p.Glu43Gln) | Hereditary pancreatitis [RCV004822651] | uncertain significance | 7 | 130381159 | 130381159 | Human | 1 | name |
| 597630418 | CV3654378 | single nucleotide variant | NM_001868.4(CPA1):c.269T>C (p.Ile90Thr) | Hereditary pancreatitis [RCV004822653] | uncertain significance | 7 | 130381751 | 130381751 | Human | 1 | name |
| 597630420 | CV3654379 | single nucleotide variant | NM_001868.4(CPA1):c.193G>A (p.Val65Ile) | Hereditary pancreatitis [RCV004822654] | uncertain significance | 7 | 130381675 | 130381675 | Human | 1 | name |
| 597630425 | CV3654381 | single nucleotide variant | NM_001868.4(CPA1):c.175C>A (p.Pro59Thr) | Hereditary pancreatitis [RCV004822656] | uncertain significance | 7 | 130381657 | 130381657 | Human | 1 | name |
| 597630430 | CV3654384 | single nucleotide variant | NM_001868.4(CPA1):c.167C>G (p.Pro56Arg) | Hereditary pancreatitis [RCV004822659] | uncertain significance | 7 | 130381649 | 130381649 | Human | 1 | name |
| 597630434 | CV3654386 | single nucleotide variant | NM_001868.4(CPA1):c.187A>G (p.Ile63Val) | Hereditary pancreatitis [RCV004822660] | uncertain significance | 7 | 130381669 | 130381669 | Human | 1 | name |
| 597630438 | CV3654388 | single nucleotide variant | NM_001868.4(CPA1):c.203C>T (p.Pro68Leu) | Hereditary pancreatitis [RCV004822662] | uncertain significance | 7 | 130381685 | 130381685 | Human | 1 | name |
| 597630463 | CV3654400 | single nucleotide variant | NM_001868.4(CPA1):c.101C>A (p.Ala34Asp) | Hereditary pancreatitis [RCV004822673] | uncertain significance | 7 | 130381133 | 130381133 | Human | 1 | name |
| 598235074 | CV3945113 | single nucleotide variant | NM_001868.4(CPA1):c.164G>C (p.Gly55Ala) | Hereditary pancreatitis [RCV005320180] | uncertain significance | 7 | 130381646 | 130381646 | Human | 1 | name |
| 598235075 | CV3945114 | single nucleotide variant | NM_001868.4(CPA1):c.1038C>G (p.Thr346=) | Hereditary pancreatitis [RCV005320181] | likely benign | 7 | 130385889 | 130385889 | Human | 1 | name |
| 598235103 | CV3945122 | single nucleotide variant | NM_001868.4(CPA1):c.106G>T (p.Val36Leu) | Hereditary pancreatitis [RCV005320189] | uncertain significance | 7 | 130381138 | 130381138 | Human | 1 | name |
| 598235130 | CV3945129 | single nucleotide variant | NM_001868.4(CPA1):c.1065G>A (p.Lys355=) | Hereditary pancreatitis [RCV005320196] | likely benign | 7 | 130385916 | 130385916 | Human | 1 | name |
| 15134707 | CV735958 | single nucleotide variant | NM_001868.4(CPA1):c.1029C>T (p.Leu343=) | Hereditary pancreatitis [RCV002319599]|not provided [RCV000898336] | benign|likely benign | 7 | 130385880 | 130385880 | Human | 1 | name |
| 15176918 | CV735959 | single nucleotide variant | NM_001868.4(CPA1):c.1209G>A (p.Thr403=) | Hereditary pancreatitis [RCV002318899]|not provided [RCV000906536] | benign|likely benign | 7 | 130387960 | 130387960 | Human | 1 | name |
| 15180983 | CV766116 | single nucleotide variant | NM_001868.4(CPA1):c.1017C>T (p.Ala339=) | Hereditary pancreatitis [RCV002318900]|not provided [RCV000930017] | likely benign | 7 | 130385868 | 130385868 | Human | 1 | name |
| 25325341 | CV808948 | single nucleotide variant | NM_001868.4(CPA1):c.159G>C (p.Trp53Cys) | Hereditary pancreatitis [RCV002319164] | uncertain significance | 7 | 130381641 | 130381641 | Human | 1 | name |
| 25328904 | CV808949 | single nucleotide variant | NM_001868.4(CPA1):c.281A>G (p.Gln94Arg) | Hereditary pancreatitis [RCV002255602]|not provided [RCV001247645] | likely benign|conflicting interpretations of pathogenicity|uncertain significance | 7 | 130381763 | 130381763 | Human | 1 | name |
| 25321610 | CV808967 | single nucleotide variant | NM_001868.4(CPA1):c.1002G>A (p.Lys334=) | Hereditary pancreatitis [RCV002318903]|not provided [RCV002549301] | likely benign | 7 | 130385853 | 130385853 | Human | 1 | name |
| 25322320 | CV808969 | single nucleotide variant | NM_001868.4(CPA1):c.1122G>A (p.Lys374=) | Hereditary pancreatitis [RCV002318908] | likely benign | 7 | 130387873 | 130387873 | Human | 1 | name |
| 25323036 | CV808970 | single nucleotide variant | NM_001868.4(CPA1):c.1203G>A (p.Lys401=) | Hereditary pancreatitis [RCV002318920]|not provided [RCV002068825] | likely benign | 7 | 130387954 | 130387954 | Human | 1 | name |
| 25323054 | CV808971 | single nucleotide variant | NM_001868.4(CPA1):c.1213C>T (p.Leu405=) | Hereditary pancreatitis [RCV002318921] | likely benign | 7 | 130387964 | 130387964 | Human | 1 | name |
| 25323227 | CV808972 | single nucleotide variant | NM_001868.4(CPA1):c.1230C>T (p.Ile410=) | Hereditary pancreatitis [RCV002318926] | likely benign | 7 | 130387981 | 130387981 | Human | 1 | name |
| 8632337 | CV87545 | single nucleotide variant | NM_001868.4(CPA1):c.151G>A (p.Asp51Asn) | Hereditary pancreatitis [RCV005320173] | likely benign|not provided | 7 | 130381633 | 130381633 | Human | 1 | name |
| 38495810 | CV955057 | single nucleotide variant | NM_001868.4(CPA1):c.137A>T (p.Glu46Val) | Hereditary pancreatitis [RCV002379929]|not provided [RCV001242172] | uncertain significance | 7 | 130381169 | 130381169 | Human | 1 | name |
| 126752104 | CV992099 | single nucleotide variant | NM_001868.4(CPA1):c.131A>C (p.Asp44Ala) | Hereditary pancreatitis [RCV002379998]|not provided [RCV001297656] | uncertain significance | 7 | 130381163 | 130381163 | Human | 1 | name |
| 126748409 | CV1007248 | single nucleotide variant | NM_001868.4(CPA1):c.523G>A (p.Asp175Asn) | Hereditary pancreatitis [RCV003294307]|not provided [RCV001326336] | uncertain significance | 7 | 130383430 | 130383430 | Human | 1 | name |
| 126725905 | CV1027781 | single nucleotide variant | NM_001868.4(CPA1):c.419C>T (p.Pro140Leu) | Hereditary pancreatitis [RCV002329335]|not provided [RCV001348298] | uncertain significance | 7 | 130382145 | 130382145 | Human | 1 | name |
| 126730531 | CV1027782 | single nucleotide variant | NM_001868.4(CPA1):c.491C>T (p.Thr164Met) | not provided [RCV001349285] | uncertain significance | 7 | 130383398 | 130383398 | Human | | name |
| 126759858 | CV1027783 | single nucleotide variant | NM_001868.4(CPA1):c.527C>T (p.Thr176Met) | Hereditary pancreatitis [RCV002350618]|not provided [RCV001340252] | uncertain significance | 7 | 130383434 | 130383434 | Human | 1 | name |
| 126774122 | CV1027784 | single nucleotide variant | NM_001868.4(CPA1):c.686C>T (p.Thr229Met) | Hereditary pancreatitis [RCV002368140]|not provided [RCV001346861] | conflicting interpretations of pathogenicity|uncertain significance | 7 | 130383784 | 130383784 | Human | 1 | name |
| 126924793 | CV1044697 | single nucleotide variant | NM_001868.4(CPA1):c.343G>C (p.Asp115His) | Hereditary pancreatitis [RCV004037010]|not provided [RCV001367442] | uncertain significance | 7 | 130381825 | 130381825 | Human | 1 | name |
| 126919076 | CV1044698 | single nucleotide variant | NM_001868.4(CPA1):c.497G>C (p.Gly166Ala) | not provided [RCV001362088] | uncertain significance | 7 | 130383404 | 130383404 | Human | | name |
| 126908495 | CV1044699 | single nucleotide variant | NM_001868.4(CPA1):c.859A>G (p.Lys287Glu) | Hereditary pancreatitis [RCV003298598]|not provided [RCV001367926] | uncertain significance | 7 | 130385217 | 130385217 | Human | 1 | name |
| 126918322 | CV1044700 | single nucleotide variant | NM_001868.4(CPA1):c.943C>A (p.Pro315Thr) | Hereditary pancreatitis [RCV004822378]|not provided [RCV001372590] | uncertain significance | 7 | 130385301 | 130385301 | Human | 1 | name |
| 127237541 | CV1074437 | single nucleotide variant | NM_001868.4(CPA1):c.410C>G (p.Ala137Gly) | Hereditary pancreatitis [RCV002322419]|not provided [RCV001414936] | likely benign|uncertain significance | 7 | 130382136 | 130382136 | Human | 1 | name |
| 151887389 | CV1341334 | single nucleotide variant | NM_001868.4(CPA1):c.751G>C (p.Val251Leu) | Hereditary pancreatitis [RCV004822940]|not provided [RCV001887752] | uncertain significance | 7 | 130384590 | 130384590 | Human | 1 | name |
| 151792881 | CV1341533 | single nucleotide variant | NM_001868.4(CPA1):c.975C>G (p.Asp325Glu) | Hereditary pancreatitis [RCV005320898]|not provided [RCV001866408] | uncertain significance | 7 | 130385333 | 130385333 | Human | 1 | name |
| 151856847 | CV1347849 | single nucleotide variant | NM_001868.4(CPA1):c.494G>A (p.Gly165Glu) | Hereditary pancreatitis [RCV004044587]|not provided [RCV001979630] | uncertain significance | 7 | 130383401 | 130383401 | Human | 1 | name |
| 151779221 | CV1352240 | single nucleotide variant | NM_001868.4(CPA1):c.779G>A (p.Gly260Asp) | Hereditary pancreatitis [RCV003375555]|not provided [RCV002009580] | uncertain significance | 7 | 130384618 | 130384618 | Human | 1 | name |
| 151861469 | CV1353316 | single nucleotide variant | NM_001868.4(CPA1):c.865A>G (p.Ile289Val) | Hereditary pancreatitis [RCV002370539]|not provided [RCV001924052] | uncertain significance | 7 | 130385223 | 130385223 | Human | 1 | name |
| 151774858 | CV1362057 | single nucleotide variant | NM_001868.4(CPA1):c.718C>T (p.Arg240Trp) | Hereditary pancreatitis [RCV002370582]|not provided [RCV001950514] | uncertain significance | 7 | 130384557 | 130384557 | Human | 1 | name |
| 151864824 | CV1370872 | single nucleotide variant | NM_001868.4(CPA1):c.389A>C (p.Asp130Ala) | Hereditary pancreatitis [RCV002359359]|not provided [RCV001884406] | likely benign|uncertain significance | 7 | 130382115 | 130382115 | Human | 1 | name |
| 151858984 | CV1377712 | single nucleotide variant | NM_001868.4(CPA1):c.834G>C (p.Lys278Asn) | Hereditary pancreatitis [RCV002441037]|not provided [RCV001938302] | uncertain significance | 7 | 130385192 | 130385192 | Human | 1 | name |
| 151730580 | CV1385173 | single nucleotide variant | NM_001868.4(CPA1):c.432C>G (p.Ser144Arg) | Hereditary pancreatitis [RCV002331550]|not provided [RCV001967066] | uncertain significance | 7 | 130382158 | 130382158 | Human | 1 | name |
| 151767085 | CV1387673 | single nucleotide variant | NM_001868.4(CPA1):c.607G>A (p.Asp203Asn) | Hereditary pancreatitis [RCV002352682]|not provided [RCV001970811] | uncertain significance | 7 | 130383705 | 130383705 | Human | 1 | name |
| 151729613 | CV1388846 | single nucleotide variant | NM_001868.4(CPA1):c.710G>A (p.Arg237His) | Hereditary pancreatitis [RCV005321039]|not provided [RCV001966967] | uncertain significance | 7 | 130384549 | 130384549 | Human | 1 | name |
| 151715263 | CV1392652 | single nucleotide variant | NM_001868.4(CPA1):c.346A>G (p.Thr116Ala) | Hereditary pancreatitis [RCV002458767]|not provided [RCV001908843] | uncertain significance | 7 | 130381828 | 130381828 | Human | 1 | name |
| 151825880 | CV1393849 | single nucleotide variant | NM_001868.4(CPA1):c.959C>G (p.Thr320Arg) | not provided [RCV002030331] | uncertain significance | 7 | 130385317 | 130385317 | Human | | name |
| 151718799 | CV1397394 | single nucleotide variant | NM_001868.4(CPA1):c.815C>T (p.Ser272Leu) | Hereditary pancreatitis [RCV002423117]|not provided [RCV001982729] | uncertain significance | 7 | 130385173 | 130385173 | Human | 1 | name |
| 151714170 | CV1399454 | single nucleotide variant | NM_001868.4(CPA1):c.851T>C (p.Val284Ala) | Hereditary pancreatitis [RCV003303311]|not provided [RCV001908630] | uncertain significance | 7 | 130385209 | 130385209 | Human | 1 | name |
| 151797020 | CV1401041 | single nucleotide variant | NM_001868.4(CPA1):c.307C>T (p.Gln103Ter) | Hereditary pancreatitis [RCV004612098]|not provided [RCV002011220] | likely benign|uncertain significance | 7 | 130381789 | 130381789 | Human | 1 | name |
| 151824414 | CV1404101 | single nucleotide variant | NM_001868.4(CPA1):c.830G>A (p.Gly277Asp) | not provided [RCV001976051] | uncertain significance | 7 | 130385188 | 130385188 | Human | | name |
| 151709403 | CV1409232 | single nucleotide variant | NM_001868.4(CPA1):c.938T>C (p.Met313Thr) | Hereditary pancreatitis [RCV002370397]|not provided [RCV001907671] | uncertain significance | 7 | 130385296 | 130385296 | Human | 1 | name |
| 151789980 | CV1413306 | single nucleotide variant | NM_001868.4(CPA1):c.763A>T (p.Arg255Trp) | Hereditary pancreatitis [RCV003303487]|not provided [RCV001989982] | uncertain significance | 7 | 130384602 | 130384602 | Human | 1 | name |
| 151723649 | CV1414183 | single nucleotide variant | NM_001868.4(CPA1):c.673G>A (p.Gly225Ser) | Hereditary pancreatitis [RCV005321081]|not provided [RCV002004001] | uncertain significance | 7 | 130383771 | 130383771 | Human | 1 | name |
| 151843614 | CV1414630 | single nucleotide variant | NM_001868.4(CPA1):c.793G>T (p.Gly265Ter) | not provided [RCV001903150] | uncertain significance | 7 | 130385151 | 130385151 | Human | | name |
| 151810535 | CV1417360 | single nucleotide variant | NM_001868.4(CPA1):c.399C>A (p.Asp133Glu) | not provided [RCV002028929] | uncertain significance | 7 | 130382125 | 130382125 | Human | | name |
| 151718082 | CV1419581 | single nucleotide variant | NM_001868.4(CPA1):c.446G>C (p.Gly149Ala) | Hereditary pancreatitis [RCV003382751]|not provided [RCV001965532] | uncertain significance | 7 | 130382172 | 130382172 | Human | 1 | name |
| 151859435 | CV1423031 | single nucleotide variant | NM_001868.4(CPA1):c.329G>A (p.Arg110Gln) | Hereditary pancreatitis [RCV002324339]|not provided [RCV001923812] | uncertain significance | 7 | 130381811 | 130381811 | Human | 1 | name |
| 151737620 | CV1469445 | single nucleotide variant | NM_001868.4(CPA1):c.793G>A (p.Gly265Arg) | Hereditary pancreatitis [RCV002422895]|not provided [RCV002041893] | uncertain significance | 7 | 130385151 | 130385151 | Human | 1 | name |
| 151871775 | CV1480557 | single nucleotide variant | NM_001868.4(CPA1):c.719G>A (p.Arg240Gln) | Hereditary pancreatitis [RCV004822957]|not provided [RCV001906582] | uncertain significance | 7 | 130384558 | 130384558 | Human | 1 | name |
| 151832653 | CV1480558 | single nucleotide variant | NM_001868.4(CPA1):c.751G>A (p.Val251Met) | Hereditary pancreatitis [RCV002388810]|not provided [RCV001935211] | uncertain significance | 7 | 130384590 | 130384590 | Human | 1 | name |
| 151879366 | CV1490841 | single nucleotide variant | NM_001868.4(CPA1):c.298G>A (p.Glu100Lys) | Hereditary pancreatitis [RCV003167348]|not provided [RCV001940800] | uncertain significance | 7 | 130381780 | 130381780 | Human | 1 | name |
| 151734951 | CV1502467 | deletion | NM_001868.4(CPA1):c.1202del (p.Lys401fs) | not provided [RCV001911283] | uncertain significance | 7 | 130387952 | 130387952 | Human | | name |
| 151818287 | CV1505953 | single nucleotide variant | NM_001868.4(CPA1):c.322C>T (p.Arg108Trp) | Hereditary pancreatitis [RCV002324236]|not provided [RCV002049535] | uncertain significance | 7 | 130381804 | 130381804 | Human | 1 | name |
| 151798708 | CV1509204 | single nucleotide variant | NM_001868.4(CPA1):c.796G>C (p.Ala266Pro) | Hereditary pancreatitis [RCV002406934]|not provided [RCV001866929] | uncertain significance | 7 | 130385154 | 130385154 | Human | 1 | name |
| 151797869 | CV1512937 | single nucleotide variant | NM_001868.4(CPA1):c.397G>C (p.Asp133His) | Hereditary pancreatitis [RCV002359291]|not provided [RCV001866853] | uncertain significance | 7 | 130382123 | 130382123 | Human | 1 | name |
| 153002494 | CV1685090 | single nucleotide variant | NM_001868.4(CPA1):c.692G>A (p.Ser231Asn) | Hereditary pancreatitis [RCV002259240]|not provided [RCV005095901] | uncertain significance | 7 | 130383790 | 130383790 | Human | 1 | name |
| 155689319 | CV1784827 | single nucleotide variant | NM_001868.4(CPA1):c.307C>G (p.Gln103Glu) | Hereditary pancreatitis [RCV002319862]|not provided [RCV003718477] | likely benign|uncertain significance | 7 | 130381789 | 130381789 | Human | 1 | name |
| 155715293 | CV1784906 | single nucleotide variant | NM_001868.4(CPA1):c.308A>G (p.Gln103Arg) | Hereditary pancreatitis [RCV002325766]|not provided [RCV005096143] | likely benign|uncertain significance | 7 | 130381790 | 130381790 | Human | 1 | name |
| 155715957 | CV1785055 | single nucleotide variant | NM_001868.4(CPA1):c.309G>C (p.Gln103His) | Hereditary pancreatitis [RCV002325915] | uncertain significance | 7 | 130381791 | 130381791 | Human | 1 | name |
| 155729837 | CV1786383 | single nucleotide variant | NM_001868.4(CPA1):c.355T>C (p.Tyr119His) | Hereditary pancreatitis [RCV002339781] | uncertain significance | 7 | 130381837 | 130381837 | Human | 1 | name |
| 155675159 | CV1786453 | single nucleotide variant | NM_001868.4(CPA1):c.356A>C (p.Tyr119Ser) | Hereditary pancreatitis [RCV002454976] | uncertain significance | 7 | 130381838 | 130381838 | Human | 1 | name |
| 155675177 | CV1786457 | single nucleotide variant | NM_001868.4(CPA1):c.356A>G (p.Tyr119Cys) | Hereditary pancreatitis [RCV002454980] | uncertain significance | 7 | 130381838 | 130381838 | Human | 1 | name |
| 155678892 | CV1786593 | single nucleotide variant | NM_001868.4(CPA1):c.370A>C (p.Thr124Pro) | Hereditary pancreatitis [RCV002353029] | uncertain significance | 7 | 130381852 | 130381852 | Human | 1 | name |
| 155664913 | CV1787133 | single nucleotide variant | NM_001868.4(CPA1):c.389A>T (p.Asp130Val) | Hereditary pancreatitis [RCV002366388] | uncertain significance | 7 | 130382115 | 130382115 | Human | 1 | name |
| 155726836 | CV1787809 | single nucleotide variant | NM_001868.4(CPA1):c.421C>A (p.His141Asn) | Hereditary pancreatitis [RCV002328021] | uncertain significance | 7 | 130382147 | 130382147 | Human | 1 | name |
| 155718351 | CV1788622 | single nucleotide variant | NM_001868.4(CPA1):c.332C>T (p.Ala111Val) | Hereditary pancreatitis [RCV002326463] | uncertain significance | 7 | 130381814 | 130381814 | Human | 1 | name |
| 155690161 | CV1789181 | single nucleotide variant | NM_001868.4(CPA1):c.350T>C (p.Phe117Ser) | Hereditary pancreatitis [RCV002459206] | uncertain significance | 7 | 130381832 | 130381832 | Human | 1 | name |
| 155664322 | CV1790159 | single nucleotide variant | NM_001868.4(CPA1):c.386A>G (p.Tyr129Cys) | Hereditary pancreatitis [RCV002366253]|not provided [RCV005096419] | uncertain significance | 7 | 130382112 | 130382112 | Human | 1 | name |
| 155725516 | CV1790945 | single nucleotide variant | NM_001868.4(CPA1):c.419C>A (p.Pro140Gln) | Hereditary pancreatitis [RCV002327823]|not provided [RCV005058357] | uncertain significance | 7 | 130382145 | 130382145 | Human | 1 | name |
| 155725525 | CV1790947 | single nucleotide variant | NM_001868.4(CPA1):c.419C>G (p.Pro140Arg) | Hereditary pancreatitis [RCV002327825] | uncertain significance | 7 | 130382145 | 130382145 | Human | 1 | name |
| 155699943 | CV1791813 | single nucleotide variant | NM_001868.4(CPA1):c.316G>A (p.Ala106Thr) | Hereditary pancreatitis [RCV002322616] | uncertain significance | 7 | 130381798 | 130381798 | Human | 1 | name |
| 155700531 | CV1791914 | single nucleotide variant | NM_001868.4(CPA1):c.317C>T (p.Ala106Val) | Hereditary pancreatitis [RCV002322717] | uncertain significance | 7 | 130381799 | 130381799 | Human | 1 | name |
| 155716859 | CV1792032 | single nucleotide variant | NM_001868.4(CPA1):c.328C>G (p.Arg110Gly) | Hereditary pancreatitis [RCV002326144] | likely benign|uncertain significance | 7 | 130381810 | 130381810 | Human | 1 | name |
| 155684379 | CV1792728 | single nucleotide variant | NM_001868.4(CPA1):c.347C>G (p.Thr116Ser) | Hereditary pancreatitis [RCV002457357] | uncertain significance | 7 | 130381829 | 130381829 | Human | 1 | name |
| 155744581 | CV1793221 | single nucleotide variant | NM_001868.4(CPA1):c.364T>A (p.Tyr122Asn) | Hereditary pancreatitis [RCV002346647] | uncertain significance | 7 | 130381846 | 130381846 | Human | 1 | name |
| 155685740 | CV1793462 | single nucleotide variant | NM_001868.4(CPA1):c.380A>G (p.Glu127Gly) | Hereditary pancreatitis [RCV002355220] | uncertain significance | 7 | 130381862 | 130381862 | Human | 1 | name |
| 155739576 | CV1794353 | single nucleotide variant | NM_001868.4(CPA1):c.434A>G (p.Lys145Arg) | Hereditary pancreatitis [RCV002332244] | uncertain significance | 7 | 130382160 | 130382160 | Human | 1 | name |
| 155711286 | CV1795199 | single nucleotide variant | NM_001868.4(CPA1):c.325T>C (p.Ser109Pro) | Hereditary pancreatitis [RCV002324960] | uncertain significance | 7 | 130381807 | 130381807 | Human | 1 | name |
| 155682867 | CV1795829 | single nucleotide variant | NM_001868.4(CPA1):c.343G>A (p.Asp115Asn) | Hereditary pancreatitis [RCV002457108] | likely benign|uncertain significance | 7 | 130381825 | 130381825 | Human | 1 | name |
| 155730380 | CV1796118 | single nucleotide variant | NM_001868.4(CPA1):c.359C>T (p.Ala120Val) | Hereditary pancreatitis [RCV002339858] | uncertain significance | 7 | 130381841 | 130381841 | Human | 1 | name |
| 155666197 | CV1796346 | single nucleotide variant | NM_001868.4(CPA1):c.374T>G (p.Leu125Arg) | Hereditary pancreatitis [RCV002349298] | uncertain significance | 7 | 130381856 | 130381856 | Human | 1 | name |
| 155734841 | CV1797790 | single nucleotide variant | NM_001868.4(CPA1):c.428T>A (p.Val143Asp) | Hereditary pancreatitis [RCV002330196]|not provided [RCV003102560] | uncertain significance | 7 | 130382154 | 130382154 | Human | 1 | name |
| 155727619 | CV1798120 | single nucleotide variant | NM_001868.4(CPA1):c.443T>C (p.Ile148Thr) | Hereditary pancreatitis [RCV002328270] | uncertain significance | 7 | 130382169 | 130382169 | Human | 1 | name |
| 155727873 | CV1798197 | single nucleotide variant | NM_001868.4(CPA1):c.444T>G (p.Ile148Met) | Hereditary pancreatitis [RCV002328348] | uncertain significance | 7 | 130382170 | 130382170 | Human | 1 | name |
| 155728418 | CV1798321 | single nucleotide variant | NM_001868.4(CPA1):c.446G>A (p.Gly149Asp) | Hereditary pancreatitis [RCV002328472]|not provided [RCV003094716] | uncertain significance | 7 | 130382172 | 130382172 | Human | 1 | name |
| 155672169 | CV1798922 | single nucleotide variant | NM_001868.4(CPA1):c.490A>T (p.Thr164Ser) | Hereditary pancreatitis [RCV002351203] | uncertain significance | 7 | 130383397 | 130383397 | Human | 1 | name |
| 155672468 | CV1799158 | single nucleotide variant | NM_001868.4(CPA1):c.493G>A (p.Gly165Arg) | Hereditary pancreatitis [RCV002351307] | uncertain significance | 7 | 130383400 | 130383400 | Human | 1 | name |
| 155739838 | CV1799218 | single nucleotide variant | NM_001868.4(CPA1):c.494G>C (p.Gly165Ala) | Hereditary pancreatitis [RCV002342724] | uncertain significance | 7 | 130383401 | 130383401 | Human | 1 | name |
| 155667317 | CV1799724 | single nucleotide variant | NM_001868.4(CPA1):c.541C>T (p.Arg181Trp) | Hereditary pancreatitis [RCV002349478]|not provided [RCV003730100] | uncertain significance | 7 | 130383448 | 130383448 | Human | 1 | name |
| 155669607 | CV1800099 | single nucleotide variant | NM_001868.4(CPA1):c.547T>G (p.Trp183Gly) | Hereditary pancreatitis [RCV002349853] | uncertain significance | 7 | 130383454 | 130383454 | Human | 1 | name |
| 155696005 | CV1800631 | single nucleotide variant | NM_001868.4(CPA1):c.598T>C (p.Tyr200His) | Hereditary pancreatitis [RCV002357889] | uncertain significance | 7 | 130383696 | 130383696 | Human | 1 | name |
| 155696930 | CV1800846 | single nucleotide variant | NM_001868.4(CPA1):c.601G>A (p.Gly201Arg) | Hereditary pancreatitis [RCV002358104] | uncertain significance | 7 | 130383699 | 130383699 | Human | 1 | name |
| 155696943 | CV1800850 | single nucleotide variant | NM_001868.4(CPA1):c.601G>C (p.Gly201Arg) | Hereditary pancreatitis [RCV002358108]|not provided [RCV003730109] | uncertain significance | 7 | 130383699 | 130383699 | Human | 1 | name |
| 155673207 | CV1801269 | single nucleotide variant | NM_001868.4(CPA1):c.631G>A (p.Asp211Asn) | Hereditary pancreatitis [RCV002368862] | uncertain significance | 7 | 130383729 | 130383729 | Human | 1 | name |
| 155735686 | CV1801734 | single nucleotide variant | NM_001868.4(CPA1):c.463C>T (p.Arg155Cys) | Hereditary pancreatitis [RCV002330430] | uncertain significance | 7 | 130382189 | 130382189 | Human | 1 | name |
| 155735779 | CV1801815 | single nucleotide variant | NM_001868.4(CPA1):c.464G>A (p.Arg155His) | Hereditary pancreatitis [RCV002330447] | uncertain significance | 7 | 130382190 | 130382190 | Human | 1 | name |
| 155734041 | CV1802195 | single nucleotide variant | NM_001868.4(CPA1):c.488G>A (p.Ser163Asn) | Hereditary pancreatitis [RCV002340539]|not provided [RCV005096687] | uncertain significance | 7 | 130383395 | 130383395 | Human | 1 | name |
| 155745403 | CV1802807 | single nucleotide variant | NM_001868.4(CPA1):c.535C>T (p.His179Tyr) | Hereditary pancreatitis [RCV002347016] | uncertain significance | 7 | 130383442 | 130383442 | Human | 1 | name |
| 155687690 | CV1803693 | single nucleotide variant | NM_001868.4(CPA1):c.592C>G (p.Gln198Glu) | Hereditary pancreatitis [RCV002355847] | uncertain significance | 7 | 130383690 | 130383690 | Human | 1 | name |
| 155665079 | CV1803995 | single nucleotide variant | NM_001868.4(CPA1):c.619A>C (p.Thr207Pro) | Hereditary pancreatitis [RCV002366426]|not provided [RCV003560976] | uncertain significance | 7 | 130383717 | 130383717 | Human | 1 | name |
| 155724831 | CV1804738 | single nucleotide variant | NM_001868.4(CPA1):c.655A>T (p.Ile219Phe) | Hereditary pancreatitis [RCV002364394]|not provided [RCV003730120] | uncertain significance | 7 | 130383753 | 130383753 | Human | 1 | name |
| 155710245 | CV1805777 | single nucleotide variant | NM_001868.4(CPA1):c.503A>C (p.Lys168Thr) | Hereditary pancreatitis [RCV002335650] | uncertain significance | 7 | 130383410 | 130383410 | Human | 1 | name |
| 155711250 | CV1805934 | single nucleotide variant | NM_001868.4(CPA1):c.505C>T (p.Arg169Cys) | Hereditary pancreatitis [RCV002335780]|not provided [RCV005096727] | uncertain significance | 7 | 130383412 | 130383412 | Human | 1 | name |
| 155743156 | CV1806651 | single nucleotide variant | NM_001868.4(CPA1):c.557A>C (p.Gln186Pro) | Hereditary pancreatitis [RCV002344732] | uncertain significance | 7 | 130383464 | 130383464 | Human | 1 | name |
| 155680951 | CV1807326 | single nucleotide variant | NM_001868.4(CPA1):c.589A>C (p.Thr197Pro) | Hereditary pancreatitis [RCV002353615] | uncertain significance | 7 | 130383687 | 130383687 | Human | 1 | name |
| 155705842 | CV1807395 | single nucleotide variant | NM_001868.4(CPA1):c.611C>A (p.Ala204Glu) | Hereditary pancreatitis [RCV002360262] | uncertain significance | 7 | 130383709 | 130383709 | Human | 1 | name |
| 155706223 | CV1807553 | single nucleotide variant | NM_001868.4(CPA1):c.614C>T (p.Ala205Val) | Hereditary pancreatitis [RCV002360420] | uncertain significance | 7 | 130383712 | 130383712 | Human | 1 | name |
| 155712503 | CV1807983 | single nucleotide variant | NM_001868.4(CPA1):c.644T>C (p.Ile215Thr) | Hereditary pancreatitis [RCV002361844] | uncertain significance | 7 | 130383742 | 130383742 | Human | 1 | name |
| 155709139 | CV1808839 | single nucleotide variant | NM_001868.4(CPA1):c.473A>G (p.Tyr158Cys) | Hereditary pancreatitis [RCV002335506] | uncertain significance | 7 | 130382199 | 130382199 | Human | 1 | name |
| 155740473 | CV1809413 | single nucleotide variant | NM_001868.4(CPA1):c.499A>G (p.Ser167Gly) | Hereditary pancreatitis [RCV002342983] | uncertain significance | 7 | 130383406 | 130383406 | Human | 1 | name |
| 155740636 | CV1809534 | single nucleotide variant | NM_001868.4(CPA1):c.500G>A (p.Ser167Asn) | Hereditary pancreatitis [RCV002343096]|not provided [RCV003096563] | likely benign|uncertain significance | 7 | 130383407 | 130383407 | Human | 1 | name |
| 155742401 | CV1809968 | single nucleotide variant | NM_001868.4(CPA1):c.526A>C (p.Thr176Pro) | Hereditary pancreatitis [RCV002344369] | uncertain significance | 7 | 130383433 | 130383433 | Human | 1 | name |
| 155669828 | CV1810036 | single nucleotide variant | NM_001868.4(CPA1):c.548G>T (p.Trp183Leu) | Hereditary pancreatitis [RCV002349898] | uncertain significance | 7 | 130383455 | 130383455 | Human | 1 | name |
| 155703324 | CV1810524 | single nucleotide variant | NM_001868.4(CPA1):c.577G>T (p.Ala193Ser) | Hereditary pancreatitis [RCV002359712]|not provided [RCV003546787] | uncertain significance | 7 | 130383484 | 130383484 | Human | 1 | name |
| 155697845 | CV1811807 | single nucleotide variant | NM_001868.4(CPA1):c.658G>A (p.Val220Ile) | Hereditary pancreatitis [RCV002375801]|not provided [RCV003718540] | uncertain significance | 7 | 130383756 | 130383756 | Human | 1 | name |
| 155725921 | CV1811808 | single nucleotide variant | NM_001868.4(CPA1):c.658G>C (p.Val220Leu) | Hereditary pancreatitis [RCV002364532] | uncertain significance | 7 | 130383756 | 130383756 | Human | 1 | name |
| 155726366 | CV1811958 | single nucleotide variant | NM_001868.4(CPA1):c.661A>G (p.Thr221Ala) | Hereditary pancreatitis [RCV002364604]|not provided [RCV003098307] | uncertain significance | 7 | 130383759 | 130383759 | Human | 1 | name |
| 155716389 | CV1812588 | single nucleotide variant | NM_001868.4(CPA1):c.697A>C (p.Asn233His) | Hereditary pancreatitis [RCV002362541] | uncertain significance | 7 | 130384536 | 130384536 | Human | 1 | name |
| 155681085 | CV1812780 | single nucleotide variant | NM_001868.4(CPA1):c.724C>A (p.His242Asn) | Hereditary pancreatitis [RCV002371093] | uncertain significance | 7 | 130384563 | 130384563 | Human | 1 | name |
| 155728495 | CV1812976 | single nucleotide variant | NM_001868.4(CPA1):c.728C>T (p.Thr243Ile) | Hereditary pancreatitis [RCV002382670] | uncertain significance | 7 | 130384567 | 130384567 | Human | 1 | name |
| 155697923 | CV1813083 | single nucleotide variant | NM_001868.4(CPA1):c.754G>C (p.Asp252His) | Hereditary pancreatitis [RCV002393982] | uncertain significance | 7 | 130384593 | 130384593 | Human | 1 | name |
| 155698304 | CV1813157 | single nucleotide variant | NM_001868.4(CPA1):c.756C>A (p.Asp252Glu) | Hereditary pancreatitis [RCV002394056] | uncertain significance | 7 | 130384595 | 130384595 | Human | 1 | name |
| 155707412 | CV1813431 | single nucleotide variant | NM_001868.4(CPA1):c.761A>G (p.Asn254Ser) | Hereditary pancreatitis [RCV002396248] | uncertain significance | 7 | 130384600 | 130384600 | Human | 1 | name |
| 155747438 | CV1813662 | single nucleotide variant | NM_001868.4(CPA1):c.794G>A (p.Gly265Glu) | Hereditary pancreatitis [RCV002416858] | uncertain significance | 7 | 130385152 | 130385152 | Human | 1 | name |
| 155708656 | CV1813969 | single nucleotide variant | NM_001868.4(CPA1):c.830G>T (p.Gly277Val) | Hereditary pancreatitis [RCV002430387] | uncertain significance | 7 | 130385188 | 130385188 | Human | 1 | name |
| 155730246 | CV1814141 | single nucleotide variant | NM_001868.4(CPA1):c.834G>T (p.Lys278Asn) | Hereditary pancreatitis [RCV002434711] | uncertain significance | 7 | 130385192 | 130385192 | Human | 1 | name |
| 155731346 | CV1814306 | single nucleotide variant | NM_001868.4(CPA1):c.839C>A (p.Ala280Asp) | Hereditary pancreatitis [RCV002434873]|not provided [RCV003560988] | uncertain significance | 7 | 130385197 | 130385197 | Human | 1 | name |
| 155683504 | CV1815031 | single nucleotide variant | NM_001868.4(CPA1):c.929A>G (p.Gln310Arg) | Hereditary pancreatitis [RCV002371494] | uncertain significance | 7 | 130385287 | 130385287 | Human | 1 | name |
| 155671247 | CV1815622 | single nucleotide variant | NM_001868.4(CPA1):c.715A>G (p.Thr239Ala) | Hereditary pancreatitis [RCV002367569] | uncertain significance | 7 | 130384554 | 130384554 | Human | 1 | name |
| 155708934 | CV1815663 | single nucleotide variant | NM_001868.4(CPA1):c.716C>G (p.Thr239Ser) | Hereditary pancreatitis [RCV002378384] | uncertain significance | 7 | 130384555 | 130384555 | Human | 1 | name |
| 155679708 | CV1815778 | single nucleotide variant | NM_001868.4(CPA1):c.718C>G (p.Arg240Gly) | Hereditary pancreatitis [RCV002370774] | uncertain significance | 7 | 130384557 | 130384557 | Human | 1 | name |
| 155687327 | CV1815963 | single nucleotide variant | NM_001868.4(CPA1):c.746T>C (p.Ile249Thr) | Hereditary pancreatitis [RCV002391462]|not provided [RCV003660944] | uncertain significance | 7 | 130384585 | 130384585 | Human | 1 | name |
| 155697833 | CV1816789 | single nucleotide variant | NM_001868.4(CPA1):c.819G>C (p.Glu273Asp) | Hereditary pancreatitis [RCV002427886] | uncertain significance | 7 | 130385177 | 130385177 | Human | 1 | name |
| 155697860 | CV1816795 | single nucleotide variant | NM_001868.4(CPA1):c.819G>T (p.Glu273Asp) | Hereditary pancreatitis [RCV002427892] | uncertain significance | 7 | 130385177 | 130385177 | Human | 1 | name |
| 155698370 | CV1816904 | single nucleotide variant | NM_001868.4(CPA1):c.821C>T (p.Thr274Ile) | Hereditary pancreatitis [RCV002427982] | uncertain significance | 7 | 130385179 | 130385179 | Human | 1 | name |
| 155742776 | CV1816988 | single nucleotide variant | NM_001868.4(CPA1):c.823T>C (p.Tyr275His) | Hereditary pancreatitis [RCV002412540] | uncertain significance | 7 | 130385181 | 130385181 | Human | 1 | name |
| 155742800 | CV1817014 | single nucleotide variant | NM_001868.4(CPA1):c.824A>G (p.Tyr275Cys) | Hereditary pancreatitis [RCV002412549] | uncertain significance | 7 | 130385182 | 130385182 | Human | 1 | name |
| 155721401 | CV1817230 | single nucleotide variant | NM_001868.4(CPA1):c.862T>C (p.Ser288Pro) | Hereditary pancreatitis [RCV002449611] | uncertain significance | 7 | 130385220 | 130385220 | Human | 1 | name |
| 155712929 | CV1818049 | single nucleotide variant | NM_001868.4(CPA1):c.918C>G (p.His306Gln) | Hereditary pancreatitis [RCV002378909] | uncertain significance | 7 | 130385276 | 130385276 | Human | 1 | name |
| 155668161 | CV1818114 | single nucleotide variant | NM_001868.4(CPA1):c.958A>G (p.Thr320Ala) | Hereditary pancreatitis [RCV002385242] | uncertain significance | 7 | 130385316 | 130385316 | Human | 1 | name |
| 155706592 | CV1818527 | single nucleotide variant | NM_001868.4(CPA1):c.674G>C (p.Gly225Ala) | Hereditary pancreatitis [RCV002377961] | uncertain significance | 7 | 130383772 | 130383772 | Human | 1 | name |
| 155728041 | CV1819004 | single nucleotide variant | NM_001868.4(CPA1):c.706T>A (p.Trp236Arg) | Hereditary pancreatitis [RCV002365090] | uncertain significance | 7 | 130384545 | 130384545 | Human | 1 | name |
| 155728046 | CV1819006 | single nucleotide variant | NM_001868.4(CPA1):c.706T>C (p.Trp236Arg) | Hereditary pancreatitis [RCV002365092] | uncertain significance | 7 | 130384545 | 130384545 | Human | 1 | name |
| 155670620 | CV1819224 | single nucleotide variant | NM_001868.4(CPA1):c.710G>T (p.Arg237Leu) | Hereditary pancreatitis [RCV002367404] | uncertain significance | 7 | 130384549 | 130384549 | Human | 1 | name |
| 155718648 | CV1819407 | single nucleotide variant | NM_001868.4(CPA1):c.739C>G (p.Leu247Val) | Hereditary pancreatitis [RCV002380492] | uncertain significance | 7 | 130384578 | 130384578 | Human | 1 | name |
| 155718656 | CV1819409 | single nucleotide variant | NM_001868.4(CPA1):c.739C>T (p.Leu247Phe) | Hereditary pancreatitis [RCV002380494] | uncertain significance | 7 | 130384578 | 130384578 | Human | 1 | name |
| 155666277 | CV1819496 | single nucleotide variant | NM_001868.4(CPA1):c.740T>C (p.Leu247Pro) | Hereditary pancreatitis [RCV002384926] | uncertain significance | 7 | 130384579 | 130384579 | Human | 1 | name |
| 155667550 | CV1819713 | single nucleotide variant | NM_001868.4(CPA1):c.745A>G (p.Ile249Val) | Hereditary pancreatitis [RCV002385144] | likely benign | 7 | 130384584 | 130384584 | Human | 1 | name |
| 155737415 | CV1819863 | single nucleotide variant | NM_001868.4(CPA1):c.774C>A (p.Asp258Glu) | Hereditary pancreatitis [RCV002409654] | uncertain significance | 7 | 130384613 | 130384613 | Human | 1 | name |
| 155737702 | CV1820098 | single nucleotide variant | NM_001868.4(CPA1):c.779G>T (p.Gly260Val) | Hereditary pancreatitis [RCV002409889] | uncertain significance | 7 | 130384618 | 130384618 | Human | 1 | name |
| 155673173 | CV1820225 | single nucleotide variant | NM_001868.4(CPA1):c.811T>G (p.Cys271Gly) | Hereditary pancreatitis [RCV002421294] | uncertain significance | 7 | 130385169 | 130385169 | Human | 1 | name |
| 155673920 | CV1820329 | single nucleotide variant | NM_001868.4(CPA1):c.814T>G (p.Ser272Ala) | Hereditary pancreatitis [RCV002421398] | uncertain significance | 7 | 130385172 | 130385172 | Human | 1 | name |
| 155697399 | CV1820445 | single nucleotide variant | NM_001868.4(CPA1):c.817G>A (p.Glu273Lys) | Hereditary pancreatitis [RCV002427805] | uncertain significance | 7 | 130385175 | 130385175 | Human | 1 | name |
| 155713303 | CV1820545 | single nucleotide variant | NM_001868.4(CPA1):c.850G>A (p.Val284Met) | Hereditary pancreatitis [RCV002447741] | uncertain significance | 7 | 130385208 | 130385208 | Human | 1 | name |
| 155700628 | CV1821112 | single nucleotide variant | NM_001868.4(CPA1):c.900G>T (p.Lys300Asn) | Hereditary pancreatitis [RCV002376394] | uncertain significance | 7 | 130385258 | 130385258 | Human | 1 | name |
| 155694726 | CV1821426 | single nucleotide variant | NM_001868.4(CPA1):c.947A>G (p.Tyr316Cys) | Hereditary pancreatitis [RCV002443509] | uncertain significance | 7 | 130385305 | 130385305 | Human | 1 | name |
| 155692961 | CV1821743 | single nucleotide variant | NM_001868.4(CPA1):c.956A>G (p.Lys319Arg) | Hereditary pancreatitis [RCV002374316] | likely benign|uncertain significance | 7 | 130385314 | 130385314 | Human | 1 | name |
| 155708160 | CV1822477 | single nucleotide variant | NM_001868.4(CPA1):c.700C>G (p.Arg234Gly) | Hereditary pancreatitis [RCV002378252] | uncertain significance | 7 | 130384539 | 130384539 | Human | 1 | name |
| 155727364 | CV1822527 | single nucleotide variant | NM_001868.4(CPA1):c.701G>A (p.Arg234His) | Hereditary pancreatitis [RCV002364863]|not provided [RCV003718544] | uncertain significance | 7 | 130384540 | 130384540 | Human | 1 | name |
| 155727603 | CV1822629 | single nucleotide variant | NM_001868.4(CPA1):c.703A>G (p.Met235Val) | Hereditary pancreatitis [RCV002364946] | uncertain significance | 7 | 130384542 | 130384542 | Human | 1 | name |
| 155716855 | CV1822816 | single nucleotide variant | NM_001868.4(CPA1):c.731C>T (p.Ala244Val) | Hereditary pancreatitis [RCV002380095] | uncertain significance | 7 | 130384570 | 130384570 | Human | 1 | name |
| 155707837 | CV1823157 | single nucleotide variant | NM_001868.4(CPA1):c.763A>G (p.Arg255Gly) | Hereditary pancreatitis [RCV002396339] | uncertain significance | 7 | 130384602 | 130384602 | Human | 1 | name |
| 155666010 | CV1823580 | single nucleotide variant | NM_001868.4(CPA1):c.800G>T (p.Ser267Ile) | Hereditary pancreatitis [RCV002419211] | uncertain significance | 7 | 130385158 | 130385158 | Human | 1 | name |
| 155690612 | CV1824395 | single nucleotide variant | NM_001868.4(CPA1):c.885C>A (p.Asp295Glu) | Hereditary pancreatitis [RCV002373844] | uncertain significance | 7 | 130385243 | 130385243 | Human | 1 | name |
| 155698726 | CV1824434 | single nucleotide variant | NM_001868.4(CPA1):c.886C>T (p.His296Tyr) | Hereditary pancreatitis [RCV002375966] | uncertain significance | 7 | 130385244 | 130385244 | Human | 1 | name |
| 155723605 | CV1824737 | single nucleotide variant | NM_001868.4(CPA1):c.895A>C (p.Ile299Leu) | Hereditary pancreatitis [RCV002449894]|not provided [RCV003100066] | uncertain significance | 7 | 130385253 | 130385253 | Human | 1 | name |
| 155690758 | CV1825034 | single nucleotide variant | NM_001868.4(CPA1):c.939G>A (p.Met313Ile) | Hereditary pancreatitis [RCV002373877]|not provided [RCV003094799] | uncertain significance | 7 | 130385297 | 130385297 | Human | 1 | name |
| 155684123 | CV1825290 | single nucleotide variant | NM_001868.4(CPA1):c.931C>T (p.Leu311Phe) | Hereditary pancreatitis [RCV002371602] | uncertain significance | 7 | 130385289 | 130385289 | Human | 1 | name |
| 155673305 | CV1825527 | single nucleotide variant | NM_001868.4(CPA1):c.975C>A (p.Asp325Glu) | Hereditary pancreatitis [RCV002387111]|not provided [RCV003718578] | uncertain significance | 7 | 130385333 | 130385333 | Human | 1 | name |
| 155703897 | CV1828734 | single nucleotide variant | NM_001868.4(CPA1):c.981T>G (p.Asp327Glu) | Hereditary pancreatitis [RCV002376847] | uncertain significance | 7 | 130385339 | 130385339 | Human | 1 | name |
| 155674224 | CV1828761 | single nucleotide variant | NM_001868.4(CPA1):c.983A>C (p.Glu328Ala) | Hereditary pancreatitis [RCV002387259] | uncertain significance | 7 | 130385341 | 130385341 | Human | 1 | name |
| 155674475 | CV1828803 | single nucleotide variant | NM_001868.4(CPA1):c.984G>C (p.Glu328Asp) | Hereditary pancreatitis [RCV002387301] | uncertain significance | 7 | 130385342 | 130385342 | Human | 1 | name |
| 155697260 | CV1854857 | single nucleotide variant | NM_001868.4(CPA1):c.304G>A (p.Glu102Lys) | Hereditary pancreatitis [RCV002444095] | uncertain significance | 7 | 130381786 | 130381786 | Human | 1 | name |
| 156061070 | CV1868081 | single nucleotide variant | NM_001868.4(CPA1):c.844T>C (p.Ser282Pro) | not provided [RCV003037262] | pathogenic|likely pathogenic | 7 | 130385202 | 130385202 | Human | | name |
| 156364438 | CV1901696 | single nucleotide variant | NM_001868.4(CPA1):c.734G>A (p.Gly245Asp) | Hereditary pancreatitis [RCV003161885]|not provided [RCV002602720] | uncertain significance | 7 | 130384573 | 130384573 | Human | 1 | name |
| 156406502 | CV1921611 | single nucleotide variant | NM_001868.4(CPA1):c.313T>C (p.Phe105Leu) | not provided [RCV002606611] | uncertain significance | 7 | 130381795 | 130381795 | Human | | name |
| 156446426 | CV1937899 | single nucleotide variant | NM_001868.4(CPA1):c.700C>T (p.Arg234Cys) | Hereditary pancreatitis [RCV004244601]|not provided [RCV003117930] | uncertain significance | 7 | 130384539 | 130384539 | Human | 1 | name |
| 156449281 | CV1944547 | single nucleotide variant | NM_001868.4(CPA1):c.412G>A (p.Glu138Lys) | Hereditary pancreatitis [RCV003162148]|not provided [RCV003121399] | uncertain significance | 7 | 130382138 | 130382138 | Human | 1 | name |
| 156165156 | CV1971456 | single nucleotide variant | NM_001868.4(CPA1):c.884A>G (p.Asp295Gly) | Hereditary pancreatitis [RCV004823044]|not provided [RCV002594601] | uncertain significance | 7 | 130385242 | 130385242 | Human | 1 | name |
| 156251665 | CV2041083 | single nucleotide variant | NM_001868.4(CPA1):c.974A>T (p.Asp325Val) | Hereditary pancreatitis [RCV003167781]|not provided [RCV002806031] | uncertain significance | 7 | 130385332 | 130385332 | Human | 1 | name |
| 155913186 | CV2081459 | single nucleotide variant | NM_001868.4(CPA1):c.926C>T (p.Ser309Phe) | Hereditary pancreatitis [RCV005321253]|not provided [RCV002858636] | uncertain significance | 7 | 130385284 | 130385284 | Human | 1 | name |
| 156022798 | CV2145396 | single nucleotide variant | NM_001868.4(CPA1):c.361A>C (p.Thr121Pro) | not provided [RCV003018310] | uncertain significance | 7 | 130381843 | 130381843 | Human | | name |
| 156332128 | CV2181153 | single nucleotide variant | NM_001868.4(CPA1):c.923A>C (p.Tyr308Ser) | not provided [RCV003047281] | uncertain significance | 7 | 130385281 | 130385281 | Human | | name |
| 156322454 | CV2182864 | single nucleotide variant | NM_001868.4(CPA1):c.758C>A (p.Pro253His) | not provided [RCV003046704] | uncertain significance | 7 | 130384597 | 130384597 | Human | | name |
| 329364143 | CV2425530 | single nucleotide variant | NM_001868.4(CPA1):c.839C>T (p.Ala280Val) | Hereditary pancreatitis [RCV003181564] | uncertain significance | 7 | 130385197 | 130385197 | Human | 1 | name |
| 329364196 | CV2425531 | single nucleotide variant | NM_001868.4(CPA1):c.536A>G (p.His179Arg) | Hereditary pancreatitis [RCV003181565] | uncertain significance | 7 | 130383443 | 130383443 | Human | 1 | name |
| 329364198 | CV2425533 | single nucleotide variant | NM_001868.4(CPA1):c.469A>C (p.Ile157Leu) | Hereditary pancreatitis [RCV003181567] | uncertain significance | 7 | 130382195 | 130382195 | Human | 1 | name |
| 329364200 | CV2425535 | single nucleotide variant | NM_001868.4(CPA1):c.353A>G (p.Asn118Ser) | Hereditary pancreatitis [RCV003181569] | uncertain significance | 7 | 130381835 | 130381835 | Human | 1 | name |
| 329364203 | CV2425538 | single nucleotide variant | NM_001868.4(CPA1):c.905T>C (p.Phe302Ser) | Hereditary pancreatitis [RCV003181571] | uncertain significance | 7 | 130385263 | 130385263 | Human | 1 | name |
| 329364206 | CV2425542 | single nucleotide variant | NM_001868.4(CPA1):c.448A>C (p.Asn150His) | Hereditary pancreatitis [RCV003181574] | uncertain significance | 7 | 130382174 | 130382174 | Human | 1 | name |
| 329364207 | CV2425543 | single nucleotide variant | NM_001868.4(CPA1):c.382A>G (p.Ile128Val) | Hereditary pancreatitis [RCV003181575]|not provided [RCV003708736] | uncertain significance | 7 | 130382108 | 130382108 | Human | 1 | name |
| 329364209 | CV2425545 | single nucleotide variant | NM_001868.4(CPA1):c.649C>A (p.Leu217Met) | Hereditary pancreatitis [RCV003181577] | uncertain significance | 7 | 130383747 | 130383747 | Human | 1 | name |
| 329364211 | CV2425547 | single nucleotide variant | NM_001868.4(CPA1):c.338C>T (p.Ser113Phe) | Hereditary pancreatitis [RCV003181579] | uncertain significance | 7 | 130381820 | 130381820 | Human | 1 | name |
| 329364213 | CV2425550 | single nucleotide variant | NM_001868.4(CPA1):c.424C>T (p.Leu142Phe) | Hereditary pancreatitis [RCV003181581] | uncertain significance | 7 | 130382150 | 130382150 | Human | 1 | name |
| 329364216 | CV2425552 | single nucleotide variant | NM_001868.4(CPA1):c.559G>A (p.Ala187Thr) | Hereditary pancreatitis [RCV003181583] | uncertain significance | 7 | 130383466 | 130383466 | Human | 1 | name |
| 329364217 | CV2425553 | single nucleotide variant | NM_001868.4(CPA1):c.503A>G (p.Lys168Arg) | Hereditary pancreatitis [RCV003181584] | uncertain significance | 7 | 130383410 | 130383410 | Human | 1 | name |
| 329363469 | CV2425554 | single nucleotide variant | NM_001868.4(CPA1):c.836T>C (p.Phe279Ser) | Hereditary pancreatitis [RCV003168240] | uncertain significance | 7 | 130385194 | 130385194 | Human | 1 | name |
| 329364218 | CV2425555 | single nucleotide variant | NM_001868.4(CPA1):c.874T>A (p.Phe292Ile) | Hereditary pancreatitis [RCV003181585] | uncertain significance | 7 | 130385232 | 130385232 | Human | 1 | name |
| 329389910 | CV2465597 | single nucleotide variant | NM_001868.4(CPA1):c.865A>T (p.Ile289Phe) | Hereditary pancreatitis [RCV003216502] | uncertain significance | 7 | 130385223 | 130385223 | Human | 1 | name |
| 329389907 | CV2465599 | single nucleotide variant | NM_001868.4(CPA1):c.989A>T (p.Asp330Val) | Hereditary pancreatitis [RCV003216504] | uncertain significance | 7 | 130385840 | 130385840 | Human | 1 | name |
| 329389906 | CV2465600 | single nucleotide variant | NM_001868.4(CPA1):c.895A>T (p.Ile299Phe) | Hereditary pancreatitis [RCV003216505]|not provided [RCV005101370] | uncertain significance | 7 | 130385253 | 130385253 | Human | 1 | name |
| 329389905 | CV2465601 | single nucleotide variant | NM_001868.4(CPA1):c.368A>G (p.His123Arg) | Hereditary pancreatitis [RCV003216506]|not provided [RCV003720808] | uncertain significance | 7 | 130381850 | 130381850 | Human | 1 | name |
| 401772413 | CV2712715 | single nucleotide variant | NM_001868.4(CPA1):c.842A>G (p.Asn281Ser) | Hereditary pancreatitis [RCV004308022] | uncertain significance | 7 | 130385200 | 130385200 | Human | 1 | name |
| 401775063 | CV2723969 | single nucleotide variant | NM_001868.4(CPA1):c.868G>T (p.Val290Leu) | Hereditary pancreatitis [RCV003305489] | uncertain significance | 7 | 130385226 | 130385226 | Human | 1 | name |
| 401775064 | CV2723970 | single nucleotide variant | NM_001868.4(CPA1):c.629T>A (p.Leu210His) | Hereditary pancreatitis [RCV003305490] | uncertain significance | 7 | 130383727 | 130383727 | Human | 1 | name |
| 401775070 | CV2723972 | single nucleotide variant | NM_001868.4(CPA1):c.539C>T (p.Ser180Phe) | Hereditary pancreatitis [RCV003305492] | uncertain significance | 7 | 130383446 | 130383446 | Human | 1 | name |
| 401775071 | CV2723973 | single nucleotide variant | NM_001868.4(CPA1):c.730G>A (p.Ala244Thr) | Hereditary pancreatitis [RCV003305493] | uncertain significance | 7 | 130384569 | 130384569 | Human | 1 | name |
| 401765393 | CV2733681 | single nucleotide variant | NM_001868.4(CPA1):c.376G>A (p.Glu126Lys) | Hereditary pancreatitis [RCV003301385] | uncertain significance | 7 | 130381858 | 130381858 | Human | 1 | name |
| 401765395 | CV2733683 | single nucleotide variant | NM_001868.4(CPA1):c.395T>A (p.Leu132Gln) | Hereditary pancreatitis [RCV003301387] | uncertain significance | 7 | 130382121 | 130382121 | Human | 1 | name |
| 401765396 | CV2733684 | single nucleotide variant | NM_001868.4(CPA1):c.463C>G (p.Arg155Gly) | Hereditary pancreatitis [RCV003301388] | uncertain significance | 7 | 130382189 | 130382189 | Human | 1 | name |
| 401765402 | CV2733689 | single nucleotide variant | NM_001868.4(CPA1):c.626T>G (p.Ile209Ser) | Hereditary pancreatitis [RCV003301393] | uncertain significance | 7 | 130383724 | 130383724 | Human | 1 | name |
| 401765405 | CV2733691 | single nucleotide variant | NM_001868.4(CPA1):c.595G>A (p.Asp199Asn) | Hereditary pancreatitis [RCV003301395] | uncertain significance | 7 | 130383693 | 130383693 | Human | 1 | name |
| 401885405 | CV2783285 | single nucleotide variant | NM_001868.4(CPA1):c.406G>A (p.Val136Met) | Hereditary pancreatitis [RCV003386787] | uncertain significance | 7 | 130382132 | 130382132 | Human | 1 | name |
| 401885474 | CV2783307 | single nucleotide variant | NM_001868.4(CPA1):c.944C>T (p.Pro315Leu) | Hereditary pancreatitis [RCV003386809] | uncertain significance | 7 | 130385302 | 130385302 | Human | 1 | name |
| 401868424 | CV2787418 | single nucleotide variant | NM_001868.4(CPA1):c.514A>G (p.Ile172Val) | Hereditary pancreatitis [RCV003380194] | uncertain significance | 7 | 130383421 | 130383421 | Human | 1 | name |
| 401868425 | CV2787419 | single nucleotide variant | NM_001868.4(CPA1):c.674G>T (p.Gly225Val) | Hereditary pancreatitis [RCV003380195] | uncertain significance | 7 | 130383772 | 130383772 | Human | 1 | name |
| 401868428 | CV2787420 | single nucleotide variant | NM_001868.4(CPA1):c.722C>G (p.Ser241Cys) | Hereditary pancreatitis [RCV003380196] | uncertain significance | 7 | 130384561 | 130384561 | Human | 1 | name |
| 401868429 | CV2787421 | single nucleotide variant | NM_001868.4(CPA1):c.532A>C (p.Ile178Leu) | Hereditary pancreatitis [RCV003380197] | uncertain significance | 7 | 130383439 | 130383439 | Human | 1 | name |
| 401868430 | CV2787422 | single nucleotide variant | NM_001868.4(CPA1):c.650T>C (p.Leu217Pro) | Hereditary pancreatitis [RCV003380198] | uncertain significance | 7 | 130383748 | 130383748 | Human | 1 | name |
| 401868432 | CV2787423 | single nucleotide variant | NM_001868.4(CPA1):c.771G>C (p.Trp257Cys) | Hereditary pancreatitis [RCV003380199] | uncertain significance | 7 | 130384610 | 130384610 | Human | 1 | name |
| 401868435 | CV2787425 | single nucleotide variant | NM_001868.4(CPA1):c.400C>A (p.Leu134Met) | Hereditary pancreatitis [RCV003380201] | uncertain significance | 7 | 130382126 | 130382126 | Human | 1 | name |
| 401868436 | CV2787426 | single nucleotide variant | NM_001868.4(CPA1):c.920G>T (p.Ser307Ile) | Hereditary pancreatitis [RCV003380202] | uncertain significance | 7 | 130385278 | 130385278 | Human | 1 | name |
| 401868438 | CV2787427 | single nucleotide variant | NM_001868.4(CPA1):c.451A>G (p.Thr151Ala) | Hereditary pancreatitis [RCV003380203] | uncertain significance | 7 | 130382177 | 130382177 | Human | 1 | name |
| 401868441 | CV2787429 | single nucleotide variant | NM_001868.4(CPA1):c.716C>T (p.Thr239Ile) | Hereditary pancreatitis [RCV003380205] | uncertain significance | 7 | 130384555 | 130384555 | Human | 1 | name |
| 405211479 | CV2917278 | single nucleotide variant | NM_001868.4(CPA1):c.527C>A (p.Thr176Lys) | not provided [RCV003567229] | uncertain significance | 7 | 130383434 | 130383434 | Human | | name |
| 405249809 | CV3000897 | single nucleotide variant | NM_001868.4(CPA1):c.331G>A (p.Ala111Thr) | not provided [RCV003721444] | uncertain significance | 7 | 130381813 | 130381813 | Human | | name |
| 405134526 | CV3115584 | single nucleotide variant | NM_001868.4(CPA1):c.341C>T (p.Thr114Ile) | Hereditary pancreatitis [RCV004366709]|not provided [RCV003816241] | uncertain significance | 7 | 130381823 | 130381823 | Human | 1 | name |
| 405083577 | CV3137593 | single nucleotide variant | NM_001868.4(CPA1):c.332C>A (p.Ala111Glu) | not provided [RCV003834302] | uncertain significance | 7 | 130381814 | 130381814 | Human | | name |
| 405208608 | CV3145725 | single nucleotide variant | NM_001868.4(CPA1):c.433A>G (p.Lys145Glu) | not provided [RCV003845455] | uncertain significance | 7 | 130382159 | 130382159 | Human | | name |
| 405655639 | CV3380129 | single nucleotide variant | NM_001868.4(CPA1):c.310A>T (p.Met104Leu) | Hereditary pancreatitis [RCV004511141] | uncertain significance | 7 | 130381792 | 130381792 | Human | 1 | name |
| 405655641 | CV3380130 | single nucleotide variant | NM_001868.4(CPA1):c.312G>A (p.Met104Ile) | Hereditary pancreatitis [RCV004511142] | uncertain significance | 7 | 130381794 | 130381794 | Human | 1 | name |
| 405655642 | CV3380131 | single nucleotide variant | NM_001868.4(CPA1):c.385T>C (p.Tyr129His) | Hereditary pancreatitis [RCV004511143] | uncertain significance | 7 | 130382111 | 130382111 | Human | 1 | name |
| 405655644 | CV3380132 | single nucleotide variant | NM_001868.4(CPA1):c.423C>G (p.His141Gln) | Hereditary pancreatitis [RCV004511144] | likely benign | 7 | 130382149 | 130382149 | Human | 1 | name |
| 405655911 | CV3380133 | single nucleotide variant | NM_001868.4(CPA1):c.431G>T (p.Ser144Ile) | Hereditary pancreatitis [RCV004511145] | uncertain significance | 7 | 130382157 | 130382157 | Human | 1 | name |
| 405655649 | CV3380135 | single nucleotide variant | NM_001868.4(CPA1):c.461G>A (p.Gly154Glu) | Hereditary pancreatitis [RCV004511147] | uncertain significance | 7 | 130382187 | 130382187 | Human | 1 | name |
| 405655650 | CV3380136 | single nucleotide variant | NM_001868.4(CPA1):c.475G>A (p.Val159Met) | Hereditary pancreatitis [RCV004511148] | uncertain significance | 7 | 130382201 | 130382201 | Human | 1 | name |
| 405655651 | CV3380137 | single nucleotide variant | NM_001868.4(CPA1):c.496G>T (p.Gly166Cys) | Hereditary pancreatitis [RCV004511149] | uncertain significance | 7 | 130383403 | 130383403 | Human | 1 | name |
| 405655655 | CV3380139 | single nucleotide variant | NM_001868.4(CPA1):c.520A>T (p.Ile174Phe) | Hereditary pancreatitis [RCV004511151] | uncertain significance | 7 | 130383427 | 130383427 | Human | 1 | name |
| 405655659 | CV3380142 | single nucleotide variant | NM_001868.4(CPA1):c.551T>C (p.Val184Ala) | Hereditary pancreatitis [RCV004511154] | uncertain significance | 7 | 130383458 | 130383458 | Human | 1 | name |
| 405655661 | CV3380143 | single nucleotide variant | NM_001868.4(CPA1):c.554C>T (p.Thr185Ile) | Hereditary pancreatitis [RCV004511155] | uncertain significance | 7 | 130383461 | 130383461 | Human | 1 | name |
| 405655662 | CV3380144 | single nucleotide variant | NM_001868.4(CPA1):c.581A>G (p.Lys194Arg) | Hereditary pancreatitis [RCV004511156] | uncertain significance | 7 | 130383488 | 130383488 | Human | 1 | name |
| 405655664 | CV3380145 | single nucleotide variant | NM_001868.4(CPA1):c.601G>T (p.Gly201Trp) | Hereditary pancreatitis [RCV004511157] | uncertain significance | 7 | 130383699 | 130383699 | Human | 1 | name |
| 405655666 | CV3380146 | single nucleotide variant | NM_001868.4(CPA1):c.602G>T (p.Gly201Val) | Hereditary pancreatitis [RCV004511158] | uncertain significance | 7 | 130383700 | 130383700 | Human | 1 | name |
| 405655669 | CV3380148 | single nucleotide variant | NM_001868.4(CPA1):c.625A>G (p.Ile209Val) | Hereditary pancreatitis [RCV004511160]|not provided [RCV005104855] | likely benign|uncertain significance | 7 | 130383723 | 130383723 | Human | 1 | name |
| 405655670 | CV3380149 | single nucleotide variant | NM_001868.4(CPA1):c.626T>C (p.Ile209Thr) | Hereditary pancreatitis [RCV004511161] | uncertain significance | 7 | 130383724 | 130383724 | Human | 1 | name |
| 405655672 | CV3380150 | single nucleotide variant | NM_001868.4(CPA1):c.638T>G (p.Leu213Trp) | Hereditary pancreatitis [RCV004511162] | uncertain significance | 7 | 130383736 | 130383736 | Human | 1 | name |
| 405655674 | CV3380151 | single nucleotide variant | NM_001868.4(CPA1):c.643A>C (p.Ile215Leu) | Hereditary pancreatitis [RCV004511163] | uncertain significance | 7 | 130383741 | 130383741 | Human | 1 | name |
| 405655676 | CV3380152 | single nucleotide variant | NM_001868.4(CPA1):c.643A>G (p.Ile215Val) | Hereditary pancreatitis [RCV004511164] | uncertain significance | 7 | 130383741 | 130383741 | Human | 1 | name |
| 405655678 | CV3380154 | single nucleotide variant | NM_001868.4(CPA1):c.656T>C (p.Ile219Thr) | Hereditary pancreatitis [RCV004511166] | uncertain significance | 7 | 130383754 | 130383754 | Human | 1 | name |
| 405655680 | CV3380155 | single nucleotide variant | NM_001868.4(CPA1):c.662C>T (p.Thr221Ile) | Hereditary pancreatitis [RCV004511167] | uncertain significance | 7 | 130383760 | 130383760 | Human | 1 | name |
| 405655682 | CV3380156 | single nucleotide variant | NM_001868.4(CPA1):c.670G>A (p.Asp224Asn) | Hereditary pancreatitis [RCV004511168]|not provided [RCV005104856] | uncertain significance | 7 | 130383768 | 130383768 | Human | 1 | name |
| 405655913 | CV3380158 | single nucleotide variant | NM_001868.4(CPA1):c.701G>T (p.Arg234Leu) | Hereditary pancreatitis [RCV004511170] | uncertain significance | 7 | 130384540 | 130384540 | Human | 1 | name |
| 405655686 | CV3380159 | single nucleotide variant | NM_001868.4(CPA1):c.762C>A (p.Asn254Lys) | Hereditary pancreatitis [RCV004511171] | uncertain significance | 7 | 130384601 | 130384601 | Human | 1 | name |
| 405655688 | CV3380160 | single nucleotide variant | NM_001868.4(CPA1):c.767A>G (p.Asn256Ser) | Hereditary pancreatitis [RCV004511172] | uncertain significance | 7 | 130384606 | 130384606 | Human | 1 | name |
| 405655691 | CV3380162 | single nucleotide variant | NM_001868.4(CPA1):c.851T>G (p.Val284Gly) | Hereditary pancreatitis [RCV004511174] | uncertain significance | 7 | 130385209 | 130385209 | Human | 1 | name |
| 405655693 | CV3380163 | single nucleotide variant | NM_001868.4(CPA1):c.904T>A (p.Phe302Ile) | Hereditary pancreatitis [RCV004511175] | uncertain significance | 7 | 130385262 | 130385262 | Human | 1 | name |
| 405655694 | CV3380164 | single nucleotide variant | NM_001868.4(CPA1):c.949G>A (p.Gly317Ser) | Hereditary pancreatitis [RCV004511176] | uncertain significance | 7 | 130385307 | 130385307 | Human | 1 | name |
| 405655696 | CV3380165 | single nucleotide variant | NM_001868.4(CPA1):c.953A>G (p.Tyr318Cys) | Hereditary pancreatitis [RCV004511177] | uncertain significance | 7 | 130385311 | 130385311 | Human | 1 | name |
| 405655703 | CV3380169 | single nucleotide variant | NM_001868.4(CPA1):c.991C>G (p.Gln331Glu) | Hereditary pancreatitis [RCV004511181] | uncertain significance | 7 | 130385842 | 130385842 | Human | 1 | name |
| 407456910 | CV3419527 | single nucleotide variant | NM_001868.4(CPA1):c.937A>C (p.Met313Leu) | Hereditary pancreatitis [RCV004610921] | likely benign | 7 | 130385295 | 130385295 | Human | 1 | name |
| 407456912 | CV3419528 | single nucleotide variant | NM_001868.4(CPA1):c.665A>T (p.Asn222Ile) | Hereditary pancreatitis [RCV004610922] | uncertain significance | 7 | 130383763 | 130383763 | Human | 1 | name |
| 407456915 | CV3419530 | single nucleotide variant | NM_001868.4(CPA1):c.724C>T (p.His242Tyr) | Hereditary pancreatitis [RCV004610924] | uncertain significance | 7 | 130384563 | 130384563 | Human | 1 | name |
| 407456919 | CV3419532 | single nucleotide variant | NM_001868.4(CPA1):c.637T>G (p.Leu213Val) | Hereditary pancreatitis [RCV004610926] | uncertain significance | 7 | 130383735 | 130383735 | Human | 1 | name |
| 407456921 | CV3419533 | single nucleotide variant | NM_001868.4(CPA1):c.845C>T (p.Ser282Phe) | Hereditary pancreatitis [RCV004610927] | uncertain significance | 7 | 130385203 | 130385203 | Human | 1 | name |
| 407456927 | CV3419537 | single nucleotide variant | NM_001868.4(CPA1):c.344A>G (p.Asp115Gly) | Hereditary pancreatitis [RCV004610931] | uncertain significance | 7 | 130381826 | 130381826 | Human | 1 | name |
| 407456932 | CV3419540 | single nucleotide variant | NM_001868.4(CPA1):c.312G>T (p.Met104Ile) | Hereditary pancreatitis [RCV004610934] | uncertain significance | 7 | 130381794 | 130381794 | Human | 1 | name |
| 407457245 | CV3419543 | single nucleotide variant | NM_001868.4(CPA1):c.807C>A (p.Asn269Lys) | Hereditary pancreatitis [RCV004610937] | uncertain significance | 7 | 130385165 | 130385165 | Human | 1 | name |
| 597630466 | CV3650896 | single nucleotide variant | NM_001868.4(CPA1):c.504G>T (p.Lys168Asn) | Hereditary pancreatitis [RCV004822675] | likely benign | 7 | 130383411 | 130383411 | Human | 1 | name |
| 597630468 | CV3650897 | single nucleotide variant | NM_001868.4(CPA1):c.326C>G (p.Ser109Cys) | Hereditary pancreatitis [RCV004822676] | uncertain significance | 7 | 130381808 | 130381808 | Human | 1 | name |
| 597630470 | CV3650898 | single nucleotide variant | NM_001868.4(CPA1):c.335G>C (p.Arg112Pro) | Hereditary pancreatitis [RCV004822677] | uncertain significance | 7 | 130381817 | 130381817 | Human | 1 | name |
| 597630472 | CV3650899 | single nucleotide variant | NM_001868.4(CPA1):c.461G>C (p.Gly154Ala) | Hereditary pancreatitis [RCV004822678] | uncertain significance | 7 | 130382187 | 130382187 | Human | 1 | name |
| 597630475 | CV3650900 | single nucleotide variant | NM_001868.4(CPA1):c.400C>G (p.Leu134Val) | Hereditary pancreatitis [RCV004822679] | uncertain significance | 7 | 130382126 | 130382126 | Human | 1 | name |
| 597630479 | CV3650902 | single nucleotide variant | NM_001868.4(CPA1):c.704T>A (p.Met235Lys) | Hereditary pancreatitis [RCV004822681] | uncertain significance | 7 | 130384543 | 130384543 | Human | 1 | name |
| 597630484 | CV3650904 | single nucleotide variant | NM_001868.4(CPA1):c.459A>C (p.Glu153Asp) | Hereditary pancreatitis [RCV004822683] | uncertain significance | 7 | 130382185 | 130382185 | Human | 1 | name |
| 597630493 | CV3650908 | single nucleotide variant | NM_001868.4(CPA1):c.901G>C (p.Ala301Pro) | Hereditary pancreatitis [RCV004822687] | uncertain significance | 7 | 130385259 | 130385259 | Human | 1 | name |
| 597630495 | CV3650909 | single nucleotide variant | NM_001868.4(CPA1):c.482A>T (p.Lys161Met) | Hereditary pancreatitis [RCV004822688] | uncertain significance | 7 | 130382208 | 130382208 | Human | 1 | name |
| 597630498 | CV3650910 | single nucleotide variant | NM_001868.4(CPA1):c.685A>C (p.Thr229Pro) | Hereditary pancreatitis [RCV004822689] | uncertain significance | 7 | 130383783 | 130383783 | Human | 1 | name |
| 597630371 | CV3654354 | single nucleotide variant | NM_001868.4(CPA1):c.334C>T (p.Arg112Cys) | Hereditary pancreatitis [RCV004822631] | likely benign | 7 | 130381816 | 130381816 | Human | 1 | name |
| 597630372 | CV3654355 | single nucleotide variant | NM_001868.4(CPA1):c.494G>T (p.Gly165Val) | Hereditary pancreatitis [RCV004822632] | uncertain significance | 7 | 130383401 | 130383401 | Human | 1 | name |
| 597630379 | CV3654358 | single nucleotide variant | NM_001868.4(CPA1):c.755A>G (p.Asp252Gly) | Hereditary pancreatitis [RCV004822635] | uncertain significance | 7 | 130384594 | 130384594 | Human | 1 | name |
| 597630383 | CV3654361 | single nucleotide variant | NM_001868.4(CPA1):c.406G>C (p.Val136Leu) | Hereditary pancreatitis [RCV004822637] | uncertain significance | 7 | 130382132 | 130382132 | Human | 1 | name |
| 597630385 | CV3654362 | single nucleotide variant | NM_001868.4(CPA1):c.532A>G (p.Ile178Val) | Hereditary pancreatitis [RCV004822638] | uncertain significance | 7 | 130383439 | 130383439 | Human | 1 | name |
| 597630388 | CV3654363 | single nucleotide variant | NM_001868.4(CPA1):c.697A>G (p.Asn233Asp) | Hereditary pancreatitis [RCV004822639] | likely benign | 7 | 130384536 | 130384536 | Human | 1 | name |
| 597630389 | CV3654364 | single nucleotide variant | NM_001868.4(CPA1):c.938T>G (p.Met313Arg) | Hereditary pancreatitis [RCV004822640] | uncertain significance | 7 | 130385296 | 130385296 | Human | 1 | name |
| 597630391 | CV3654365 | single nucleotide variant | NM_001868.4(CPA1):c.618C>A (p.Phe206Leu) | Hereditary pancreatitis [RCV004822641] | likely benign | 7 | 130383716 | 130383716 | Human | 1 | name |
| 597630396 | CV3654367 | single nucleotide variant | NM_001868.4(CPA1):c.329G>T (p.Arg110Leu) | Hereditary pancreatitis [RCV004822643] | uncertain significance | 7 | 130381811 | 130381811 | Human | 1 | name |
| 597630402 | CV3654370 | single nucleotide variant | NM_001868.4(CPA1):c.973G>A (p.Asp325Asn) | Hereditary pancreatitis [RCV004822646] | uncertain significance | 7 | 130385331 | 130385331 | Human | 1 | name |
| 597630422 | CV3654380 | single nucleotide variant | NM_001868.4(CPA1):c.545A>T (p.Glu182Val) | Hereditary pancreatitis [RCV004822655]|not provided [RCV005110154] | uncertain significance | 7 | 130383452 | 130383452 | Human | 1 | name |
| 597630435 | CV3654387 | single nucleotide variant | NM_001868.4(CPA1):c.467C>G (p.Pro156Arg) | Hereditary pancreatitis [RCV004822661] | uncertain significance | 7 | 130382193 | 130382193 | Human | 1 | name |
| 597630444 | CV3654391 | single nucleotide variant | NM_001868.4(CPA1):c.344A>T (p.Asp115Val) | Hereditary pancreatitis [RCV004822665] | uncertain significance | 7 | 130381826 | 130381826 | Human | 1 | name |
| 597630446 | CV3654392 | single nucleotide variant | NM_001868.4(CPA1):c.842A>C (p.Asn281Thr) | Hereditary pancreatitis [RCV004822666] | uncertain significance | 7 | 130385200 | 130385200 | Human | 1 | name |
| 597630449 | CV3654393 | single nucleotide variant | NM_001868.4(CPA1):c.573G>T (p.Trp191Cys) | Hereditary pancreatitis [RCV004822667] | uncertain significance | 7 | 130383480 | 130383480 | Human | 1 | name |
| 597630451 | CV3654394 | single nucleotide variant | NM_001868.4(CPA1):c.704T>G (p.Met235Arg) | Hereditary pancreatitis [RCV004822668] | uncertain significance | 7 | 130384543 | 130384543 | Human | 1 | name |
| 597630454 | CV3654395 | single nucleotide variant | NM_001868.4(CPA1):c.721T>A (p.Ser241Thr) | Hereditary pancreatitis [RCV004822669] | uncertain significance | 7 | 130384560 | 130384560 | Human | 1 | name |
| 597630456 | CV3654397 | single nucleotide variant | NM_001868.4(CPA1):c.455A>G (p.Tyr152Cys) | Hereditary pancreatitis [RCV004822670] | uncertain significance | 7 | 130382181 | 130382181 | Human | 1 | name |
| 597630457 | CV3654398 | single nucleotide variant | NM_001868.4(CPA1):c.808C>T (p.Pro270Ser) | Hereditary pancreatitis [RCV004822671] | uncertain significance | 7 | 130385166 | 130385166 | Human | 1 | name |
| 597630464 | CV3654401 | single nucleotide variant | NM_001868.4(CPA1):c.371C>A (p.Thr124Asn) | Hereditary pancreatitis [RCV004822674] | uncertain significance | 7 | 130381853 | 130381853 | Human | 1 | name |
| 12840276 | CV368929 | single nucleotide variant | NM_001868.4(CPA1):c.657C>G (p.Ile219Met) | Hereditary pancreatitis [RCV002365575]|not provided [RCV000430381] | uncertain significance | 7 | 130383755 | 130383755 | Human | 1 | name |
| 597887220 | CV3741909 | single nucleotide variant | NM_001868.4(CPA1):c.491C>A (p.Thr164Lys) | not provided [RCV005070629] | uncertain significance | 7 | 130383398 | 130383398 | Human | | name |
| 597900917 | CV3796633 | single nucleotide variant | NM_001868.4(CPA1):c.404T>G (p.Leu135Arg) | not provided [RCV005152715] | uncertain significance | 7 | 130382130 | 130382130 | Human | | name |
| 597888798 | CV3859560 | single nucleotide variant | NM_001868.4(CPA1):c.907A>G (p.Ile303Val) | not provided [RCV005200216] | uncertain significance | 7 | 130385265 | 130385265 | Human | | name |
| 598235036 | CV3945104 | single nucleotide variant | NM_001868.4(CPA1):c.383T>G (p.Ile128Ser) | Hereditary pancreatitis [RCV005320170] | uncertain significance | 7 | 130382109 | 130382109 | Human | 1 | name |
| 598235053 | CV3945108 | single nucleotide variant | NM_001868.4(CPA1):c.959C>T (p.Thr320Ile) | Hereditary pancreatitis [RCV005320175] | uncertain significance | 7 | 130385317 | 130385317 | Human | 1 | name |
| 598235067 | CV3945111 | single nucleotide variant | NM_001868.4(CPA1):c.853G>A (p.Glu285Lys) | Hereditary pancreatitis [RCV005320178] | uncertain significance | 7 | 130385211 | 130385211 | Human | 1 | name |
| 598235090 | CV3945117 | single nucleotide variant | NM_001868.4(CPA1):c.490A>C (p.Thr164Pro) | Hereditary pancreatitis [RCV005320184] | uncertain significance | 7 | 130383397 | 130383397 | Human | 1 | name |
| 598235098 | CV3945120 | single nucleotide variant | NM_001868.4(CPA1):c.417C>A (p.Asn139Lys) | Hereditary pancreatitis [RCV005320187] | uncertain significance | 7 | 130382143 | 130382143 | Human | 1 | name |
| 598235124 | CV3945127 | single nucleotide variant | NM_001868.4(CPA1):c.985C>G (p.Leu329Val) | Hereditary pancreatitis [RCV005320194] | uncertain significance | 7 | 130385343 | 130385343 | Human | 1 | name |
| 598235135 | CV3945130 | single nucleotide variant | NM_001868.4(CPA1):c.748G>C (p.Gly250Arg) | Hereditary pancreatitis [RCV005320197] | uncertain significance | 7 | 130384587 | 130384587 | Human | 1 | name |
| 598235138 | CV3945131 | single nucleotide variant | NM_001868.4(CPA1):c.418C>T (p.Pro140Ser) | Hereditary pancreatitis [RCV005320198] | uncertain significance | 7 | 130382144 | 130382144 | Human | 1 | name |
| 13445797 | CV438371 | single nucleotide variant | NM_001868.4(CPA1):c.497G>A (p.Gly166Asp) | CPA1-related disorder [RCV003902818]|Hereditary pancreatitis [RCV002256328]|not provided [RCV000512869] | likely benign|conflicting interpretations of pathogenicity|uncertain significance | 7 | 130383404 | 130383404 | Human | 1 | name , trait , alternate_id |
| 13485790 | CV444065 | single nucleotide variant | NM_001868.4(CPA1):c.847G>A (p.Glu283Lys) | Hereditary pancreatitis [RCV002448571]|not provided [RCV000522708] | uncertain significance | 7 | 130385205 | 130385205 | Human | 1 | name |
| 15138262 | CV710771 | single nucleotide variant | NM_001868.4(CPA1):c.604C>A (p.Gln202Lys) | Hereditary pancreatitis [RCV002346171]|not provided [RCV000965760] | benign|likely benign | 7 | 130383702 | 130383702 | Human | 1 | name |
| 25316723 | CV808950 | single nucleotide variant | NM_001868.4(CPA1):c.358G>A (p.Ala120Thr) | Hereditary pancreatitis [RCV002319265]|not provided [RCV001242987] | uncertain significance | 7 | 130381840 | 130381840 | Human | 1 | name |
| 25317295 | CV808951 | single nucleotide variant | NM_001868.4(CPA1):c.371C>T (p.Thr124Ile) | CPA1-related disorder [RCV003928665]|Hereditary pancreatitis [RCV002258086]|not provided [RCV001516447] | benign|likely benign | 7 | 130381853 | 130381853 | Human | 1 | name , trait , alternate_id |
| 25318217 | CV808952 | single nucleotide variant | NM_001868.4(CPA1):c.401T>G (p.Leu134Arg) | Hereditary pancreatitis [RCV002319306] | uncertain significance | 7 | 130382127 | 130382127 | Human | 1 | name |
| 25318659 | CV808954 | single nucleotide variant | NM_001868.4(CPA1):c.421C>T (p.His141Tyr) | Hereditary pancreatitis [RCV002319330] | uncertain significance | 7 | 130382147 | 130382147 | Human | 1 | name |
| 25322624 | CV808956 | single nucleotide variant | NM_001868.4(CPA1):c.506G>A (p.Arg169His) | Hereditary pancreatitis [RCV002319395]|not provided [RCV002067663] | likely benign|uncertain significance | 7 | 130383413 | 130383413 | Human | 1 | name |
| 25323569 | CV808957 | single nucleotide variant | NM_001868.4(CPA1):c.542G>A (p.Arg181Gln) | Hereditary pancreatitis [RCV002319633]|not provided [RCV002551887] | uncertain significance | 7 | 130383449 | 130383449 | Human | 1 | name |
| 25324692 | CV808959 | single nucleotide variant | NM_001868.4(CPA1):c.622G>A (p.Ala208Thr) | Hereditary pancreatitis [RCV002354932]|not provided [RCV001517260] | benign|likely benign | 7 | 130383720 | 130383720 | Human | 1 | name |
| 25325543 | CV808961 | single nucleotide variant | NM_001868.4(CPA1):c.686C>A (p.Thr229Lys) | Hereditary pancreatitis [RCV002382256]|not provided [RCV003769613] | uncertain significance | 7 | 130383784 | 130383784 | Human | 1 | name |
| 25325643 | CV808962 | single nucleotide variant | NM_001868.4(CPA1):c.695C>T (p.Thr232Met) | Hereditary pancreatitis [RCV002391083]|not provided [RCV001517271] | benign|likely benign | 7 | 130383793 | 130383793 | Human | 1 | name |
| 25327222 | CV808964 | single nucleotide variant | NM_001868.4(CPA1):c.820A>G (p.Thr274Ala) | Hereditary pancreatitis [RCV002445189] | uncertain significance | 7 | 130385178 | 130385178 | Human | 1 | name |
| 25327336 | CV808965 | single nucleotide variant | NM_001868.4(CPA1):c.829G>A (p.Gly277Ser) | CPA1-related disorder [RCV004758136]|Hereditary pancreatitis [RCV002445197]|not provided [RCV001229837] | likely pathogenic|uncertain significance | 7 | 130385187 | 130385187 | Human | 1 | name , trait , alternate_id |
| 26884894 | CV833136 | single nucleotide variant | NM_001868.4(CPA1):c.322C>G (p.Arg108Gly) | not provided [RCV001052781] | uncertain significance | 7 | 130381804 | 130381804 | Human | | name |
| 26904363 | CV833138 | single nucleotide variant | NM_001868.4(CPA1):c.496G>A (p.Gly166Ser) | Hereditary pancreatitis [RCV004030756]|not provided [RCV001070606] | uncertain significance | 7 | 130383403 | 130383403 | Human | 1 | name |
| 26922161 | CV833139 | single nucleotide variant | NM_001868.4(CPA1):c.775G>T (p.Ala259Ser) | Hereditary pancreatitis [RCV002409432]|not provided [RCV001051580] | uncertain significance | 7 | 130384614 | 130384614 | Human | 1 | name |
| 26917101 | CV833140 | single nucleotide variant | NM_001868.4(CPA1):c.845C>G (p.Ser282Cys) | not provided [RCV001041312] | uncertain significance | 7 | 130385203 | 130385203 | Human | | name |
| 28883924 | CV859586 | single nucleotide variant | NM_001868.4(CPA1):c.768C>G (p.Asn256Lys) | not provided [RCV001091495] | likely pathogenic | 7 | 130384607 | 130384607 | Human | | name |
| 38461053 | CV945429 | single nucleotide variant | NM_001868.4(CPA1):c.709C>T (p.Arg237Cys) | Hereditary pancreatitis [RCV002366025]|not provided [RCV001229465] | uncertain significance | 7 | 130384548 | 130384548 | Human | 1 | name |
| 38494979 | CV955058 | single nucleotide variant | NM_001868.4(CPA1):c.691A>G (p.Ser231Gly) | Hereditary pancreatitis [RCV002375277]|not provided [RCV001241677] | uncertain significance | 7 | 130383789 | 130383789 | Human | 1 | name |
| 38498506 | CV955059 | single nucleotide variant | NM_001868.4(CPA1):c.713A>C (p.Lys238Thr) | not provided [RCV001243875] | uncertain significance | 7 | 130384552 | 130384552 | Human | | name |
| 126750192 | CV992100 | single nucleotide variant | NM_001868.4(CPA1):c.409G>A (p.Ala137Thr) | Hereditary pancreatitis [RCV003166659]|not provided [RCV001297279] | likely benign|uncertain significance | 7 | 130382135 | 130382135 | Human | 1 | name |
| 126732364 | CV992101 | single nucleotide variant | NM_001868.4(CPA1):c.635C>A (p.Thr212Asn) | Hereditary pancreatitis [RCV002366145]|not provided [RCV001304073] | likely benign|uncertain significance | 7 | 130383733 | 130383733 | Human | 1 | name |
| 126755553 | CV992102 | single nucleotide variant | NM_001868.4(CPA1):c.635C>G (p.Thr212Ser) | Hereditary pancreatitis [RCV002366126]|not provided [RCV001298380] | likely benign|uncertain significance | 7 | 130383733 | 130383733 | Human | 1 | name |
| 126755476 | CV992103 | single nucleotide variant | NM_001868.4(CPA1):c.776C>T (p.Ala259Val) | Hereditary pancreatitis [RCV003166754]|not provided [RCV001307869] | uncertain significance | 7 | 130384615 | 130384615 | Human | 1 | name |
| 126744512 | CV1007249 | single nucleotide variant | NM_001868.4(CPA1):c.1016C>A (p.Ala339Asp) | Hereditary pancreatitis [RCV002350573]|not provided [RCV001314949] | uncertain significance | 7 | 130385867 | 130385867 | Human | 1 | name |
| 126757325 | CV1007250 | single nucleotide variant | NM_001868.4(CPA1):c.1145G>A (p.Arg382Gln) | Hereditary pancreatitis [RCV002456424]|not provided [RCV001317457] | uncertain significance | 7 | 130387896 | 130387896 | Human | 1 | name |
| 126745216 | CV1027788 | single nucleotide variant | NM_001868.4(CPA1):c.1157G>A (p.Arg386His) | Hereditary pancreatitis [RCV002357174]|not provided [RCV001337182] | likely benign|uncertain significance | 7 | 130387908 | 130387908 | Human | 1 | name |
| 126774123 | CV1027789 | single nucleotide variant | NM_001868.4(CPA1):c.1193C>T (p.Pro398Leu) | Hereditary pancreatitis [RCV002350640]|not provided [RCV001346862] | uncertain significance | 7 | 130387944 | 130387944 | Human | 1 | name |
| 126921987 | CV1044701 | single nucleotide variant | NM_001868.4(CPA1):c.1033G>A (p.Gly345Arg) | Hereditary pancreatitis [RCV004822375]|not provided [RCV001364134] | uncertain significance | 7 | 130385884 | 130385884 | Human | 1 | name |
| 126915339 | CV1044702 | single nucleotide variant | NM_001868.4(CPA1):c.1137C>A (p.Phe379Leu) | Hereditary pancreatitis [RCV004037483]|not provided [RCV001370858] | uncertain significance | 7 | 130387888 | 130387888 | Human | 1 | name |
| 151771209 | CV1340248 | single nucleotide variant | NM_001868.4(CPA1):c.1228A>G (p.Ile410Val) | Hereditary pancreatitis [RCV003303252]|not provided [RCV001874465] | uncertain significance | 7 | 130387979 | 130387979 | Human | 1 | name |
| 151742044 | CV1386779 | single nucleotide variant | NM_001868.4(CPA1):c.1192C>T (p.Pro398Ser) | Hereditary pancreatitis [RCV002334823]|not provided [RCV001893361] | uncertain significance | 7 | 130387943 | 130387943 | Human | 1 | name |
| 151856278 | CV1387541 | single nucleotide variant | NM_001868.4(CPA1):c.1217C>T (p.Ala406Val) | Hereditary pancreatitis [RCV002352636]|not provided [RCV001996577] | uncertain significance | 7 | 130387968 | 130387968 | Human | 1 | name |
| 151880409 | CV1388489 | single nucleotide variant | NM_001868.4(CPA1):c.1151C>T (p.Thr384Ile) | Hereditary pancreatitis [RCV002352628]|not provided [RCV001982458] | uncertain significance | 7 | 130387902 | 130387902 | Human | 1 | name |
| 151881035 | CV1406057 | single nucleotide variant | NM_001868.4(CPA1):c.1112A>G (p.Gln371Arg) | Hereditary pancreatitis [RCV002441068]|not provided [RCV001941038] | uncertain significance | 7 | 130387863 | 130387863 | Human | 1 | name |
| 151862249 | CV1448698 | single nucleotide variant | NM_001868.4(CPA1):c.1009G>C (p.Val337Leu) | not provided [RCV001959369] | uncertain significance | 7 | 130385860 | 130385860 | Human | | name |
| 151847520 | CV1484016 | single nucleotide variant | NM_001868.4(CPA1):c.1153G>A (p.Gly385Arg) | not provided [RCV001903638] | uncertain significance | 7 | 130387904 | 130387904 | Human | | name |
| 151721781 | CV1491780 | single nucleotide variant | NM_001868.4(CPA1):c.1022C>A (p.Ala341Asp) | Hereditary pancreatitis [RCV003170404]|not provided [RCV002003779] | uncertain significance | 7 | 130385873 | 130385873 | Human | 1 | name |
| 153349759 | CV1693925 | single nucleotide variant | NM_001868.4(CPA1):c.1085G>A (p.Gly362Glu) | not provided [RCV002276177] | likely pathogenic | 7 | 130387836 | 130387836 | Human | | name |
| 155703378 | CV1774795 | single nucleotide variant | NM_001868.4(CPA1):c.1117A>C (p.Ile373Leu) | not provided [RCV002300074] | uncertain significance | 7 | 130387868 | 130387868 | Human | | name |
| 155664439 | CV1786539 | single nucleotide variant | NM_001868.4(CPA1):c.1151C>G (p.Thr384Ser) | Hereditary pancreatitis [RCV002348946] | uncertain significance | 7 | 130387902 | 130387902 | Human | 1 | name |
| 155719247 | CV1788769 | single nucleotide variant | NM_001868.4(CPA1):c.1138G>C (p.Glu380Gln) | Hereditary pancreatitis [RCV002326611] | uncertain significance | 7 | 130387889 | 130387889 | Human | 1 | name |
| 155704184 | CV1795298 | single nucleotide variant | NM_001868.4(CPA1):c.1135T>C (p.Phe379Leu) | Hereditary pancreatitis [RCV002445709] | uncertain significance | 7 | 130387886 | 130387886 | Human | 1 | name |
| 155682741 | CV1795809 | single nucleotide variant | NM_001868.4(CPA1):c.1141C>G (p.Leu381Val) | Hereditary pancreatitis [RCV002457088] | uncertain significance | 7 | 130387892 | 130387892 | Human | 1 | name |
| 155668398 | CV1799892 | single nucleotide variant | NM_001868.4(CPA1):c.1201A>C (p.Lys401Gln) | Hereditary pancreatitis [RCV002349646] | likely benign | 7 | 130387952 | 130387952 | Human | 1 | name |
| 155669502 | CV1800086 | single nucleotide variant | NM_001868.4(CPA1):c.1202A>G (p.Lys401Arg) | Hereditary pancreatitis [RCV002349840] | likely benign | 7 | 130387953 | 130387953 | Human | 1 | name |
| 155746695 | CV1800294 | single nucleotide variant | NM_001868.4(CPA1):c.1208C>T (p.Thr403Met) | Hereditary pancreatitis [RCV002347665]|not provided [RCV003096851] | uncertain significance | 7 | 130387959 | 130387959 | Human | 1 | name |
| 155687641 | CV1803679 | single nucleotide variant | NM_001868.4(CPA1):c.1211G>T (p.Trp404Leu) | Hereditary pancreatitis [RCV002355833] | uncertain significance | 7 | 130387962 | 130387962 | Human | 1 | name |
| 155666133 | CV1804254 | single nucleotide variant | NM_001868.4(CPA1):c.1219C>T (p.Leu407Phe) | Hereditary pancreatitis [RCV002366632]|not provided [RCV003718531] | uncertain significance | 7 | 130387970 | 130387970 | Human | 1 | name |
| 155737245 | CV1805457 | single nucleotide variant | NM_001868.4(CPA1):c.1185G>T (p.Gln395His) | Hereditary pancreatitis [RCV002330752]|not provided [RCV003660934] | uncertain significance | 7 | 130387936 | 130387936 | Human | 1 | name |
| 155721875 | CV1805607 | single nucleotide variant | NM_001868.4(CPA1):c.1186A>T (p.Ile396Phe) | Hereditary pancreatitis [RCV002338106] | uncertain significance | 7 | 130387937 | 130387937 | Human | 1 | name |
| 155713395 | CV1808097 | single nucleotide variant | NM_001868.4(CPA1):c.1223T>G (p.Leu408Arg) | Hereditary pancreatitis [RCV002361953] | uncertain significance | 7 | 130387974 | 130387974 | Human | 1 | name |
| 155730634 | CV1808471 | single nucleotide variant | NM_001868.4(CPA1):c.1177G>C (p.Ala393Pro) | Hereditary pancreatitis [RCV002339886] | uncertain significance | 7 | 130387928 | 130387928 | Human | 1 | name |
| 155726650 | CV1812617 | single nucleotide variant | NM_001868.4(CPA1):c.1234G>A (p.Glu412Lys) | Hereditary pancreatitis [RCV002364654] | uncertain significance | 7 | 130387985 | 130387985 | Human | 1 | name |
| 155715035 | CV1815446 | single nucleotide variant | NM_001868.4(CPA1):c.1232T>A (p.Met411Lys) | Hereditary pancreatitis [RCV002362240] | uncertain significance | 7 | 130387983 | 130387983 | Human | 1 | name |
| 155742295 | CV1816629 | single nucleotide variant | NM_001868.4(CPA1):c.1252C>G (p.Pro418Ala) | Hereditary pancreatitis [RCV002412327] | uncertain significance | 7 | 130388003 | 130388003 | Human | 1 | name |
| 155742318 | CV1816642 | single nucleotide variant | NM_001868.4(CPA1):c.1252C>T (p.Pro418Ser) | Hereditary pancreatitis [RCV002412340] | uncertain significance | 7 | 130388003 | 130388003 | Human | 1 | name |
| 155722321 | CV1817549 | single nucleotide variant | NM_001868.4(CPA1):c.1001A>G (p.Lys334Arg) | Hereditary pancreatitis [RCV002449737] | uncertain significance | 7 | 130385852 | 130385852 | Human | 1 | name |
| 155670829 | CV1819305 | single nucleotide variant | NM_001868.4(CPA1):c.1238A>G (p.His413Arg) | Hereditary pancreatitis [RCV002367457] | uncertain significance | 7 | 130387989 | 130387989 | Human | 1 | name |
| 155666527 | CV1819539 | single nucleotide variant | NM_001868.4(CPA1):c.1243C>A (p.Leu415Met) | Hereditary pancreatitis [RCV002384969] | uncertain significance | 7 | 130387994 | 130387994 | Human | 1 | name |
| 155726825 | CV1822302 | single nucleotide variant | NM_001868.4(CPA1):c.1234G>C (p.Glu412Gln) | Hereditary pancreatitis [RCV002364689] | likely benign|uncertain significance | 7 | 130387985 | 130387985 | Human | 1 | name |
| 155717272 | CV1822923 | single nucleotide variant | NM_001868.4(CPA1):c.1241C>T (p.Thr414Ile) | Hereditary pancreatitis [RCV002380202] | uncertain significance | 7 | 130387992 | 130387992 | Human | 1 | name |
| 155728942 | CV1823423 | single nucleotide variant | NM_001868.4(CPA1):c.1249C>T (p.His417Tyr) | Hereditary pancreatitis [RCV002400563] | uncertain significance | 7 | 130388000 | 130388000 | Human | 1 | name |
| 155694017 | CV1827506 | single nucleotide variant | NM_001868.4(CPA1):c.1003G>A (p.Ala335Thr) | Hereditary pancreatitis [RCV002392651]|not provided [RCV003096968] | uncertain significance | 7 | 130385854 | 130385854 | Human | 1 | name |
| 155718706 | CV1827819 | single nucleotide variant | NM_001868.4(CPA1):c.1003G>C (p.Ala335Pro) | Hereditary pancreatitis [RCV002398537] | uncertain significance | 7 | 130385854 | 130385854 | Human | 1 | name |
| 155700610 | CV1828473 | single nucleotide variant | NM_001868.4(CPA1):c.1058T>G (p.Ile353Ser) | Hereditary pancreatitis [RCV002401457] | uncertain significance | 7 | 130385909 | 130385909 | Human | 1 | name |
| 155720072 | CV1835727 | single nucleotide variant | NM_001868.4(CPA1):c.1025C>G (p.Ser342Cys) | Hereditary pancreatitis [RCV002380728] | uncertain significance | 7 | 130385876 | 130385876 | Human | 1 | name |
| 155720167 | CV1835741 | single nucleotide variant | NM_001868.4(CPA1):c.1025C>T (p.Ser342Phe) | Hereditary pancreatitis [RCV002380742] | uncertain significance | 7 | 130385876 | 130385876 | Human | 1 | name |
| 155706424 | CV1837164 | single nucleotide variant | NM_001868.4(CPA1):c.1042T>G (p.Phe348Val) | Hereditary pancreatitis [RCV002402971] | uncertain significance | 7 | 130385893 | 130385893 | Human | 1 | name |
| 155730861 | CV1837531 | single nucleotide variant | NM_001868.4(CPA1):c.1049A>G (p.Tyr350Cys) | Hereditary pancreatitis [RCV002400874] | uncertain significance | 7 | 130385900 | 130385900 | Human | 1 | name |
| 155723990 | CV1837964 | single nucleotide variant | NM_001868.4(CPA1):c.1054A>C (p.Ser352Arg) | Hereditary pancreatitis [RCV002406103] | uncertain significance | 7 | 130385905 | 130385905 | Human | 1 | name |
| 155714583 | CV1841911 | single nucleotide variant | NM_001868.4(CPA1):c.1100G>A (p.Trp367Ter) | Hereditary pancreatitis [RCV002431146] | likely benign | 7 | 130387851 | 130387851 | Human | 1 | name |
| 155694790 | CV1844480 | single nucleotide variant | NM_001868.4(CPA1):c.1089C>G (p.Ser363Arg) | Hereditary pancreatitis [RCV002443528] | uncertain significance | 7 | 130387840 | 130387840 | Human | 1 | name |
| 155670901 | CV1848993 | single nucleotide variant | NM_001868.4(CPA1):c.1009G>A (p.Val337Met) | Hereditary pancreatitis [RCV002453182]|not provided [RCV005098253] | uncertain significance | 7 | 130385860 | 130385860 | Human | 1 | name |
| 155664013 | CV1849406 | single nucleotide variant | NM_001868.4(CPA1):c.1117A>T (p.Ile373Phe) | Hereditary pancreatitis [RCV002435034] | uncertain significance | 7 | 130387868 | 130387868 | Human | 1 | name |
| 155684596 | CV1849892 | single nucleotide variant | NM_001868.4(CPA1):c.1006G>T (p.Ala336Ser) | Hereditary pancreatitis [RCV002423946] | uncertain significance | 7 | 130385857 | 130385857 | Human | 1 | name |
| 155684848 | CV1849960 | single nucleotide variant | NM_001868.4(CPA1):c.1079C>G (p.Ala360Gly) | Hereditary pancreatitis [RCV002424014] | uncertain significance | 7 | 130387830 | 130387830 | Human | 1 | name |
| 155703110 | CV1852290 | single nucleotide variant | NM_001868.4(CPA1):c.1109G>A (p.Ser370Asn) | Hereditary pancreatitis [RCV002428801] | likely benign | 7 | 130387860 | 130387860 | Human | 1 | name |
| 155703309 | CV1852324 | single nucleotide variant | NM_001868.4(CPA1):c.1109G>T (p.Ser370Ile) | Hereditary pancreatitis [RCV002428825] | uncertain significance | 7 | 130387860 | 130387860 | Human | 1 | name |
| 155697275 | CV1854860 | single nucleotide variant | NM_001868.4(CPA1):c.1126T>C (p.Ser376Pro) | Hereditary pancreatitis [RCV002444098]|not provided [RCV005098403] | uncertain significance | 7 | 130387877 | 130387877 | Human | 1 | name |
| 155798681 | CV1860750 | single nucleotide variant | NM_001868.4(CPA1):c.1124A>G (p.Tyr375Cys) | Hereditary pancreatitis [RCV002467392] | uncertain significance | 7 | 130387875 | 130387875 | Human | 1 | name |
| 156305029 | CV1868082 | single nucleotide variant | NM_001868.4(CPA1):c.1138G>A (p.Glu380Lys) | not provided [RCV003062143] | uncertain significance | 7 | 130387889 | 130387889 | Human | | name |
| 156398939 | CV1897334 | single nucleotide variant | NM_001868.4(CPA1):c.1199C>T (p.Ala400Val) | Hereditary pancreatitis [RCV003294521]|not provided [RCV002584665] | uncertain significance | 7 | 130387950 | 130387950 | Human | 1 | name |
| 156442343 | CV1938569 | single nucleotide variant | NM_001868.4(CPA1):c.1129T>C (p.Phe377Leu) | Hereditary pancreatitis [RCV003384357]|not provided [RCV003112684] | uncertain significance | 7 | 130387880 | 130387880 | Human | 1 | name |
| 329364197 | CV2425532 | single nucleotide variant | NM_001868.4(CPA1):c.1033G>T (p.Gly345Trp) | Hereditary pancreatitis [RCV003181566] | uncertain significance | 7 | 130385884 | 130385884 | Human | 1 | name |
| 329389922 | CV2465587 | single nucleotide variant | NM_001868.4(CPA1):c.1010T>C (p.Val337Ala) | Hereditary pancreatitis [RCV003216492] | uncertain significance | 7 | 130385861 | 130385861 | Human | 1 | name |
| 329389921 | CV2465588 | single nucleotide variant | NM_001868.4(CPA1):c.1180T>C (p.Ser394Pro) | Hereditary pancreatitis [RCV003216493] | uncertain significance | 7 | 130387931 | 130387931 | Human | 1 | name |
| 329389920 | CV2465589 | single nucleotide variant | NM_001868.4(CPA1):c.1256A>G (p.Tyr419Cys) | Hereditary pancreatitis [RCV003216494]|not provided [RCV003779759] | uncertain significance | 7 | 130388007 | 130388007 | Human | 1 | name |
| 329389919 | CV2465590 | single nucleotide variant | NM_001868.4(CPA1):c.1110C>G (p.Ser370Arg) | Hereditary pancreatitis [RCV003216495] | uncertain significance | 7 | 130387861 | 130387861 | Human | 1 | name |
| 401765394 | CV2733682 | single nucleotide variant | NM_001868.4(CPA1):c.1103C>T (p.Thr368Ile) | Hereditary pancreatitis [RCV003301386] | uncertain significance | 7 | 130387854 | 130387854 | Human | 1 | name |
| 401885267 | CV2783218 | single nucleotide variant | NM_001868.4(CPA1):c.1142T>A (p.Leu381His) | Hereditary pancreatitis [RCV003386720] | uncertain significance | 7 | 130387893 | 130387893 | Human | 1 | name |
| 401885366 | CV2783248 | single nucleotide variant | NM_001868.4(CPA1):c.1069A>G (p.Ile357Val) | Hereditary pancreatitis [RCV003386750] | uncertain significance | 7 | 130385920 | 130385920 | Human | 1 | name |
| 401885381 | CV2783277 | single nucleotide variant | NM_001868.4(CPA1):c.1141C>T (p.Leu381Phe) | Hereditary pancreatitis [RCV003386779]|not provided [RCV005104178] | uncertain significance | 7 | 130387892 | 130387892 | Human | 1 | name |
| 401868434 | CV2787424 | single nucleotide variant | NM_001868.4(CPA1):c.1105T>C (p.Tyr369His) | Hereditary pancreatitis [RCV003380200] | uncertain significance | 7 | 130387856 | 130387856 | Human | 1 | name |
| 405194912 | CV2982236 | single nucleotide variant | NM_001868.4(CPA1):c.1101G>C (p.Trp367Cys) | not provided [RCV003706811] | uncertain significance | 7 | 130387852 | 130387852 | Human | | name |
| 405144039 | CV3056057 | single nucleotide variant | NM_001868.4(CPA1):c.1251C>A (p.His417Gln) | Hereditary pancreatitis [RCV004374097]|not provided [RCV003725805] | uncertain significance | 7 | 130388002 | 130388002 | Human | 1 | name |
| 405123798 | CV3136369 | single nucleotide variant | NM_001868.4(CPA1):c.1120A>G (p.Lys374Glu) | not provided [RCV003837699] | uncertain significance | 7 | 130387871 | 130387871 | Human | | name |
| 405229943 | CV3153793 | single nucleotide variant | NM_001868.4(CPA1):c.1007C>T (p.Ala336Val) | not provided [RCV003848660] | uncertain significance | 7 | 130385858 | 130385858 | Human | | name |
| 405685812 | CV3235788 | single nucleotide variant | NM_001868.4(CPA1):c.1073A>G (p.Tyr358Cys) | Hereditary pancreatitis [RCV004372302] | uncertain significance | 7 | 130387824 | 130387824 | Human | 1 | name |
| 405685819 | CV3235790 | single nucleotide variant | NM_001868.4(CPA1):c.1180T>A (p.Ser394Thr) | Hereditary pancreatitis [RCV004372304]|not provided [RCV005064993] | uncertain significance | 7 | 130387931 | 130387931 | Human | 1 | name |
| 405655603 | CV3383118 | single nucleotide variant | NM_001868.4(CPA1):c.1061T>A (p.Ile354Asn) | Hereditary pancreatitis [RCV004511119] | uncertain significance | 7 | 130385912 | 130385912 | Human | 1 | name |
| 405655607 | CV3383120 | single nucleotide variant | NM_001868.4(CPA1):c.1133C>A (p.Thr378Asn) | Hereditary pancreatitis [RCV004511121] | uncertain significance | 7 | 130387884 | 130387884 | Human | 1 | name |
| 405655616 | CV3383125 | single nucleotide variant | NM_001868.4(CPA1):c.1156C>A (p.Arg386Ser) | Hereditary pancreatitis [RCV004511126] | uncertain significance | 7 | 130387907 | 130387907 | Human | 1 | name |
| 405655622 | CV3383129 | single nucleotide variant | NM_001868.4(CPA1):c.1226C>A (p.Thr409Asn) | Hereditary pancreatitis [RCV004511130] | uncertain significance | 7 | 130387977 | 130387977 | Human | 1 | name |
| 405655624 | CV3383130 | single nucleotide variant | NM_001868.4(CPA1):c.1232T>C (p.Met411Thr) | Hereditary pancreatitis [RCV004511131] | uncertain significance | 7 | 130387983 | 130387983 | Human | 1 | name |
| 405655625 | CV3383131 | single nucleotide variant | NM_001868.4(CPA1):c.1233G>T (p.Met411Ile) | Hereditary pancreatitis [RCV004511132] | uncertain significance | 7 | 130387984 | 130387984 | Human | 1 | name |
| 405655627 | CV3383132 | single nucleotide variant | NM_001868.4(CPA1):c.1247A>C (p.Asn416Thr) | Hereditary pancreatitis [RCV004511133] | uncertain significance | 7 | 130387998 | 130387998 | Human | 1 | name |
| 407456896 | CV3419519 | single nucleotide variant | NM_001868.4(CPA1):c.1137C>G (p.Phe379Leu) | Hereditary pancreatitis [RCV004610913] | uncertain significance | 7 | 130387888 | 130387888 | Human | 1 | name |
| 407456909 | CV3419526 | single nucleotide variant | NM_001868.4(CPA1):c.1063A>G (p.Lys355Glu) | Hereditary pancreatitis [RCV004610920] | uncertain significance | 7 | 130385914 | 130385914 | Human | 1 | name |
| 407456923 | CV3419534 | single nucleotide variant | NM_001868.4(CPA1):c.1177G>T (p.Ala393Ser) | Hereditary pancreatitis [RCV004610928] | uncertain significance | 7 | 130387928 | 130387928 | Human | 1 | name |
| 407456930 | CV3419539 | single nucleotide variant | NM_001868.4(CPA1):c.1174C>T (p.Pro392Ser) | Hereditary pancreatitis [RCV004610933] | uncertain significance | 7 | 130387925 | 130387925 | Human | 1 | name |
| 407457244 | CV3419544 | single nucleotide variant | NM_001868.4(CPA1):c.1041G>C (p.Lys347Asn) | Hereditary pancreatitis [RCV004610938] | uncertain significance | 7 | 130385892 | 130385892 | Human | 1 | name |
| 597630486 | CV3650905 | single nucleotide variant | NM_001868.4(CPA1):c.1237C>T (p.His413Tyr) | Hereditary pancreatitis [RCV004822684] | uncertain significance | 7 | 130387988 | 130387988 | Human | 1 | name |
| 597630398 | CV3654368 | single nucleotide variant | NM_001868.4(CPA1):c.1178C>T (p.Ala393Val) | Hereditary pancreatitis [RCV004822644] | uncertain significance | 7 | 130387929 | 130387929 | Human | 1 | name |
| 597630405 | CV3654371 | single nucleotide variant | NM_001868.4(CPA1):c.1130T>C (p.Phe377Ser) | Hereditary pancreatitis [RCV004822647] | uncertain significance | 7 | 130387881 | 130387881 | Human | 1 | name |
| 597630442 | CV3654390 | single nucleotide variant | NM_001868.4(CPA1):c.1250A>G (p.His417Arg) | Hereditary pancreatitis [RCV004822664] | uncertain significance | 7 | 130388001 | 130388001 | Human | 1 | name |
| 597944740 | CV3812614 | single nucleotide variant | NM_001868.4(CPA1):c.1000A>C (p.Lys334Gln) | not provided [RCV005159824] | uncertain significance | 7 | 130385851 | 130385851 | Human | | name |
| 597958416 | CV3849121 | single nucleotide variant | NM_001868.4(CPA1):c.1031A>G (p.Tyr344Cys) | not provided [RCV005192122] | uncertain significance | 7 | 130385882 | 130385882 | Human | | name |
| 598235070 | CV3945112 | single nucleotide variant | NM_001868.4(CPA1):c.1236G>T (p.Glu412Asp) | Hereditary pancreatitis [RCV005320179] | uncertain significance | 7 | 130387987 | 130387987 | Human | 1 | name |
| 598235085 | CV3945116 | single nucleotide variant | NM_001868.4(CPA1):c.1202A>C (p.Lys401Thr) | Hereditary pancreatitis [RCV005320183] | likely benign | 7 | 130387953 | 130387953 | Human | 1 | name |
| 598235095 | CV3945119 | single nucleotide variant | NM_001868.4(CPA1):c.1231A>G (p.Met411Val) | Hereditary pancreatitis [RCV005320186] | uncertain significance | 7 | 130387982 | 130387982 | Human | 1 | name |
| 598235107 | CV3945123 | single nucleotide variant | NM_001868.4(CPA1):c.1112A>T (p.Gln371Leu) | Hereditary pancreatitis [RCV005320190] | uncertain significance | 7 | 130387863 | 130387863 | Human | 1 | name |
| 25329082 | CV808968 | single nucleotide variant | NM_001868.4(CPA1):c.1021G>A (p.Ala341Thr) | Hereditary pancreatitis [RCV002258085]|not provided [RCV001402994] | benign|likely benign | 7 | 130385872 | 130385872 | Human | 3 | name |
| 25329082 | CV808968 | single nucleotide variant | NM_001868.4(CPA1):c.1021G>A (p.Ala341Thr) | Hereditary pancreatitis [RCV002258085]|not provided [RCV001402994] | benign|likely benign | 7 | 130385872 | 130385873 | Human | 3 | name |
| 25323450 | CV808973 | single nucleotide variant | NM_001868.4(CPA1):c.1258T>C (p.Ter420Arg) | Hereditary pancreatitis [RCV002318932] | uncertain significance | 7 | 130388009 | 130388009 | Human | 1 | name |
| 26922155 | CV833141 | single nucleotide variant | NM_001868.4(CPA1):c.1099T>C (p.Trp367Arg) | not provided [RCV001051575] | uncertain significance | 7 | 130387850 | 130387850 | Human | | name |
| 26905205 | CV833142 | single nucleotide variant | NM_001868.4(CPA1):c.1156C>T (p.Arg386Cys) | Hereditary pancreatitis [RCV002365786]|not provided [RCV001071696] | uncertain significance | 7 | 130387907 | 130387907 | Human | 1 | name |
| 38458286 | CV945430 | single nucleotide variant | NM_001868.4(CPA1):c.1212G>C (p.Trp404Cys) | Hereditary pancreatitis [RCV002356978]|not provided [RCV001228881] | uncertain significance | 7 | 130387963 | 130387963 | Human | 1 | name |
| 38456776 | CV955060 | single nucleotide variant | NM_001868.4(CPA1):c.1144C>T (p.Arg382Trp) | Early-onset chronic pancreatitis [RCV003225166]|Hereditary pancreatitis [RCV002451599]|not provided [RCV001245889] | uncertain significance | 7 | 130387895 | 130387895 | Human | 1 | name |
| 405142634 | CV3155437 | microsatellite | NM_001868.4(CPA1):c.261_262dup (p.Thr88fs) | not provided [RCV003855675] | uncertain significance | 7 | 130381740 | 130381741 | Human | | name |
| 151710646 | CV1365608 | deletion | NM_001868.4(CPA1):c.937_938del (p.Met313fs) | not provided [RCV001907926] | uncertain significance | 7 | 130385295 | 130385296 | Human | | name |
| 155747782 | CV1849780 | indel | NM_001868.4(CPA1):c.2_8delinsGCA (p.Met1fs) | Hereditary pancreatitis [RCV002417158] | likely benign | 7 | 130380522 | 130380528 | Human | | name |
| 156194251 | CV2066516 | deletion | NM_001868.4(CPA1):c.1201_1203del (p.Lys401del) | not provided [RCV002828713] | uncertain significance | 7 | 130387952 | 130387954 | Human | | name |
| 25324380 | CV808958 | indel | NM_001868.4(CPA1):c.599_600delinsG (p.Tyr200fs) | Hereditary pancreatitis [RCV002346224] | likely benign | 7 | 130383697 | 130383698 | Human | | name |
| 156372360 | CV2059083 | indel | NM_001868.4(CPA1):c.409_410delinsTT (p.Ala137Leu) | not provided [RCV002814399] | uncertain significance | 7 | 130382135 | 130382136 | Human | | name |
| 597948985 | CV3772254 | indel | NM_001868.4(CPA1):c.925_926delinsAA (p.Ser309Asn) | not provided [RCV005120573] | uncertain significance | 7 | 130385283 | 130385284 | Human | | name |
| 151857069 | CV1363740 | deletion | NM_001868.4(CPA1):c.1243del (p.Thr414_Leu415insTer) | not provided [RCV001904818] | uncertain significance | 7 | 130387992 | 130387992 | Human | | name |
| 405244387 | CV3050585 | deletion | NM_001868.4(CPA1):c.257_258del (p.Ser85_Tyr86insTer) | not provided [RCV003719970] | uncertain significance | 7 | 130381738 | 130381739 | Human | | name |
| 155692736 | CV1821658 | deletion | NM_001868.4(CPA1):c.954_955del (p.Tyr318_Lys319delinsTer) | Hereditary pancreatitis [RCV002374272]|not provided [RCV005097350] | likely benign|uncertain significance | 7 | 130385311 | 130385312 | Human | 1 | name |
| 156067214 | CV2166993 | duplication | NM_001868.4(CPA1):c.115_123dup (p.Glu41_Leu42insValLysGlu) | not provided [RCV003019927] | uncertain significance | 7 | 130381144 | 130381145 | Human | | name |
| 597630415 | CV3654377 | microsatellite | NM_001868.4(CPA1):c.298GAGCAG[3] (p.Gln103_Met104insGluGln) | Hereditary pancreatitis [RCV004822652] | uncertain significance | 7 | 130381777 | 130381778 | Human | | name |
| 155667765 | CV1812179 | duplication | NM_001868.4(CPA1):c.1228_1251dup (p.His417_Pro418insIleMetGluHisThrLeuAsnHis) | Hereditary pancreatitis [RCV002366885]|not provided [RCV003103313] | uncertain significance | 7 | 130387977 | 130387978 | Human | 1 | name |
| 151788372 | CV1376927 | insertion | NM_001868.4(CPA1):c.607_608insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCACCACGATGGGAGGCCGAGGCGCGCGGATCACGAGGTCAAGANNNNNNNNNNAAAAAAAAAAAAAAAAAAAAAAGACTACGGGCAGG (p.Asp203fs) | not provided [RCV001897932] | uncertain significance | 7 | 130383690 | 130383691 | Human | | name |