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Pathways
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)


945 records found for search term Cpa1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155696512CV1800742single nucleotide variantNM_001868.4(CPA1):c.-5G>CHereditary pancreatitis [RCV002358000]uncertain significance7130380516130380516Human1name
155747739CV1849743single nucleotide variantNM_001868.4(CPA1):c.-1C>GHereditary pancreatitis [RCV002417121]uncertain significance7130380520130380520Human1name
150535060CV1306797single nucleotide variantNM_001868.4(CPA1):c.*97A>Cnot provided [RCV001757795]likely benign7130388108130388108Humanname
153303610CV1690377single nucleotide variantNM_001868.4(CPA1):c.*16C>Anot provided [RCV002269420]likely benign7130388027130388027Humanname
127329053CV1138521single nucleotide variantNM_001868.4(CPA1):c.65+3A>GHereditary pancreatitis [RCV002368494]|not provided [RCV001487203]likely benign|uncertain significance7130380588130380588Human1name
151812087CV1510362single nucleotide variantNM_001868.4(CPA1):c.65+4G>Anot provided [RCV001918712]uncertain significance7130380589130380589Humanname
155667134CV1812080single nucleotide variantNM_001868.4(CPA1):c.66-3C>THereditary pancreatitis [RCV002366785]uncertain significance7130381095130381095Human1name
156238670CV1882296deletionNM_001868.4(CPA1):c.66-3delnot provided [RCV003085660]likely benign7130381093130381093Humanname
405049847CV3025456duplicationNM_001868.4(CPA1):c.65+1dupnot provided [RCV003696902]uncertain significance7130380582130380583Humanname
25325095CV815376deletionNM_001868.4(CPA1):c.65+3delHereditary pancreatitis [RCV002354953]|not provided [RCV001419046]likely benign|uncertain significance7130380588130380588Human1name
126752760CV1007247single nucleotide variantNM_001868.4(CPA1):c.483+4A>Gnot provided [RCV001316372]uncertain significance7130382213130382213Humanname
126761239CV1027786single nucleotide variantNM_001868.4(CPA1):c.696+5C>THereditary pancreatitis [RCV002259106]|not provided [RCV001340634]uncertain significance7130383799130383799Human1name
127277062CV1074436single nucleotide variantNM_001868.4(CPA1):c.381+9G>Anot provided [RCV001407536]likely benign7130381872130381872Humanname
127264434CV1074438single nucleotide variantNM_001868.4(CPA1):c.585+7C>Tnot provided [RCV001403280]likely benign7130383499130383499Humanname
127297689CV1138522single nucleotide variantNM_001868.4(CPA1):c.148-4C>THereditary pancreatitis [RCV002388534]|not provided [RCV001497827]likely benign|uncertain significance7130381626130381626Human1name
127320899CV1138523single nucleotide variantNM_001868.4(CPA1):c.585+8C>Tnot provided [RCV001484379]likely benign7130383500130383500Humanname
150496754CV1271608single nucleotide variantNM_001868.4(CPA1):c.66-90G>Anot provided [RCV001688909]benign7130381008130381008Humanname
151863972CV1374536single nucleotide variantNM_001868.4(CPA1):c.147+4A>CHereditary pancreatitis [RCV002388772]|not provided [RCV001884307]uncertain significance7130381183130381183Human1name
151775968CV1440261single nucleotide variantNM_001868.4(CPA1):c.787+1G>AHereditary pancreatitis [RCV004040570]|not provided [RCV001874904]likely benign|uncertain significance7130384627130384627Human1name
151802003CV1442353single nucleotide variantNM_001868.4(CPA1):c.586-2A>GHereditary pancreatitis [RCV002352741]|not provided [RCV002011660]uncertain significance7130383682130383682Human1name
152124333CV1527656single nucleotide variantNM_001868.4(CPA1):c.65+14G>Anot provided [RCV002082000]likely benign7130380599130380599Humanname
152163152CV1561207single nucleotide variantNM_001868.4(CPA1):c.788-6C>Gnot provided [RCV002104183]benign7130385140130385140Humanname
152137931CV1563459single nucleotide variantNM_001868.4(CPA1):c.66-11A>THereditary pancreatitis [RCV002256902]|not provided [RCV002200197]likely benign|uncertain significance7130381087130381087Human1name
152135726CV1595024single nucleotide variantNM_001868.4(CPA1):c.788-5C>AHereditary pancreatitis [RCV002407364]|not provided [RCV002199914]likely benign|uncertain significance7130385141130385141Human1name
152056889CV1656463single nucleotide variantNM_001868.4(CPA1):c.988-7T>Cnot provided [RCV002109654]likely benign7130385832130385832Humanname
153002495CV1685091single nucleotide variantNM_001868.4(CPA1):c.696+6G>AHereditary pancreatitis [RCV002259241]likely benign7130383800130383800Human1name
155680091CV1807127single nucleotide variantNM_001868.4(CPA1):c.586-1G>THereditary pancreatitis [RCV002353416]uncertain significance7130383683130383683Human1name
155742197CV1816585single nucleotide variantNM_001868.4(CPA1):c.787+2T>AHereditary pancreatitis [RCV002412283]uncertain significance7130384628130384628Human1name
155675107CV1828898single nucleotide variantNM_001868.4(CPA1):c.988-3C>THereditary pancreatitis [RCV002387397]uncertain significance7130385836130385836Human1name
156163494CV1903215single nucleotide variantNM_001868.4(CPA1):c.696+4C>Gnot provided [RCV003082989]uncertain significance7130383798130383798Humanname
155958292CV1903875single nucleotide variantNM_001868.4(CPA1):c.586-8C>Tnot provided [RCV003095707]likely benign7130383676130383676Humanname
156446986CV1948680single nucleotide variantNM_001868.4(CPA1):c.148-6C>Gnot provided [RCV003118510]uncertain significance7130381624130381624Humanname
156385901CV1971993single nucleotide variantNM_001868.4(CPA1):c.483+5C>Tnot provided [RCV002604292]uncertain significance7130382214130382214Humanname
156395140CV2016012single nucleotide variantNM_001868.4(CPA1):c.697-9C>Tnot provided [RCV002725475]likely benign7130384527130384527Humanname
11542908CV252618single nucleotide variantNM_001868.4(CPA1):c.788-5C>GHereditary pancreatitis [RCV002256184]|not provided [RCV001312152]|not specified [RCV000241762]benign|likely benign7130385141130385141Human1name
401765390CV2733679single nucleotide variantNM_001868.4(CPA1):c.382-4T>AHereditary pancreatitis [RCV003301383]likely benign7130382104130382104Human1name
405202921CV3036368single nucleotide variantNM_001868.4(CPA1):c.586-6C>Anot provided [RCV003707635]uncertain significance7130383678130383678Humanname
405177994CV3049573duplicationNM_001868.4(CPA1):c.381+7dupnot provided [RCV003728451]likely benign7130381867130381868Humanname
402500182CV3170492single nucleotide variantNM_001868.4(CPA1):c.586-3C>Gnot provided [RCV003877864]uncertain significance7130383681130383681Humanname
405259672CV3186372single nucleotide variantNM_001868.4(CPA1):c.147+5G>Cnot provided [RCV003884131]likely benign7130381184130381184Humanname
407456878CV3419509single nucleotide variantNM_001868.4(CPA1):c.988-2A>GHereditary pancreatitis [RCV004610903]likely benign7130385837130385837Human1name
597630374CV3654356single nucleotide variantNM_001868.4(CPA1):c.788-4A>CHereditary pancreatitis [RCV004822633]likely benign7130385142130385142Human1name
597630380CV3654360single nucleotide variantNM_001868.4(CPA1):c.788-5C>THereditary pancreatitis [RCV004822636]uncertain significance7130385141130385141Human1name
597630406CV3654372single nucleotide variantNM_001868.4(CPA1):c.788-3C>GHereditary pancreatitis [RCV004822648]uncertain significance7130385143130385143Human1name
597970460CV3832488single nucleotide variantNM_001868.4(CPA1):c.586-8C>Anot provided [RCV005166567]likely benign7130383676130383676Humanname
598235051CV3945107single nucleotide variantNM_001868.4(CPA1):c.381+2T>CHereditary pancreatitis [RCV005320174]uncertain significance7130381865130381865Human1name
15194414CV730466single nucleotide variantNM_001868.4(CPA1):c.585+9G>Anot provided [RCV000889218]likely benign7130383501130383501Humanname
15131941CV759514single nucleotide variantNM_001868.4(CPA1):c.381+7G>Cnot provided [RCV000920251]likely benign7130381870130381870Humanname
25324213CV815377single nucleotide variantNM_001868.4(CPA1):c.586-3C>AHereditary pancreatitis [RCV002337077]|not provided [RCV002067676]benign|likely benign7130383681130383681Human1name
150447808CV1216169single nucleotide variantNM_001868.4(CPA1):c.65+143A>Gnot provided [RCV001611467]benign7130380728130380728Humanname
150430361CV1230841single nucleotide variantNM_001868.4(CPA1):c.381+57T>Cnot provided [RCV001641390]benign7130381920130381920Humanname
150501399CV1238387duplicationNM_001868.4(CPA1):c.697-63dupnot provided [RCV001656817]benign7130384467130384468Humanname
150487097CV1262683deletionNM_001868.4(CPA1):c.696+27delnot provided [RCV001687080]benign7130383817130383817Humanname
150496207CV1272824single nucleotide variantNM_001868.4(CPA1):c.484-53A>Gnot provided [RCV001688747]benign7130383338130383338Humanname
150536161CV1309157single nucleotide variantNM_001868.4(CPA1):c.65+174C>Tnot provided [RCV001759364]likely benign7130380759130380759Humanname
151759780CV1343124single nucleotide variantNM_001868.4(CPA1):c.987+12C>Anot provided [RCV002024225]likely benign7130385357130385357Humanname
151816511CV1344573single nucleotide variantNM_001868.4(CPA1):c.484-20C>Gnot provided [RCV001919137]likely benign|uncertain significance7130383371130383371Humanname
152077657CV1531356single nucleotide variantNM_001868.4(CPA1):c.696+14C>Anot provided [RCV002210809]likely benign7130383808130383808Humanname
152069718CV1535466single nucleotide variantNM_001868.4(CPA1):c.484-18C>Anot provided [RCV002091418]likely benign7130383373130383373Humanname
152109215CV1556483single nucleotide variantNM_001868.4(CPA1):c.484-20C>Anot provided [RCV002096615]likely benign7130383371130383371Humanname
152089366CV1580648single nucleotide variantNM_001868.4(CPA1):c.586-20C>Tnot provided [RCV002093955]likely benign7130383664130383664Humanname
152037493CV1596288single nucleotide variantNM_001868.4(CPA1):c.586-15C>Gnot provided [RCV002125584]benign7130383669130383669Humanname
152082845CV1623630deletionNM_001868.4(CPA1):c.148-11delnot provided [RCV002149540]benign7130381619130381619Humanname
152155842CV1629613single nucleotide variantNM_001868.4(CPA1):c.381+18G>Anot provided [RCV002202634]likely benign7130381881130381881Humanname
156446273CV1951309single nucleotide variantNM_001868.4(CPA1):c.697-20G>Cnot provided [RCV003117244]likely benign7130384516130384516Humanname
155937725CV2125832single nucleotide variantNM_001868.4(CPA1):c.1073-6C>Anot provided [RCV002971068]likely benign|uncertain significance7130387818130387818Humanname
405136316CV2906896single nucleotide variantNM_001868.4(CPA1):c.788-11T>Cnot provided [RCV003560431]likely benign7130385135130385135Humanname
405208719CV2909386single nucleotide variantNM_001868.4(CPA1):c.1073-1G>Anot provided [RCV003566851]uncertain significance7130387823130387823Humanname
405222840CV2976290single nucleotide variantNM_001868.4(CPA1):c.788-10C>Anot provided [RCV003680890]likely benign7130385136130385136Humanname
405225612CV3058221single nucleotide variantNM_001868.4(CPA1):c.987+16G>Anot provided [RCV003733850]likely benign7130385361130385361Humanname
405224768CV3058229single nucleotide variantNM_001868.4(CPA1):c.787+20G>Cnot provided [RCV003733854]likely benign7130384646130384646Humanname
405223374CV3061283single nucleotide variantNM_001868.4(CPA1):c.148-18G>Tnot provided [RCV003733655]uncertain significance7130381612130381612Humanname
405223561CV3061348single nucleotide variantNM_001868.4(CPA1):c.148-18G>Anot provided [RCV003733683]uncertain significance7130381612130381612Humanname
405224539CV3061474single nucleotide variantNM_001868.4(CPA1):c.987+14T>Cnot provided [RCV003733731]likely benign7130385359130385359Humanname
405226811CV3068387single nucleotide variantNM_001868.4(CPA1):c.381+20C>Tnot provided [RCV003733989]likely benign7130381883130381883Humanname
405086657CV3137690single nucleotide variantNM_001868.4(CPA1):c.585+10G>Tnot provided [RCV003834399]likely benign7130383502130383502Humanname
405234681CV3155568single nucleotide variantNM_001868.4(CPA1):c.381+11C>Tnot provided [RCV003853546]likely benign7130381874130381874Humanname
597936793CV3774575single nucleotide variantNM_001868.4(CPA1):c.988-14G>Cnot provided [RCV005117608]likely benign7130385825130385825Humanname
597948983CV3848794single nucleotide variantNM_001868.4(CPA1):c.987+15C>Tnot provided [RCV005189731]likely benign7130385360130385360Humanname
597957651CV3848912single nucleotide variantNM_001868.4(CPA1):c.787+17C>Gnot provided [RCV005191913]likely benign7130384643130384643Humanname
597949398CV3852553single nucleotide variantNM_001868.4(CPA1):c.148-11G>Cnot provided [RCV005189631]likely benign7130381619130381619Humanname
597869034CV3858328single nucleotide variantNM_001868.4(CPA1):c.1073-1G>Tnot provided [RCV005197071]uncertain significance7130387823130387823Humanname
25329172CV815378single nucleotide variantNM_001868.4(CPA1):c.1072+1G>THereditary pancreatitis [RCV002320219]uncertain significance7130385924130385924Human1name
26919955CV852066single nucleotide variantNM_001868.4(CPA1):c.988-10T>Anot provided [RCV001046727]likely benign|uncertain significance7130385829130385829Humanname
127266241CV1096075single nucleotide variantNM_001868.4(CPA1):c.1072+10C>Tnot provided [RCV001429349]likely benign7130385933130385933Humanname
150333498CV1169222single nucleotide variantNM_001868.4(CPA1):c.148-140C>Tnot provided [RCV001537366]benign7130381490130381490Humanname
150499143CV1224539single nucleotide variantNM_001868.4(CPA1):c.1073-32A>Gnot provided [RCV001620370]benign7130387792130387792Humanname
150458575CV1235950single nucleotide variantNM_001868.4(CPA1):c.697-260C>Gnot provided [RCV001648920]benign7130384276130384276Humanname
150446641CV1261393single nucleotide variantNM_001868.4(CPA1):c.787+234G>Cnot provided [RCV001680067]benign7130384860130384860Humanname
150445005CV1269365single nucleotide variantNM_001868.4(CPA1):c.987+182G>Cnot provided [RCV001691052]benign7130385527130385527Human1name
150445005CV1269365single nucleotide variantNM_001868.4(CPA1):c.987+182G>Cnot provided [RCV001691052]benign7130385527130385528Human1name
152061974CV1594875single nucleotide variantNM_001868.4(CPA1):c.1072+18C>Tnot provided [RCV002190632]likely benign7130385941130385941Humanname
152157041CV1629792single nucleotide variantNM_001868.4(CPA1):c.1073-11T>Cnot provided [RCV002202775]likely benign7130387813130387813Humanname
152120805CV1662069single nucleotide variantNM_001868.4(CPA1):c.1072+16G>Cnot provided [RCV002117826]benign|likely benign7130385939130385939Humanname
153001884CV1685089single nucleotide variantNM_001868.4(CPA1):c.1073-10C>THereditary pancreatitis [RCV002257295]uncertain significance7130387814130387814Human1name
405225123CV3058202single nucleotide variantNM_001868.4(CPA1):c.1072+11G>Anot provided [RCV003733846]likely benign7130385934130385934Humanname
150484854CV1250109single nucleotide variantNM_001868.4(CPA1):c.1072+131A>Gnot provided [RCV001673722]benign7130386054130386054Human2name
150484854CV1250109single nucleotide variantNM_001868.4(CPA1):c.1072+131A>Gnot provided [RCV001673722]benign7130386054130386055Human2name
150461013CV1264254single nucleotide variantNM_001868.4(CPA1):c.1072+289G>Cnot provided [RCV001682171]benign7130386212130386212Humanname
155731288CV1825928single nucleotide variantNM_001868.4(CPA1):c.9G>A (p.Gly3=)Hereditary pancreatitis [RCV002383145]likely benign7130380529130380529Human1name
155731351CV1825941single nucleotide variantNM_001868.4(CPA1):c.9G>T (p.Gly3=)Hereditary pancreatitis [RCV002383158]|not provided [RCV003718581]likely benign7130380529130380529Human1name
155719504CV1837378single nucleotide variantNM_001868.4(CPA1):c.15G>A (p.Leu5=)Hereditary pancreatitis [RCV002398665]|not provided [RCV005097626]likely benign|uncertain significance7130380535130380535Human1name
155747714CV1849722single nucleotide variantNM_001868.4(CPA1):c.19T>C (p.Leu7=)Hereditary pancreatitis [RCV002417100]likely benign7130380539130380539Human1name
405167770CV2950950single nucleotide variantNM_001868.4(CPA1):c.12G>A (p.Leu4=)not provided [RCV003675170]likely benign7130380532130380532Humanname
597630488CV3650906single nucleotide variantNM_001868.4(CPA1):c.27C>G (p.Val9=)Hereditary pancreatitis [RCV004822685]likely benign7130380547130380547Human1name
150514238CV1228123duplicationNM_001868.4(CPA1):c.697-64_697-63dupnot provided [RCV001638401]benign7130384467130384468Humanname
151852900CV1376173single nucleotide variantNM_001868.4(CPA1):c.93C>T (p.Ala31=)Hereditary pancreatitis [RCV002370686]|not provided [RCV001996189]likely benign7130381125130381125Human1name
152142365CV1526660single nucleotide variantNM_001868.4(CPA1):c.93C>G (p.Ala31=)Hereditary pancreatitis [RCV002372965]|not provided [RCV002084331]likely benign7130381125130381125Human1name
152164512CV1557652single nucleotide variantNM_001868.4(CPA1):c.75G>C (p.Val25=)Hereditary pancreatitis [RCV002391265]|not provided [RCV002141536]likely benign7130381107130381107Human1name
152099522CV1595589single nucleotide variantNM_001868.4(CPA1):c.36G>A (p.Gly12=)Hereditary pancreatitis [RCV002352953]|not provided [RCV002213815]likely benign7130380556130380556Human1name
152098654CV1611758deletionNM_001868.4(CPA1):c.148-13_148-12delnot provided [RCV002172806]likely benign7130381617130381618Humanname
155716114CV1785096single nucleotide variantNM_001868.4(CPA1):c.30G>A (p.Leu10=)Hereditary pancreatitis [RCV002325956]likely benign7130380550130380550Human1name
155716142CV1785104single nucleotide variantNM_001868.4(CPA1):c.30G>C (p.Leu10=)Hereditary pancreatitis [RCV002325964]likely benign7130380550130380550Human1name
155702337CV1788433single nucleotide variantNM_001868.4(CPA1):c.31T>C (p.Leu11=)Hereditary pancreatitis [RCV002322966]|not provided [RCV003099286]likely benign7130380551130380551Human1name
155735050CV1797886single nucleotide variantNM_001868.4(CPA1):c.42C>A (p.Val14=)Hereditary pancreatitis [RCV002330292]likely benign7130380562130380562Human1name
155738415CV1797894single nucleotide variantNM_001868.4(CPA1):c.42C>T (p.Val14=)Hereditary pancreatitis [RCV002331862]likely benign7130380562130380562Human1name
155704293CV1810663single nucleotide variantNM_001868.4(CPA1):c.57C>T (p.Asp19=)Hereditary pancreatitis [RCV002359852]likely benign7130380577130380577Human1name
155705559CV1811244single nucleotide variantNM_001868.4(CPA1):c.60T>C (p.Phe20=)Hereditary pancreatitis [RCV002360171]likely benign7130380580130380580Human1name
155699069CV1813336single nucleotide variantNM_001868.4(CPA1):c.75G>A (p.Val25=)Hereditary pancreatitis [RCV002394235]likely benign7130381107130381107Human1name
155665620CV1813874single nucleotide variantNM_001868.4(CPA1):c.79C>A (p.Arg27=)Hereditary pancreatitis [RCV002419140]likely benign7130381111130381111Human1name
155702476CV1825344single nucleotide variantNM_001868.4(CPA1):c.96T>C (p.Asp32=)Hereditary pancreatitis [RCV002376666]likely benign7130381128130381128Human1name
329364212CV2425548single nucleotide variantNM_001868.4(CPA1):c.84C>A (p.Ile28=)Hereditary pancreatitis [RCV003181580]likely benign7130381116130381116Human1name
401885439CV2783296single nucleotide variantNM_001868.4(CPA1):c.8G>T (p.Gly3Val)Hereditary pancreatitis [RCV003386798]uncertain significance7130380528130380528Human1name
401868442CV2787430single nucleotide variantNM_001868.4(CPA1):c.63G>A (p.Val21=)Hereditary pancreatitis [RCV003380206]likely benign7130380583130380583Human1name
405137449CV2907186single nucleotide variantNM_001868.4(CPA1):c.3G>T (p.Met1Ile)not provided [RCV003560564]uncertain significance7130380523130380523Humanname
405655653CV3380138single nucleotide variantNM_001868.4(CPA1):c.51G>A (p.Lys17=)Hereditary pancreatitis [RCV004511150]likely benign7130380571130380571Human1name
405655683CV3380157single nucleotide variantNM_001868.4(CPA1):c.69T>C (p.His23=)Hereditary pancreatitis [RCV004511169]likely benign7130381101130381101Human1name
405655690CV3380161single nucleotide variantNM_001868.4(CPA1):c.84C>T (p.Ile28=)Hereditary pancreatitis [RCV004511173]likely benign7130381116130381116Human1name
405655704CV3380170single nucleotide variantNM_001868.4(CPA1):c.99G>A (p.Glu33=)Hereditary pancreatitis [RCV004511182]likely benign7130381131130381131Human1name
407456886CV3419512single nucleotide variantNM_001868.4(CPA1):c.5G>C (p.Arg2Pro)Hereditary pancreatitis [RCV004610906]uncertain significance7130380525130380525Human1name
597630481CV3650903single nucleotide variantNM_001868.4(CPA1):c.63G>C (p.Val21=)Hereditary pancreatitis [RCV004822682]likely benign7130380583130380583Human1name
597630367CV3654353single nucleotide variantNM_001868.4(CPA1):c.45T>C (p.Phe15=)Hereditary pancreatitis [RCV004822630]likely benign7130380565130380565Human1name
598235047CV3945106single nucleotide variantNM_001868.4(CPA1):c.54G>A (p.Glu18=)Hereditary pancreatitis [RCV005320172]likely benign7130380574130380574Human1name
25329589CV808946single nucleotide variantNM_001868.4(CPA1):c.2T>C (p.Met1Thr)Hereditary pancreatitis [RCV002346217]|not provided [RCV002549469]likely benign|uncertain significance7130380522130380522Human1name
25324410CV808947single nucleotide variantNM_001868.4(CPA1):c.5G>A (p.Arg2Gln)CPA1-related disorder [RCV003918646]|Hereditary pancreatitis [RCV002346226]|not provided [RCV001475985]benign|likely benign7130380525130380525Human1name , trait , alternate_id
126743901CV992097single nucleotide variantNM_001868.4(CPA1):c.4C>T (p.Arg2Trp)Hereditary pancreatitis [RCV002339720]|not provided [RCV001296259]uncertain significance7130380524130380524Human1name
127249459CV1074435single nucleotide variantNM_001868.4(CPA1):c.273G>A (p.Glu91=)Hereditary pancreatitis [RCV002438916]|not provided [RCV001399603]likely benign7130381755130381755Human1name
127248433CV1096072single nucleotide variantNM_001868.4(CPA1):c.201G>T (p.Val67=)Hereditary pancreatitis [RCV002420953]|not provided [RCV001424927]likely benign|uncertain significance7130381683130381683Human1name
127316401CV1117592single nucleotide variantNM_001868.4(CPA1):c.276C>T (p.Asp92=)Hereditary pancreatitis [RCV002439103]|not provided [RCV001465530]likely benign7130381758130381758Human1name
151893327CV1338109single nucleotide variantNM_001868.4(CPA1):c.23G>T (p.Ser8Ile)Hereditary pancreatitis [RCV002449500]|not provided [RCV001944924]uncertain significance7130380543130380543Human1name
152051335CV1527952single nucleotide variantNM_001868.4(CPA1):c.222G>T (p.Ala74=)Hereditary pancreatitis [RCV002416464]|not provided [RCV002089197]likely benign7130381704130381704Human1name
152165617CV1543822single nucleotide variantNM_001868.4(CPA1):c.291G>A (p.Leu97=)Hereditary pancreatitis [RCV002434554]|not provided [RCV002124051]likely benign7130381773130381773Human1name
152145486CV1553787single nucleotide variantNM_001868.4(CPA1):c.204C>T (p.Pro68=)Hereditary pancreatitis [RCV002416493]|not provided [RCV002138746]likely benign7130381686130381686Human1name
152154526CV1560799single nucleotide variantNM_001868.4(CPA1):c.160C>A (p.Arg54=)Hereditary pancreatitis [RCV002391229]|not provided [RCV002102742]likely benign7130381642130381642Human1name
152092173CV1602979single nucleotide variantNM_001868.4(CPA1):c.165G>A (p.Gly55=)Hereditary pancreatitis [RCV002391356]|not provided [RCV002194440]likely benign7130381647130381647Human1name
152032832CV1643191single nucleotide variantNM_001868.4(CPA1):c.141C>T (p.His47=)Hereditary pancreatitis [RCV002391186]|not provided [RCV002205055]likely benign7130381173130381173Human1name
155681248CV1812813single nucleotide variantNM_001868.4(CPA1):c.123G>A (p.Glu41=)Hereditary pancreatitis [RCV002371126]likely benign7130381155130381155Human1name
155665833CV1823552duplicationNM_001868.4(CPA1):c.8_9dup (p.Leu4fs)Hereditary pancreatitis [RCV002419183]|not provided [RCV003776471]likely benign|uncertain significance7130380524130380525Human1name
155704496CV1827961single nucleotide variantNM_001868.4(CPA1):c.165G>T (p.Gly55=)Hereditary pancreatitis [RCV002395089]likely benign7130381647130381647Human1name
155700457CV1836745single nucleotide variantNM_001868.4(CPA1):c.144G>A (p.Leu48=)Hereditary pancreatitis [RCV002394558]likely benign7130381176130381176Human1name
155700491CV1836753single nucleotide variantNM_001868.4(CPA1):c.144G>C (p.Leu48=)Hereditary pancreatitis [RCV002394566]likely benign7130381176130381176Human1name
155746185CV1838993single nucleotide variantNM_001868.4(CPA1):c.186C>T (p.Pro62=)Hereditary pancreatitis [RCV002415064]likely benign7130381668130381668Human1name
155743352CV1839377single nucleotide variantNM_001868.4(CPA1):c.183C>G (p.Ser61=)Hereditary pancreatitis [RCV002412796]likely benign7130381665130381665Human1name
155713960CV1841761single nucleotide variantNM_001868.4(CPA1):c.249C>T (p.Gly83=)Hereditary pancreatitis [RCV002431041]likely benign7130381731130381731Human1name
155693576CV1842201single nucleotide variantNM_001868.4(CPA1):c.261G>A (p.Glu87=)Hereditary pancreatitis [RCV002426390]likely benign7130381743130381743Human1name
155709541CV1843915single nucleotide variantNM_001868.4(CPA1):c.213C>T (p.Ser71=)Hereditary pancreatitis [RCV002430510]likely benign7130381695130381695Human1name
155717202CV1844875single nucleotide variantNM_001868.4(CPA1):c.235C>T (p.Leu79=)Hereditary pancreatitis [RCV002448515]likely benign7130381717130381717Human1name
155711698CV1845181single nucleotide variantNM_001868.4(CPA1):c.246C>T (p.His82=)Hereditary pancreatitis [RCV002430775]likely benign7130381728130381728Human1name
155699379CV1847524single nucleotide variantNM_001868.4(CPA1):c.222G>A (p.Ala74=)Hereditary pancreatitis [RCV002428227]likely benign7130381704130381704Human1name
155694530CV1848114single nucleotide variantNM_001868.4(CPA1):c.243C>T (p.Ser81=)Hereditary pancreatitis [RCV002460002]likely benign7130381725130381725Human1name
155674951CV1855857single nucleotide variantNM_001868.4(CPA1):c.288G>C (p.Leu96=)Hereditary pancreatitis [RCV002437908]likely benign7130381770130381770Human1name
156227638CV2176538single nucleotide variantNM_001868.4(CPA1):c.204C>G (p.Pro68=)not provided [RCV003059183]likely benign7130381686130381686Humanname
329364205CV2425540single nucleotide variantNM_001868.4(CPA1):c.17T>C (p.Val6Ala)Hereditary pancreatitis [RCV003181573]uncertain significance7130380537130380537Human1name
329364215CV2425551single nucleotide variantNM_001868.4(CPA1):c.196C>A (p.Arg66=)Hereditary pancreatitis [RCV003181582]likely benign7130381678130381678Human1name
329389912CV2465595single nucleotide variantNM_001868.4(CPA1):c.297G>A (p.Glu99=)Hereditary pancreatitis [RCV003216500]|not provided [RCV005061115]likely benign7130381779130381779Human1name
329389904CV2465602single nucleotide variantNM_001868.4(CPA1):c.14T>C (p.Leu5Pro)Hereditary pancreatitis [RCV003216507]uncertain significance7130380534130380534Human1name
11543296CV252615single nucleotide variantNM_001868.4(CPA1):c.165G>C (p.Gly55=)Hereditary pancreatitis [RCV002318975]|not provided [RCV001511899]|not specified [RCV000242274]benign7130381647130381647Human3name
401775062CV2723968single nucleotide variantNM_001868.4(CPA1):c.285G>A (p.Ser95=)Hereditary pancreatitis [RCV003305488]likely benign7130381767130381767Human1name
401885646CV2783259single nucleotide variantNM_001868.4(CPA1):c.120G>A (p.Lys40=)Hereditary pancreatitis [RCV003386761]likely benign7130381152130381152Human1name
401884966CV2786633single nucleotide variantNM_001868.4(CPA1):c.102C>T (p.Ala34=)Hereditary pancreatitis [RCV003386627]likely benign7130381134130381134Human1name
401885096CV2786673single nucleotide variantNM_001868.4(CPA1):c.216C>A (p.Ile72=)Hereditary pancreatitis [RCV003386667]likely benign7130381698130381698Human1name
405655636CV3380127single nucleotide variantNM_001868.4(CPA1):c.294C>T (p.Asp98=)Hereditary pancreatitis [RCV004511139]likely benign7130381776130381776Human1name
405655605CV3383119single nucleotide variantNM_001868.4(CPA1):c.10T>A (p.Leu4Met)Hereditary pancreatitis [RCV004511120]uncertain significance7130380530130380530Human1name
405655628CV3383133single nucleotide variantNM_001868.4(CPA1):c.126G>A (p.Leu42=)Hereditary pancreatitis [RCV004511134]likely benign7130381158130381158Human1name
405655630CV3383134single nucleotide variantNM_001868.4(CPA1):c.156C>T (p.Phe52=)Hereditary pancreatitis [RCV004511135]likely benign7130381638130381638Human1name
407456889CV3419514single nucleotide variantNM_001868.4(CPA1):c.279G>A (p.Val93=)Hereditary pancreatitis [RCV004610908]likely benign7130381761130381761Human1name
407456895CV3419518single nucleotide variantNM_001868.4(CPA1):c.270C>T (p.Ile90=)Hereditary pancreatitis [RCV004610912]likely benign7130381752130381752Human1name
597630490CV3650907single nucleotide variantNM_001868.4(CPA1):c.243C>G (p.Ser81=)Hereditary pancreatitis [RCV004822686]likely benign7130381725130381725Human1name
597630399CV3654369single nucleotide variantNM_001868.4(CPA1):c.148C>T (p.Leu50=)Hereditary pancreatitis [RCV004822645]likely benign7130381630130381630Human1name
597630409CV3654373single nucleotide variantNM_001868.4(CPA1):c.282G>A (p.Gln94=)Hereditary pancreatitis [RCV004822649]likely benign7130381764130381764Human1name
597630427CV3654382single nucleotide variantNM_001868.4(CPA1):c.171C>T (p.Ala57=)Hereditary pancreatitis [RCV004822657]likely benign7130381653130381653Human1name
597630429CV3654383single nucleotide variantNM_001868.4(CPA1):c.16G>C (p.Val6Leu)Hereditary pancreatitis [RCV004822658]uncertain significance7130380536130380536Human1name
598235057CV3945109single nucleotide variantNM_001868.4(CPA1):c.11T>G (p.Leu4Trp)Hereditary pancreatitis [RCV005320176]uncertain significance7130380531130380531Human1name
598235109CV3945124single nucleotide variantNM_001868.4(CPA1):c.288G>A (p.Leu96=)Hereditary pancreatitis [RCV005320191]likely benign7130381770130381770Human1name
598235127CV3945128single nucleotide variantNM_001868.4(CPA1):c.195C>T (p.Val65=)Hereditary pancreatitis [RCV005320195]likely benign7130381677130381677Human1name
126748221CV1027785single nucleotide variantNM_001868.4(CPA1):c.696G>A (p.Thr232=)Hereditary pancreatitis [RCV002377496]|not provided [RCV001351821]uncertain significance7130383794130383794Human1name
126922771CV1044695single nucleotide variantNM_001868.4(CPA1):c.86C>G (p.Ser29Cys)Hereditary pancreatitis [RCV002447470]|not provided [RCV001365061]uncertain significance7130381118130381118Human1name
127268345CV1074439single nucleotide variantNM_001868.4(CPA1):c.828C>T (p.His276=)Hereditary pancreatitis [RCV002432114]|not provided [RCV001404365]likely benign7130385186130385186Human1name
127236633CV1096073single nucleotide variantNM_001868.4(CPA1):c.582G>A (p.Lys194=)Hereditary pancreatitis [RCV002358971]|not provided [RCV001433382]likely benign7130383489130383489Human1name
127278514CV1096074single nucleotide variantNM_001868.4(CPA1):c.606G>A (p.Gln202=)not provided [RCV001445118]likely benign7130383704130383704Humanname
127328986CV1117593single nucleotide variantNM_001868.4(CPA1):c.522C>T (p.Ile174=)Hereditary pancreatitis [RCV002342057]|not provided [RCV001469919]likely benign7130383429130383429Human1name
127292659CV1117594single nucleotide variantNM_001868.4(CPA1):c.792C>G (p.Ser264=)Hereditary pancreatitis [RCV002421020]|not provided [RCV001451803]likely benign7130385150130385150Human1name
127291621CV1117595single nucleotide variantNM_001868.4(CPA1):c.834G>A (p.Lys278=)Hereditary pancreatitis [RCV002439139]|not provided [RCV001476134]likely benign7130385192130385192Human1name
127291787CV1117596single nucleotide variantNM_001868.4(CPA1):c.861G>A (p.Lys287=)Hereditary pancreatitis [RCV002449263]|not provided [RCV001476168]likely benign7130385219130385219Human1name
127320085CV1138524single nucleotide variantNM_001868.4(CPA1):c.657C>T (p.Ile219=)Hereditary pancreatitis [RCV002377881]|not provided [RCV001504292]likely benign7130383755130383755Human1name
127302970CV1138525single nucleotide variantNM_001868.4(CPA1):c.825C>T (p.Tyr275=)CPA1-related disorder [RCV003980405]|Hereditary pancreatitis [RCV002432342]|not provided [RCV001479108]likely benign7130385183130385183Human1name , trait , alternate_id
151736012CV1351268single nucleotide variantNM_001868.4(CPA1):c.80G>A (p.Arg27Gln)Hereditary pancreatitis [RCV002423129]|not provided [RCV002021822]uncertain significance7130381112130381112Human1name
151866017CV1354645single nucleotide variantNM_001868.4(CPA1):c.71A>T (p.Gln24Leu)not provided [RCV001924612]uncertain significance7130381103130381103Humanname
151886020CV1367201single nucleotide variantNM_001868.4(CPA1):c.52G>A (p.Glu18Lys)not provided [RCV002000603]uncertain significance7130380572130380572Humanname
151843935CV1457698single nucleotide variantNM_001868.4(CPA1):c.40G>C (p.Val14Leu)Hereditary pancreatitis [RCV002324351]|not provided [RCV001936456]likely benign|uncertain significance7130380560130380560Human1name
151716982CV1465069single nucleotide variantNM_001868.4(CPA1):c.55G>T (p.Asp19Tyr)not provided [RCV002003073]uncertain significance7130380575130380575Humanname
152042097CV1553684single nucleotide variantNM_001868.4(CPA1):c.894C>T (p.Asn298=)Hereditary pancreatitis [RCV002372888]|not provided [RCV002088096]likely benign7130385252130385252Human1name
152128004CV1554308single nucleotide variantNM_001868.4(CPA1):c.774C>T (p.Asp258=)Hereditary pancreatitis [RCV002255733]|not provided [RCV002176421]likely benign7130384613130384613Human1name
152046881CV1561516single nucleotide variantNM_001868.4(CPA1):c.546G>A (p.Glu182=)Hereditary pancreatitis [RCV002346479]|not provided [RCV002108444]likely benign7130383453130383453Human1name
152116243CV1566843single nucleotide variantNM_001868.4(CPA1):c.759C>G (p.Pro253=)Hereditary pancreatitis [RCV002391226]|not provided [RCV002097527]likely benign7130384598130384598Human1name
152170421CV1567614single nucleotide variantNM_001868.4(CPA1):c.633C>T (p.Asp211=)Hereditary pancreatitis [RCV002363631]|not provided [RCV002183144]likely benign7130383731130383731Human1name
152167531CV1577467single nucleotide variantNM_001868.4(CPA1):c.345C>T (p.Asp115=)Hereditary pancreatitis [RCV002454392]|not provided [RCV002204728]likely benign7130381827130381827Human1name
152168856CV1613966single nucleotide variantNM_001868.4(CPA1):c.762C>T (p.Asn254=)Hereditary pancreatitis [RCV002391335]|not provided [RCV002161256]likely benign7130384601130384601Human1name
152139873CV1628678single nucleotide variantNM_001868.4(CPA1):c.792C>T (p.Ser264=)Hereditary pancreatitis [RCV002416417]|not provided [RCV002100625]likely benign7130385150130385150Human1name
155715932CV1785048single nucleotide variantNM_001868.4(CPA1):c.309G>A (p.Gln103=)Hereditary pancreatitis [RCV002325908]likely benign7130381791130381791Human1name
155732255CV1785696single nucleotide variantNM_001868.4(CPA1):c.336C>T (p.Arg112=)Hereditary pancreatitis [RCV002451716]likely benign7130381818130381818Human1name
155664567CV1786960single nucleotide variantNM_001868.4(CPA1):c.387T>C (p.Tyr129=)Hereditary pancreatitis [RCV002366308]likely benign7130382113130382113Human1name
155704350CV1787578single nucleotide variantNM_001868.4(CPA1):c.408G>A (p.Val136=)Hereditary pancreatitis [RCV002323205]likely benign7130382134130382134Human1name
155701296CV1788265single nucleotide variantNM_001868.4(CPA1):c.318C>G (p.Ala106=)Hereditary pancreatitis [RCV002322833]likely benign7130381800130381800Human1name
155688595CV1788959single nucleotide variantNM_001868.4(CPA1):c.348T>A (p.Thr116=)Hereditary pancreatitis [RCV002459013]likely benign7130381830130381830Human1name
155664169CV1789783single nucleotide variantNM_001868.4(CPA1):c.369C>T (p.His123=)Hereditary pancreatitis [RCV002348875]likely benign7130381851130381851Human1name
155696231CV1790658single nucleotide variantNM_001868.4(CPA1):c.405G>A (p.Leu135=)Hereditary pancreatitis [RCV002321378]likely benign7130382131130382131Human1name
155721166CV1793386single nucleotide variantNM_001868.4(CPA1):c.37G>A (p.Ala13Thr)Hereditary pancreatitis [RCV002363957]uncertain significance7130380557130380557Human1name
155739902CV1794441single nucleotide variantNM_001868.4(CPA1):c.435G>A (p.Lys145=)Hereditary pancreatitis [RCV002332332]likely benign7130382161130382161Human1name
155710710CV1795078single nucleotide variantNM_001868.4(CPA1):c.324G>C (p.Arg108=)Hereditary pancreatitis [RCV002324879]likely benign7130381806130381806Human1name
155704346CV1795382single nucleotide variantNM_001868.4(CPA1):c.327C>T (p.Ser109=)Hereditary pancreatitis [RCV002445740]likely benign7130381809130381809Human1name
155664532CV1795424single nucleotide variantNM_001868.4(CPA1):c.33G>T (p.Leu11Phe)Hereditary pancreatitis [RCV002452059]uncertain significance7130380553130380553Human1name
155717521CV1795713single nucleotide variantNM_001868.4(CPA1):c.342C>G (p.Thr114=)Hereditary pancreatitis [RCV002337448]|not provided [RCV003718485]likely benign7130381824130381824Human1name
155682215CV1795719single nucleotide variantNM_001868.4(CPA1):c.342C>T (p.Thr114=)Hereditary pancreatitis [RCV002457008]likely benign7130381824130381824Human1name
155675777CV1795949single nucleotide variantNM_001868.4(CPA1):c.357C>T (p.Tyr119=)Hereditary pancreatitis [RCV002455074]|not provided [RCV003102397]likely benign7130381839130381839Human1name
155705594CV1797230single nucleotide variantNM_001868.4(CPA1):c.411G>A (p.Ala137=)Hereditary pancreatitis [RCV002323484]|not provided [RCV003560958]likely benign7130382137130382137Human1name
155735004CV1797866single nucleotide variantNM_001868.4(CPA1):c.429C>T (p.Val143=)Hereditary pancreatitis [RCV002330272]likely benign7130382155130382155Human1name
155735970CV1798450single nucleotide variantNM_001868.4(CPA1):c.465T>C (p.Arg155=)Hereditary pancreatitis [RCV002330486]likely benign7130382191130382191Human1name
155736275CV1798652single nucleotide variantNM_001868.4(CPA1):c.468C>T (p.Pro156=)Hereditary pancreatitis [RCV002330555]likely benign7130382194130382194Human1name
155734720CV1799084single nucleotide variantNM_001868.4(CPA1):c.492G>C (p.Thr164=)Hereditary pancreatitis [RCV002340760]likely benign7130383399130383399Human1name
155739582CV1799089single nucleotide variantNM_001868.4(CPA1):c.492G>T (p.Thr164=)Hereditary pancreatitis [RCV002342624]likely benign7130383399130383399Human1name
155668105CV1799843single nucleotide variantNM_001868.4(CPA1):c.543G>A (p.Arg181=)Hereditary pancreatitis [RCV002349597]likely benign7130383450130383450Human1name
155746576CV1800233single nucleotide variantNM_001868.4(CPA1):c.570C>G (p.Val190=)Hereditary pancreatitis [RCV002347604]likely benign7130383477130383477Human1name
155672442CV1801030single nucleotide variantNM_001868.4(CPA1):c.627T>C (p.Ile209=)Hereditary pancreatitis [RCV002368690]likely benign7130383725130383725Human1name
155673029CV1801212single nucleotide variantNM_001868.4(CPA1):c.630C>G (p.Leu210=)Hereditary pancreatitis [RCV002368828]likely benign7130383728130383728Human1name
155739353CV1801671single nucleotide variantNM_001868.4(CPA1):c.462G>T (p.Gly154=)Hereditary pancreatitis [RCV002342562]likely benign7130382188130382188Human1name
155740117CV1802245single nucleotide variantNM_001868.4(CPA1):c.489C>T (p.Ser163=)Hereditary pancreatitis [RCV002332395]|not provided [RCV003102649]likely benign7130383396130383396Human1name
155722526CV1802646single nucleotide variantNM_001868.4(CPA1):c.513C>T (p.Ala171=)Hereditary pancreatitis [RCV002338195]|not provided [RCV003776040]likely benign7130383420130383420Human1name
155666896CV1803106single nucleotide variantNM_001868.4(CPA1):c.540C>T (p.Ser180=)Hereditary pancreatitis [RCV002349407]likely benign7130383447130383447Human1name
155744107CV1803319single nucleotide variantNM_001868.4(CPA1):c.564T>C (p.Ser188=)Hereditary pancreatitis [RCV002345195]likely benign7130383471130383471Human1name
155746196CV1803466single nucleotide variantNM_001868.4(CPA1):c.567G>A (p.Gly189=)Hereditary pancreatitis [RCV002347415]likely benign7130383474130383474Human1name
155687559CV1803656single nucleotide variantNM_001868.4(CPA1):c.591T>C (p.Thr197=)Hereditary pancreatitis [RCV002355810]likely benign7130383689130383689Human1name
155689282CV1803968single nucleotide variantNM_001868.4(CPA1):c.597C>T (p.Asp199=)Hereditary pancreatitis [RCV002356122]likely benign7130383695130383695Human1name
155713872CV1804424single nucleotide variantNM_001868.4(CPA1):c.649C>T (p.Leu217=)Hereditary pancreatitis [RCV002362021]|not provided [RCV003574931]likely benign7130383747130383747Human1name
155722599CV1804452single nucleotide variantNM_001868.4(CPA1):c.64G>A (p.Gly22Arg)Hereditary pancreatitis [RCV002364130]uncertain significance7130380584130380584Human1name
155725608CV1804834single nucleotide variantNM_001868.4(CPA1):c.657C>A (p.Ile219=)Hereditary pancreatitis [RCV002364487]likely benign7130383755130383755Human1name
155738089CV1805004single nucleotide variantNM_001868.4(CPA1):c.456T>C (p.Tyr152=)Hereditary pancreatitis [RCV002342127]likely benign7130382182130382182Human1name
155738579CV1805194single nucleotide variantNM_001868.4(CPA1):c.459A>G (p.Glu153=)Hereditary pancreatitis [RCV002342318]likely benign7130382185130382185Human1name
155720548CV1805405single nucleotide variantNM_001868.4(CPA1):c.480G>A (p.Leu160=)Hereditary pancreatitis [RCV002337942]likely benign7130382206130382206Human1name
155737182CV1805418single nucleotide variantNM_001868.4(CPA1):c.480G>T (p.Leu160=)Hereditary pancreatitis [RCV002330739]likely benign7130382206130382206Human1name
155742695CV1806167single nucleotide variantNM_001868.4(CPA1):c.528G>A (p.Thr176=)Hereditary pancreatitis [RCV002344509]|not provided [RCV003096679]likely benign7130383435130383435Human1name
155743078CV1806349single nucleotide variantNM_001868.4(CPA1):c.531C>A (p.Gly177=)Hereditary pancreatitis [RCV002344693]|not provided [RCV003718518]likely benign7130383438130383438Human1name
155743082CV1806352single nucleotide variantNM_001868.4(CPA1):c.531C>T (p.Gly177=)Hereditary pancreatitis [RCV002344696]|not provided [RCV003730098]likely benign|uncertain significance7130383438130383438Human1name
155676456CV1806526single nucleotide variantNM_001868.4(CPA1):c.555C>G (p.Thr185=)Hereditary pancreatitis [RCV002351968]|not provided [RCV003730104]likely benign7130383462130383462Human1name
155681193CV1807636single nucleotide variantNM_001868.4(CPA1):c.615T>G (p.Ala205=)Hereditary pancreatitis [RCV002353662]likely benign7130383713130383713Human1name
155690044CV1808191single nucleotide variantNM_001868.4(CPA1):c.648C>T (p.Phe216=)Hereditary pancreatitis [RCV002356237]|not provided [RCV005096947]likely benign7130383746130383746Human1name
155731822CV1808705single nucleotide variantNM_001868.4(CPA1):c.453C>T (p.Thr151=)Hereditary pancreatitis [RCV002340089]likely benign7130382179130382179Human1name
155739998CV1809177single nucleotide variantNM_001868.4(CPA1):c.495G>A (p.Gly165=)Hereditary pancreatitis [RCV002342787]likely benign7130383402130383402Human1name
155675561CV1810312single nucleotide variantNM_001868.4(CPA1):c.552C>T (p.Val184=)Hereditary pancreatitis [RCV002351813]likely benign7130383459130383459Human1name
155683629CV1811496single nucleotide variantNM_001868.4(CPA1):c.637T>C (p.Leu213=)Hereditary pancreatitis [RCV002354068]likely benign7130383735130383735Human1name
155726159CV1811869single nucleotide variantNM_001868.4(CPA1):c.65G>C (p.Gly22Ala)Hereditary pancreatitis [RCV002364564]uncertain significance7130380585130380585Human1name
155726250CV1811912single nucleotide variantNM_001868.4(CPA1):c.660C>T (p.Val220=)Hereditary pancreatitis [RCV002364582]likely benign7130383758130383758Human1name
155707135CV1812280single nucleotide variantNM_001868.4(CPA1):c.690C>T (p.His230=)Hereditary pancreatitis [RCV002378079]likely benign7130383788130383788Human1name
155698899CV1813289single nucleotide variantNM_001868.4(CPA1):c.759C>A (p.Pro253=)Hereditary pancreatitis [RCV002394188]likely benign7130384598130384598Human1name
155742411CV1813692single nucleotide variantNM_001868.4(CPA1):c.795A>G (p.Gly265=)Hereditary pancreatitis [RCV002412381]likely benign7130385153130385153Human1name
155665262CV1813800single nucleotide variantNM_001868.4(CPA1):c.798C>T (p.Ala266=)Hereditary pancreatitis [RCV002419071]likely benign7130385156130385156Human1name
155690139CV1814622single nucleotide variantNM_001868.4(CPA1):c.882G>A (p.Lys294=)Hereditary pancreatitis [RCV002373768]likely benign7130385240130385240Human1name
155683685CV1815061single nucleotide variantNM_001868.4(CPA1):c.92C>T (p.Ala31Val)Hereditary pancreatitis [RCV002371525]uncertain significance7130381124130381124Human1name
155677565CV1815106single nucleotide variantNM_001868.4(CPA1):c.681C>T (p.Ala227=)Hereditary pancreatitis [RCV002369579]likely benign7130383779130383779Human1name
155706827CV1815423single nucleotide variantNM_001868.4(CPA1):c.687G>A (p.Thr229=)Hereditary pancreatitis [RCV002378016]|not provided [RCV003730126]likely benign7130383785130383785Human1name
155706838CV1815432single nucleotide variantNM_001868.4(CPA1):c.687G>T (p.Thr229=)Hereditary pancreatitis [RCV002378019]likely benign7130383785130383785Human1name
155679542CV1815730single nucleotide variantNM_001868.4(CPA1):c.717T>A (p.Thr239=)Hereditary pancreatitis [RCV002370726]likely benign7130384556130384556Human1name
155696737CV1816157single nucleotide variantNM_001868.4(CPA1):c.750C>T (p.Gly250=)Hereditary pancreatitis [RCV002393750]|not provided [RCV003718552]likely benign7130384589130384589Human1name
155742160CV1816572single nucleotide variantNM_001868.4(CPA1):c.786G>A (p.Gly262=)Hereditary pancreatitis [RCV002412270]likely benign7130384625130384625Human1name
155747168CV1816707single nucleotide variantNM_001868.4(CPA1):c.789G>A (p.Leu263=)Hereditary pancreatitis [RCV002416620]likely benign7130385147130385147Human1name
155721556CV1817290single nucleotide variantNM_001868.4(CPA1):c.864C>T (p.Ser288=)Hereditary pancreatitis [RCV002449633]likely benign7130385222130385222Human1name
155722218CV1817509single nucleotide variantNM_001868.4(CPA1):c.870A>G (p.Val290=)Hereditary pancreatitis [RCV002449723]likely benign7130385228130385228Human1name
155712289CV1817944single nucleotide variantNM_001868.4(CPA1):c.915C>T (p.Ile305=)Hereditary pancreatitis [RCV002378823]likely benign7130385273130385273Human1name
155712957CV1818053single nucleotide variantNM_001868.4(CPA1):c.918C>T (p.His306=)Hereditary pancreatitis [RCV002378913]|not provided [RCV003738230]likely benign7130385276130385276Human1name
155701994CV1818486single nucleotide variantNM_001868.4(CPA1):c.969C>G (p.Val323=)Hereditary pancreatitis [RCV002376605]likely benign7130385327130385327Human1name
155718327CV1819351single nucleotide variantNM_001868.4(CPA1):c.738C>T (p.Ser246=)Hereditary pancreatitis [RCV002380436]|not provided [RCV005097106]likely benign7130384577130384577Human1name
155737729CV1820122single nucleotide variantNM_001868.4(CPA1):c.77T>G (p.Leu26Arg)Hereditary pancreatitis [RCV002409913]uncertain significance7130381109130381109Human1name
155713736CV1820617single nucleotide variantNM_001868.4(CPA1):c.852G>A (p.Val284=)Hereditary pancreatitis [RCV002447799]likely benign7130385210130385210Human1name
155744771CV1820627single nucleotide variantNM_001868.4(CPA1):c.852G>T (p.Val284=)Hereditary pancreatitis [RCV002414435]likely benign7130385210130385210Human1name
155700583CV1821103single nucleotide variantNM_001868.4(CPA1):c.900G>A (p.Lys300=)Hereditary pancreatitis [RCV002376385]likely benign7130385258130385258Human1name
155710071CV1821294single nucleotide variantNM_001868.4(CPA1):c.906C>T (p.Phe302=)Hereditary pancreatitis [RCV002378543]likely benign7130385264130385264Human1name
155692003CV1821514single nucleotide variantNM_001868.4(CPA1):c.94G>A (p.Asp32Asn)Hereditary pancreatitis [RCV002374133]|not provided [RCV003718573]uncertain significance7130381126130381126Human1name
155729015CV1823438single nucleotide variantNM_001868.4(CPA1):c.76C>G (p.Leu26Val)Hereditary pancreatitis [RCV002400578]uncertain significance7130381108130381108Human1name
155704965CV1824001single nucleotide variantNM_001868.4(CPA1):c.840C>G (p.Ala280=)Hereditary pancreatitis [RCV002445855]likely benign7130385198130385198Human1name
155711959CV1824210single nucleotide variantNM_001868.4(CPA1):c.846C>T (p.Ser282=)Hereditary pancreatitis [RCV002447581]likely benign7130385204130385204Human1name
155698611CV1824400single nucleotide variantNM_001868.4(CPA1):c.885C>T (p.Asp295=)Hereditary pancreatitis [RCV002375943]likely benign7130385243130385243Human1name
155699314CV1824605single nucleotide variantNM_001868.4(CPA1):c.891G>A (p.Gly297=)Hereditary pancreatitis [RCV002376120]likely benign7130385249130385249Human1name
155684372CV1824862single nucleotide variantNM_001868.4(CPA1):c.933C>T (p.Leu311=)Hereditary pancreatitis [RCV002371660]likely benign7130385291130385291Human1name
155684583CV1824938single nucleotide variantNM_001868.4(CPA1):c.936C>A (p.Leu312=)Hereditary pancreatitis [RCV002371716]likely benign7130385294130385294Human1name
155683962CV1825257single nucleotide variantNM_001868.4(CPA1):c.930G>A (p.Gln310=)Hereditary pancreatitis [RCV002371569]likely benign7130385288130385288Human1name
155730827CV1825852single nucleotide variantNM_001868.4(CPA1):c.999C>T (p.Ser333=)Hereditary pancreatitis [RCV002383069]likely benign7130385850130385850Human1name
155690703CV1826880deletionNM_001868.4(CPA1):c.142del (p.Leu48fs)Hereditary pancreatitis [RCV002392030]likely benign7130381173130381173Human1name
156323988CV2072180single nucleotide variantNM_001868.4(CPA1):c.921C>T (p.Ser307=)not provided [RCV002834892]likely benign7130385279130385279Humanname
156260946CV2381262single nucleotide variantNM_001868.4(CPA1):c.49A>C (p.Lys17Gln)Hereditary pancreatitis [RCV004227325]uncertain significance7130380569130380569Human1name
329364199CV2425534single nucleotide variantNM_001868.4(CPA1):c.816G>C (p.Ser272=)Hereditary pancreatitis [RCV003181568]likely benign7130385174130385174Human1name
329363464CV2425536single nucleotide variantNM_001868.4(CPA1):c.411G>C (p.Ala137=)Hereditary pancreatitis [RCV003168237]likely benign7130382137130382137Human1name
329363467CV2425541single nucleotide variantNM_001868.4(CPA1):c.420G>C (p.Pro140=)Hereditary pancreatitis [RCV003168238]likely benign7130382146130382146Human1name
329364210CV2425546single nucleotide variantNM_001868.4(CPA1):c.342C>A (p.Thr114=)Hereditary pancreatitis [RCV003181578]likely benign7130381824130381824Human1name
329363468CV2425549single nucleotide variantNM_001868.4(CPA1):c.612A>C (p.Ala204=)Hereditary pancreatitis [RCV003168239]likely benign7130383710130383710Human1name
329363470CV2425556single nucleotide variantNM_001868.4(CPA1):c.756C>T (p.Asp252=)Hereditary pancreatitis [RCV003168241]likely benign7130384595130384595Human1name
329389925CV2465585single nucleotide variantNM_001868.4(CPA1):c.420G>A (p.Pro140=)Hereditary pancreatitis [RCV003216490]|not provided [RCV003730475]likely benign7130382146130382146Human1name
11545214CV252616single nucleotide variantNM_001868.4(CPA1):c.474C>T (p.Tyr158=)Hereditary pancreatitis [RCV002318976]|not provided [RCV001515482]|not specified [RCV000244832]benign7130382200130382200Human1name
11548966CV252617single nucleotide variantNM_001868.4(CPA1):c.600C>T (p.Tyr200=)Hereditary pancreatitis [RCV002347957]|not provided [RCV001515483]|not specified [RCV000249795]benign7130383698130383698Human1name
401775058CV2723966single nucleotide variantNM_001868.4(CPA1):c.471T>C (p.Ile157=)Hereditary pancreatitis [RCV003305486]likely benign7130382197130382197Human1name
401765397CV2733685single nucleotide variantNM_001868.4(CPA1):c.423C>T (p.His141=)Hereditary pancreatitis [RCV003301389]likely benign7130382149130382149Human1name
401765401CV2733688single nucleotide variantNM_001868.4(CPA1):c.741C>A (p.Leu247=)Hereditary pancreatitis [RCV003301392]likely benign7130384580130384580Human1name
401765403CV2733690single nucleotide variantNM_001868.4(CPA1):c.933C>A (p.Leu311=)Hereditary pancreatitis [RCV003301394]likely benign7130385291130385291Human1name
401885200CV2786705single nucleotide variantNM_001868.4(CPA1):c.948T>C (p.Tyr316=)Hereditary pancreatitis [RCV003386699]|not provided [RCV005104177]likely benign7130385306130385306Human1name
405193550CV2984895single nucleotide variantNM_001868.4(CPA1):c.420G>T (p.Pro140=)Hereditary pancreatitis [RCV004823179]|not provided [RCV003706540]likely benign7130382146130382146Human1name
405215080CV2985163single nucleotide variantNM_001868.4(CPA1):c.522C>A (p.Ile174=)not provided [RCV003709087]likely benign7130383429130383429Humanname
402514911CV2991517single nucleotide variantNM_001868.4(CPA1):c.402G>A (p.Leu134=)not provided [RCV003689773]likely benign7130382128130382128Humanname
405127983CV3167029single nucleotide variantNM_001868.4(CPA1):c.315C>T (p.Phe105=)not provided [RCV003854284]likely benign7130381797130381797Humanname
405655638CV3380128single nucleotide variantNM_001868.4(CPA1):c.300G>A (p.Glu100=)Hereditary pancreatitis [RCV004511140]|not provided [RCV005065180]likely benign7130381782130381782Human1name
405655647CV3380134single nucleotide variantNM_001868.4(CPA1):c.447C>T (p.Gly149=)Hereditary pancreatitis [RCV004511146]likely benign7130382173130382173Human1name
405655656CV3380140single nucleotide variantNM_001868.4(CPA1):c.537T>C (p.His179=)Hereditary pancreatitis [RCV004511152]likely benign7130383444130383444Human1name
405655658CV3380141single nucleotide variantNM_001868.4(CPA1):c.54G>C (p.Glu18Asp)Hereditary pancreatitis [RCV004511153]uncertain significance7130380574130380574Human1name
405655667CV3380147single nucleotide variantNM_001868.4(CPA1):c.61G>C (p.Val21Leu)Hereditary pancreatitis [RCV004511159]uncertain significance7130380581130380581Human1name
405655677CV3380153single nucleotide variantNM_001868.4(CPA1):c.64G>C (p.Gly22Arg)Hereditary pancreatitis [RCV004511165]uncertain significance7130380584130380584Human1name
405655698CV3380166single nucleotide variantNM_001868.4(CPA1):c.95A>G (p.Asp32Gly)Hereditary pancreatitis [RCV004511178]likely benign7130381127130381127Human1name
405655700CV3380167single nucleotide variantNM_001868.4(CPA1):c.972T>C (p.Pro324=)Hereditary pancreatitis [RCV004511179]likely benign7130385330130385330Human1name
405655701CV3380168single nucleotide variantNM_001868.4(CPA1):c.985C>T (p.Leu329=)Hereditary pancreatitis [RCV004511180]likely benign7130385343130385343Human1name
407456893CV3419516single nucleotide variantNM_001868.4(CPA1):c.348T>C (p.Thr116=)Hereditary pancreatitis [RCV004610910]likely benign7130381830130381830Human1name
407456894CV3419517single nucleotide variantNM_001868.4(CPA1):c.903C>G (p.Ala301=)Hereditary pancreatitis [RCV004610911]likely benign7130385261130385261Human1name
407456898CV3419520single nucleotide variantNM_001868.4(CPA1):c.318C>T (p.Ala106=)Hereditary pancreatitis [RCV004610914]likely benign7130381800130381800Human1name
407456905CV3419523single nucleotide variantNM_001868.4(CPA1):c.414G>A (p.Glu138=)Hereditary pancreatitis [RCV004610917]likely benign7130382140130382140Human1name
407456924CV3419535single nucleotide variantNM_001868.4(CPA1):c.654G>A (p.Glu218=)Hereditary pancreatitis [RCV004610929]likely benign7130383752130383752Human1name
407456925CV3419536single nucleotide variantNM_001868.4(CPA1):c.528G>T (p.Thr176=)Hereditary pancreatitis [RCV004610930]likely benign7130383435130383435Human1name
407456928CV3419538single nucleotide variantNM_001868.4(CPA1):c.837T>C (p.Phe279=)Hereditary pancreatitis [RCV004610932]likely benign7130385195130385195Human1name
597630412CV3654375single nucleotide variantNM_001868.4(CPA1):c.555C>T (p.Thr185=)Hereditary pancreatitis [RCV004822650]likely benign7130383462130383462Human1name
597630441CV3654389single nucleotide variantNM_001868.4(CPA1):c.807C>T (p.Asn269=)Hereditary pancreatitis [RCV004822663]likely benign7130385165130385165Human1name
597630459CV3654399single nucleotide variantNM_001868.4(CPA1):c.373C>T (p.Leu125=)Hereditary pancreatitis [RCV004822672]likely benign7130381855130381855Human1name
597854220CV3821640single nucleotide variantNM_001868.4(CPA1):c.618C>T (p.Phe206=)not provided [RCV005174118]likely benign7130383716130383716Humanname
597937965CV3852717single nucleotide variantNM_001868.4(CPA1):c.669T>C (p.Pro223=)not provided [RCV005187116]likely benign7130383767130383767Humanname
598235092CV3945118single nucleotide variantNM_001868.4(CPA1):c.92C>A (p.Ala31Asp)Hereditary pancreatitis [RCV005320185]uncertain significance7130381124130381124Human1name
598235100CV3945121single nucleotide variantNM_001868.4(CPA1):c.717T>G (p.Thr239=)Hereditary pancreatitis [RCV005320188]likely benign7130384556130384556Human1name
598235120CV3945126single nucleotide variantNM_001868.4(CPA1):c.57C>G (p.Asp19Glu)Hereditary pancreatitis [RCV005320193]likely benign7130380577130380577Human1name
15186355CV699851single nucleotide variantNM_001868.4(CPA1):c.867T>C (p.Ile289=)CPA1-related disorder [RCV004758103]|Hereditary pancreatitis [RCV002255596]|not provided [RCV000953258]benign|likely benign7130385225130385225Human1name , trait , alternate_id
15184658CV710770single nucleotide variantNM_001868.4(CPA1):c.321C>T (p.Phe107=)CPA1-related disorder [RCV003962927]|Hereditary pancreatitis [RCV002409288]|not provided [RCV000975167]benign7130381803130381803Human1name , trait , alternate_id
15191542CV735957single nucleotide variantNM_001868.4(CPA1):c.79C>T (p.Arg27Ter)Hereditary pancreatitis [RCV002255574]|not provided [RCV000910277]likely benign7130381111130381111Human1name
15148065CV750424single nucleotide variantNM_001868.4(CPA1):c.621C>T (p.Thr207=)CPA1-related disorder [RCV003923298]|Hereditary pancreatitis [RCV002256602]|not provided [RCV000923027]benign|likely benign7130383719130383719Human1name , trait , alternate_id
15193923CV750425single nucleotide variantNM_001868.4(CPA1):c.726C>T (p.His242=)Hereditary pancreatitis [RCV002382068]|not provided [RCV000910977]likely benign7130384565130384565Human1name
15148070CV750426single nucleotide variantNM_001868.4(CPA1):c.816G>A (p.Ser272=)CPA1-related disorder [RCV003913105]|Hereditary pancreatitis [RCV002256603]|not provided [RCV000923028]benign|likely benign7130385174130385174Human1name , trait , alternate_id
15191134CV766115single nucleotide variantNM_001868.4(CPA1):c.492G>A (p.Thr164=)CPA1-related disorder [RCV003925804]|Hereditary pancreatitis [RCV002319130]|not provided [RCV000932716]likely benign7130383399130383399Human1name , trait , alternate_id
25318317CV808953single nucleotide variantNM_001868.4(CPA1):c.405G>C (p.Leu135=)Hereditary pancreatitis [RCV002319310]|not provided [RCV001424455]likely benign7130382131130382131Human1name
25321986CV808955single nucleotide variantNM_001868.4(CPA1):c.486C>T (p.Phe162=)Hereditary pancreatitis [RCV002319376]|not provided [RCV001519647]benign|likely benign7130383393130383393Human1name
25324803CV808960single nucleotide variantNM_001868.4(CPA1):c.630C>T (p.Leu210=)Hereditary pancreatitis [RCV002354937]|not provided [RCV001428447]likely benign7130383728130383728Human1name
25326811CV808963single nucleotide variantNM_001868.4(CPA1):c.787T>C (p.Leu263=)Hereditary pancreatitis [RCV002434413]|not provided [RCV001343037]likely benign|uncertain significance7130384626130384626Human1name
25329524CV808966single nucleotide variantNM_001868.4(CPA1):c.846C>A (p.Ser282=)Hereditary pancreatitis [RCV002346215]likely benign7130385204130385204Human1name
26900678CV833137single nucleotide variantNM_001868.4(CPA1):c.330G>T (p.Arg110=)Hereditary pancreatitis [RCV002320341]|not provided [RCV001067977]likely benign|uncertain significance7130381812130381812Human1name
38495864CV955056single nucleotide variantNM_001868.4(CPA1):c.41T>C (p.Val14Ala)Hereditary pancreatitis [RCV002327585]|not provided [RCV001242201]likely benign|uncertain significance7130380561130380561Human1name
126746052CV992098single nucleotide variantNM_001868.4(CPA1):c.92C>G (p.Ala31Gly)not provided [RCV001296526]uncertain significance7130381124130381124Humanname
126771592CV1007246single nucleotide variantNM_001868.4(CPA1):c.226A>G (p.Lys76Glu)Hereditary pancreatitis [RCV002447367]|not provided [RCV001323251]uncertain significance7130381708130381708Human1name
126731313CV1027780single nucleotide variantNM_001868.4(CPA1):c.221C>T (p.Ala74Val)Hereditary pancreatitis [RCV002431988]|not provided [RCV001349405]uncertain significance7130381703130381703Human1name
126768944CV1027787single nucleotide variantNM_001868.4(CPA1):c.1071T>A (p.Ile357=)Hereditary pancreatitis [RCV003169654]|not provided [RCV001343646]likely benign|uncertain significance7130385922130385922Human1name
126908103CV1044696single nucleotide variantNM_001868.4(CPA1):c.284C>T (p.Ser95Leu)Hereditary pancreatitis [RCV002438856]|not provided [RCV001367593]uncertain significance7130381766130381766Human1name
127276237CV1096076single nucleotide variantNM_001868.4(CPA1):c.1137C>T (p.Phe379=)Hereditary pancreatitis [RCV002322469]|not provided [RCV001443725]likely benign7130387888130387888Human1name
127298608CV1117597single nucleotide variantNM_001868.4(CPA1):c.1032C>T (p.Tyr344=)Hereditary pancreatitis [RCV002396084]|not provided [RCV001460599]likely benign7130385883130385883Human1name
151713887CV1379585single nucleotide variantNM_001868.4(CPA1):c.197G>A (p.Arg66Gln)Hereditary pancreatitis [RCV002423076]|not provided [RCV001964837]uncertain significance7130381679130381679Human1name
151846163CV1395246single nucleotide variantNM_001868.4(CPA1):c.203C>A (p.Pro68His)not provided [RCV001995362]uncertain significance7130381685130381685Humanname
151875981CV1406077single nucleotide variantNM_001868.4(CPA1):c.295G>A (p.Glu99Lys)Hereditary pancreatitis [RCV002441069]|not provided [RCV001981907]uncertain significance7130381777130381777Human1name
151768852CV1409609deletionNM_001868.4(CPA1):c.401del (p.Leu134fs)Hereditary pancreatitis [RCV002370461]|not provided [RCV001896133]uncertain significance7130382127130382127Human1name
151814297CV1460575single nucleotide variantNM_001868.4(CPA1):c.218A>G (p.Gln73Arg)Hereditary pancreatitis [RCV002425123]|not provided [RCV001878583]uncertain significance7130381700130381700Human1name
151827733CV1479846single nucleotide variantNM_001868.4(CPA1):c.114G>C (p.Lys38Asn)Hereditary pancreatitis [RCV002458769]|not provided [RCV001901498]uncertain significance7130381146130381146Human1name
151886766CV1514055single nucleotide variantNM_001868.4(CPA1):c.208C>T (p.Pro70Ser)Hereditary pancreatitis [RCV004042989]|not provided [RCV001962832]uncertain significance7130381690130381690Human1name
152164460CV1560701single nucleotide variantNM_001868.4(CPA1):c.1089C>T (p.Ser363=)Hereditary pancreatitis [RCV002443194]|not provided [RCV002160253]likely benign7130387840130387840Human1name
152105968CV1614797single nucleotide variantNM_001868.4(CPA1):c.1107C>T (p.Tyr369=)not provided [RCV002079614]likely benign7130387858130387858Humanname
152146253CV1649505single nucleotide variantNM_001868.4(CPA1):c.1173G>A (p.Leu391=)not provided [RCV002121085]likely benign7130387924130387924Humanname
152056879CV1656462single nucleotide variantNM_001868.4(CPA1):c.1218G>A (p.Ala406=)Hereditary pancreatitis [RCV002363608]|not provided [RCV002109653]likely benign7130387969130387969Human1name
155744868CV1771518single nucleotide variantNM_001868.4(CPA1):c.211A>T (p.Ser71Cys)not provided [RCV002303299]uncertain significance7130381693130381693Humanname
155703249CV1785584single nucleotide variantNM_001868.4(CPA1):c.1134C>T (p.Thr378=)Hereditary pancreatitis [RCV002445597]likely benign7130387885130387885Human1name
155704223CV1787556single nucleotide variantNM_001868.4(CPA1):c.1164C>A (p.Gly388=)Hereditary pancreatitis [RCV002323183]likely benign7130387915130387915Human1name
155700148CV1791855single nucleotide variantNM_001868.4(CPA1):c.1131C>T (p.Phe377=)Hereditary pancreatitis [RCV002322658]likely benign7130387882130387882Human1name
155665363CV1792875single nucleotide variantNM_001868.4(CPA1):c.1149C>T (p.Asp383=)Hereditary pancreatitis [RCV002452237]likely benign7130387900130387900Human1name
155697342CV1794051single nucleotide variantNM_001868.4(CPA1):c.1161T>C (p.Tyr387=)Hereditary pancreatitis [RCV002375712]likely benign7130387912130387912Human1name
155664605CV1795441single nucleotide variantNM_001868.4(CPA1):c.1011G>A (p.Val337=)Hereditary pancreatitis [RCV002452076]likely benign7130385862130385862Human1name
155665880CV1796279single nucleotide variantNM_001868.4(CPA1):c.1152T>A (p.Thr384=)Hereditary pancreatitis [RCV002349246]likely benign7130387903130387903Human1name
155720039CV1796284single nucleotide variantNM_001868.4(CPA1):c.1152T>C (p.Thr384=)Hereditary pancreatitis [RCV002363788]likely benign7130387903130387903Human1name
155687228CV1796874single nucleotide variantNM_001868.4(CPA1):c.115G>A (p.Val39Met)Hereditary pancreatitis [RCV002373278]uncertain significance7130381147130381147Human1name
155735007CV1797868single nucleotide variantNM_001868.4(CPA1):c.1170G>A (p.Leu390=)Hereditary pancreatitis [RCV002330274]likely benign7130387921130387921Human1name
155738454CV1797910single nucleotide variantNM_001868.4(CPA1):c.1170G>C (p.Leu390=)Hereditary pancreatitis [RCV002331878]likely benign7130387921130387921Human1name
155707687CV1798703single nucleotide variantNM_001868.4(CPA1):c.1182C>T (p.Ser394=)Hereditary pancreatitis [RCV002335274]likely benign7130387933130387933Human1name
155672877CV1801176single nucleotide variantNM_001868.4(CPA1):c.121G>A (p.Glu41Lys)Hereditary pancreatitis [RCV002368800]uncertain significance7130381153130381153Human1name
155713914CV1804435single nucleotide variantNM_001868.4(CPA1):c.1224G>A (p.Leu408=)Hereditary pancreatitis [RCV002362027]likely benign7130387975130387975Human1name
155734907CV1809687single nucleotide variantNM_001868.4(CPA1):c.1197A>G (p.Thr399=)Hereditary pancreatitis [RCV002340835]likely benign7130387948130387948Human1name
155667675CV1812163single nucleotide variantNM_001868.4(CPA1):c.101C>G (p.Ala34Gly)Hereditary pancreatitis [RCV002366869]uncertain significance7130381133130381133Human1name
155742415CV1813704single nucleotide variantNM_001868.4(CPA1):c.1254C>A (p.Pro418=)Hereditary pancreatitis [RCV002412384]likely benign7130388005130388005Human1name
155697572CV1816332single nucleotide variantNM_001868.4(CPA1):c.1245G>C (p.Leu415=)Hereditary pancreatitis [RCV002393925]likely benign7130387996130387996Human1name
155741501CV1816413single nucleotide variantNM_001868.4(CPA1):c.1251C>T (p.His417=)Hereditary pancreatitis [RCV002412110]likely benign7130388002130388002Human1name
155729729CV1819757single nucleotide variantNM_001868.4(CPA1):c.124C>G (p.Leu42Val)Hereditary pancreatitis [RCV002400705]uncertain significance7130381156130381156Human1name
155669155CV1821804single nucleotide variantNM_001868.4(CPA1):c.130G>A (p.Asp44Asn)Hereditary pancreatitis [RCV002385410]|not provided [RCV003718583]likely benign|uncertain significance7130381162130381162Human1name
155718078CV1823105single nucleotide variantNM_001868.4(CPA1):c.1242C>T (p.Thr414=)Hereditary pancreatitis [RCV002380385]likely benign7130387993130387993Human1name
155688997CV1826625single nucleotide variantNM_001868.4(CPA1):c.141C>A (p.His47Gln)Hereditary pancreatitis [RCV002391775]uncertain significance7130381173130381173Human1name
155690090CV1826783single nucleotide variantNM_001868.4(CPA1):c.1035G>A (p.Gly345=)Hereditary pancreatitis [RCV002391933]likely benign7130385886130385886Human1name
155690585CV1826859single nucleotide variantNM_001868.4(CPA1):c.1035G>C (p.Gly345=)Hereditary pancreatitis [RCV002392009]likely benign7130385886130385886Human1name
155691954CV1827380single nucleotide variantNM_001868.4(CPA1):c.1041G>A (p.Lys347=)Hereditary pancreatitis [RCV002392276]likely benign7130385892130385892Human1name
155694060CV1827534single nucleotide variantNM_001868.4(CPA1):c.1047C>T (p.Asn349=)Hereditary pancreatitis [RCV002392658]likely benign7130385898130385898Human1name
155718064CV1827689single nucleotide variantNM_001868.4(CPA1):c.158G>C (p.Trp53Ser)Hereditary pancreatitis [RCV002398406]uncertain significance7130381640130381640Human1name
155730075CV1828370single nucleotide variantNM_001868.4(CPA1):c.173A>T (p.His58Leu)Hereditary pancreatitis [RCV002407476]uncertain significance7130381655130381655Human1name
155710365CV1830991single nucleotide variantNM_001868.4(CPA1):c.1050T>C (p.Tyr350=)Hereditary pancreatitis [RCV002403591]|not provided [RCV003720589]likely benign7130385901130385901Human1name
155680638CV1832923single nucleotide variantNM_001868.4(CPA1):c.139C>T (p.His47Tyr)Hereditary pancreatitis [RCV002389204]uncertain significance7130381171130381171Human1name
155711628CV1833213single nucleotide variantNM_001868.4(CPA1):c.146A>G (p.Gln49Arg)Hereditary pancreatitis [RCV002396893]uncertain significance7130381178130381178Human1name
155731746CV1833854single nucleotide variantNM_001868.4(CPA1):c.161G>A (p.Arg54Gln)Hereditary pancreatitis [RCV002401046]likely benign|uncertain significance7130381643130381643Human1name
155732010CV1835038single nucleotide variantNM_001868.4(CPA1):c.179G>A (p.Gly60Asp)Hereditary pancreatitis [RCV002407852]uncertain significance7130381661130381661Human1name
155733596CV1836154single nucleotide variantNM_001868.4(CPA1):c.136G>A (p.Glu46Lys)Hereditary pancreatitis [RCV002383673]uncertain significance7130381168130381168Human1name
155738979CV1839182single nucleotide variantNM_001868.4(CPA1):c.182C>A (p.Ser61Tyr)Hereditary pancreatitis [RCV002410506]uncertain significance7130381664130381664Human1name
155738992CV1839187single nucleotide variantNM_001868.4(CPA1):c.182C>T (p.Ser61Phe)Hereditary pancreatitis [RCV002410511]uncertain significance7130381664130381664Human1name
155682983CV1839880single nucleotide variantNM_001868.4(CPA1):c.197G>C (p.Arg66Pro)Hereditary pancreatitis [RCV002423656]uncertain significance7130381679130381679Human1name
155692082CV1841448single nucleotide variantNM_001868.4(CPA1):c.238G>A (p.Glu80Lys)Hereditary pancreatitis [RCV002459561]uncertain significance7130381720130381720Human1name
155723003CV1842031single nucleotide variantNM_001868.4(CPA1):c.1008T>A (p.Ala336=)Hereditary pancreatitis [RCV002432969]likely benign7130385859130385859Human1name
155701634CV1842450single nucleotide variantNM_001868.4(CPA1):c.263C>T (p.Thr88Ile)Hereditary pancreatitis [RCV002428627]likely benign7130381745130381745Human1name
155744195CV1842983single nucleotide variantNM_001868.4(CPA1):c.193G>T (p.Val65Phe)Hereditary pancreatitis [RCV002413165]uncertain significance7130381675130381675Human1name
155676845CV1843730single nucleotide variantNM_001868.4(CPA1):c.1077A>G (p.Gln359=)Hereditary pancreatitis [RCV002421834]uncertain significance7130387828130387828Human1name
155711667CV1845175single nucleotide variantNM_001868.4(CPA1):c.246C>A (p.His82Gln)Hereditary pancreatitis [RCV002430772]uncertain significance7130381728130381728Human1name
155696610CV1845333single nucleotide variantNM_001868.4(CPA1):c.247G>C (p.Gly83Arg)Hereditary pancreatitis [RCV002443946]|not provided [RCV003101868]uncertain significance7130381729130381729Human1name
155668335CV1846583single nucleotide variantNM_001868.4(CPA1):c.1074T>C (p.Tyr358=)Hereditary pancreatitis [RCV002419552]likely benign7130387825130387825Human1name
155698716CV1847343single nucleotide variantNM_001868.4(CPA1):c.221C>G (p.Ala74Gly)Hereditary pancreatitis [RCV002428057]uncertain significance7130381703130381703Human1name
155669051CV1848859single nucleotide variantNM_001868.4(CPA1):c.257A>G (p.Tyr86Cys)Hereditary pancreatitis [RCV002452823]|not provided [RCV003730222]uncertain significance7130381739130381739Human1name
155672213CV1849247single nucleotide variantNM_001868.4(CPA1):c.270C>G (p.Ile90Met)Hereditary pancreatitis [RCV002437437]|not provided [RCV003720637]uncertain significance7130381752130381752Human1name
155684827CV1850754single nucleotide variantNM_001868.4(CPA1):c.228G>C (p.Lys76Asn)Hereditary pancreatitis [RCV002457468]uncertain significance7130381710130381710Human1name
155678769CV1851883single nucleotide variantNM_001868.4(CPA1):c.1008T>G (p.Ala336=)Hereditary pancreatitis [RCV002455788]likely benign7130385859130385859Human1name
155680587CV1853265single nucleotide variantNM_001868.4(CPA1):c.277G>A (p.Val93Met)Hereditary pancreatitis [RCV002439716]|not provided [RCV003102208]uncertain significance7130381759130381759Human1name
155680611CV1853271single nucleotide variantNM_001868.4(CPA1):c.277G>T (p.Val93Leu)Hereditary pancreatitis [RCV002439722]uncertain significance7130381759130381759Human1name
155683236CV1853514single nucleotide variantNM_001868.4(CPA1):c.293A>T (p.Asp98Val)Hereditary pancreatitis [RCV002440145]uncertain significance7130381775130381775Human1name
155687448CV1853634single nucleotide variantNM_001868.4(CPA1):c.294C>G (p.Asp98Glu)Hereditary pancreatitis [RCV002441829]uncertain significance7130381776130381776Human1name
155681107CV1854491single nucleotide variantNM_001868.4(CPA1):c.290T>C (p.Leu97Pro)Hereditary pancreatitis [RCV002439823]uncertain significance7130381772130381772Human1name
155681123CV1854493single nucleotide variantNM_001868.4(CPA1):c.290T>G (p.Leu97Arg)Hereditary pancreatitis [RCV002439825]uncertain significance7130381772130381772Human1name
155698536CV1855082deletionNM_001868.4(CPA1):c.306del (p.Glu102fs)Hereditary pancreatitis [RCV002444321]|not provided [RCV003546853]likely benign|uncertain significance7130381788130381788Human1name
155668597CV1856167single nucleotide variantNM_001868.4(CPA1):c.1125C>T (p.Tyr375=)Hereditary pancreatitis [RCV002435869]|not provided [RCV003775444]likely benign7130387876130387876Human1name
155689766CV1856528single nucleotide variantNM_001868.4(CPA1):c.297G>C (p.Glu99Asp)Hereditary pancreatitis [RCV002442202]uncertain significance7130381779130381779Human1name
155955127CV1907097single nucleotide variantNM_001868.4(CPA1):c.196C>T (p.Arg66Ter)Hereditary pancreatitis [RCV004614357]|not provided [RCV003095541]likely benign|uncertain significance7130381678130381678Human1name
156370742CV1920206single nucleotide variantNM_001868.4(CPA1):c.179G>C (p.Gly60Ala)Hereditary pancreatitis [RCV003294537]|not provided [RCV002603154]uncertain significance7130381661130381661Human1name
156119698CV1982685single nucleotide variantNM_001868.4(CPA1):c.179G>T (p.Gly60Val)Hereditary pancreatitis [RCV004823048]|not provided [RCV002622896]uncertain significance7130381661130381661Human1name
156225382CV2005982single nucleotide variantNM_001868.4(CPA1):c.267G>A (p.Met89Ile)not provided [RCV002667381]uncertain significance7130381749130381749Humanname
156358069CV2006757single nucleotide variantNM_001868.4(CPA1):c.157T>G (p.Trp53Gly)not provided [RCV002676060]uncertain significance7130381639130381639Humanname
156116591CV2017004single nucleotide variantNM_001868.4(CPA1):c.241T>C (p.Ser81Pro)not provided [RCV002740038]uncertain significance7130381723130381723Humanname
156006967CV2042003single nucleotide variantNM_001868.4(CPA1):c.209C>T (p.Pro70Leu)Hereditary pancreatitis [RCV003167724]|not provided [RCV002756479]uncertain significance7130381691130381691Human1name
155999512CV2045462single nucleotide variantNM_001868.4(CPA1):c.143T>C (p.Leu48Pro)Hereditary pancreatitis [RCV005321232]|not provided [RCV002756130]uncertain significance7130381175130381175Human1name
329364202CV2425537single nucleotide variantNM_001868.4(CPA1):c.1254C>T (p.Pro418=)Hereditary pancreatitis [RCV003181570]likely benign7130388005130388005Human1name
329364204CV2425539single nucleotide variantNM_001868.4(CPA1):c.1215G>A (p.Leu405=)Hereditary pancreatitis [RCV003181572]likely benign7130387966130387966Human1name
329364208CV2425544single nucleotide variantNM_001868.4(CPA1):c.176C>G (p.Pro59Arg)Hereditary pancreatitis [RCV003181576]uncertain significance7130381658130381658Human1name
329389928CV2465583single nucleotide variantNM_001868.4(CPA1):c.149T>G (p.Leu50Arg)Hereditary pancreatitis [RCV003216488]uncertain significance7130381631130381631Human1name
329389918CV2465591single nucleotide variantNM_001868.4(CPA1):c.178G>A (p.Gly60Ser)Hereditary pancreatitis [RCV003216496]uncertain significance7130381660130381660Human1name
329389916CV2465592single nucleotide variantNM_001868.4(CPA1):c.143T>G (p.Leu48Arg)Hereditary pancreatitis [RCV003216497]uncertain significance7130381175130381175Human1name
329389913CV2465594single nucleotide variantNM_001868.4(CPA1):c.1158C>T (p.Arg386=)Hereditary pancreatitis [RCV003216499]likely benign7130387909130387909Human1name
329389911CV2465596single nucleotide variantNM_001868.4(CPA1):c.164G>A (p.Gly55Glu)Hereditary pancreatitis [RCV003216501]|not provided [RCV005101369]uncertain significance7130381646130381646Human1name
401775072CV2723974single nucleotide variantNM_001868.4(CPA1):c.1164C>T (p.Gly388=)Hereditary pancreatitis [RCV003305494]likely benign7130387915130387915Human1name
401765391CV2733680single nucleotide variantNM_001868.4(CPA1):c.1236G>A (p.Glu412=)Hereditary pancreatitis [RCV003301384]likely benign7130387987130387987Human1name
401765398CV2733686single nucleotide variantNM_001868.4(CPA1):c.265A>G (p.Met89Val)Hereditary pancreatitis [RCV003301390]uncertain significance7130381747130381747Human1name
401885235CV2786716single nucleotide variantNM_001868.4(CPA1):c.163G>T (p.Gly55Trp)Hereditary pancreatitis [RCV003386710]|not provided [RCV003720872]uncertain significance7130381645130381645Human1name
401868440CV2787428single nucleotide variantNM_001868.4(CPA1):c.1017C>G (p.Ala339=)Hereditary pancreatitis [RCV003380204]likely benign7130385868130385868Human1name
405073349CV2941240single nucleotide variantNM_001868.4(CPA1):c.149T>C (p.Leu50Pro)not provided [RCV003664117]uncertain significance7130381631130381631Humanname
405187745CV2964107single nucleotide variantNM_001868.4(CPA1):c.1023C>T (p.Ala341=)Hereditary pancreatitis [RCV005323514]|not provided [RCV003676834]likely benign7130385874130385874Human1name
405082398CV3046840single nucleotide variantNM_001868.4(CPA1):c.160C>T (p.Arg54Trp)Hereditary pancreatitis [RCV004823188]|not provided [RCV003717234]likely benign|uncertain significance7130381642130381642Human1name
405685814CV3235789single nucleotide variantNM_001868.4(CPA1):c.116T>C (p.Val39Ala)Hereditary pancreatitis [RCV004372303]uncertain significance7130381148130381148Human1name
405655631CV3380124single nucleotide variantNM_001868.4(CPA1):c.212G>A (p.Ser71Asn)Hereditary pancreatitis [RCV004511136]uncertain significance7130381694130381694Human1name
405655633CV3380125single nucleotide variantNM_001868.4(CPA1):c.236T>C (p.Leu79Pro)Hereditary pancreatitis [RCV004511137]uncertain significance7130381718130381718Human1name
405655635CV3380126single nucleotide variantNM_001868.4(CPA1):c.247G>A (p.Gly83Ser)Hereditary pancreatitis [RCV004511138]uncertain significance7130381729130381729Human1name
405655608CV3383121single nucleotide variantNM_001868.4(CPA1):c.1134C>A (p.Thr378=)Hereditary pancreatitis [RCV004511122]likely benign7130387885130387885Human1name
405655909CV3383122single nucleotide variantNM_001868.4(CPA1):c.1134C>G (p.Thr378=)Hereditary pancreatitis [RCV004511123]likely benign7130387885130387885Human1name
405655614CV3383124single nucleotide variantNM_001868.4(CPA1):c.1143C>G (p.Leu381=)Hereditary pancreatitis [RCV004511125]|not provided [RCV005104854]likely benign7130387894130387894Human1name
405655617CV3383126single nucleotide variantNM_001868.4(CPA1):c.1158C>A (p.Arg386=)Hereditary pancreatitis [RCV004511127]likely benign7130387909130387909Human1name
405655619CV3383127single nucleotide variantNM_001868.4(CPA1):c.1179C>A (p.Ala393=)Hereditary pancreatitis [RCV004511128]likely benign7130387930130387930Human1name
405655620CV3383128single nucleotide variantNM_001868.4(CPA1):c.1209G>T (p.Thr403=)Hereditary pancreatitis [RCV004511129]likely benign7130387960130387960Human1name
407456881CV3419510single nucleotide variantNM_001868.4(CPA1):c.134T>C (p.Leu45Pro)Hereditary pancreatitis [RCV004610904]uncertain significance7130381166130381166Human1name
407456891CV3419515single nucleotide variantNM_001868.4(CPA1):c.131A>T (p.Asp44Val)Hereditary pancreatitis [RCV004610909]uncertain significance7130381163130381163Human1name
407456902CV3419522single nucleotide variantNM_001868.4(CPA1):c.272A>G (p.Glu91Gly)Hereditary pancreatitis [RCV004610916]uncertain significance7130381754130381754Human1name
407456906CV3419524single nucleotide variantNM_001868.4(CPA1):c.184C>G (p.Pro62Ala)Hereditary pancreatitis [RCV004610918]uncertain significance7130381666130381666Human1name
407456908CV3419525single nucleotide variantNM_001868.4(CPA1):c.125T>G (p.Leu42Arg)Hereditary pancreatitis [RCV004610919]uncertain significance7130381157130381157Human1name
407456914CV3419529deletionNM_001868.4(CPA1):c.986del (p.Leu329fs)Hereditary pancreatitis [RCV004610923]likely benign7130385344130385344Human1name
407456933CV3419541single nucleotide variantNM_001868.4(CPA1):c.1191C>T (p.Ile397=)Hereditary pancreatitis [RCV004610935]likely benign7130387942130387942Human1name
597630477CV3650901single nucleotide variantNM_001868.4(CPA1):c.1152T>G (p.Thr384=)Hereditary pancreatitis [RCV004822680]likely benign7130387903130387903Human1name
597630500CV3650911single nucleotide variantNM_001868.4(CPA1):c.228G>T (p.Lys76Asn)Hereditary pancreatitis [RCV004822690]uncertain significance7130381710130381710Human1name
597630377CV3654357deletionNM_001868.4(CPA1):c.530del (p.Gly177fs)Hereditary pancreatitis [RCV004822634]likely benign7130383435130383435Human1name
597630393CV3654366single nucleotide variantNM_001868.4(CPA1):c.199G>A (p.Val67Met)Hereditary pancreatitis [RCV004822642]uncertain significance7130381681130381681Human1name
597630414CV3654376single nucleotide variantNM_001868.4(CPA1):c.127G>C (p.Glu43Gln)Hereditary pancreatitis [RCV004822651]uncertain significance7130381159130381159Human1name
597630418CV3654378single nucleotide variantNM_001868.4(CPA1):c.269T>C (p.Ile90Thr)Hereditary pancreatitis [RCV004822653]uncertain significance7130381751130381751Human1name
597630420CV3654379single nucleotide variantNM_001868.4(CPA1):c.193G>A (p.Val65Ile)Hereditary pancreatitis [RCV004822654]uncertain significance7130381675130381675Human1name
597630425CV3654381single nucleotide variantNM_001868.4(CPA1):c.175C>A (p.Pro59Thr)Hereditary pancreatitis [RCV004822656]uncertain significance7130381657130381657Human1name
597630430CV3654384single nucleotide variantNM_001868.4(CPA1):c.167C>G (p.Pro56Arg)Hereditary pancreatitis [RCV004822659]uncertain significance7130381649130381649Human1name
597630434CV3654386single nucleotide variantNM_001868.4(CPA1):c.187A>G (p.Ile63Val)Hereditary pancreatitis [RCV004822660]uncertain significance7130381669130381669Human1name
597630438CV3654388single nucleotide variantNM_001868.4(CPA1):c.203C>T (p.Pro68Leu)Hereditary pancreatitis [RCV004822662]uncertain significance7130381685130381685Human1name
597630463CV3654400single nucleotide variantNM_001868.4(CPA1):c.101C>A (p.Ala34Asp)Hereditary pancreatitis [RCV004822673]uncertain significance7130381133130381133Human1name
598235074CV3945113single nucleotide variantNM_001868.4(CPA1):c.164G>C (p.Gly55Ala)Hereditary pancreatitis [RCV005320180]uncertain significance7130381646130381646Human1name
598235075CV3945114single nucleotide variantNM_001868.4(CPA1):c.1038C>G (p.Thr346=)Hereditary pancreatitis [RCV005320181]likely benign7130385889130385889Human1name
598235103CV3945122single nucleotide variantNM_001868.4(CPA1):c.106G>T (p.Val36Leu)Hereditary pancreatitis [RCV005320189]uncertain significance7130381138130381138Human1name
598235130CV3945129single nucleotide variantNM_001868.4(CPA1):c.1065G>A (p.Lys355=)Hereditary pancreatitis [RCV005320196]likely benign7130385916130385916Human1name
15134707CV735958single nucleotide variantNM_001868.4(CPA1):c.1029C>T (p.Leu343=)Hereditary pancreatitis [RCV002319599]|not provided [RCV000898336]benign|likely benign7130385880130385880Human1name
15176918CV735959single nucleotide variantNM_001868.4(CPA1):c.1209G>A (p.Thr403=)Hereditary pancreatitis [RCV002318899]|not provided [RCV000906536]benign|likely benign7130387960130387960Human1name
15180983CV766116single nucleotide variantNM_001868.4(CPA1):c.1017C>T (p.Ala339=)Hereditary pancreatitis [RCV002318900]|not provided [RCV000930017]likely benign7130385868130385868Human1name
25325341CV808948single nucleotide variantNM_001868.4(CPA1):c.159G>C (p.Trp53Cys)Hereditary pancreatitis [RCV002319164]uncertain significance7130381641130381641Human1name
25328904CV808949single nucleotide variantNM_001868.4(CPA1):c.281A>G (p.Gln94Arg)Hereditary pancreatitis [RCV002255602]|not provided [RCV001247645]likely benign|conflicting interpretations of pathogenicity|uncertain significance7130381763130381763Human1name
25321610CV808967single nucleotide variantNM_001868.4(CPA1):c.1002G>A (p.Lys334=)Hereditary pancreatitis [RCV002318903]|not provided [RCV002549301]likely benign7130385853130385853Human1name
25322320CV808969single nucleotide variantNM_001868.4(CPA1):c.1122G>A (p.Lys374=)Hereditary pancreatitis [RCV002318908]likely benign7130387873130387873Human1name
25323036CV808970single nucleotide variantNM_001868.4(CPA1):c.1203G>A (p.Lys401=)Hereditary pancreatitis [RCV002318920]|not provided [RCV002068825]likely benign7130387954130387954Human1name
25323054CV808971single nucleotide variantNM_001868.4(CPA1):c.1213C>T (p.Leu405=)Hereditary pancreatitis [RCV002318921]likely benign7130387964130387964Human1name
25323227CV808972single nucleotide variantNM_001868.4(CPA1):c.1230C>T (p.Ile410=)Hereditary pancreatitis [RCV002318926]likely benign7130387981130387981Human1name
8632337CV87545single nucleotide variantNM_001868.4(CPA1):c.151G>A (p.Asp51Asn)Hereditary pancreatitis [RCV005320173]likely benign|not provided7130381633130381633Human1name
38495810CV955057single nucleotide variantNM_001868.4(CPA1):c.137A>T (p.Glu46Val)Hereditary pancreatitis [RCV002379929]|not provided [RCV001242172]uncertain significance7130381169130381169Human1name
126752104CV992099single nucleotide variantNM_001868.4(CPA1):c.131A>C (p.Asp44Ala)Hereditary pancreatitis [RCV002379998]|not provided [RCV001297656]uncertain significance7130381163130381163Human1name
126748409CV1007248single nucleotide variantNM_001868.4(CPA1):c.523G>A (p.Asp175Asn)Hereditary pancreatitis [RCV003294307]|not provided [RCV001326336]uncertain significance7130383430130383430Human1name
126725905CV1027781single nucleotide variantNM_001868.4(CPA1):c.419C>T (p.Pro140Leu)Hereditary pancreatitis [RCV002329335]|not provided [RCV001348298]uncertain significance7130382145130382145Human1name
126730531CV1027782single nucleotide variantNM_001868.4(CPA1):c.491C>T (p.Thr164Met)not provided [RCV001349285]uncertain significance7130383398130383398Humanname
126759858CV1027783single nucleotide variantNM_001868.4(CPA1):c.527C>T (p.Thr176Met)Hereditary pancreatitis [RCV002350618]|not provided [RCV001340252]uncertain significance7130383434130383434Human1name
126774122CV1027784single nucleotide variantNM_001868.4(CPA1):c.686C>T (p.Thr229Met)Hereditary pancreatitis [RCV002368140]|not provided [RCV001346861]conflicting interpretations of pathogenicity|uncertain significance7130383784130383784Human1name
126924793CV1044697single nucleotide variantNM_001868.4(CPA1):c.343G>C (p.Asp115His)Hereditary pancreatitis [RCV004037010]|not provided [RCV001367442]uncertain significance7130381825130381825Human1name
126919076CV1044698single nucleotide variantNM_001868.4(CPA1):c.497G>C (p.Gly166Ala)not provided [RCV001362088]uncertain significance7130383404130383404Humanname
126908495CV1044699single nucleotide variantNM_001868.4(CPA1):c.859A>G (p.Lys287Glu)Hereditary pancreatitis [RCV003298598]|not provided [RCV001367926]uncertain significance7130385217130385217Human1name
126918322CV1044700single nucleotide variantNM_001868.4(CPA1):c.943C>A (p.Pro315Thr)Hereditary pancreatitis [RCV004822378]|not provided [RCV001372590]uncertain significance7130385301130385301Human1name
127237541CV1074437single nucleotide variantNM_001868.4(CPA1):c.410C>G (p.Ala137Gly)Hereditary pancreatitis [RCV002322419]|not provided [RCV001414936]likely benign|uncertain significance7130382136130382136Human1name
151887389CV1341334single nucleotide variantNM_001868.4(CPA1):c.751G>C (p.Val251Leu)Hereditary pancreatitis [RCV004822940]|not provided [RCV001887752]uncertain significance7130384590130384590Human1name
151792881CV1341533single nucleotide variantNM_001868.4(CPA1):c.975C>G (p.Asp325Glu)Hereditary pancreatitis [RCV005320898]|not provided [RCV001866408]uncertain significance7130385333130385333Human1name
151856847CV1347849single nucleotide variantNM_001868.4(CPA1):c.494G>A (p.Gly165Glu)Hereditary pancreatitis [RCV004044587]|not provided [RCV001979630]uncertain significance7130383401130383401Human1name
151779221CV1352240single nucleotide variantNM_001868.4(CPA1):c.779G>A (p.Gly260Asp)Hereditary pancreatitis [RCV003375555]|not provided [RCV002009580]uncertain significance7130384618130384618Human1name
151861469CV1353316single nucleotide variantNM_001868.4(CPA1):c.865A>G (p.Ile289Val)Hereditary pancreatitis [RCV002370539]|not provided [RCV001924052]uncertain significance7130385223130385223Human1name
151774858CV1362057single nucleotide variantNM_001868.4(CPA1):c.718C>T (p.Arg240Trp)Hereditary pancreatitis [RCV002370582]|not provided [RCV001950514]uncertain significance7130384557130384557Human1name
151864824CV1370872single nucleotide variantNM_001868.4(CPA1):c.389A>C (p.Asp130Ala)Hereditary pancreatitis [RCV002359359]|not provided [RCV001884406]likely benign|uncertain significance7130382115130382115Human1name
151858984CV1377712single nucleotide variantNM_001868.4(CPA1):c.834G>C (p.Lys278Asn)Hereditary pancreatitis [RCV002441037]|not provided [RCV001938302]uncertain significance7130385192130385192Human1name
151730580CV1385173single nucleotide variantNM_001868.4(CPA1):c.432C>G (p.Ser144Arg)Hereditary pancreatitis [RCV002331550]|not provided [RCV001967066]uncertain significance7130382158130382158Human1name
151767085CV1387673single nucleotide variantNM_001868.4(CPA1):c.607G>A (p.Asp203Asn)Hereditary pancreatitis [RCV002352682]|not provided [RCV001970811]uncertain significance7130383705130383705Human1name
151729613CV1388846single nucleotide variantNM_001868.4(CPA1):c.710G>A (p.Arg237His)Hereditary pancreatitis [RCV005321039]|not provided [RCV001966967]uncertain significance7130384549130384549Human1name
151715263CV1392652single nucleotide variantNM_001868.4(CPA1):c.346A>G (p.Thr116Ala)Hereditary pancreatitis [RCV002458767]|not provided [RCV001908843]uncertain significance7130381828130381828Human1name
151825880CV1393849single nucleotide variantNM_001868.4(CPA1):c.959C>G (p.Thr320Arg)not provided [RCV002030331]uncertain significance7130385317130385317Humanname
151718799CV1397394single nucleotide variantNM_001868.4(CPA1):c.815C>T (p.Ser272Leu)Hereditary pancreatitis [RCV002423117]|not provided [RCV001982729]uncertain significance7130385173130385173Human1name
151714170CV1399454single nucleotide variantNM_001868.4(CPA1):c.851T>C (p.Val284Ala)Hereditary pancreatitis [RCV003303311]|not provided [RCV001908630]uncertain significance7130385209130385209Human1name
151797020CV1401041single nucleotide variantNM_001868.4(CPA1):c.307C>T (p.Gln103Ter)Hereditary pancreatitis [RCV004612098]|not provided [RCV002011220]likely benign|uncertain significance7130381789130381789Human1name
151824414CV1404101single nucleotide variantNM_001868.4(CPA1):c.830G>A (p.Gly277Asp)not provided [RCV001976051]uncertain significance7130385188130385188Humanname
151709403CV1409232single nucleotide variantNM_001868.4(CPA1):c.938T>C (p.Met313Thr)Hereditary pancreatitis [RCV002370397]|not provided [RCV001907671]uncertain significance7130385296130385296Human1name
151789980CV1413306single nucleotide variantNM_001868.4(CPA1):c.763A>T (p.Arg255Trp)Hereditary pancreatitis [RCV003303487]|not provided [RCV001989982]uncertain significance7130384602130384602Human1name
151723649CV1414183single nucleotide variantNM_001868.4(CPA1):c.673G>A (p.Gly225Ser)Hereditary pancreatitis [RCV005321081]|not provided [RCV002004001]uncertain significance7130383771130383771Human1name
151843614CV1414630single nucleotide variantNM_001868.4(CPA1):c.793G>T (p.Gly265Ter)not provided [RCV001903150]uncertain significance7130385151130385151Humanname
151810535CV1417360single nucleotide variantNM_001868.4(CPA1):c.399C>A (p.Asp133Glu)not provided [RCV002028929]uncertain significance7130382125130382125Humanname
151718082CV1419581single nucleotide variantNM_001868.4(CPA1):c.446G>C (p.Gly149Ala)Hereditary pancreatitis [RCV003382751]|not provided [RCV001965532]uncertain significance7130382172130382172Human1name
151859435CV1423031single nucleotide variantNM_001868.4(CPA1):c.329G>A (p.Arg110Gln)Hereditary pancreatitis [RCV002324339]|not provided [RCV001923812]uncertain significance7130381811130381811Human1name
151737620CV1469445single nucleotide variantNM_001868.4(CPA1):c.793G>A (p.Gly265Arg)Hereditary pancreatitis [RCV002422895]|not provided [RCV002041893]uncertain significance7130385151130385151Human1name
151871775CV1480557single nucleotide variantNM_001868.4(CPA1):c.719G>A (p.Arg240Gln)Hereditary pancreatitis [RCV004822957]|not provided [RCV001906582]uncertain significance7130384558130384558Human1name
151832653CV1480558single nucleotide variantNM_001868.4(CPA1):c.751G>A (p.Val251Met)Hereditary pancreatitis [RCV002388810]|not provided [RCV001935211]uncertain significance7130384590130384590Human1name
151879366CV1490841single nucleotide variantNM_001868.4(CPA1):c.298G>A (p.Glu100Lys)Hereditary pancreatitis [RCV003167348]|not provided [RCV001940800]uncertain significance7130381780130381780Human1name
151734951CV1502467deletionNM_001868.4(CPA1):c.1202del (p.Lys401fs)not provided [RCV001911283]uncertain significance7130387952130387952Humanname
151818287CV1505953single nucleotide variantNM_001868.4(CPA1):c.322C>T (p.Arg108Trp)Hereditary pancreatitis [RCV002324236]|not provided [RCV002049535]uncertain significance7130381804130381804Human1name
151798708CV1509204single nucleotide variantNM_001868.4(CPA1):c.796G>C (p.Ala266Pro)Hereditary pancreatitis [RCV002406934]|not provided [RCV001866929]uncertain significance7130385154130385154Human1name
151797869CV1512937single nucleotide variantNM_001868.4(CPA1):c.397G>C (p.Asp133His)Hereditary pancreatitis [RCV002359291]|not provided [RCV001866853]uncertain significance7130382123130382123Human1name
153002494CV1685090single nucleotide variantNM_001868.4(CPA1):c.692G>A (p.Ser231Asn)Hereditary pancreatitis [RCV002259240]|not provided [RCV005095901]uncertain significance7130383790130383790Human1name
155689319CV1784827single nucleotide variantNM_001868.4(CPA1):c.307C>G (p.Gln103Glu)Hereditary pancreatitis [RCV002319862]|not provided [RCV003718477]likely benign|uncertain significance7130381789130381789Human1name
155715293CV1784906single nucleotide variantNM_001868.4(CPA1):c.308A>G (p.Gln103Arg)Hereditary pancreatitis [RCV002325766]|not provided [RCV005096143]likely benign|uncertain significance7130381790130381790Human1name
155715957CV1785055single nucleotide variantNM_001868.4(CPA1):c.309G>C (p.Gln103His)Hereditary pancreatitis [RCV002325915]uncertain significance7130381791130381791Human1name
155729837CV1786383single nucleotide variantNM_001868.4(CPA1):c.355T>C (p.Tyr119His)Hereditary pancreatitis [RCV002339781]uncertain significance7130381837130381837Human1name
155675159CV1786453single nucleotide variantNM_001868.4(CPA1):c.356A>C (p.Tyr119Ser)Hereditary pancreatitis [RCV002454976]uncertain significance7130381838130381838Human1name
155675177CV1786457single nucleotide variantNM_001868.4(CPA1):c.356A>G (p.Tyr119Cys)Hereditary pancreatitis [RCV002454980]uncertain significance7130381838130381838Human1name
155678892CV1786593single nucleotide variantNM_001868.4(CPA1):c.370A>C (p.Thr124Pro)Hereditary pancreatitis [RCV002353029]uncertain significance7130381852130381852Human1name
155664913CV1787133single nucleotide variantNM_001868.4(CPA1):c.389A>T (p.Asp130Val)Hereditary pancreatitis [RCV002366388]uncertain significance7130382115130382115Human1name
155726836CV1787809single nucleotide variantNM_001868.4(CPA1):c.421C>A (p.His141Asn)Hereditary pancreatitis [RCV002328021]uncertain significance7130382147130382147Human1name
155718351CV1788622single nucleotide variantNM_001868.4(CPA1):c.332C>T (p.Ala111Val)Hereditary pancreatitis [RCV002326463]uncertain significance7130381814130381814Human1name
155690161CV1789181single nucleotide variantNM_001868.4(CPA1):c.350T>C (p.Phe117Ser)Hereditary pancreatitis [RCV002459206]uncertain significance7130381832130381832Human1name
155664322CV1790159single nucleotide variantNM_001868.4(CPA1):c.386A>G (p.Tyr129Cys)Hereditary pancreatitis [RCV002366253]|not provided [RCV005096419]uncertain significance7130382112130382112Human1name
155725516CV1790945single nucleotide variantNM_001868.4(CPA1):c.419C>A (p.Pro140Gln)Hereditary pancreatitis [RCV002327823]|not provided [RCV005058357]uncertain significance7130382145130382145Human1name
155725525CV1790947single nucleotide variantNM_001868.4(CPA1):c.419C>G (p.Pro140Arg)Hereditary pancreatitis [RCV002327825]uncertain significance7130382145130382145Human1name
155699943CV1791813single nucleotide variantNM_001868.4(CPA1):c.316G>A (p.Ala106Thr)Hereditary pancreatitis [RCV002322616]uncertain significance7130381798130381798Human1name
155700531CV1791914single nucleotide variantNM_001868.4(CPA1):c.317C>T (p.Ala106Val)Hereditary pancreatitis [RCV002322717]uncertain significance7130381799130381799Human1name
155716859CV1792032single nucleotide variantNM_001868.4(CPA1):c.328C>G (p.Arg110Gly)Hereditary pancreatitis [RCV002326144]likely benign|uncertain significance7130381810130381810Human1name
155684379CV1792728single nucleotide variantNM_001868.4(CPA1):c.347C>G (p.Thr116Ser)Hereditary pancreatitis [RCV002457357]uncertain significance7130381829130381829Human1name
155744581CV1793221single nucleotide variantNM_001868.4(CPA1):c.364T>A (p.Tyr122Asn)Hereditary pancreatitis [RCV002346647]uncertain significance7130381846130381846Human1name
155685740CV1793462single nucleotide variantNM_001868.4(CPA1):c.380A>G (p.Glu127Gly)Hereditary pancreatitis [RCV002355220]uncertain significance7130381862130381862Human1name
155739576CV1794353single nucleotide variantNM_001868.4(CPA1):c.434A>G (p.Lys145Arg)Hereditary pancreatitis [RCV002332244]uncertain significance7130382160130382160Human1name
155711286CV1795199single nucleotide variantNM_001868.4(CPA1):c.325T>C (p.Ser109Pro)Hereditary pancreatitis [RCV002324960]uncertain significance7130381807130381807Human1name
155682867CV1795829single nucleotide variantNM_001868.4(CPA1):c.343G>A (p.Asp115Asn)Hereditary pancreatitis [RCV002457108]likely benign|uncertain significance7130381825130381825Human1name
155730380CV1796118single nucleotide variantNM_001868.4(CPA1):c.359C>T (p.Ala120Val)Hereditary pancreatitis [RCV002339858]uncertain significance7130381841130381841Human1name
155666197CV1796346single nucleotide variantNM_001868.4(CPA1):c.374T>G (p.Leu125Arg)Hereditary pancreatitis [RCV002349298]uncertain significance7130381856130381856Human1name
155734841CV1797790single nucleotide variantNM_001868.4(CPA1):c.428T>A (p.Val143Asp)Hereditary pancreatitis [RCV002330196]|not provided [RCV003102560]uncertain significance7130382154130382154Human1name
155727619CV1798120single nucleotide variantNM_001868.4(CPA1):c.443T>C (p.Ile148Thr)Hereditary pancreatitis [RCV002328270]uncertain significance7130382169130382169Human1name
155727873CV1798197single nucleotide variantNM_001868.4(CPA1):c.444T>G (p.Ile148Met)Hereditary pancreatitis [RCV002328348]uncertain significance7130382170130382170Human1name
155728418CV1798321single nucleotide variantNM_001868.4(CPA1):c.446G>A (p.Gly149Asp)Hereditary pancreatitis [RCV002328472]|not provided [RCV003094716]uncertain significance7130382172130382172Human1name
155672169CV1798922single nucleotide variantNM_001868.4(CPA1):c.490A>T (p.Thr164Ser)Hereditary pancreatitis [RCV002351203]uncertain significance7130383397130383397Human1name
155672468CV1799158single nucleotide variantNM_001868.4(CPA1):c.493G>A (p.Gly165Arg)Hereditary pancreatitis [RCV002351307]uncertain significance7130383400130383400Human1name
155739838CV1799218single nucleotide variantNM_001868.4(CPA1):c.494G>C (p.Gly165Ala)Hereditary pancreatitis [RCV002342724]uncertain significance7130383401130383401Human1name
155667317CV1799724single nucleotide variantNM_001868.4(CPA1):c.541C>T (p.Arg181Trp)Hereditary pancreatitis [RCV002349478]|not provided [RCV003730100]uncertain significance7130383448130383448Human1name
155669607CV1800099single nucleotide variantNM_001868.4(CPA1):c.547T>G (p.Trp183Gly)Hereditary pancreatitis [RCV002349853]uncertain significance7130383454130383454Human1name
155696005CV1800631single nucleotide variantNM_001868.4(CPA1):c.598T>C (p.Tyr200His)Hereditary pancreatitis [RCV002357889]uncertain significance7130383696130383696Human1name
155696930CV1800846single nucleotide variantNM_001868.4(CPA1):c.601G>A (p.Gly201Arg)Hereditary pancreatitis [RCV002358104]uncertain significance7130383699130383699Human1name
155696943CV1800850single nucleotide variantNM_001868.4(CPA1):c.601G>C (p.Gly201Arg)Hereditary pancreatitis [RCV002358108]|not provided [RCV003730109]uncertain significance7130383699130383699Human1name
155673207CV1801269single nucleotide variantNM_001868.4(CPA1):c.631G>A (p.Asp211Asn)Hereditary pancreatitis [RCV002368862]uncertain significance7130383729130383729Human1name
155735686CV1801734single nucleotide variantNM_001868.4(CPA1):c.463C>T (p.Arg155Cys)Hereditary pancreatitis [RCV002330430]uncertain significance7130382189130382189Human1name
155735779CV1801815single nucleotide variantNM_001868.4(CPA1):c.464G>A (p.Arg155His)Hereditary pancreatitis [RCV002330447]uncertain significance7130382190130382190Human1name
155734041CV1802195single nucleotide variantNM_001868.4(CPA1):c.488G>A (p.Ser163Asn)Hereditary pancreatitis [RCV002340539]|not provided [RCV005096687]uncertain significance7130383395130383395Human1name
155745403CV1802807single nucleotide variantNM_001868.4(CPA1):c.535C>T (p.His179Tyr)Hereditary pancreatitis [RCV002347016]uncertain significance7130383442130383442Human1name
155687690CV1803693single nucleotide variantNM_001868.4(CPA1):c.592C>G (p.Gln198Glu)Hereditary pancreatitis [RCV002355847]uncertain significance7130383690130383690Human1name
155665079CV1803995single nucleotide variantNM_001868.4(CPA1):c.619A>C (p.Thr207Pro)Hereditary pancreatitis [RCV002366426]|not provided [RCV003560976]uncertain significance7130383717130383717Human1name
155724831CV1804738single nucleotide variantNM_001868.4(CPA1):c.655A>T (p.Ile219Phe)Hereditary pancreatitis [RCV002364394]|not provided [RCV003730120]uncertain significance7130383753130383753Human1name
155710245CV1805777single nucleotide variantNM_001868.4(CPA1):c.503A>C (p.Lys168Thr)Hereditary pancreatitis [RCV002335650]uncertain significance7130383410130383410Human1name
155711250CV1805934single nucleotide variantNM_001868.4(CPA1):c.505C>T (p.Arg169Cys)Hereditary pancreatitis [RCV002335780]|not provided [RCV005096727]uncertain significance7130383412130383412Human1name
155743156CV1806651single nucleotide variantNM_001868.4(CPA1):c.557A>C (p.Gln186Pro)Hereditary pancreatitis [RCV002344732]uncertain significance7130383464130383464Human1name
155680951CV1807326single nucleotide variantNM_001868.4(CPA1):c.589A>C (p.Thr197Pro)Hereditary pancreatitis [RCV002353615]uncertain significance7130383687130383687Human1name
155705842CV1807395single nucleotide variantNM_001868.4(CPA1):c.611C>A (p.Ala204Glu)Hereditary pancreatitis [RCV002360262]uncertain significance7130383709130383709Human1name
155706223CV1807553single nucleotide variantNM_001868.4(CPA1):c.614C>T (p.Ala205Val)Hereditary pancreatitis [RCV002360420]uncertain significance7130383712130383712Human1name
155712503CV1807983single nucleotide variantNM_001868.4(CPA1):c.644T>C (p.Ile215Thr)Hereditary pancreatitis [RCV002361844]uncertain significance7130383742130383742Human1name
155709139CV1808839single nucleotide variantNM_001868.4(CPA1):c.473A>G (p.Tyr158Cys)Hereditary pancreatitis [RCV002335506]uncertain significance7130382199130382199Human1name
155740473CV1809413single nucleotide variantNM_001868.4(CPA1):c.499A>G (p.Ser167Gly)Hereditary pancreatitis [RCV002342983]uncertain significance7130383406130383406Human1name
155740636CV1809534single nucleotide variantNM_001868.4(CPA1):c.500G>A (p.Ser167Asn)Hereditary pancreatitis [RCV002343096]|not provided [RCV003096563]likely benign|uncertain significance7130383407130383407Human1name
155742401CV1809968single nucleotide variantNM_001868.4(CPA1):c.526A>C (p.Thr176Pro)Hereditary pancreatitis [RCV002344369]uncertain significance7130383433130383433Human1name
155669828CV1810036single nucleotide variantNM_001868.4(CPA1):c.548G>T (p.Trp183Leu)Hereditary pancreatitis [RCV002349898]uncertain significance7130383455130383455Human1name
155703324CV1810524single nucleotide variantNM_001868.4(CPA1):c.577G>T (p.Ala193Ser)Hereditary pancreatitis [RCV002359712]|not provided [RCV003546787]uncertain significance7130383484130383484Human1name
155697845CV1811807single nucleotide variantNM_001868.4(CPA1):c.658G>A (p.Val220Ile)Hereditary pancreatitis [RCV002375801]|not provided [RCV003718540]uncertain significance7130383756130383756Human1name
155725921CV1811808single nucleotide variantNM_001868.4(CPA1):c.658G>C (p.Val220Leu)Hereditary pancreatitis [RCV002364532]uncertain significance7130383756130383756Human1name
155726366CV1811958single nucleotide variantNM_001868.4(CPA1):c.661A>G (p.Thr221Ala)Hereditary pancreatitis [RCV002364604]|not provided [RCV003098307]uncertain significance7130383759130383759Human1name
155716389CV1812588single nucleotide variantNM_001868.4(CPA1):c.697A>C (p.Asn233His)Hereditary pancreatitis [RCV002362541]uncertain significance7130384536130384536Human1name
155681085CV1812780single nucleotide variantNM_001868.4(CPA1):c.724C>A (p.His242Asn)Hereditary pancreatitis [RCV002371093]uncertain significance7130384563130384563Human1name
155728495CV1812976single nucleotide variantNM_001868.4(CPA1):c.728C>T (p.Thr243Ile)Hereditary pancreatitis [RCV002382670]uncertain significance7130384567130384567Human1name
155697923CV1813083single nucleotide variantNM_001868.4(CPA1):c.754G>C (p.Asp252His)Hereditary pancreatitis [RCV002393982]uncertain significance7130384593130384593Human1name
155698304CV1813157single nucleotide variantNM_001868.4(CPA1):c.756C>A (p.Asp252Glu)Hereditary pancreatitis [RCV002394056]uncertain significance7130384595130384595Human1name
155707412CV1813431single nucleotide variantNM_001868.4(CPA1):c.761A>G (p.Asn254Ser)Hereditary pancreatitis [RCV002396248]uncertain significance7130384600130384600Human1name
155747438CV1813662single nucleotide variantNM_001868.4(CPA1):c.794G>A (p.Gly265Glu)Hereditary pancreatitis [RCV002416858]uncertain significance7130385152130385152Human1name
155708656CV1813969single nucleotide variantNM_001868.4(CPA1):c.830G>T (p.Gly277Val)Hereditary pancreatitis [RCV002430387]uncertain significance7130385188130385188Human1name
155730246CV1814141single nucleotide variantNM_001868.4(CPA1):c.834G>T (p.Lys278Asn)Hereditary pancreatitis [RCV002434711]uncertain significance7130385192130385192Human1name
155731346CV1814306single nucleotide variantNM_001868.4(CPA1):c.839C>A (p.Ala280Asp)Hereditary pancreatitis [RCV002434873]|not provided [RCV003560988]uncertain significance7130385197130385197Human1name
155683504CV1815031single nucleotide variantNM_001868.4(CPA1):c.929A>G (p.Gln310Arg)Hereditary pancreatitis [RCV002371494]uncertain significance7130385287130385287Human1name
155671247CV1815622single nucleotide variantNM_001868.4(CPA1):c.715A>G (p.Thr239Ala)Hereditary pancreatitis [RCV002367569]uncertain significance7130384554130384554Human1name
155708934CV1815663single nucleotide variantNM_001868.4(CPA1):c.716C>G (p.Thr239Ser)Hereditary pancreatitis [RCV002378384]uncertain significance7130384555130384555Human1name
155679708CV1815778single nucleotide variantNM_001868.4(CPA1):c.718C>G (p.Arg240Gly)Hereditary pancreatitis [RCV002370774]uncertain significance7130384557130384557Human1name
155687327CV1815963single nucleotide variantNM_001868.4(CPA1):c.746T>C (p.Ile249Thr)Hereditary pancreatitis [RCV002391462]|not provided [RCV003660944]uncertain significance7130384585130384585Human1name
155697833CV1816789single nucleotide variantNM_001868.4(CPA1):c.819G>C (p.Glu273Asp)Hereditary pancreatitis [RCV002427886]uncertain significance7130385177130385177Human1name
155697860CV1816795single nucleotide variantNM_001868.4(CPA1):c.819G>T (p.Glu273Asp)Hereditary pancreatitis [RCV002427892]uncertain significance7130385177130385177Human1name
155698370CV1816904single nucleotide variantNM_001868.4(CPA1):c.821C>T (p.Thr274Ile)Hereditary pancreatitis [RCV002427982]uncertain significance7130385179130385179Human1name
155742776CV1816988single nucleotide variantNM_001868.4(CPA1):c.823T>C (p.Tyr275His)Hereditary pancreatitis [RCV002412540]uncertain significance7130385181130385181Human1name
155742800CV1817014single nucleotide variantNM_001868.4(CPA1):c.824A>G (p.Tyr275Cys)Hereditary pancreatitis [RCV002412549]uncertain significance7130385182130385182Human1name
155721401CV1817230single nucleotide variantNM_001868.4(CPA1):c.862T>C (p.Ser288Pro)Hereditary pancreatitis [RCV002449611]uncertain significance7130385220130385220Human1name
155712929CV1818049single nucleotide variantNM_001868.4(CPA1):c.918C>G (p.His306Gln)Hereditary pancreatitis [RCV002378909]uncertain significance7130385276130385276Human1name
155668161CV1818114single nucleotide variantNM_001868.4(CPA1):c.958A>G (p.Thr320Ala)Hereditary pancreatitis [RCV002385242]uncertain significance7130385316130385316Human1name
155706592CV1818527single nucleotide variantNM_001868.4(CPA1):c.674G>C (p.Gly225Ala)Hereditary pancreatitis [RCV002377961]uncertain significance7130383772130383772Human1name
155728041CV1819004single nucleotide variantNM_001868.4(CPA1):c.706T>A (p.Trp236Arg)Hereditary pancreatitis [RCV002365090]uncertain significance7130384545130384545Human1name
155728046CV1819006single nucleotide variantNM_001868.4(CPA1):c.706T>C (p.Trp236Arg)Hereditary pancreatitis [RCV002365092]uncertain significance7130384545130384545Human1name
155670620CV1819224single nucleotide variantNM_001868.4(CPA1):c.710G>T (p.Arg237Leu)Hereditary pancreatitis [RCV002367404]uncertain significance7130384549130384549Human1name
155718648CV1819407single nucleotide variantNM_001868.4(CPA1):c.739C>G (p.Leu247Val)Hereditary pancreatitis [RCV002380492]uncertain significance7130384578130384578Human1name
155718656CV1819409single nucleotide variantNM_001868.4(CPA1):c.739C>T (p.Leu247Phe)Hereditary pancreatitis [RCV002380494]uncertain significance7130384578130384578Human1name
155666277CV1819496single nucleotide variantNM_001868.4(CPA1):c.740T>C (p.Leu247Pro)Hereditary pancreatitis [RCV002384926]uncertain significance7130384579130384579Human1name
155667550CV1819713single nucleotide variantNM_001868.4(CPA1):c.745A>G (p.Ile249Val)Hereditary pancreatitis [RCV002385144]likely benign7130384584130384584Human1name
155737415CV1819863single nucleotide variantNM_001868.4(CPA1):c.774C>A (p.Asp258Glu)Hereditary pancreatitis [RCV002409654]uncertain significance7130384613130384613Human1name
155737702CV1820098single nucleotide variantNM_001868.4(CPA1):c.779G>T (p.Gly260Val)Hereditary pancreatitis [RCV002409889]uncertain significance7130384618130384618Human1name
155673173CV1820225single nucleotide variantNM_001868.4(CPA1):c.811T>G (p.Cys271Gly)Hereditary pancreatitis [RCV002421294]uncertain significance7130385169130385169Human1name
155673920CV1820329single nucleotide variantNM_001868.4(CPA1):c.814T>G (p.Ser272Ala)Hereditary pancreatitis [RCV002421398]uncertain significance7130385172130385172Human1name
155697399CV1820445single nucleotide variantNM_001868.4(CPA1):c.817G>A (p.Glu273Lys)Hereditary pancreatitis [RCV002427805]uncertain significance7130385175130385175Human1name
155713303CV1820545single nucleotide variantNM_001868.4(CPA1):c.850G>A (p.Val284Met)Hereditary pancreatitis [RCV002447741]uncertain significance7130385208130385208Human1name
155700628CV1821112single nucleotide variantNM_001868.4(CPA1):c.900G>T (p.Lys300Asn)Hereditary pancreatitis [RCV002376394]uncertain significance7130385258130385258Human1name
155694726CV1821426single nucleotide variantNM_001868.4(CPA1):c.947A>G (p.Tyr316Cys)Hereditary pancreatitis [RCV002443509]uncertain significance7130385305130385305Human1name
155692961CV1821743single nucleotide variantNM_001868.4(CPA1):c.956A>G (p.Lys319Arg)Hereditary pancreatitis [RCV002374316]likely benign|uncertain significance7130385314130385314Human1name
155708160CV1822477single nucleotide variantNM_001868.4(CPA1):c.700C>G (p.Arg234Gly)Hereditary pancreatitis [RCV002378252]uncertain significance7130384539130384539Human1name
155727364CV1822527single nucleotide variantNM_001868.4(CPA1):c.701G>A (p.Arg234His)Hereditary pancreatitis [RCV002364863]|not provided [RCV003718544]uncertain significance7130384540130384540Human1name
155727603CV1822629single nucleotide variantNM_001868.4(CPA1):c.703A>G (p.Met235Val)Hereditary pancreatitis [RCV002364946]uncertain significance7130384542130384542Human1name
155716855CV1822816single nucleotide variantNM_001868.4(CPA1):c.731C>T (p.Ala244Val)Hereditary pancreatitis [RCV002380095]uncertain significance7130384570130384570Human1name
155707837CV1823157single nucleotide variantNM_001868.4(CPA1):c.763A>G (p.Arg255Gly)Hereditary pancreatitis [RCV002396339]uncertain significance7130384602130384602Human1name
155666010CV1823580single nucleotide variantNM_001868.4(CPA1):c.800G>T (p.Ser267Ile)Hereditary pancreatitis [RCV002419211]uncertain significance7130385158130385158Human1name
155690612CV1824395single nucleotide variantNM_001868.4(CPA1):c.885C>A (p.Asp295Glu)Hereditary pancreatitis [RCV002373844]uncertain significance7130385243130385243Human1name
155698726CV1824434single nucleotide variantNM_001868.4(CPA1):c.886C>T (p.His296Tyr)Hereditary pancreatitis [RCV002375966]uncertain significance7130385244130385244Human1name
155723605CV1824737single nucleotide variantNM_001868.4(CPA1):c.895A>C (p.Ile299Leu)Hereditary pancreatitis [RCV002449894]|not provided [RCV003100066]uncertain significance7130385253130385253Human1name
155690758CV1825034single nucleotide variantNM_001868.4(CPA1):c.939G>A (p.Met313Ile)Hereditary pancreatitis [RCV002373877]|not provided [RCV003094799]uncertain significance7130385297130385297Human1name
155684123CV1825290single nucleotide variantNM_001868.4(CPA1):c.931C>T (p.Leu311Phe)Hereditary pancreatitis [RCV002371602]uncertain significance7130385289130385289Human1name
155673305CV1825527single nucleotide variantNM_001868.4(CPA1):c.975C>A (p.Asp325Glu)Hereditary pancreatitis [RCV002387111]|not provided [RCV003718578]uncertain significance7130385333130385333Human1name
155703897CV1828734single nucleotide variantNM_001868.4(CPA1):c.981T>G (p.Asp327Glu)Hereditary pancreatitis [RCV002376847]uncertain significance7130385339130385339Human1name
155674224CV1828761single nucleotide variantNM_001868.4(CPA1):c.983A>C (p.Glu328Ala)Hereditary pancreatitis [RCV002387259]uncertain significance7130385341130385341Human1name
155674475CV1828803single nucleotide variantNM_001868.4(CPA1):c.984G>C (p.Glu328Asp)Hereditary pancreatitis [RCV002387301]uncertain significance7130385342130385342Human1name
155697260CV1854857single nucleotide variantNM_001868.4(CPA1):c.304G>A (p.Glu102Lys)Hereditary pancreatitis [RCV002444095]uncertain significance7130381786130381786Human1name
156061070CV1868081single nucleotide variantNM_001868.4(CPA1):c.844T>C (p.Ser282Pro)not provided [RCV003037262]pathogenic|likely pathogenic7130385202130385202Humanname
156364438CV1901696single nucleotide variantNM_001868.4(CPA1):c.734G>A (p.Gly245Asp)Hereditary pancreatitis [RCV003161885]|not provided [RCV002602720]uncertain significance7130384573130384573Human1name
156406502CV1921611single nucleotide variantNM_001868.4(CPA1):c.313T>C (p.Phe105Leu)not provided [RCV002606611]uncertain significance7130381795130381795Humanname
156446426CV1937899single nucleotide variantNM_001868.4(CPA1):c.700C>T (p.Arg234Cys)Hereditary pancreatitis [RCV004244601]|not provided [RCV003117930]uncertain significance7130384539130384539Human1name
156449281CV1944547single nucleotide variantNM_001868.4(CPA1):c.412G>A (p.Glu138Lys)Hereditary pancreatitis [RCV003162148]|not provided [RCV003121399]uncertain significance7130382138130382138Human1name
156165156CV1971456single nucleotide variantNM_001868.4(CPA1):c.884A>G (p.Asp295Gly)Hereditary pancreatitis [RCV004823044]|not provided [RCV002594601]uncertain significance7130385242130385242Human1name
156251665CV2041083single nucleotide variantNM_001868.4(CPA1):c.974A>T (p.Asp325Val)Hereditary pancreatitis [RCV003167781]|not provided [RCV002806031]uncertain significance7130385332130385332Human1name
155913186CV2081459single nucleotide variantNM_001868.4(CPA1):c.926C>T (p.Ser309Phe)Hereditary pancreatitis [RCV005321253]|not provided [RCV002858636]uncertain significance7130385284130385284Human1name
156022798CV2145396single nucleotide variantNM_001868.4(CPA1):c.361A>C (p.Thr121Pro)not provided [RCV003018310]uncertain significance7130381843130381843Humanname
156332128CV2181153single nucleotide variantNM_001868.4(CPA1):c.923A>C (p.Tyr308Ser)not provided [RCV003047281]uncertain significance7130385281130385281Humanname
156322454CV2182864single nucleotide variantNM_001868.4(CPA1):c.758C>A (p.Pro253His)not provided [RCV003046704]uncertain significance7130384597130384597Humanname
329364143CV2425530single nucleotide variantNM_001868.4(CPA1):c.839C>T (p.Ala280Val)Hereditary pancreatitis [RCV003181564]uncertain significance7130385197130385197Human1name
329364196CV2425531single nucleotide variantNM_001868.4(CPA1):c.536A>G (p.His179Arg)Hereditary pancreatitis [RCV003181565]uncertain significance7130383443130383443Human1name
329364198CV2425533single nucleotide variantNM_001868.4(CPA1):c.469A>C (p.Ile157Leu)Hereditary pancreatitis [RCV003181567]uncertain significance7130382195130382195Human1name
329364200CV2425535single nucleotide variantNM_001868.4(CPA1):c.353A>G (p.Asn118Ser)Hereditary pancreatitis [RCV003181569]uncertain significance7130381835130381835Human1name
329364203CV2425538single nucleotide variantNM_001868.4(CPA1):c.905T>C (p.Phe302Ser)Hereditary pancreatitis [RCV003181571]uncertain significance7130385263130385263Human1name
329364206CV2425542single nucleotide variantNM_001868.4(CPA1):c.448A>C (p.Asn150His)Hereditary pancreatitis [RCV003181574]uncertain significance7130382174130382174Human1name
329364207CV2425543single nucleotide variantNM_001868.4(CPA1):c.382A>G (p.Ile128Val)Hereditary pancreatitis [RCV003181575]|not provided [RCV003708736]uncertain significance7130382108130382108Human1name
329364209CV2425545single nucleotide variantNM_001868.4(CPA1):c.649C>A (p.Leu217Met)Hereditary pancreatitis [RCV003181577]uncertain significance7130383747130383747Human1name
329364211CV2425547single nucleotide variantNM_001868.4(CPA1):c.338C>T (p.Ser113Phe)Hereditary pancreatitis [RCV003181579]uncertain significance7130381820130381820Human1name
329364213CV2425550single nucleotide variantNM_001868.4(CPA1):c.424C>T (p.Leu142Phe)Hereditary pancreatitis [RCV003181581]uncertain significance7130382150130382150Human1name
329364216CV2425552single nucleotide variantNM_001868.4(CPA1):c.559G>A (p.Ala187Thr)Hereditary pancreatitis [RCV003181583]uncertain significance7130383466130383466Human1name
329364217CV2425553single nucleotide variantNM_001868.4(CPA1):c.503A>G (p.Lys168Arg)Hereditary pancreatitis [RCV003181584]uncertain significance7130383410130383410Human1name
329363469CV2425554single nucleotide variantNM_001868.4(CPA1):c.836T>C (p.Phe279Ser)Hereditary pancreatitis [RCV003168240]uncertain significance7130385194130385194Human1name
329364218CV2425555single nucleotide variantNM_001868.4(CPA1):c.874T>A (p.Phe292Ile)Hereditary pancreatitis [RCV003181585]uncertain significance7130385232130385232Human1name
329389910CV2465597single nucleotide variantNM_001868.4(CPA1):c.865A>T (p.Ile289Phe)Hereditary pancreatitis [RCV003216502]uncertain significance7130385223130385223Human1name
329389907CV2465599single nucleotide variantNM_001868.4(CPA1):c.989A>T (p.Asp330Val)Hereditary pancreatitis [RCV003216504]uncertain significance7130385840130385840Human1name
329389906CV2465600single nucleotide variantNM_001868.4(CPA1):c.895A>T (p.Ile299Phe)Hereditary pancreatitis [RCV003216505]|not provided [RCV005101370]uncertain significance7130385253130385253Human1name
329389905CV2465601single nucleotide variantNM_001868.4(CPA1):c.368A>G (p.His123Arg)Hereditary pancreatitis [RCV003216506]|not provided [RCV003720808]uncertain significance7130381850130381850Human1name
401772413CV2712715single nucleotide variantNM_001868.4(CPA1):c.842A>G (p.Asn281Ser)Hereditary pancreatitis [RCV004308022]uncertain significance7130385200130385200Human1name
401775063CV2723969single nucleotide variantNM_001868.4(CPA1):c.868G>T (p.Val290Leu)Hereditary pancreatitis [RCV003305489]uncertain significance7130385226130385226Human1name
401775064CV2723970single nucleotide variantNM_001868.4(CPA1):c.629T>A (p.Leu210His)Hereditary pancreatitis [RCV003305490]uncertain significance7130383727130383727Human1name
401775070CV2723972single nucleotide variantNM_001868.4(CPA1):c.539C>T (p.Ser180Phe)Hereditary pancreatitis [RCV003305492]uncertain significance7130383446130383446Human1name
401775071CV2723973single nucleotide variantNM_001868.4(CPA1):c.730G>A (p.Ala244Thr)Hereditary pancreatitis [RCV003305493]uncertain significance7130384569130384569Human1name
401765393CV2733681single nucleotide variantNM_001868.4(CPA1):c.376G>A (p.Glu126Lys)Hereditary pancreatitis [RCV003301385]uncertain significance7130381858130381858Human1name
401765395CV2733683single nucleotide variantNM_001868.4(CPA1):c.395T>A (p.Leu132Gln)Hereditary pancreatitis [RCV003301387]uncertain significance7130382121130382121Human1name
401765396CV2733684single nucleotide variantNM_001868.4(CPA1):c.463C>G (p.Arg155Gly)Hereditary pancreatitis [RCV003301388]uncertain significance7130382189130382189Human1name
401765402CV2733689single nucleotide variantNM_001868.4(CPA1):c.626T>G (p.Ile209Ser)Hereditary pancreatitis [RCV003301393]uncertain significance7130383724130383724Human1name
401765405CV2733691single nucleotide variantNM_001868.4(CPA1):c.595G>A (p.Asp199Asn)Hereditary pancreatitis [RCV003301395]uncertain significance7130383693130383693Human1name
401885405CV2783285single nucleotide variantNM_001868.4(CPA1):c.406G>A (p.Val136Met)Hereditary pancreatitis [RCV003386787]uncertain significance7130382132130382132Human1name
401885474CV2783307single nucleotide variantNM_001868.4(CPA1):c.944C>T (p.Pro315Leu)Hereditary pancreatitis [RCV003386809]uncertain significance7130385302130385302Human1name
401868424CV2787418single nucleotide variantNM_001868.4(CPA1):c.514A>G (p.Ile172Val)Hereditary pancreatitis [RCV003380194]uncertain significance7130383421130383421Human1name
401868425CV2787419single nucleotide variantNM_001868.4(CPA1):c.674G>T (p.Gly225Val)Hereditary pancreatitis [RCV003380195]uncertain significance7130383772130383772Human1name
401868428CV2787420single nucleotide variantNM_001868.4(CPA1):c.722C>G (p.Ser241Cys)Hereditary pancreatitis [RCV003380196]uncertain significance7130384561130384561Human1name
401868429CV2787421single nucleotide variantNM_001868.4(CPA1):c.532A>C (p.Ile178Leu)Hereditary pancreatitis [RCV003380197]uncertain significance7130383439130383439Human1name
401868430CV2787422single nucleotide variantNM_001868.4(CPA1):c.650T>C (p.Leu217Pro)Hereditary pancreatitis [RCV003380198]uncertain significance7130383748130383748Human1name
401868432CV2787423single nucleotide variantNM_001868.4(CPA1):c.771G>C (p.Trp257Cys)Hereditary pancreatitis [RCV003380199]uncertain significance7130384610130384610Human1name
401868435CV2787425single nucleotide variantNM_001868.4(CPA1):c.400C>A (p.Leu134Met)Hereditary pancreatitis [RCV003380201]uncertain significance7130382126130382126Human1name
401868436CV2787426single nucleotide variantNM_001868.4(CPA1):c.920G>T (p.Ser307Ile)Hereditary pancreatitis [RCV003380202]uncertain significance7130385278130385278Human1name
401868438CV2787427single nucleotide variantNM_001868.4(CPA1):c.451A>G (p.Thr151Ala)Hereditary pancreatitis [RCV003380203]uncertain significance7130382177130382177Human1name
401868441CV2787429single nucleotide variantNM_001868.4(CPA1):c.716C>T (p.Thr239Ile)Hereditary pancreatitis [RCV003380205]uncertain significance7130384555130384555Human1name
405211479CV2917278single nucleotide variantNM_001868.4(CPA1):c.527C>A (p.Thr176Lys)not provided [RCV003567229]uncertain significance7130383434130383434Humanname
405249809CV3000897single nucleotide variantNM_001868.4(CPA1):c.331G>A (p.Ala111Thr)not provided [RCV003721444]uncertain significance7130381813130381813Humanname
405134526CV3115584single nucleotide variantNM_001868.4(CPA1):c.341C>T (p.Thr114Ile)Hereditary pancreatitis [RCV004366709]|not provided [RCV003816241]uncertain significance7130381823130381823Human1name
405083577CV3137593single nucleotide variantNM_001868.4(CPA1):c.332C>A (p.Ala111Glu)not provided [RCV003834302]uncertain significance7130381814130381814Humanname
405208608CV3145725single nucleotide variantNM_001868.4(CPA1):c.433A>G (p.Lys145Glu)not provided [RCV003845455]uncertain significance7130382159130382159Humanname
405655639CV3380129single nucleotide variantNM_001868.4(CPA1):c.310A>T (p.Met104Leu)Hereditary pancreatitis [RCV004511141]uncertain significance7130381792130381792Human1name
405655641CV3380130single nucleotide variantNM_001868.4(CPA1):c.312G>A (p.Met104Ile)Hereditary pancreatitis [RCV004511142]uncertain significance7130381794130381794Human1name
405655642CV3380131single nucleotide variantNM_001868.4(CPA1):c.385T>C (p.Tyr129His)Hereditary pancreatitis [RCV004511143]uncertain significance7130382111130382111Human1name
405655644CV3380132single nucleotide variantNM_001868.4(CPA1):c.423C>G (p.His141Gln)Hereditary pancreatitis [RCV004511144]likely benign7130382149130382149Human1name
405655911CV3380133single nucleotide variantNM_001868.4(CPA1):c.431G>T (p.Ser144Ile)Hereditary pancreatitis [RCV004511145]uncertain significance7130382157130382157Human1name
405655649CV3380135single nucleotide variantNM_001868.4(CPA1):c.461G>A (p.Gly154Glu)Hereditary pancreatitis [RCV004511147]uncertain significance7130382187130382187Human1name
405655650CV3380136single nucleotide variantNM_001868.4(CPA1):c.475G>A (p.Val159Met)Hereditary pancreatitis [RCV004511148]uncertain significance7130382201130382201Human1name
405655651CV3380137single nucleotide variantNM_001868.4(CPA1):c.496G>T (p.Gly166Cys)Hereditary pancreatitis [RCV004511149]uncertain significance7130383403130383403Human1name
405655655CV3380139single nucleotide variantNM_001868.4(CPA1):c.520A>T (p.Ile174Phe)Hereditary pancreatitis [RCV004511151]uncertain significance7130383427130383427Human1name
405655659CV3380142single nucleotide variantNM_001868.4(CPA1):c.551T>C (p.Val184Ala)Hereditary pancreatitis [RCV004511154]uncertain significance7130383458130383458Human1name
405655661CV3380143single nucleotide variantNM_001868.4(CPA1):c.554C>T (p.Thr185Ile)Hereditary pancreatitis [RCV004511155]uncertain significance7130383461130383461Human1name
405655662CV3380144single nucleotide variantNM_001868.4(CPA1):c.581A>G (p.Lys194Arg)Hereditary pancreatitis [RCV004511156]uncertain significance7130383488130383488Human1name
405655664CV3380145single nucleotide variantNM_001868.4(CPA1):c.601G>T (p.Gly201Trp)Hereditary pancreatitis [RCV004511157]uncertain significance7130383699130383699Human1name
405655666CV3380146single nucleotide variantNM_001868.4(CPA1):c.602G>T (p.Gly201Val)Hereditary pancreatitis [RCV004511158]uncertain significance7130383700130383700Human1name
405655669CV3380148single nucleotide variantNM_001868.4(CPA1):c.625A>G (p.Ile209Val)Hereditary pancreatitis [RCV004511160]|not provided [RCV005104855]likely benign|uncertain significance7130383723130383723Human1name
405655670CV3380149single nucleotide variantNM_001868.4(CPA1):c.626T>C (p.Ile209Thr)Hereditary pancreatitis [RCV004511161]uncertain significance7130383724130383724Human1name
405655672CV3380150single nucleotide variantNM_001868.4(CPA1):c.638T>G (p.Leu213Trp)Hereditary pancreatitis [RCV004511162]uncertain significance7130383736130383736Human1name
405655674CV3380151single nucleotide variantNM_001868.4(CPA1):c.643A>C (p.Ile215Leu)Hereditary pancreatitis [RCV004511163]uncertain significance7130383741130383741Human1name
405655676CV3380152single nucleotide variantNM_001868.4(CPA1):c.643A>G (p.Ile215Val)Hereditary pancreatitis [RCV004511164]uncertain significance7130383741130383741Human1name
405655678CV3380154single nucleotide variantNM_001868.4(CPA1):c.656T>C (p.Ile219Thr)Hereditary pancreatitis [RCV004511166]uncertain significance7130383754130383754Human1name
405655680CV3380155single nucleotide variantNM_001868.4(CPA1):c.662C>T (p.Thr221Ile)Hereditary pancreatitis [RCV004511167]uncertain significance7130383760130383760Human1name
405655682CV3380156single nucleotide variantNM_001868.4(CPA1):c.670G>A (p.Asp224Asn)Hereditary pancreatitis [RCV004511168]|not provided [RCV005104856]uncertain significance7130383768130383768Human1name
405655913CV3380158single nucleotide variantNM_001868.4(CPA1):c.701G>T (p.Arg234Leu)Hereditary pancreatitis [RCV004511170]uncertain significance7130384540130384540Human1name
405655686CV3380159single nucleotide variantNM_001868.4(CPA1):c.762C>A (p.Asn254Lys)Hereditary pancreatitis [RCV004511171]uncertain significance7130384601130384601Human1name
405655688CV3380160single nucleotide variantNM_001868.4(CPA1):c.767A>G (p.Asn256Ser)Hereditary pancreatitis [RCV004511172]uncertain significance7130384606130384606Human1name
405655691CV3380162single nucleotide variantNM_001868.4(CPA1):c.851T>G (p.Val284Gly)Hereditary pancreatitis [RCV004511174]uncertain significance7130385209130385209Human1name
405655693CV3380163single nucleotide variantNM_001868.4(CPA1):c.904T>A (p.Phe302Ile)Hereditary pancreatitis [RCV004511175]uncertain significance7130385262130385262Human1name
405655694CV3380164single nucleotide variantNM_001868.4(CPA1):c.949G>A (p.Gly317Ser)Hereditary pancreatitis [RCV004511176]uncertain significance7130385307130385307Human1name
405655696CV3380165single nucleotide variantNM_001868.4(CPA1):c.953A>G (p.Tyr318Cys)Hereditary pancreatitis [RCV004511177]uncertain significance7130385311130385311Human1name
405655703CV3380169single nucleotide variantNM_001868.4(CPA1):c.991C>G (p.Gln331Glu)Hereditary pancreatitis [RCV004511181]uncertain significance7130385842130385842Human1name
407456910CV3419527single nucleotide variantNM_001868.4(CPA1):c.937A>C (p.Met313Leu)Hereditary pancreatitis [RCV004610921]likely benign7130385295130385295Human1name
407456912CV3419528single nucleotide variantNM_001868.4(CPA1):c.665A>T (p.Asn222Ile)Hereditary pancreatitis [RCV004610922]uncertain significance7130383763130383763Human1name
407456915CV3419530single nucleotide variantNM_001868.4(CPA1):c.724C>T (p.His242Tyr)Hereditary pancreatitis [RCV004610924]uncertain significance7130384563130384563Human1name
407456919CV3419532single nucleotide variantNM_001868.4(CPA1):c.637T>G (p.Leu213Val)Hereditary pancreatitis [RCV004610926]uncertain significance7130383735130383735Human1name
407456921CV3419533single nucleotide variantNM_001868.4(CPA1):c.845C>T (p.Ser282Phe)Hereditary pancreatitis [RCV004610927]uncertain significance7130385203130385203Human1name
407456927CV3419537single nucleotide variantNM_001868.4(CPA1):c.344A>G (p.Asp115Gly)Hereditary pancreatitis [RCV004610931]uncertain significance7130381826130381826Human1name
407456932CV3419540single nucleotide variantNM_001868.4(CPA1):c.312G>T (p.Met104Ile)Hereditary pancreatitis [RCV004610934]uncertain significance7130381794130381794Human1name
407457245CV3419543single nucleotide variantNM_001868.4(CPA1):c.807C>A (p.Asn269Lys)Hereditary pancreatitis [RCV004610937]uncertain significance7130385165130385165Human1name
597630466CV3650896single nucleotide variantNM_001868.4(CPA1):c.504G>T (p.Lys168Asn)Hereditary pancreatitis [RCV004822675]likely benign7130383411130383411Human1name
597630468CV3650897single nucleotide variantNM_001868.4(CPA1):c.326C>G (p.Ser109Cys)Hereditary pancreatitis [RCV004822676]uncertain significance7130381808130381808Human1name
597630470CV3650898single nucleotide variantNM_001868.4(CPA1):c.335G>C (p.Arg112Pro)Hereditary pancreatitis [RCV004822677]uncertain significance7130381817130381817Human1name
597630472CV3650899single nucleotide variantNM_001868.4(CPA1):c.461G>C (p.Gly154Ala)Hereditary pancreatitis [RCV004822678]uncertain significance7130382187130382187Human1name
597630475CV3650900single nucleotide variantNM_001868.4(CPA1):c.400C>G (p.Leu134Val)Hereditary pancreatitis [RCV004822679]uncertain significance7130382126130382126Human1name
597630479CV3650902single nucleotide variantNM_001868.4(CPA1):c.704T>A (p.Met235Lys)Hereditary pancreatitis [RCV004822681]uncertain significance7130384543130384543Human1name
597630484CV3650904single nucleotide variantNM_001868.4(CPA1):c.459A>C (p.Glu153Asp)Hereditary pancreatitis [RCV004822683]uncertain significance7130382185130382185Human1name
597630493CV3650908single nucleotide variantNM_001868.4(CPA1):c.901G>C (p.Ala301Pro)Hereditary pancreatitis [RCV004822687]uncertain significance7130385259130385259Human1name
597630495CV3650909single nucleotide variantNM_001868.4(CPA1):c.482A>T (p.Lys161Met)Hereditary pancreatitis [RCV004822688]uncertain significance7130382208130382208Human1name
597630498CV3650910single nucleotide variantNM_001868.4(CPA1):c.685A>C (p.Thr229Pro)Hereditary pancreatitis [RCV004822689]uncertain significance7130383783130383783Human1name
597630371CV3654354single nucleotide variantNM_001868.4(CPA1):c.334C>T (p.Arg112Cys)Hereditary pancreatitis [RCV004822631]likely benign7130381816130381816Human1name
597630372CV3654355single nucleotide variantNM_001868.4(CPA1):c.494G>T (p.Gly165Val)Hereditary pancreatitis [RCV004822632]uncertain significance7130383401130383401Human1name
597630379CV3654358single nucleotide variantNM_001868.4(CPA1):c.755A>G (p.Asp252Gly)Hereditary pancreatitis [RCV004822635]uncertain significance7130384594130384594Human1name
597630383CV3654361single nucleotide variantNM_001868.4(CPA1):c.406G>C (p.Val136Leu)Hereditary pancreatitis [RCV004822637]uncertain significance7130382132130382132Human1name
597630385CV3654362single nucleotide variantNM_001868.4(CPA1):c.532A>G (p.Ile178Val)Hereditary pancreatitis [RCV004822638]uncertain significance7130383439130383439Human1name
597630388CV3654363single nucleotide variantNM_001868.4(CPA1):c.697A>G (p.Asn233Asp)Hereditary pancreatitis [RCV004822639]likely benign7130384536130384536Human1name
597630389CV3654364single nucleotide variantNM_001868.4(CPA1):c.938T>G (p.Met313Arg)Hereditary pancreatitis [RCV004822640]uncertain significance7130385296130385296Human1name
597630391CV3654365single nucleotide variantNM_001868.4(CPA1):c.618C>A (p.Phe206Leu)Hereditary pancreatitis [RCV004822641]likely benign7130383716130383716Human1name
597630396CV3654367single nucleotide variantNM_001868.4(CPA1):c.329G>T (p.Arg110Leu)Hereditary pancreatitis [RCV004822643]uncertain significance7130381811130381811Human1name
597630402CV3654370single nucleotide variantNM_001868.4(CPA1):c.973G>A (p.Asp325Asn)Hereditary pancreatitis [RCV004822646]uncertain significance7130385331130385331Human1name
597630422CV3654380single nucleotide variantNM_001868.4(CPA1):c.545A>T (p.Glu182Val)Hereditary pancreatitis [RCV004822655]|not provided [RCV005110154]uncertain significance7130383452130383452Human1name
597630435CV3654387single nucleotide variantNM_001868.4(CPA1):c.467C>G (p.Pro156Arg)Hereditary pancreatitis [RCV004822661]uncertain significance7130382193130382193Human1name
597630444CV3654391single nucleotide variantNM_001868.4(CPA1):c.344A>T (p.Asp115Val)Hereditary pancreatitis [RCV004822665]uncertain significance7130381826130381826Human1name
597630446CV3654392single nucleotide variantNM_001868.4(CPA1):c.842A>C (p.Asn281Thr)Hereditary pancreatitis [RCV004822666]uncertain significance7130385200130385200Human1name
597630449CV3654393single nucleotide variantNM_001868.4(CPA1):c.573G>T (p.Trp191Cys)Hereditary pancreatitis [RCV004822667]uncertain significance7130383480130383480Human1name
597630451CV3654394single nucleotide variantNM_001868.4(CPA1):c.704T>G (p.Met235Arg)Hereditary pancreatitis [RCV004822668]uncertain significance7130384543130384543Human1name
597630454CV3654395single nucleotide variantNM_001868.4(CPA1):c.721T>A (p.Ser241Thr)Hereditary pancreatitis [RCV004822669]uncertain significance7130384560130384560Human1name
597630456CV3654397single nucleotide variantNM_001868.4(CPA1):c.455A>G (p.Tyr152Cys)Hereditary pancreatitis [RCV004822670]uncertain significance7130382181130382181Human1name
597630457CV3654398single nucleotide variantNM_001868.4(CPA1):c.808C>T (p.Pro270Ser)Hereditary pancreatitis [RCV004822671]uncertain significance7130385166130385166Human1name
597630464CV3654401single nucleotide variantNM_001868.4(CPA1):c.371C>A (p.Thr124Asn)Hereditary pancreatitis [RCV004822674]uncertain significance7130381853130381853Human1name
12840276CV368929single nucleotide variantNM_001868.4(CPA1):c.657C>G (p.Ile219Met)Hereditary pancreatitis [RCV002365575]|not provided [RCV000430381]uncertain significance7130383755130383755Human1name
597887220CV3741909single nucleotide variantNM_001868.4(CPA1):c.491C>A (p.Thr164Lys)not provided [RCV005070629]uncertain significance7130383398130383398Humanname
597900917CV3796633single nucleotide variantNM_001868.4(CPA1):c.404T>G (p.Leu135Arg)not provided [RCV005152715]uncertain significance7130382130130382130Humanname
597888798CV3859560single nucleotide variantNM_001868.4(CPA1):c.907A>G (p.Ile303Val)not provided [RCV005200216]uncertain significance7130385265130385265Humanname
598235036CV3945104single nucleotide variantNM_001868.4(CPA1):c.383T>G (p.Ile128Ser)Hereditary pancreatitis [RCV005320170]uncertain significance7130382109130382109Human1name
598235053CV3945108single nucleotide variantNM_001868.4(CPA1):c.959C>T (p.Thr320Ile)Hereditary pancreatitis [RCV005320175]uncertain significance7130385317130385317Human1name
598235067CV3945111single nucleotide variantNM_001868.4(CPA1):c.853G>A (p.Glu285Lys)Hereditary pancreatitis [RCV005320178]uncertain significance7130385211130385211Human1name
598235090CV3945117single nucleotide variantNM_001868.4(CPA1):c.490A>C (p.Thr164Pro)Hereditary pancreatitis [RCV005320184]uncertain significance7130383397130383397Human1name
598235098CV3945120single nucleotide variantNM_001868.4(CPA1):c.417C>A (p.Asn139Lys)Hereditary pancreatitis [RCV005320187]uncertain significance7130382143130382143Human1name
598235124CV3945127single nucleotide variantNM_001868.4(CPA1):c.985C>G (p.Leu329Val)Hereditary pancreatitis [RCV005320194]uncertain significance7130385343130385343Human1name
598235135CV3945130single nucleotide variantNM_001868.4(CPA1):c.748G>C (p.Gly250Arg)Hereditary pancreatitis [RCV005320197]uncertain significance7130384587130384587Human1name
598235138CV3945131single nucleotide variantNM_001868.4(CPA1):c.418C>T (p.Pro140Ser)Hereditary pancreatitis [RCV005320198]uncertain significance7130382144130382144Human1name
13445797CV438371single nucleotide variantNM_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 significance7130383404130383404Human1name , trait , alternate_id
13485790CV444065single nucleotide variantNM_001868.4(CPA1):c.847G>A (p.Glu283Lys)Hereditary pancreatitis [RCV002448571]|not provided [RCV000522708]uncertain significance7130385205130385205Human1name
15138262CV710771single nucleotide variantNM_001868.4(CPA1):c.604C>A (p.Gln202Lys)Hereditary pancreatitis [RCV002346171]|not provided [RCV000965760]benign|likely benign7130383702130383702Human1name
25316723CV808950single nucleotide variantNM_001868.4(CPA1):c.358G>A (p.Ala120Thr)Hereditary pancreatitis [RCV002319265]|not provided [RCV001242987]uncertain significance7130381840130381840Human1name
25317295CV808951single nucleotide variantNM_001868.4(CPA1):c.371C>T (p.Thr124Ile)CPA1-related disorder [RCV003928665]|Hereditary pancreatitis [RCV002258086]|not provided [RCV001516447]benign|likely benign7130381853130381853Human1name , trait , alternate_id
25318217CV808952single nucleotide variantNM_001868.4(CPA1):c.401T>G (p.Leu134Arg)Hereditary pancreatitis [RCV002319306]uncertain significance7130382127130382127Human1name
25318659CV808954single nucleotide variantNM_001868.4(CPA1):c.421C>T (p.His141Tyr)Hereditary pancreatitis [RCV002319330]uncertain significance7130382147130382147Human1name
25322624CV808956single nucleotide variantNM_001868.4(CPA1):c.506G>A (p.Arg169His)Hereditary pancreatitis [RCV002319395]|not provided [RCV002067663]likely benign|uncertain significance7130383413130383413Human1name
25323569CV808957single nucleotide variantNM_001868.4(CPA1):c.542G>A (p.Arg181Gln)Hereditary pancreatitis [RCV002319633]|not provided [RCV002551887]uncertain significance7130383449130383449Human1name
25324692CV808959single nucleotide variantNM_001868.4(CPA1):c.622G>A (p.Ala208Thr)Hereditary pancreatitis [RCV002354932]|not provided [RCV001517260]benign|likely benign7130383720130383720Human1name
25325543CV808961single nucleotide variantNM_001868.4(CPA1):c.686C>A (p.Thr229Lys)Hereditary pancreatitis [RCV002382256]|not provided [RCV003769613]uncertain significance7130383784130383784Human1name
25325643CV808962single nucleotide variantNM_001868.4(CPA1):c.695C>T (p.Thr232Met)Hereditary pancreatitis [RCV002391083]|not provided [RCV001517271]benign|likely benign7130383793130383793Human1name
25327222CV808964single nucleotide variantNM_001868.4(CPA1):c.820A>G (p.Thr274Ala)Hereditary pancreatitis [RCV002445189]uncertain significance7130385178130385178Human1name
25327336CV808965single nucleotide variantNM_001868.4(CPA1):c.829G>A (p.Gly277Ser)CPA1-related disorder [RCV004758136]|Hereditary pancreatitis [RCV002445197]|not provided [RCV001229837]likely pathogenic|uncertain significance7130385187130385187Human1name , trait , alternate_id
26884894CV833136single nucleotide variantNM_001868.4(CPA1):c.322C>G (p.Arg108Gly)not provided [RCV001052781]uncertain significance7130381804130381804Humanname
26904363CV833138single nucleotide variantNM_001868.4(CPA1):c.496G>A (p.Gly166Ser)Hereditary pancreatitis [RCV004030756]|not provided [RCV001070606]uncertain significance7130383403130383403Human1name
26922161CV833139single nucleotide variantNM_001868.4(CPA1):c.775G>T (p.Ala259Ser)Hereditary pancreatitis [RCV002409432]|not provided [RCV001051580]uncertain significance7130384614130384614Human1name
26917101CV833140single nucleotide variantNM_001868.4(CPA1):c.845C>G (p.Ser282Cys)not provided [RCV001041312]uncertain significance7130385203130385203Humanname
28883924CV859586single nucleotide variantNM_001868.4(CPA1):c.768C>G (p.Asn256Lys)not provided [RCV001091495]likely pathogenic7130384607130384607Humanname
38461053CV945429single nucleotide variantNM_001868.4(CPA1):c.709C>T (p.Arg237Cys)Hereditary pancreatitis [RCV002366025]|not provided [RCV001229465]uncertain significance7130384548130384548Human1name
38494979CV955058single nucleotide variantNM_001868.4(CPA1):c.691A>G (p.Ser231Gly)Hereditary pancreatitis [RCV002375277]|not provided [RCV001241677]uncertain significance7130383789130383789Human1name
38498506CV955059single nucleotide variantNM_001868.4(CPA1):c.713A>C (p.Lys238Thr)not provided [RCV001243875]uncertain significance7130384552130384552Humanname
126750192CV992100single nucleotide variantNM_001868.4(CPA1):c.409G>A (p.Ala137Thr)Hereditary pancreatitis [RCV003166659]|not provided [RCV001297279]likely benign|uncertain significance7130382135130382135Human1name
126732364CV992101single nucleotide variantNM_001868.4(CPA1):c.635C>A (p.Thr212Asn)Hereditary pancreatitis [RCV002366145]|not provided [RCV001304073]likely benign|uncertain significance7130383733130383733Human1name
126755553CV992102single nucleotide variantNM_001868.4(CPA1):c.635C>G (p.Thr212Ser)Hereditary pancreatitis [RCV002366126]|not provided [RCV001298380]likely benign|uncertain significance7130383733130383733Human1name
126755476CV992103single nucleotide variantNM_001868.4(CPA1):c.776C>T (p.Ala259Val)Hereditary pancreatitis [RCV003166754]|not provided [RCV001307869]uncertain significance7130384615130384615Human1name
126744512CV1007249single nucleotide variantNM_001868.4(CPA1):c.1016C>A (p.Ala339Asp)Hereditary pancreatitis [RCV002350573]|not provided [RCV001314949]uncertain significance7130385867130385867Human1name
126757325CV1007250single nucleotide variantNM_001868.4(CPA1):c.1145G>A (p.Arg382Gln)Hereditary pancreatitis [RCV002456424]|not provided [RCV001317457]uncertain significance7130387896130387896Human1name
126745216CV1027788single nucleotide variantNM_001868.4(CPA1):c.1157G>A (p.Arg386His)Hereditary pancreatitis [RCV002357174]|not provided [RCV001337182]likely benign|uncertain significance7130387908130387908Human1name
126774123CV1027789single nucleotide variantNM_001868.4(CPA1):c.1193C>T (p.Pro398Leu)Hereditary pancreatitis [RCV002350640]|not provided [RCV001346862]uncertain significance7130387944130387944Human1name
126921987CV1044701single nucleotide variantNM_001868.4(CPA1):c.1033G>A (p.Gly345Arg)Hereditary pancreatitis [RCV004822375]|not provided [RCV001364134]uncertain significance7130385884130385884Human1name
126915339CV1044702single nucleotide variantNM_001868.4(CPA1):c.1137C>A (p.Phe379Leu)Hereditary pancreatitis [RCV004037483]|not provided [RCV001370858]uncertain significance7130387888130387888Human1name
151771209CV1340248single nucleotide variantNM_001868.4(CPA1):c.1228A>G (p.Ile410Val)Hereditary pancreatitis [RCV003303252]|not provided [RCV001874465]uncertain significance7130387979130387979Human1name
151742044CV1386779single nucleotide variantNM_001868.4(CPA1):c.1192C>T (p.Pro398Ser)Hereditary pancreatitis [RCV002334823]|not provided [RCV001893361]uncertain significance7130387943130387943Human1name
151856278CV1387541single nucleotide variantNM_001868.4(CPA1):c.1217C>T (p.Ala406Val)Hereditary pancreatitis [RCV002352636]|not provided [RCV001996577]uncertain significance7130387968130387968Human1name
151880409CV1388489single nucleotide variantNM_001868.4(CPA1):c.1151C>T (p.Thr384Ile)Hereditary pancreatitis [RCV002352628]|not provided [RCV001982458]uncertain significance7130387902130387902Human1name
151881035CV1406057single nucleotide variantNM_001868.4(CPA1):c.1112A>G (p.Gln371Arg)Hereditary pancreatitis [RCV002441068]|not provided [RCV001941038]uncertain significance7130387863130387863Human1name
151862249CV1448698single nucleotide variantNM_001868.4(CPA1):c.1009G>C (p.Val337Leu)not provided [RCV001959369]uncertain significance7130385860130385860Humanname
151847520CV1484016single nucleotide variantNM_001868.4(CPA1):c.1153G>A (p.Gly385Arg)not provided [RCV001903638]uncertain significance7130387904130387904Humanname
151721781CV1491780single nucleotide variantNM_001868.4(CPA1):c.1022C>A (p.Ala341Asp)Hereditary pancreatitis [RCV003170404]|not provided [RCV002003779]uncertain significance7130385873130385873Human1name
153349759CV1693925single nucleotide variantNM_001868.4(CPA1):c.1085G>A (p.Gly362Glu)not provided [RCV002276177]likely pathogenic7130387836130387836Humanname
155703378CV1774795single nucleotide variantNM_001868.4(CPA1):c.1117A>C (p.Ile373Leu)not provided [RCV002300074]uncertain significance7130387868130387868Humanname
155664439CV1786539single nucleotide variantNM_001868.4(CPA1):c.1151C>G (p.Thr384Ser)Hereditary pancreatitis [RCV002348946]uncertain significance7130387902130387902Human1name
155719247CV1788769single nucleotide variantNM_001868.4(CPA1):c.1138G>C (p.Glu380Gln)Hereditary pancreatitis [RCV002326611]uncertain significance7130387889130387889Human1name
155704184CV1795298single nucleotide variantNM_001868.4(CPA1):c.1135T>C (p.Phe379Leu)Hereditary pancreatitis [RCV002445709]uncertain significance7130387886130387886Human1name
155682741CV1795809single nucleotide variantNM_001868.4(CPA1):c.1141C>G (p.Leu381Val)Hereditary pancreatitis [RCV002457088]uncertain significance7130387892130387892Human1name
155668398CV1799892single nucleotide variantNM_001868.4(CPA1):c.1201A>C (p.Lys401Gln)Hereditary pancreatitis [RCV002349646]likely benign7130387952130387952Human1name
155669502CV1800086single nucleotide variantNM_001868.4(CPA1):c.1202A>G (p.Lys401Arg)Hereditary pancreatitis [RCV002349840]likely benign7130387953130387953Human1name
155746695CV1800294single nucleotide variantNM_001868.4(CPA1):c.1208C>T (p.Thr403Met)Hereditary pancreatitis [RCV002347665]|not provided [RCV003096851]uncertain significance7130387959130387959Human1name
155687641CV1803679single nucleotide variantNM_001868.4(CPA1):c.1211G>T (p.Trp404Leu)Hereditary pancreatitis [RCV002355833]uncertain significance7130387962130387962Human1name
155666133CV1804254single nucleotide variantNM_001868.4(CPA1):c.1219C>T (p.Leu407Phe)Hereditary pancreatitis [RCV002366632]|not provided [RCV003718531]uncertain significance7130387970130387970Human1name
155737245CV1805457single nucleotide variantNM_001868.4(CPA1):c.1185G>T (p.Gln395His)Hereditary pancreatitis [RCV002330752]|not provided [RCV003660934]uncertain significance7130387936130387936Human1name
155721875CV1805607single nucleotide variantNM_001868.4(CPA1):c.1186A>T (p.Ile396Phe)Hereditary pancreatitis [RCV002338106]uncertain significance7130387937130387937Human1name
155713395CV1808097single nucleotide variantNM_001868.4(CPA1):c.1223T>G (p.Leu408Arg)Hereditary pancreatitis [RCV002361953]uncertain significance7130387974130387974Human1name
155730634CV1808471single nucleotide variantNM_001868.4(CPA1):c.1177G>C (p.Ala393Pro)Hereditary pancreatitis [RCV002339886]uncertain significance7130387928130387928Human1name
155726650CV1812617single nucleotide variantNM_001868.4(CPA1):c.1234G>A (p.Glu412Lys)Hereditary pancreatitis [RCV002364654]uncertain significance7130387985130387985Human1name
155715035CV1815446single nucleotide variantNM_001868.4(CPA1):c.1232T>A (p.Met411Lys)Hereditary pancreatitis [RCV002362240]uncertain significance7130387983130387983Human1name
155742295CV1816629single nucleotide variantNM_001868.4(CPA1):c.1252C>G (p.Pro418Ala)Hereditary pancreatitis [RCV002412327]uncertain significance7130388003130388003Human1name
155742318CV1816642single nucleotide variantNM_001868.4(CPA1):c.1252C>T (p.Pro418Ser)Hereditary pancreatitis [RCV002412340]uncertain significance7130388003130388003Human1name
155722321CV1817549single nucleotide variantNM_001868.4(CPA1):c.1001A>G (p.Lys334Arg)Hereditary pancreatitis [RCV002449737]uncertain significance7130385852130385852Human1name
155670829CV1819305single nucleotide variantNM_001868.4(CPA1):c.1238A>G (p.His413Arg)Hereditary pancreatitis [RCV002367457]uncertain significance7130387989130387989Human1name
155666527CV1819539single nucleotide variantNM_001868.4(CPA1):c.1243C>A (p.Leu415Met)Hereditary pancreatitis [RCV002384969]uncertain significance7130387994130387994Human1name
155726825CV1822302single nucleotide variantNM_001868.4(CPA1):c.1234G>C (p.Glu412Gln)Hereditary pancreatitis [RCV002364689]likely benign|uncertain significance7130387985130387985Human1name
155717272CV1822923single nucleotide variantNM_001868.4(CPA1):c.1241C>T (p.Thr414Ile)Hereditary pancreatitis [RCV002380202]uncertain significance7130387992130387992Human1name
155728942CV1823423single nucleotide variantNM_001868.4(CPA1):c.1249C>T (p.His417Tyr)Hereditary pancreatitis [RCV002400563]uncertain significance7130388000130388000Human1name
155694017CV1827506single nucleotide variantNM_001868.4(CPA1):c.1003G>A (p.Ala335Thr)Hereditary pancreatitis [RCV002392651]|not provided [RCV003096968]uncertain significance7130385854130385854Human1name
155718706CV1827819single nucleotide variantNM_001868.4(CPA1):c.1003G>C (p.Ala335Pro)Hereditary pancreatitis [RCV002398537]uncertain significance7130385854130385854Human1name
155700610CV1828473single nucleotide variantNM_001868.4(CPA1):c.1058T>G (p.Ile353Ser)Hereditary pancreatitis [RCV002401457]uncertain significance7130385909130385909Human1name
155720072CV1835727single nucleotide variantNM_001868.4(CPA1):c.1025C>G (p.Ser342Cys)Hereditary pancreatitis [RCV002380728]uncertain significance7130385876130385876Human1name
155720167CV1835741single nucleotide variantNM_001868.4(CPA1):c.1025C>T (p.Ser342Phe)Hereditary pancreatitis [RCV002380742]uncertain significance7130385876130385876Human1name
155706424CV1837164single nucleotide variantNM_001868.4(CPA1):c.1042T>G (p.Phe348Val)Hereditary pancreatitis [RCV002402971]uncertain significance7130385893130385893Human1name
155730861CV1837531single nucleotide variantNM_001868.4(CPA1):c.1049A>G (p.Tyr350Cys)Hereditary pancreatitis [RCV002400874]uncertain significance7130385900130385900Human1name
155723990CV1837964single nucleotide variantNM_001868.4(CPA1):c.1054A>C (p.Ser352Arg)Hereditary pancreatitis [RCV002406103]uncertain significance7130385905130385905Human1name
155714583CV1841911single nucleotide variantNM_001868.4(CPA1):c.1100G>A (p.Trp367Ter)Hereditary pancreatitis [RCV002431146]likely benign7130387851130387851Human1name
155694790CV1844480single nucleotide variantNM_001868.4(CPA1):c.1089C>G (p.Ser363Arg)Hereditary pancreatitis [RCV002443528]uncertain significance7130387840130387840Human1name
155670901CV1848993single nucleotide variantNM_001868.4(CPA1):c.1009G>A (p.Val337Met)Hereditary pancreatitis [RCV002453182]|not provided [RCV005098253]uncertain significance7130385860130385860Human1name
155664013CV1849406single nucleotide variantNM_001868.4(CPA1):c.1117A>T (p.Ile373Phe)Hereditary pancreatitis [RCV002435034]uncertain significance7130387868130387868Human1name
155684596CV1849892single nucleotide variantNM_001868.4(CPA1):c.1006G>T (p.Ala336Ser)Hereditary pancreatitis [RCV002423946]uncertain significance7130385857130385857Human1name
155684848CV1849960single nucleotide variantNM_001868.4(CPA1):c.1079C>G (p.Ala360Gly)Hereditary pancreatitis [RCV002424014]uncertain significance7130387830130387830Human1name
155703110CV1852290single nucleotide variantNM_001868.4(CPA1):c.1109G>A (p.Ser370Asn)Hereditary pancreatitis [RCV002428801]likely benign7130387860130387860Human1name
155703309CV1852324single nucleotide variantNM_001868.4(CPA1):c.1109G>T (p.Ser370Ile)Hereditary pancreatitis [RCV002428825]uncertain significance7130387860130387860Human1name
155697275CV1854860single nucleotide variantNM_001868.4(CPA1):c.1126T>C (p.Ser376Pro)Hereditary pancreatitis [RCV002444098]|not provided [RCV005098403]uncertain significance7130387877130387877Human1name
155798681CV1860750single nucleotide variantNM_001868.4(CPA1):c.1124A>G (p.Tyr375Cys)Hereditary pancreatitis [RCV002467392]uncertain significance7130387875130387875Human1name
156305029CV1868082single nucleotide variantNM_001868.4(CPA1):c.1138G>A (p.Glu380Lys)not provided [RCV003062143]uncertain significance7130387889130387889Humanname
156398939CV1897334single nucleotide variantNM_001868.4(CPA1):c.1199C>T (p.Ala400Val)Hereditary pancreatitis [RCV003294521]|not provided [RCV002584665]uncertain significance7130387950130387950Human1name
156442343CV1938569single nucleotide variantNM_001868.4(CPA1):c.1129T>C (p.Phe377Leu)Hereditary pancreatitis [RCV003384357]|not provided [RCV003112684]uncertain significance7130387880130387880Human1name
329364197CV2425532single nucleotide variantNM_001868.4(CPA1):c.1033G>T (p.Gly345Trp)Hereditary pancreatitis [RCV003181566]uncertain significance7130385884130385884Human1name
329389922CV2465587single nucleotide variantNM_001868.4(CPA1):c.1010T>C (p.Val337Ala)Hereditary pancreatitis [RCV003216492]uncertain significance7130385861130385861Human1name
329389921CV2465588single nucleotide variantNM_001868.4(CPA1):c.1180T>C (p.Ser394Pro)Hereditary pancreatitis [RCV003216493]uncertain significance7130387931130387931Human1name
329389920CV2465589single nucleotide variantNM_001868.4(CPA1):c.1256A>G (p.Tyr419Cys)Hereditary pancreatitis [RCV003216494]|not provided [RCV003779759]uncertain significance7130388007130388007Human1name
329389919CV2465590single nucleotide variantNM_001868.4(CPA1):c.1110C>G (p.Ser370Arg)Hereditary pancreatitis [RCV003216495]uncertain significance7130387861130387861Human1name
401765394CV2733682single nucleotide variantNM_001868.4(CPA1):c.1103C>T (p.Thr368Ile)Hereditary pancreatitis [RCV003301386]uncertain significance7130387854130387854Human1name
401885267CV2783218single nucleotide variantNM_001868.4(CPA1):c.1142T>A (p.Leu381His)Hereditary pancreatitis [RCV003386720]uncertain significance7130387893130387893Human1name
401885366CV2783248single nucleotide variantNM_001868.4(CPA1):c.1069A>G (p.Ile357Val)Hereditary pancreatitis [RCV003386750]uncertain significance7130385920130385920Human1name
401885381CV2783277single nucleotide variantNM_001868.4(CPA1):c.1141C>T (p.Leu381Phe)Hereditary pancreatitis [RCV003386779]|not provided [RCV005104178]uncertain significance7130387892130387892Human1name
401868434CV2787424single nucleotide variantNM_001868.4(CPA1):c.1105T>C (p.Tyr369His)Hereditary pancreatitis [RCV003380200]uncertain significance7130387856130387856Human1name
405194912CV2982236single nucleotide variantNM_001868.4(CPA1):c.1101G>C (p.Trp367Cys)not provided [RCV003706811]uncertain significance7130387852130387852Humanname
405144039CV3056057single nucleotide variantNM_001868.4(CPA1):c.1251C>A (p.His417Gln)Hereditary pancreatitis [RCV004374097]|not provided [RCV003725805]uncertain significance7130388002130388002Human1name
405123798CV3136369single nucleotide variantNM_001868.4(CPA1):c.1120A>G (p.Lys374Glu)not provided [RCV003837699]uncertain significance7130387871130387871Humanname
405229943CV3153793single nucleotide variantNM_001868.4(CPA1):c.1007C>T (p.Ala336Val)not provided [RCV003848660]uncertain significance7130385858130385858Humanname
405685812CV3235788single nucleotide variantNM_001868.4(CPA1):c.1073A>G (p.Tyr358Cys)Hereditary pancreatitis [RCV004372302]uncertain significance7130387824130387824Human1name
405685819CV3235790single nucleotide variantNM_001868.4(CPA1):c.1180T>A (p.Ser394Thr)Hereditary pancreatitis [RCV004372304]|not provided [RCV005064993]uncertain significance7130387931130387931Human1name
405655603CV3383118single nucleotide variantNM_001868.4(CPA1):c.1061T>A (p.Ile354Asn)Hereditary pancreatitis [RCV004511119]uncertain significance7130385912130385912Human1name
405655607CV3383120single nucleotide variantNM_001868.4(CPA1):c.1133C>A (p.Thr378Asn)Hereditary pancreatitis [RCV004511121]uncertain significance7130387884130387884Human1name
405655616CV3383125single nucleotide variantNM_001868.4(CPA1):c.1156C>A (p.Arg386Ser)Hereditary pancreatitis [RCV004511126]uncertain significance7130387907130387907Human1name
405655622CV3383129single nucleotide variantNM_001868.4(CPA1):c.1226C>A (p.Thr409Asn)Hereditary pancreatitis [RCV004511130]uncertain significance7130387977130387977Human1name
405655624CV3383130single nucleotide variantNM_001868.4(CPA1):c.1232T>C (p.Met411Thr)Hereditary pancreatitis [RCV004511131]uncertain significance7130387983130387983Human1name
405655625CV3383131single nucleotide variantNM_001868.4(CPA1):c.1233G>T (p.Met411Ile)Hereditary pancreatitis [RCV004511132]uncertain significance7130387984130387984Human1name
405655627CV3383132single nucleotide variantNM_001868.4(CPA1):c.1247A>C (p.Asn416Thr)Hereditary pancreatitis [RCV004511133]uncertain significance7130387998130387998Human1name
407456896CV3419519single nucleotide variantNM_001868.4(CPA1):c.1137C>G (p.Phe379Leu)Hereditary pancreatitis [RCV004610913]uncertain significance7130387888130387888Human1name
407456909CV3419526single nucleotide variantNM_001868.4(CPA1):c.1063A>G (p.Lys355Glu)Hereditary pancreatitis [RCV004610920]uncertain significance7130385914130385914Human1name
407456923CV3419534single nucleotide variantNM_001868.4(CPA1):c.1177G>T (p.Ala393Ser)Hereditary pancreatitis [RCV004610928]uncertain significance7130387928130387928Human1name
407456930CV3419539single nucleotide variantNM_001868.4(CPA1):c.1174C>T (p.Pro392Ser)Hereditary pancreatitis [RCV004610933]uncertain significance7130387925130387925Human1name
407457244CV3419544single nucleotide variantNM_001868.4(CPA1):c.1041G>C (p.Lys347Asn)Hereditary pancreatitis [RCV004610938]uncertain significance7130385892130385892Human1name
597630486CV3650905single nucleotide variantNM_001868.4(CPA1):c.1237C>T (p.His413Tyr)Hereditary pancreatitis [RCV004822684]uncertain significance7130387988130387988Human1name
597630398CV3654368single nucleotide variantNM_001868.4(CPA1):c.1178C>T (p.Ala393Val)Hereditary pancreatitis [RCV004822644]uncertain significance7130387929130387929Human1name
597630405CV3654371single nucleotide variantNM_001868.4(CPA1):c.1130T>C (p.Phe377Ser)Hereditary pancreatitis [RCV004822647]uncertain significance7130387881130387881Human1name
597630442CV3654390single nucleotide variantNM_001868.4(CPA1):c.1250A>G (p.His417Arg)Hereditary pancreatitis [RCV004822664]uncertain significance7130388001130388001Human1name
597944740CV3812614single nucleotide variantNM_001868.4(CPA1):c.1000A>C (p.Lys334Gln)not provided [RCV005159824]uncertain significance7130385851130385851Humanname
597958416CV3849121single nucleotide variantNM_001868.4(CPA1):c.1031A>G (p.Tyr344Cys)not provided [RCV005192122]uncertain significance7130385882130385882Humanname
598235070CV3945112single nucleotide variantNM_001868.4(CPA1):c.1236G>T (p.Glu412Asp)Hereditary pancreatitis [RCV005320179]uncertain significance7130387987130387987Human1name
598235085CV3945116single nucleotide variantNM_001868.4(CPA1):c.1202A>C (p.Lys401Thr)Hereditary pancreatitis [RCV005320183]likely benign7130387953130387953Human1name
598235095CV3945119single nucleotide variantNM_001868.4(CPA1):c.1231A>G (p.Met411Val)Hereditary pancreatitis [RCV005320186]uncertain significance7130387982130387982Human1name
598235107CV3945123single nucleotide variantNM_001868.4(CPA1):c.1112A>T (p.Gln371Leu)Hereditary pancreatitis [RCV005320190]uncertain significance7130387863130387863Human1name
25329082CV808968single nucleotide variantNM_001868.4(CPA1):c.1021G>A (p.Ala341Thr)Hereditary pancreatitis [RCV002258085]|not provided [RCV001402994]benign|likely benign7130385872130385872Human3name
25329082CV808968single nucleotide variantNM_001868.4(CPA1):c.1021G>A (p.Ala341Thr)Hereditary pancreatitis [RCV002258085]|not provided [RCV001402994]benign|likely benign7130385872130385873Human3name
25323450CV808973single nucleotide variantNM_001868.4(CPA1):c.1258T>C (p.Ter420Arg)Hereditary pancreatitis [RCV002318932]uncertain significance7130388009130388009Human1name
26922155CV833141single nucleotide variantNM_001868.4(CPA1):c.1099T>C (p.Trp367Arg)not provided [RCV001051575]uncertain significance7130387850130387850Humanname
26905205CV833142single nucleotide variantNM_001868.4(CPA1):c.1156C>T (p.Arg386Cys)Hereditary pancreatitis [RCV002365786]|not provided [RCV001071696]uncertain significance7130387907130387907Human1name
38458286CV945430single nucleotide variantNM_001868.4(CPA1):c.1212G>C (p.Trp404Cys)Hereditary pancreatitis [RCV002356978]|not provided [RCV001228881]uncertain significance7130387963130387963Human1name
38456776CV955060single nucleotide variantNM_001868.4(CPA1):c.1144C>T (p.Arg382Trp)Early-onset chronic pancreatitis [RCV003225166]|Hereditary pancreatitis [RCV002451599]|not provided [RCV001245889]uncertain significance7130387895130387895Human1name
405142634CV3155437microsatelliteNM_001868.4(CPA1):c.261_262dup (p.Thr88fs)not provided [RCV003855675]uncertain significance7130381740130381741Humanname
151710646CV1365608deletionNM_001868.4(CPA1):c.937_938del (p.Met313fs)not provided [RCV001907926]uncertain significance7130385295130385296Humanname
155747782CV1849780indelNM_001868.4(CPA1):c.2_8delinsGCA (p.Met1fs)Hereditary pancreatitis [RCV002417158]likely benign7130380522130380528Humanname
156194251CV2066516deletionNM_001868.4(CPA1):c.1201_1203del (p.Lys401del)not provided [RCV002828713]uncertain significance7130387952130387954Humanname
25324380CV808958indelNM_001868.4(CPA1):c.599_600delinsG (p.Tyr200fs)Hereditary pancreatitis [RCV002346224]likely benign7130383697130383698Humanname
156372360CV2059083indelNM_001868.4(CPA1):c.409_410delinsTT (p.Ala137Leu)not provided [RCV002814399]uncertain significance7130382135130382136Humanname
597948985CV3772254indelNM_001868.4(CPA1):c.925_926delinsAA (p.Ser309Asn)not provided [RCV005120573]uncertain significance7130385283130385284Humanname
151857069CV1363740deletionNM_001868.4(CPA1):c.1243del (p.Thr414_Leu415insTer)not provided [RCV001904818]uncertain significance7130387992130387992Humanname
405244387CV3050585deletionNM_001868.4(CPA1):c.257_258del (p.Ser85_Tyr86insTer)not provided [RCV003719970]uncertain significance7130381738130381739Humanname
155692736CV1821658deletionNM_001868.4(CPA1):c.954_955del (p.Tyr318_Lys319delinsTer)Hereditary pancreatitis [RCV002374272]|not provided [RCV005097350]likely benign|uncertain significance7130385311130385312Human1name
156067214CV2166993duplicationNM_001868.4(CPA1):c.115_123dup (p.Glu41_Leu42insValLysGlu)not provided [RCV003019927]uncertain significance7130381144130381145Humanname
597630415CV3654377microsatelliteNM_001868.4(CPA1):c.298GAGCAG[3] (p.Gln103_Met104insGluGln)Hereditary pancreatitis [RCV004822652]uncertain significance7130381777130381778Humanname
155667765CV1812179duplicationNM_001868.4(CPA1):c.1228_1251dup (p.His417_Pro418insIleMetGluHisThrLeuAsnHis)Hereditary pancreatitis [RCV002366885]|not provided [RCV003103313]uncertain significance7130387977130387978Human1name
151788372CV1376927insertionNM_001868.4(CPA1):c.607_608insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCACCACGATGGGAGGCCGAGGCGCGCGGATCACGAGGTCAAGANNNNNNNNNNAAAAAAAAAAAAAAAAAAAAAAGACTACGGGCAGG (p.Asp203fs)not provided [RCV001897932]uncertain significance7130383690130383691Humanname