Palld Variant Search Result - Rat Genome Database

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
11632883	CV292725	single nucleotide variant	NM_001166108.2(PALLD):c.-8G>A	Pancreatic cancer, susceptibility to, 1 [RCV000293974]	benign\|likely benign	4	168511497	168511497	Human	1	name
126913053	CV1042670	single nucleotide variant	NM_001166108.2(PALLD):c.*33C>A	Pancreatic adenocarcinoma [RCV001359033]\|not specified [RCV005394976]	uncertain significance	4	168926213	168926213	Human	2	name
126917858	CV1042671	single nucleotide variant	NM_001166108.2(PALLD):c.*40G>C	Pancreatic adenocarcinoma [RCV001372320]	uncertain significance	4	168926220	168926220	Human	2	name
151735755	CV1435757	single nucleotide variant	NM_001166108.2(PALLD):c.*71A>G	Pancreatic adenocarcinoma [RCV001946551]	uncertain significance	4	168926251	168926251	Human	2	name
151741048	CV1466649	single nucleotide variant	NM_001166108.2(PALLD):c.*33C>T	Pancreatic adenocarcinoma [RCV001911931]\|not specified [RCV005397093]	uncertain significance	4	168926213	168926213	Human	2	name
151834244	CV1479344	single nucleotide variant	NM_001166108.2(PALLD):c.*69A>T	Pancreatic adenocarcinoma [RCV002051031]	uncertain significance	4	168926249	168926249	Human	2	name
151759581	CV1499826	single nucleotide variant	NM_001166108.2(PALLD):c.*41C>T	Pancreatic adenocarcinoma [RCV001895149]	uncertain significance	4	168926221	168926221	Human	2	name
152027197	CV1562546	single nucleotide variant	NM_001166108.2(PALLD):c.*67A>G	Pancreatic adenocarcinoma [RCV002104812]\|not specified [RCV005382388]	likely benign	4	168926247	168926247	Human	2	name
152066664	CV1601713	single nucleotide variant	NM_001166108.2(PALLD):c.*43T>C	Pancreatic adenocarcinoma [RCV002168753]	likely benign	4	168926223	168926223	Human	2	name
156079629	CV1883405	single nucleotide variant	NM_001166108.2(PALLD):c.*37G>T	Pancreatic adenocarcinoma [RCV003079824]	uncertain significance	4	168926217	168926217	Human	2	name
156418673	CV1922476	single nucleotide variant	NM_001166108.2(PALLD):c.*93G>A	Pancreatic adenocarcinoma [RCV002611874]\|not specified [RCV005399134]	uncertain significance	4	168926273	168926273	Human	2	name
156066992	CV2092906	single nucleotide variant	NM_001166108.2(PALLD):c.*96A>T	Pancreatic adenocarcinoma [RCV002886690]\|not specified [RCV004066190]	uncertain significance	4	168926276	168926276	Human	2	name
156148923	CV2128493	single nucleotide variant	NM_001166108.2(PALLD):c.*63A>G	Pancreatic adenocarcinoma [RCV002928831]	uncertain significance	4	168926243	168926243	Human	2	name
405142224	CV2909633	deletion	NM_001166108.2(PALLD):c.*57del	Pancreatic adenocarcinoma [RCV003584267]	uncertain significance	4	168926237	168926237	Human	2	name
405249564	CV2983295	single nucleotide variant	NM_001166108.2(PALLD):c.*73A>T	Pancreatic adenocarcinoma [RCV003747180]	uncertain significance	4	168926253	168926253	Human	2	name
405757282	CV3367717	single nucleotide variant	NM_001166108.2(PALLD):c.*93G>C	not specified [RCV004500037]	uncertain significance	4	168926273	168926273	Human		name
597657545	CV3574907	single nucleotide variant	NM_001166108.2(PALLD):c.*78G>A	not specified [RCV004827642]	uncertain significance	4	168926258	168926258	Human		name
597872179	CV3805273	single nucleotide variant	NM_001166108.2(PALLD):c.*60C>A	Pancreatic adenocarcinoma [RCV005148551]	uncertain significance	4	168926240	168926240	Human	2	name
12880648	CV393906	single nucleotide variant	NM_001166108.2(PALLD):c.*77C>T	Pancreatic adenocarcinoma [RCV000456395]	uncertain significance	4	168926257	168926257	Human	2	name
598258319	CV4005594	single nucleotide variant	NM_001166108.2(PALLD):c.*69A>G	not specified [RCV005386254]	uncertain significance	4	168926249	168926249	Human		name
598258364	CV4005605	single nucleotide variant	NM_001166108.2(PALLD):c.*74G>A	not specified [RCV005386263]	uncertain significance	4	168926254	168926254	Human		name
598258420	CV4005617	single nucleotide variant	NM_001166108.2(PALLD):c.*58C>T	not specified [RCV005386276]	likely benign	4	168926238	168926238	Human		name
598258481	CV4005631	single nucleotide variant	NM_001166108.2(PALLD):c.*61C>T	not specified [RCV005386289]	likely benign	4	168926241	168926241	Human		name
598258488	CV4005633	single nucleotide variant	NM_001166108.2(PALLD):c.*75T>G	not specified [RCV005386291]	uncertain significance	4	168926255	168926255	Human		name
598258547	CV4005645	single nucleotide variant	NM_001166108.2(PALLD):c.*68A>G	not specified [RCV005386302]	uncertain significance	4	168926248	168926248	Human		name
598258552	CV4005646	single nucleotide variant	NM_001166108.2(PALLD):c.*55G>A	not specified [RCV005386303]	likely benign	4	168926235	168926235	Human		name
126768057	CV1025750	single nucleotide variant	NM_001166108.2(PALLD):c.*135C>T	Pancreatic adenocarcinoma [RCV001343122]\|not specified [RCV005385048]	uncertain significance	4	168926315	168926315	Human	2	name
126774755	CV1025751	single nucleotide variant	NM_001166108.2(PALLD):c.*161C>T	Pancreatic adenocarcinoma [RCV001347595]	uncertain significance	4	168926341	168926341	Human	2	name
126771760	CV1025752	single nucleotide variant	NM_001166108.2(PALLD):c.*185G>T	Pancreatic adenocarcinoma [RCV001345231]	uncertain significance	4	168926365	168926365	Human	2	name
127336554	CV1135588	single nucleotide variant	NM_001166108.2(PALLD):c.*109G>A	Pancreatic adenocarcinoma [RCV001492232]\|not specified [RCV004837806]	likely benign	4	168926289	168926289	Human	2	name
152070049	CV1601005	single nucleotide variant	NM_001166108.2(PALLD):c.*172G>A	Pancreatic adenocarcinoma [RCV002091462]\|not specified [RCV005382386]	likely benign	4	168926352	168926352	Human	2	name
152146448	CV1606061	single nucleotide variant	NM_001166108.2(PALLD):c.*196G>A	Pancreatic adenocarcinoma [RCV002178793]\|not specified [RCV004827877]	likely benign	4	168926376	168926376	Human	2	name
152148678	CV1618933	single nucleotide variant	NM_001166108.2(PALLD):c.*100A>G	Pancreatic adenocarcinoma [RCV002121439]	likely benign	4	168926280	168926280	Human	2	name
152033823	CV1621376	single nucleotide variant	NM_001166108.2(PALLD):c.*124C>T	Pancreatic adenocarcinoma [RCV002205245]\|not specified [RCV004837841]	likely benign	4	168926304	168926304	Human	2	name
10041314	CV186024	single nucleotide variant	NM_001166108.2(PALLD):c.*153A>G	Pancreatic adenocarcinoma [RCV000168268]	uncertain significance	4	168926333	168926333	Human	2	name
10407743	CV212380	single nucleotide variant	NM_001166108.2(PALLD):c.33-4G>A	PALLD-related disorder [RCV003947654]\|Pancreatic adenocarcinoma [RCV000197648]\|Pancreatic cancer, susceptibility to, 1 [RCV000286156]\|not specified [RCV004827762]	benign\|likely benign	4	168926209	168926209	Human	3	name , alternate_id
10405869	CV212381	single nucleotide variant	NM_001166108.2(PALLD):c.*108C>T	Pancreatic adenocarcinoma [RCV000199118]\|Pancreatic cancer, susceptibility to, 1 [RCV005031747]\|not specified [RCV004837753]	uncertain significance	4	168926288	168926288	Human	3	name
405141608	CV2903655	single nucleotide variant	NM_001166108.2(PALLD):c.*112C>T	Pancreatic adenocarcinoma [RCV003584177]	likely benign	4	168926292	168926292	Human	2	name
11659485	CV292715	single nucleotide variant	NM_001166108.2(PALLD):c.-178G>A	Pancreatic cancer, susceptibility to, 1 [RCV000358552]	uncertain significance	4	168497099	168497099	Human	1	name
11633246	CV292720	single nucleotide variant	NM_001166108.2(PALLD):c.-161A>T	Pancreatic cancer, susceptibility to, 1 [RCV000323708]\|not provided [RCV001712088]	benign	4	168497116	168497116	Human	1	name
11646215	CV292721	single nucleotide variant	NM_001166108.2(PALLD):c.-139G>T	Carcinoma of pancreas [RCV000269757]	uncertain significance	4	168497138	168497138	Human	1	name
11632569	CV294083	single nucleotide variant	NM_001166108.2(PALLD):c.-172C>A	Pancreatic cancer, susceptibility to, 1 [RCV000268581]	uncertain significance	4	168497105	168497105	Human	1	name
11633266	CV294114	deletion	NM_001166108.2(PALLD):c.*325del	Carcinoma of pancreas [RCV000324866]\|not provided [RCV001653674]	benign	4	168926496	168926496	Human	1	name
11633594	CV294117	single nucleotide variant	NM_001166108.2(PALLD):c.*946C>A	Pancreatic cancer, susceptibility to, 1 [RCV000350510]\|not provided [RCV004716175]	benign\|likely benign	4	168927126	168927126	Human	1	name
11634103	CV294118	single nucleotide variant	NM_001166108.2(PALLD):c.*992A>G	Pancreatic cancer, susceptibility to, 1 [RCV000396199]	benign\|likely benign	4	168927172	168927172	Human	1	name
11633948	CV297545	single nucleotide variant	NM_001166108.2(PALLD):c.*317A>T	Pancreatic cancer, susceptibility to, 1 [RCV000381767]	likely benign	4	168926497	168926497	Human	1	name
11633557	CV297548	single nucleotide variant	NM_001166108.2(PALLD):c.*492A>G	Pancreatic cancer, susceptibility to, 1 [RCV000347025]	benign\|likely benign	4	168926672	168926672	Human	1	name
11662333	CV297568	duplication	NM_001166108.2(PALLD):c.*829dup	Carcinoma of pancreas [RCV000385204]	uncertain significance	4	168927001	168927002	Human	1	name
11650464	CV297571	single nucleotide variant	NM_001166108.2(PALLD):c.*908A>G	Pancreatic cancer, susceptibility to, 1 [RCV000293190]	uncertain significance	4	168927088	168927088	Human	1	name
11632985	CV297623	single nucleotide variant	NM_001166108.2(PALLD):c.-179G>C	Pancreatic cancer, susceptibility to, 1 [RCV000303785]	benign\|likely benign	4	168497098	168497098	Human	1	name
11633958	CV297624	single nucleotide variant	NM_001166108.2(PALLD):c.-143A>G	Pancreatic cancer, susceptibility to, 1 [RCV000382717]	likely benign\|uncertain significance	4	168497134	168497134	Human	1	name
405246687	CV3007265	single nucleotide variant	NM_001166108.2(PALLD):c.*136G>T	Pancreatic adenocarcinoma [RCV003746078]	likely benign	4	168926316	168926316	Human	2	name
405220408	CV3157760	single nucleotide variant	NM_001166108.2(PALLD):c.*136G>C	Pancreatic adenocarcinoma [RCV003863452]	likely benign	4	168926316	168926316	Human	2	name
405160302	CV3159938	single nucleotide variant	NM_001166108.2(PALLD):c.*182T>A	Pancreatic adenocarcinoma [RCV003857009]\|not specified [RCV005387281]	uncertain significance	4	168926362	168926362	Human	2	name
597715671	CV3574905	single nucleotide variant	NM_001166108.2(PALLD):c.*151C>T	not specified [RCV004841356]	likely benign	4	168926331	168926331	Human		name
597893303	CV3857064	single nucleotide variant	NM_001166108.2(PALLD):c.*168C>A	Pancreatic adenocarcinoma [RCV005200927]	uncertain significance	4	168926348	168926348	Human	2	name
12883659	CV394323	single nucleotide variant	NM_001166108.2(PALLD):c.*163C>T	Pancreatic adenocarcinoma [RCV001445639]	likely benign	4	168926343	168926343	Human	2	name
598258434	CV4005621	single nucleotide variant	NM_001166108.2(PALLD):c.*175T>A	not specified [RCV005386279]	uncertain significance	4	168926355	168926355	Human		name
598258571	CV4005651	single nucleotide variant	NM_001166108.2(PALLD):c.*110G>A	not specified [RCV005386307]	uncertain significance	4	168926290	168926290	Human		name
598258726	CV4005685	single nucleotide variant	NM_001166108.2(PALLD):c.*197G>A	not specified [RCV005386336]	uncertain significance	4	168926377	168926377	Human		name
13493501	CV453045	single nucleotide variant	NM_001166108.2(PALLD):c.*187A>G	Pancreatic adenocarcinoma [RCV000558235]	likely benign	4	168926367	168926367	Human	2	name
13625505	CV520074	single nucleotide variant	NM_001166108.2(PALLD):c.*136G>A	Pancreatic adenocarcinoma [RCV000653485]	likely benign	4	168926316	168926316	Human	2	name
13806856	CV559633	single nucleotide variant	NM_001166108.2(PALLD):c.*155C>G	Pancreatic adenocarcinoma [RCV000686406]\|not specified [RCV004837774]	uncertain significance	4	168926335	168926335	Human	2	name
13821267	CV561970	single nucleotide variant	NM_001166108.2(PALLD):c.*127C>G	Pancreatic adenocarcinoma [RCV000695641]\|not specified [RCV005392301]	uncertain significance	4	168926307	168926307	Human	2	name
26923577	CV828955	single nucleotide variant	NM_001166108.2(PALLD):c.*194G>C	Pancreatic adenocarcinoma [RCV001064251]\|not specified [RCV005384930]	uncertain significance	4	168926374	168926374	Human	2	name
26886691	CV828956	single nucleotide variant	NM_001166108.2(PALLD):c.*203T>A	Pancreatic adenocarcinoma [RCV001066220]	uncertain significance	4	168926383	168926383	Human	2	name
28877241	CV890388	single nucleotide variant	NM_001166108.2(PALLD):c.-162C>T	Pancreatic cancer, susceptibility to, 1 [RCV001148281]	benign	4	168497115	168497115	Human	1	name
28877245	CV890389	single nucleotide variant	NM_001166108.2(PALLD):c.-135A>G	Pancreatic cancer, susceptibility to, 1 [RCV001148282]	uncertain significance	4	168497142	168497142	Human	1	name
28877251	CV890390	single nucleotide variant	NM_001166108.2(PALLD):c.-115C>G	Pancreatic cancer, susceptibility to, 1 [RCV001148283]	uncertain significance	4	168497162	168497162	Human	1	name
28882779	CV890413	single nucleotide variant	NM_001166108.2(PALLD):c.*386T>C	Pancreatic cancer, susceptibility to, 1 [RCV001150070]	uncertain significance	4	168926566	168926566	Human	1	name
28882784	CV890414	single nucleotide variant	NM_001166108.2(PALLD):c.*400T>C	Pancreatic cancer, susceptibility to, 1 [RCV001150071]	uncertain significance	4	168926580	168926580	Human	1	name
28882787	CV890415	single nucleotide variant	NM_001166108.2(PALLD):c.*439T>C	Pancreatic cancer, susceptibility to, 1 [RCV001150072]	uncertain significance	4	168926619	168926619	Human	1	name
28882793	CV890416	single nucleotide variant	NM_001166108.2(PALLD):c.*461G>A	Pancreatic cancer, susceptibility to, 1 [RCV001150073]	uncertain significance	4	168926641	168926641	Human	1	name
28903248	CV890417	single nucleotide variant	NM_001166108.2(PALLD):c.*994A>G	Pancreatic cancer, susceptibility to, 1 [RCV001143947]	benign	4	168927174	168927174	Human	1	name
38483399	CV932250	single nucleotide variant	NM_001166108.2(PALLD):c.*110G>C	Pancreatic adenocarcinoma [RCV001207631]\|not specified [RCV004837788]	uncertain significance	4	168926290	168926290	Human	2	name
9834686	CV180159	single nucleotide variant	NM_001166108.2(PALLD):c.-83+8A>G	Pancreatic cancer, susceptibility to, 1 [RCV000329451]\|not specified [RCV000160880]	benign\|likely benign	4	168497202	168497202	Human	1	name
156019449	CV1914918	single nucleotide variant	NM_001166108.2(PALLD):c.*33-8C>T	Pancreatic adenocarcinoma [RCV002636635]	likely benign	4	168926205	168926205	Human	2	name
11634031	CV292770	deletion	NM_001166108.2(PALLD):c.*2156del	Carcinoma of pancreas [RCV000389268]	benign	4	168928327	168928327	Human	1	name
11633459	CV292773	single nucleotide variant	NM_001166108.2(PALLD):c.*2184G>A	Pancreatic cancer, susceptibility to, 1 [RCV000339397]	uncertain significance	4	168928364	168928364	Human	1	name
11633976	CV294084	single nucleotide variant	NM_001166108.2(PALLD):c.-83+9G>A	Pancreatic cancer, susceptibility to, 1 [RCV000384008]	likely benign\|uncertain significance	4	168497203	168497203	Human	1	name
11633661	CV294119	single nucleotide variant	NM_001166108.2(PALLD):c.*1594T>C	Pancreatic cancer, susceptibility to, 1 [RCV000357157]	benign\|likely benign	4	168927774	168927774	Human	1	name
11659641	CV294121	single nucleotide variant	NM_001166108.2(PALLD):c.*1787T>C	Pancreatic cancer, susceptibility to, 1 [RCV000360071]	uncertain significance	4	168927967	168927967	Human	1	name
11633952	CV294124	single nucleotide variant	NM_001166108.2(PALLD):c.*1829T>C	Pancreatic cancer, susceptibility to, 1 [RCV000382024]	benign\|likely benign	4	168928009	168928009	Human	1	name
11632624	CV294126	single nucleotide variant	NM_001166108.2(PALLD):c.*1906G>A	Pancreatic cancer, susceptibility to, 1 [RCV000271034]\|not provided [RCV001675853]	benign	4	168928086	168928086	Human	1	name
11632959	CV297574	single nucleotide variant	NM_001166108.2(PALLD):c.*1164T>G	Pancreatic cancer, susceptibility to, 1 [RCV000299921]	benign\|likely benign	4	168927344	168927344	Human	1	name
11633267	CV297575	single nucleotide variant	NM_001166108.2(PALLD):c.*1808C>T	Pancreatic cancer, susceptibility to, 1 [RCV000325058]	likely benign\|uncertain significance	4	168927988	168927988	Human	1	name
11634020	CV297578	single nucleotide variant	NM_001166108.2(PALLD):c.*2058C>G	Pancreatic cancer, susceptibility to, 1 [RCV000385400]\|not provided [RCV001618621]	benign	4	168928238	168928238	Human	1	name
11650559	CV297579	single nucleotide variant	NM_001166108.2(PALLD):c.*2070G>C	Pancreatic cancer, susceptibility to, 1 [RCV000293432]	uncertain significance	4	168928250	168928250	Human	1	name
11658661	CV297580	duplication	NM_001166108.2(PALLD):c.*2156dup	Carcinoma of pancreas [RCV000350998]\|not provided [RCV004695783]	uncertain significance	4	168928326	168928327	Human	1	name
11634104	CV297586	single nucleotide variant	NM_001166108.2(PALLD):c.*2214C>T	Pancreatic cancer, susceptibility to, 1 [RCV000396315]	benign\|likely benign	4	168928394	168928394	Human	1	name
11633400	CV297657	single nucleotide variant	NM_001166108.2(PALLD):c.*1131T>G	Pancreatic cancer, susceptibility to, 1 [RCV000334998]	uncertain significance	4	168927311	168927311	Human	1	name
11634174	CV297658	single nucleotide variant	NM_001166108.2(PALLD):c.*1132T>C	Pancreatic cancer, susceptibility to, 1 [RCV000401967]	benign\|likely benign	4	168927312	168927312	Human	1	name
11645287	CV297659	single nucleotide variant	NM_001166108.2(PALLD):c.*1757T>G	Pancreatic cancer, susceptibility to, 1 [RCV000264861]	uncertain significance	4	168927937	168927937	Human	1	name
11632582	CV297662	single nucleotide variant	NM_001166108.2(PALLD):c.*1792T>A	Pancreatic cancer, susceptibility to, 1 [RCV000267723]	likely benign\|uncertain significance	4	168927972	168927972	Human	1	name
11655777	CV297665	single nucleotide variant	NM_001166108.2(PALLD):c.*2022A>G	Pancreatic cancer, susceptibility to, 1 [RCV000328416]	uncertain significance	4	168928202	168928202	Human	1	name
11663457	CV297668	single nucleotide variant	NM_001166108.2(PALLD):c.*2166A>G	Pancreatic cancer, susceptibility to, 1 [RCV000396316]	uncertain significance	4	168928346	168928346	Human	1	name
11651762	CV297683	single nucleotide variant	NM_001166108.2(PALLD):c.*2168C>A	Pancreatic cancer, susceptibility to, 1 [RCV000300945]	uncertain significance	4	168928348	168928348	Human	1	name
28871416	CV890418	single nucleotide variant	NM_001166108.2(PALLD):c.*1655A>T	Pancreatic cancer, susceptibility to, 1 [RCV001145839]	uncertain significance	4	168927835	168927835	Human	1	name
28871418	CV890419	single nucleotide variant	NM_001166108.2(PALLD):c.*1713T>C	Pancreatic cancer, susceptibility to, 1 [RCV001145840]	uncertain significance	4	168927893	168927893	Human	1	name
28878201	CV890420	single nucleotide variant	NM_001166108.2(PALLD):c.*2027T>C	Pancreatic cancer, susceptibility to, 1 [RCV001148606]	uncertain significance	4	168928207	168928207	Human	1	name
28878208	CV890421	single nucleotide variant	NM_001166108.2(PALLD):c.*2141A>G	Pancreatic cancer, susceptibility to, 1 [RCV001148607]	uncertain significance	4	168928321	168928321	Human	1	name
28883194	CV890422	single nucleotide variant	NM_001166108.2(PALLD):c.*2171T>C	Pancreatic cancer, susceptibility to, 1 [RCV001150188]	uncertain significance	4	168928351	168928351	Human	1	name
28877584	CV891769	single nucleotide variant	NM_001166108.2(PALLD):c.908+3A>G	Pancreatic cancer, susceptibility to, 1 [RCV001148391]	uncertain significance	4	168512415	168512415	Human	1	name
126766997	CV1025749	deletion	NM_001166108.2(PALLD):c.3059-6del	PALLD-related disorder [RCV003946004]\|Pancreatic adenocarcinoma [RCV001342644]	benign\|likely benign\|uncertain significance	4	168924246	168924246	Human	3	name , alternate_id
127303451	CV1114687	single nucleotide variant	NM_001166108.2(PALLD):c.2851-6A>G	Pancreatic adenocarcinoma [RCV001454755]	likely benign	4	168921528	168921528	Human	2	name
127317784	CV1135585	single nucleotide variant	NM_001166108.2(PALLD):c.1965-8T>C	Pancreatic adenocarcinoma [RCV001483262]	likely benign	4	168890914	168890914	Human	2	name
150339536	CV1167314	single nucleotide variant	NM_001166108.2(PALLD):c.1155-9A>G	not provided [RCV001534305]	benign	4	168682989	168682989	Human		name
150473700	CV1217674	single nucleotide variant	NM_001166108.2(PALLD):c.-83+87T>C	not provided [RCV001615685]	benign	4	168497281	168497281	Human		name
150472188	CV1236298	deletion	NM_001166108.2(PALLD):c.-83+67del	not provided [RCV001651383]	benign	4	168497249	168497249	Human		name
151755388	CV1387791	single nucleotide variant	NM_001166108.2(PALLD):c.2101-3T>C	Pancreatic adenocarcinoma [RCV001969617]	uncertain significance	4	168894576	168894576	Human	2	name
8689795	CV139722	single nucleotide variant	NM_001166108.2(PALLD):c.2101-9G>A	PALLD-related disorder [RCV003905178]\|Pancreatic adenocarcinoma [RCV000123176]	likely benign\|uncertain significance	4	168894570	168894570	Human	3	name , alternate_id
8689796	CV139723	single nucleotide variant	NM_001166108.2(PALLD):c.2199+8G>A	Pancreatic adenocarcinoma [RCV001083018]\|Pancreatic cancer, susceptibility to, 1 [RCV000310521]\|not provided [RCV003389731]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	4	168894685	168894685	Human	3	name
152170769	CV1536543	single nucleotide variant	NM_001166108.2(PALLD):c.2622+8A>G	Pancreatic adenocarcinoma [RCV002183271]	likely benign	4	168903914	168903914	Human	2	name
152143576	CV1538425	single nucleotide variant	NM_001166108.2(PALLD):c.*33-14C>G	Pancreatic adenocarcinoma [RCV002219697]	likely benign	4	168926199	168926199	Human	2	name
152169720	CV1538682	single nucleotide variant	NM_001166108.2(PALLD):c.2623-8T>C	Pancreatic adenocarcinoma [RCV002182899]	likely benign	4	168913919	168913919	Human	2	name
152025925	CV1586626	single nucleotide variant	NM_001166108.2(PALLD):c.2473-4A>G	Pancreatic adenocarcinoma [RCV002184983]	likely benign	4	168903753	168903753	Human	2	name
152152746	CV1631211	single nucleotide variant	NM_001166108.2(PALLD):c.2850+8T>G	Pancreatic adenocarcinoma [RCV002139769]	likely benign	4	168916035	168916035	Human	2	name
10405838	CV212369	duplication	NM_001166108.2(PALLD):c.1965-9dup	PALLD-related disorder [RCV003895266]\|Pancreatic adenocarcinoma [RCV001465295]	likely benign	4	168890912	168890913	Human	3	name , alternate_id
155911788	CV2141723	single nucleotide variant	NM_001166108.2(PALLD):c.2718-3A>C	Pancreatic adenocarcinoma [RCV002968109]	uncertain significance	4	168915892	168915892	Human	2	name
156354348	CV2154095	single nucleotide variant	NM_001166108.2(PALLD):c.2100+5T>C	Pancreatic adenocarcinoma [RCV003031115]	uncertain significance	4	168891062	168891062	Human	2	name
10767555	CV221450	deletion	NM_001166110.1(PALLD):c.738+4delC	Pancreatic adenocarcinoma [RCV000204907]	benign	4	168894681	168894681	Human	1	name
10768559	CV221458	single nucleotide variant	NM_001166108.2(PALLD):c.3358+9C>G	Pancreatic adenocarcinoma [RCV001500484]	likely benign	4	168925087	168925087	Human	2	name
11351451	CV239349	deletion	NM_001166108.2(PALLD):c.2199+5del	Pancreatic adenocarcinoma [RCV000227731]\|not specified [RCV004837760]	benign\|likely benign	4	168894681	168894681	Human	2	name
11633883	CV292763	single nucleotide variant	NM_001166108.2(PALLD):c.3359-4G>A	Pancreatic cancer, susceptibility to, 1 [RCV000376121]\|not provided [RCV001675852]\|not specified [RCV004021958]	benign\|likely benign	4	168925229	168925229	Human	1	name
405248281	CV2937510	single nucleotide variant	NM_001166108.2(PALLD):c.2622+3A>G	Pancreatic adenocarcinoma [RCV003746727]	uncertain significance	4	168903909	168903909	Human	2	name
405248466	CV2949292	single nucleotide variant	NM_001166108.2(PALLD):c.2850+4A>C	Pancreatic adenocarcinoma [RCV003746783]	uncertain significance	4	168916031	168916031	Human	2	name
405247501	CV3046723	single nucleotide variant	NM_001166108.2(PALLD):c.2472+8G>A	Pancreatic adenocarcinoma [RCV003746394]	likely benign	4	168898722	168898722	Human	2	name
405247650	CV3055070	single nucleotide variant	NM_001166108.2(PALLD):c.3059-6T>C	Pancreatic adenocarcinoma [RCV003746453]	likely benign	4	168924249	168924249	Human	2	name
405261127	CV3216178	single nucleotide variant	NM_001166108.2(PALLD):c.1622-7T>G	PALLD-related disorder [RCV003944342]	likely benign	4	168711574	168711574	Human		name , trait , alternate_id
597654872	CV3721380	single nucleotide variant	NM_001166108.2(PALLD):c.1502-9C>T	Pancreatic cancer, susceptibility to, 1 [RCV005027303]	uncertain significance	4	168709019	168709019	Human	1	name
597957480	CV3755087	single nucleotide variant	NM_001166108.2(PALLD):c.2101-6G>A	Pancreatic adenocarcinoma [RCV005080757]	likely benign	4	168894573	168894573	Human	2	name
597862688	CV3813942	single nucleotide variant	NM_001166108.2(PALLD):c.*33-16C>T	Pancreatic adenocarcinoma [RCV005147011]	likely benign	4	168926197	168926197	Human	2	name
597931797	CV3863278	single nucleotide variant	NM_001166108.2(PALLD):c.2472+5G>A	Pancreatic adenocarcinoma [RCV005206804]	uncertain significance	4	168898719	168898719	Human	2	name
12887994	CV394314	single nucleotide variant	NM_001166108.2(PALLD):c.2199+4C>T	Pancreatic adenocarcinoma [RCV000470091]	uncertain significance	4	168894681	168894681	Human	2	name
15151291	CV759281	single nucleotide variant	NM_001166108.2(PALLD):c.2622+9G>A	Pancreatic adenocarcinoma [RCV001398853]	likely benign	4	168903915	168903915	Human	2	name
28882466	CV891770	single nucleotide variant	NM_001166108.2(PALLD):c.1260+8T>C	Pancreatic cancer, susceptibility to, 1 [RCV001149954]	uncertain significance	4	168683111	168683111	Human	1	name
126766724	CV990020	single nucleotide variant	NM_001166108.2(PALLD):c.1965-7C>G	Pancreatic adenocarcinoma [RCV001302005]	likely benign\|uncertain significance	4	168890915	168890915	Human	2	name
127281136	CV1093138	single nucleotide variant	NM_001166108.2(PALLD):c.2851-10T>C	Pancreatic adenocarcinoma [RCV001446912]	likely benign	4	168921524	168921524	Human	2	name
127307421	CV1154708	single nucleotide variant	NM_001166108.2(PALLD):c.1965-10T>A	PALLD-related disorder [RCV003900769]\|Pancreatic adenocarcinoma [RCV001517098]	benign\|likely benign	4	168890912	168890912	Human	3	name , alternate_id
150339296	CV1167313	duplication	NM_001166108.2(PALLD):c.-82-309dup	not provided [RCV001534127]	benign	4	168511112	168511113	Human		name
150334357	CV1171225	single nucleotide variant	NM_001166108.2(PALLD):c.909-127T>C	not provided [RCV001540001]	benign	4	168668063	168668063	Human		name
150437687	CV1220761	single nucleotide variant	NM_001166108.2(PALLD):c.2251-55G>A	not provided [RCV001609746]	benign	4	168898438	168898438	Human		name
150504510	CV1240768	single nucleotide variant	NM_001166108.2(PALLD):c.1335+68C>T	not provided [RCV001657611]	benign	4	168685627	168685627	Human		name
150506708	CV1242280	single nucleotide variant	NM_001166108.2(PALLD):c.-82-231T>C	not provided [RCV001658635]	benign	4	168511192	168511192	Human		name
150439105	CV1247675	single nucleotide variant	NM_001166108.2(PALLD):c.2100+41C>T	not provided [RCV001666042]	benign	4	168891098	168891098	Human		name
150470564	CV1248018	single nucleotide variant	NM_001166108.2(PALLD):c.1501+85C>T	not provided [RCV001671054]	benign	4	168691377	168691377	Human		name
150461264	CV1253219	single nucleotide variant	NM_001166108.2(PALLD):c.3058+28C>G	not provided [RCV001669548]	benign	4	168921769	168921769	Human		name
150448310	CV1253532	single nucleotide variant	NM_001166108.2(PALLD):c.2718-85T>C	not provided [RCV001667460]	benign	4	168915810	168915810	Human		name
150453626	CV1260542	single nucleotide variant	NM_001166108.2(PALLD):c.3358+26T>C	not provided [RCV001681034]	benign	4	168925104	168925104	Human		name
150484731	CV1263240	single nucleotide variant	NM_001166108.2(PALLD):c.2623-30C>G	not provided [RCV001686640]	benign	4	168913897	168913897	Human		name
150445047	CV1269372	single nucleotide variant	NM_001166108.2(PALLD):c.3058+84T>C	not provided [RCV001691059]	benign	4	168921825	168921825	Human		name
150464580	CV1276426	single nucleotide variant	NM_001166108.2(PALLD):c.1155-47G>A	not provided [RCV001710371]	benign	4	168682951	168682951	Human		name
150479443	CV1282278	duplication	NM_001166108.2(PALLD):c.1155-57dup	not provided [RCV001714467]	benign	4	168682929	168682930	Human		name
150488429	CV1284018	single nucleotide variant	NM_001166108.2(PALLD):c.1335+58C>T	not provided [RCV001716101]	benign	4	168685617	168685617	Human		name
150508523	CV1284303	deletion	NM_001166108.2(PALLD):c.*33-237del	not provided [RCV001720411]	benign	4	168925965	168925965	Human		name
150512180	CV1284883	single nucleotide variant	NM_001166108.2(PALLD):c.-82-280C>T	not provided [RCV001721752]	benign	4	168511143	168511143	Human		name
151744885	CV1460730	single nucleotide variant	NM_001166108.2(PALLD):c.3224+14A>G	Pancreatic adenocarcinoma [RCV001871401]	likely benign\|uncertain significance	4	168924434	168924434	Human	2	name
151829141	CV1489254	single nucleotide variant	NM_001166108.2(PALLD):c.3358+17C>T	Pancreatic adenocarcinoma [RCV001934884]	likely benign	4	168925095	168925095	Human	2	name
152165182	CV1543712	single nucleotide variant	NM_001166108.2(PALLD):c.2100+12T>G	Pancreatic adenocarcinoma [RCV002123959]	likely benign	4	168891069	168891069	Human	2	name
152167281	CV1600555	single nucleotide variant	NM_001166108.2(PALLD):c.2472+13A>G	Pancreatic adenocarcinoma [RCV002160830]	benign	4	168898727	168898727	Human	2	name
152037451	CV1605626	single nucleotide variant	NM_001166108.2(PALLD):c.2850+15T>C	Pancreatic adenocarcinoma [RCV002087455]	likely benign	4	168916042	168916042	Human	2	name
156058264	CV1867880	single nucleotide variant	NM_001166108.2(PALLD):c.2199+18A>G	Pancreatic adenocarcinoma [RCV003037165]	likely benign	4	168894695	168894695	Human	2	name
156215759	CV1869308	single nucleotide variant	NM_001166108.2(PALLD):c.3058+15G>A	Pancreatic adenocarcinoma [RCV003058718]	likely benign	4	168921756	168921756	Human	2	name
155910267	CV2017613	single nucleotide variant	NM_001166108.2(PALLD):c.2199+16G>A	Pancreatic adenocarcinoma [RCV002681664]	likely benign	4	168894693	168894693	Human	2	name
156021627	CV2019394	duplication	NM_001166108.2(PALLD):c.71_73dup	Pancreatic adenocarcinoma [RCV002691029]	uncertain significance	4	168926246	168926247	Human	2	name
155975133	CV2079459	single nucleotide variant	NM_001166108.2(PALLD):c.3059-20T>C	Pancreatic adenocarcinoma [RCV002881668]	likely benign	4	168924235	168924235	Human	2	name
156104087	CV2113517	single nucleotide variant	NM_001166108.2(PALLD):c.1965-17G>C	Pancreatic adenocarcinoma [RCV002952847]	likely benign	4	168890905	168890905	Human	2	name
156301539	CV2129521	single nucleotide variant	NM_001166108.2(PALLD):c.2251-12T>C	Pancreatic adenocarcinoma [RCV002962165]	likely benign	4	168898481	168898481	Human	2	name
155938146	CV2146412	single nucleotide variant	NM_001166108.2(PALLD):c.2101-20T>G	Pancreatic adenocarcinoma [RCV003014084]	likely benign	4	168894559	168894559	Human	2	name
405141341	CV2900173	single nucleotide variant	NM_001166108.2(PALLD):c.2473-10C>G	Pancreatic adenocarcinoma [RCV003584151]	likely benign	4	168903747	168903747	Human	2	name
405248598	CV2958712	single nucleotide variant	NM_001166108.2(PALLD):c.3224+18G>A	Pancreatic adenocarcinoma [RCV003746849]	likely benign	4	168924438	168924438	Human	2	name
11632822	CV297641	microsatellite	NM_001166108.2(PALLD):c.*333ATA[3]	Carcinoma of pancreas [RCV000289470]	likely benign	4	168926511	168926512	Human		name
405249617	CV2983628	single nucleotide variant	NM_001166108.2(PALLD):c.3225-18C>G	Pancreatic adenocarcinoma [RCV003747203]	likely benign	4	168924927	168924927	Human	2	name
405247482	CV3053309	single nucleotide variant	NM_001166108.2(PALLD):c.1965-19T>C	Pancreatic adenocarcinoma [RCV003746387]	likely benign	4	168890903	168890903	Human	2	name
405250553	CV3070666	duplication	NM_001166108.2(PALLD):c.2101-11dup	Pancreatic adenocarcinoma [RCV003747578]	likely benign	4	168894567	168894568	Human	2	name
405250676	CV3080632	single nucleotide variant	NM_001166108.2(PALLD):c.2473-18C>T	Pancreatic adenocarcinoma [RCV003747652]	likely benign	4	168903739	168903739	Human	2	name
405250735	CV3080727	single nucleotide variant	NM_001166108.2(PALLD):c.3059-13C>T	Pancreatic adenocarcinoma [RCV003747676]	likely benign	4	168924242	168924242	Human	2	name
597743120	CV3721379	single nucleotide variant	NM_001166108.2(PALLD):c.1155-16C>A	Pancreatic cancer, susceptibility to, 1 [RCV005039056]	uncertain significance	4	168682982	168682982	Human	1	name
597840183	CV3825273	single nucleotide variant	NM_001166108.2(PALLD):c.2473-14G>C	Pancreatic adenocarcinoma [RCV005171956]	likely benign	4	168903743	168903743	Human	2	name
597970652	CV3832569	single nucleotide variant	NM_001166108.2(PALLD):c.3224+16G>A	Pancreatic adenocarcinoma [RCV005166648]	likely benign	4	168924436	168924436	Human	2	name
597924316	CV3863080	single nucleotide variant	NM_001166108.2(PALLD):c.2622+17G>T	Pancreatic adenocarcinoma [RCV005205568]	likely benign	4	168903923	168903923	Human	2	name
15160883	CV689751	single nucleotide variant	NM_001166108.2(PALLD):c.2101-10C>T	Pancreatic adenocarcinoma [RCV001478088]	likely benign	4	168894569	168894569	Human	2	name
150451444	CV1220863	single nucleotide variant	NM_001166108.2(PALLD):c.1088-111C>T	not provided [RCV001611957]	benign	4	168681221	168681221	Human		name
150482590	CV1223449	single nucleotide variant	NM_001166108.2(PALLD):c.3224+149C>T	not provided [RCV001617162]	benign	4	168924569	168924569	Human		name
150507462	CV1226598	single nucleotide variant	NM_001166108.2(PALLD):c.2199+277A>T	not provided [RCV001635966]	benign	4	168894954	168894954	Human		name
150513570	CV1229052	single nucleotide variant	NM_001166108.2(PALLD):c.1087+159C>T	not provided [RCV001637894]	benign	4	168668527	168668527	Human		name
150509189	CV1229827	single nucleotide variant	NM_001166108.2(PALLD):c.1965-316T>C	not provided [RCV001636407]	benign	4	168890606	168890606	Human		name
150430497	CV1243334	single nucleotide variant	NM_001166108.2(PALLD):c.1335+163G>A	not provided [RCV001662951]	benign	4	168685722	168685722	Human		name
150440791	CV1246631	single nucleotide variant	NM_001166108.2(PALLD):c.3058+150A>T	not provided [RCV001666284]	benign	4	168921891	168921891	Human		name
150438235	CV1247143	single nucleotide variant	NM_001166108.2(PALLD):c.2101-258T>G	not provided [RCV001665912]	benign	4	168894321	168894321	Human		name
150465085	CV1252823	single nucleotide variant	NM_001166108.2(PALLD):c.2100+105T>C	not provided [RCV001670147]	benign	4	168891162	168891162	Human		name
150507742	CV1257214	single nucleotide variant	NM_001166108.2(PALLD):c.1261-264G>A	not provided [RCV001678513]	benign	4	168685221	168685221	Human		name
150452426	CV1260394	single nucleotide variant	NM_001166108.2(PALLD):c.2717+152T>G	not provided [RCV001680884]	benign	4	168914173	168914173	Human		name
150458636	CV1265163	single nucleotide variant	NM_001166108.2(PALLD):c.1477+167C>T	not provided [RCV001681796]	benign	4	168690911	168690911	Human		name
150459892	CV1268408	single nucleotide variant	NM_001166108.2(PALLD):c.1335+143A>G	not provided [RCV001693405]	benign	4	168685702	168685702	Human		name
150477211	CV1272013	deletion	NM_001166108.2(PALLD):c.2851-108del	not provided [RCV001696298]	benign	4	168921407	168921407	Human		name
150498665	CV1282194	duplication	NM_001166108.2(PALLD):c.2851-108dup	not provided [RCV001718058]	benign	4	168921406	168921407	Human		name
9834685	CV180162	microsatellite	NM_001166108.2(PALLD):c.3359-24CT[5]	Hereditary cancer-predisposing syndrome [RCV000160879]	benign	4	168925209	168925210	Human		name
11656699	CV292771	microsatellite	NM_001166108.2(PALLD):c.*2162ATCA[2]	Carcinoma of pancreas [RCV000335736]\|not provided [RCV001672639]	benign	4	168928342	168928345	Human		name
126741484	CV1005166	deletion	NM_001166108.2(PALLD):c.1965-13001del	Pancreatic adenocarcinoma [RCV001325352]	uncertain significance	4	168877917	168877917	Human	2	name
126770151	CV1005167	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12735C>A	Pancreatic adenocarcinoma [RCV001322394]	uncertain significance	4	168878187	168878187	Human	2	name
126769787	CV1005168	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12723C>T	Pancreatic adenocarcinoma [RCV001322179]\|not specified [RCV005385035]	uncertain significance	4	168878199	168878199	Human	2	name
126748170	CV1005169	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12579C>T	Pancreatic adenocarcinoma [RCV001326289]\|not specified [RCV004035198]	uncertain significance	4	168878343	168878343	Human	2	name
126750122	CV1005170	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12532C>A	Pancreatic adenocarcinoma [RCV001315855]\|not specified [RCV005385033]	uncertain significance	4	168878390	168878390	Human	2	name
126768651	CV1025736	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12928G>A	Pancreatic adenocarcinoma [RCV001343481]\|not specified [RCV005385049]	uncertain significance	4	168877994	168877994	Human	2	name
126770910	CV1025737	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12859C>T	Pancreatic adenocarcinoma [RCV001344738]	uncertain significance	4	168878063	168878063	Human	2	name
126733906	CV1025738	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12772T>C	Pancreatic adenocarcinoma [RCV001349856]\|not specified [RCV004036598]	likely benign\|uncertain significance	4	168878150	168878150	Human	2	name
126767301	CV1025740	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12696C>T	Pancreatic adenocarcinoma [RCV001342769]\|not specified [RCV004837796]	uncertain significance	4	168878226	168878226	Human	2	name
126730999	CV1025741	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12543A>G	Pancreatic adenocarcinoma [RCV001349354]	uncertain significance	4	168878379	168878379	Human	2	name
126913143	CV1042658	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12923G>A	Pancreatic adenocarcinoma [RCV001369993]\|not specified [RCV005385077]	likely benign\|uncertain significance	4	168877999	168877999	Human	2	name
126918864	CV1042659	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12882T>A	Pancreatic adenocarcinoma [RCV001372904]\|not specified [RCV004651631]	uncertain significance	4	168878040	168878040	Human	2	name
126917848	CV1042660	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12841G>A	Pancreatic adenocarcinoma [RCV001372314]\|not specified [RCV005385082]	uncertain significance	4	168878081	168878081	Human	2	name
127243725	CV1071529	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12971C>T	Pancreatic adenocarcinoma [RCV001398449]\|not specified [RCV005385084]	likely benign	4	168877951	168877951	Human	2	name
127281975	CV1071530	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12890G>A	Pancreatic adenocarcinoma [RCV001410814]\|not specified [RCV004837803]	likely benign	4	168878032	168878032	Human	2	name
127233227	CV1071531	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12836C>G	Pancreatic adenocarcinoma [RCV001396041]	likely benign	4	168878086	168878086	Human	2	name
127255562	CV1071532	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12773G>C	Pancreatic adenocarcinoma [RCV001418786]\|not specified [RCV005385089]	likely benign	4	168878149	168878149	Human	2	name
127257476	CV1071533	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12703C>T	Pancreatic adenocarcinoma [RCV001419306]	likely benign	4	168878219	168878219	Human	2	name
127265303	CV1071534	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12665G>A	Pancreatic adenocarcinoma [RCV001403538]	likely benign	4	168878257	168878257	Human	2	name
127258187	CV1071535	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12575G>C	Pancreatic adenocarcinoma [RCV001419505]\|not specified [RCV005385090]	likely benign	4	168878347	168878347	Human	2	name
127232412	CV1071536	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12574C>T	Pancreatic adenocarcinoma [RCV001413428]\|not specified [RCV004038105]	likely benign\|uncertain significance	4	168878348	168878348	Human	2	name
127234009	CV1071537	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12563C>T	Pancreatic adenocarcinoma [RCV001414116]\|not specified [RCV004837804]	likely benign	4	168878359	168878359	Human	2	name
127262606	CV1093132	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12974C>T	Pancreatic adenocarcinoma [RCV001439026]\|not specified [RCV004827819]	likely benign	4	168877948	168877948	Human	2	name
127244368	CV1093133	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12878G>A	Pancreatic adenocarcinoma [RCV001435008]\|not specified [RCV005385096]	likely benign	4	168878044	168878044	Human	2	name
127239628	CV1093134	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12812C>T	Pancreatic adenocarcinoma [RCV001434011]\|not specified [RCV005385094]	likely benign	4	168878110	168878110	Human	2	name
127291665	CV1114683	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12986C>T	Pancreatic adenocarcinoma [RCV001451559]\|not specified [RCV005385100]	likely benign	4	168877936	168877936	Human	2	name
127295046	CV1114684	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12536C>T	Pancreatic adenocarcinoma [RCV001452390]	likely benign	4	168878386	168878386	Human	2	name
127316900	CV1135581	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12962C>T	Pancreatic adenocarcinoma [RCV001503183]\|not specified [RCV004837808]	likely benign	4	168877960	168877960	Human	2	name
127326781	CV1135582	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12782C>A	Pancreatic adenocarcinoma [RCV001486140]	likely benign	4	168878140	168878140	Human	2	name
127302770	CV1135583	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12735C>G	Pancreatic adenocarcinoma [RCV001479029]\|not specified [RCV004827822]	likely benign\|uncertain significance	4	168878187	168878187	Human	2	name
127296407	CV1135584	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12602C>T	PALLD-related disorder [RCV004751996]\|Pancreatic adenocarcinoma [RCV001497459]\|not specified [RCV004837807]	likely benign	4	168878320	168878320	Human	3	name , alternate_id
127290979	CV1154706	single nucleotide variant	NM_001166108.2(PALLD):c.1964+44318A>G	Pancreatic adenocarcinoma [RCV001510107]\|not provided [RCV004716721]	benign	4	168756241	168756241	Human	2	name
150340454	CV1168011	duplication	NM_001166108.2(PALLD):c.1965-12229dup	not provided [RCV001535390]	benign	4	168878682	168878683	Human		name
150331226	CV1169035	single nucleotide variant	NM_001166108.2(PALLD):c.1965-58894A>C	not provided [RCV001536390]	benign	4	168832028	168832028	Human		name
150473792	CV1217690	duplication	NM_001166108.2(PALLD):c.1965-12240dup	not provided [RCV001615701]	benign	4	168878681	168878682	Human		name
150502956	CV1223347	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12447C>T	not provided [RCV001621282]	benign	4	168878475	168878475	Human		name
150498277	CV1224110	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13095C>A	not provided [RCV001620222]	benign	4	168877827	168877827	Human		name
150453638	CV1260544	single nucleotide variant	NM_001166108.2(PALLD):c.1965-58860G>A	not provided [RCV001681036]	benign	4	168832062	168832062	Human		name
150494140	CV1267292	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12239G>T	not provided [RCV001688320]	benign	4	168878683	168878683	Human		name
150455930	CV1269005	deletion	NM_001166108.2(PALLD):c.1965-12229del	not provided [RCV001692829]	benign	4	168878683	168878683	Human		name
151871426	CV1340625	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13000G>C	Pancreatic adenocarcinoma [RCV001939855]\|not provided [RCV004693941]	uncertain significance	4	168877922	168877922	Human	2	name
151791392	CV1341275	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12931C>T	Pancreatic adenocarcinoma [RCV001866280]\|not specified [RCV004038990]	uncertain significance	4	168877991	168877991	Human	2	name
151831086	CV1359040	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12709T>C	Pancreatic adenocarcinoma [RCV001993718]	uncertain significance	4	168878213	168878213	Human	2	name
151882828	CV1383943	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12838C>G	Pancreatic adenocarcinoma [RCV001886806]	uncertain significance	4	168878084	168878084	Human	2	name
151870926	CV1384573	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12612C>A	Pancreatic adenocarcinoma [RCV001981289]\|not specified [RCV005382297]	uncertain significance	4	168878310	168878310	Human	2	name
151820624	CV1390895	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12697C>T	Pancreatic adenocarcinoma [RCV001992732]	uncertain significance	4	168878225	168878225	Human	2	name
8689779	CV139706	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12928G>C	Pancreatic adenocarcinoma [RCV000123160]	uncertain significance	4	168877994	168877994	Human	2	name
8689780	CV139707	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12910C>G	PALLD-related disorder [RCV003952630]\|Pancreatic adenocarcinoma [RCV000123161]\|not specified [RCV004837748]	benign\|uncertain significance	4	168878012	168878012	Human	3	name , alternate_id
8689783	CV139710	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12875G>A	Pancreatic adenocarcinoma [RCV000123164]	likely benign\|uncertain significance	4	168878047	168878047	Human	2	name
8689786	CV139713	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12840C>G	PALLD-related disorder [RCV003925221]\|Pancreatic adenocarcinoma [RCV000123167]\|Pancreatic cancer, susceptibility to, 1 [RCV005235026]\|not specified [RCV004019707]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	4	168878082	168878082	Human	3	name , alternate_id
8689787	CV139714	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12830G>T	Pancreatic adenocarcinoma [RCV000123168]	likely benign\|uncertain significance	4	168878092	168878092	Human	2	name
8689788	CV139715	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12812C>A	Pancreatic adenocarcinoma [RCV000123169]\|not specified [RCV004019708]	uncertain significance	4	168878110	168878110	Human	2	name
8689789	CV139716	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12795C>T	Pancreatic adenocarcinoma [RCV000123170]\|not specified [RCV005384657]	uncertain significance	4	168878127	168878127	Human	2	name
8689790	CV139717	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12665G>C	Pancreatic adenocarcinoma [RCV001083802]\|Pancreatic cancer, susceptibility to, 1 [RCV005235027]\|not provided [RCV000123171]\|not specified [RCV004837749]	benign\|likely benign\|uncertain significance	4	168878257	168878257	Human	3	name
8689791	CV139718	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12636G>A	Pancreatic adenocarcinoma [RCV000123172]\|not provided [RCV003436939]\|not specified [RCV000160874]	benign\|likely benign\|uncertain significance	4	168878286	168878286	Human	2	name
8689792	CV139719	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12594T>G	Pancreatic adenocarcinoma [RCV001079639]\|Pancreatic cancer, susceptibility to, 1 [RCV003315814]\|not provided [RCV000123173]\|not specified [RCV004837750]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	4	168878328	168878328	Human	3	name
8689793	CV139720	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12570C>T	Pancreatic adenocarcinoma [RCV000123174]	uncertain significance	4	168878352	168878352	Human	2	name
8689794	CV139721	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12565G>A	Pancreatic adenocarcinoma [RCV000123175]\|Pancreatic cancer, susceptibility to, 1 [RCV003315815]\|not specified [RCV001356302]	benign\|likely benign\|uncertain significance	4	168878357	168878357	Human	3	name
151731933	CV1419342	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12639C>G	Pancreatic adenocarcinoma [RCV001946139]	uncertain significance	4	168878283	168878283	Human	2	name
151888012	CV1434354	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12534C>A	Pancreatic adenocarcinoma [RCV001887875]\|not specified [RCV004837813]	uncertain significance	4	168878388	168878388	Human	2	name
151882659	CV1443264	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12813T>C	Pancreatic adenocarcinoma [RCV002037183]	uncertain significance	4	168878109	168878109	Human	2	name
151835391	CV1463342	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12671G>A	Pancreatic adenocarcinoma [RCV001880727]\|not specified [RCV004837817]	likely benign\|uncertain significance	4	168878251	168878251	Human	2	name
151754114	CV1467498	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12687C>T	Pancreatic adenocarcinoma [RCV001948444]\|not specified [RCV004837825]	uncertain significance	4	168878235	168878235	Human	2	name
151870919	CV1476938	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12997A>T	Pancreatic adenocarcinoma [RCV001906463]	uncertain significance	4	168877925	168877925	Human	2	name
151827829	CV1479860	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12708T>G	Pancreatic adenocarcinoma [RCV001901507]	uncertain significance	4	168878214	168878214	Human	2	name
151721073	CV1491657	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12597C>T	Pancreatic adenocarcinoma [RCV002003676]	uncertain significance	4	168878325	168878325	Human	2	name
151708782	CV1495121	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12869G>A	Pancreatic adenocarcinoma [RCV002001518]\|not specified [RCV005382327]	uncertain significance	4	168878053	168878053	Human	2	name
151760156	CV1499972	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12598G>C	Pancreatic adenocarcinoma [RCV001895212]	uncertain significance	4	168878324	168878324	Human	2	name
151718626	CV1506774	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12580C>G	Pancreatic adenocarcinoma [RCV001909375]	uncertain significance	4	168878342	168878342	Human	2	name
152095020	CV1533919	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12947C>G	Pancreatic adenocarcinoma [RCV002151089]	likely benign	4	168877975	168877975	Human	2	name
152164304	CV1557560	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12968G>A	Pancreatic adenocarcinoma [RCV002141493]	likely benign	4	168877954	168877954	Human	2	name
152095946	CV1559684	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12944G>A	Pancreatic adenocarcinoma [RCV002213358]	likely benign	4	168877978	168877978	Human	2	name
152141988	CV1583568	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12514G>A	Pancreatic adenocarcinoma [RCV002120499]	likely benign	4	168878408	168878408	Human	2	name
152077433	CV1601857	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12872C>T	Pancreatic adenocarcinoma [RCV002148872]	likely benign	4	168878050	168878050	Human	2	name
152115311	CV1628202	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13025C>T	Pancreatic adenocarcinoma [RCV002197319]\|not specified [RCV005382382]	likely benign	4	168877897	168877897	Human	2	name
152166845	CV1632673	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12950C>T	Pancreatic adenocarcinoma [RCV002182017]\|not specified [RCV004837840]	likely benign	4	168877972	168877972	Human	2	name
152113638	CV1639412	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12635C>T	Pancreatic adenocarcinoma [RCV002197111]\|not specified [RCV005382381]	likely benign	4	168878287	168878287	Human	2	name
8595820	CV17611	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12616C>T	PALLD-related disorder [RCV003894786]\|Pancreatic adenocarcinoma [RCV000168440]\|Pancreatic cancer, susceptibility to, 1 [RCV000002681]\|not specified [RCV000160876]	risk factor\|benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	4	168878306	168878306	Human	3	name , alternate_id
155737402	CV1774539	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12906C>A	Pancreatic adenocarcinoma [RCV002301995]	uncertain significance	4	168878016	168878016	Human	2	name
155721327	CV1776443	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12744T>C	Pancreatic adenocarcinoma [RCV002296713]	uncertain significance	4	168878178	168878178	Human	2	name
155696513	CV1787388	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12625A>C	not specified [RCV004051254]	uncertain significance	4	168878297	168878297	Human		name
155702603	CV1791426	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12591T>G	not specified [RCV004050651]	uncertain significance	4	168878331	168878331	Human		name
155677174	CV1792835	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12671G>C	Pancreatic adenocarcinoma [RCV003585253]\|not specified [RCV004049240]	likely benign	4	168878251	168878251	Human	2	name
155738675	CV1797975	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12601A>C	not specified [RCV004049967]	uncertain significance	4	168878321	168878321	Human		name
155696210	CV1800676	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12972A>C	not specified [RCV004052543]	uncertain significance	4	168877950	168877950	Human		name
9834683	CV180160	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12625A>G	Pancreatic adenocarcinoma [RCV000547431]\|Pancreatic cancer, susceptibility to, 1 [RCV003315965]\|not provided [RCV004715748]\|not specified [RCV000456012]	benign	4	168878297	168878297	Human	3	name
155733966	CV1802178	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12543A>C	not specified [RCV004050154]	uncertain significance	4	168878379	168878379	Human		name
155745726	CV1802966	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13020T>G	not specified [RCV004053004]	uncertain significance	4	168877902	168877902	Human		name
155729416	CV1808388	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12582A>C	not specified [RCV004050808]	uncertain significance	4	168878340	168878340	Human		name
155740549	CV1809455	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12982T>G	not specified [RCV004050870]	uncertain significance	4	168877940	168877940	Human		name
155683589	CV1815045	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12939A>C	not specified [RCV004055663]	uncertain significance	4	168877983	168877983	Human		name
155679945	CV1815832	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12960A>C	not specified [RCV004055745]	uncertain significance	4	168877962	168877962	Human		name
155681679	CV1839686	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12835G>C	not specified [RCV004061584]	uncertain significance	4	168878087	168878087	Human		name
155744292	CV1843064	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12925T>G	not specified [RCV004060980]	uncertain significance	4	168877997	168877997	Human		name
155664226	CV1855151	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12749G>C	PALLD-related disorder [RCV003926395]\|not specified [RCV004062361]	likely benign	4	168878173	168878173	Human	1	name , alternate_id
10041330	CV186022	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13000G>T	Pancreatic adenocarcinoma [RCV000168348]\|not specified [RCV004020005]	uncertain significance	4	168877922	168877922	Human	2	name
156375628	CV1868646	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12916G>A	Pancreatic adenocarcinoma [RCV003066691]	uncertain significance	4	168878006	168878006	Human	2	name
156217042	CV1869411	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12854G>A	Pancreatic adenocarcinoma [RCV003058769]	likely benign	4	168878068	168878068	Human	2	name
156217228	CV1869425	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12515C>G	Pancreatic adenocarcinoma [RCV003058776]	likely benign	4	168878407	168878407	Human	2	name
156349636	CV1885908	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12590G>A	Pancreatic adenocarcinoma [RCV003090867]	likely benign	4	168878332	168878332	Human	2	name
156075365	CV1890161	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12916G>T	Pancreatic adenocarcinoma [RCV003079683]	uncertain significance	4	168878006	168878006	Human	2	name
156380148	CV1899631	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12879C>G	Pancreatic adenocarcinoma [RCV003093207]	uncertain significance	4	168878043	168878043	Human	2	name
156414552	CV1912512	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12762C>G	Pancreatic adenocarcinoma [RCV002588672]\|not specified [RCV005382560]	uncertain significance	4	168878160	168878160	Human	2	name
156183457	CV1924603	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12883C>T	Pancreatic adenocarcinoma [RCV002625121]	uncertain significance	4	168878039	168878039	Human	2	name
156357793	CV1925193	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12648C>T	Pancreatic adenocarcinoma [RCV002651414]\|not specified [RCV004827945]	uncertain significance	4	168878274	168878274	Human	2	name
156367355	CV1925673	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12663C>T	Pancreatic adenocarcinoma [RCV002633114]\|not specified [RCV005382577]	likely benign\|uncertain significance	4	168878259	168878259	Human	2	name
156043792	CV1927007	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12601A>G	Pancreatic adenocarcinoma [RCV002637685]	uncertain significance	4	168878321	168878321	Human	2	name
156170672	CV1930171	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12926G>C	Pancreatic adenocarcinoma [RCV002624697]	likely benign	4	168877996	168877996	Human	2	name
156446167	CV1951201	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12938C>A	Pancreatic adenocarcinoma [RCV003117133]	uncertain significance	4	168877984	168877984	Human	2	name
156148078	CV1970784	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13012C>T	Pancreatic adenocarcinoma [RCV002594056]	uncertain significance	4	168877910	168877910	Human	2	name
155909216	CV1980005	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12540G>A	Pancreatic adenocarcinoma [RCV002613865]	uncertain significance	4	168878382	168878382	Human	2	name
156390443	CV1991156	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12658C>T	Pancreatic adenocarcinoma [RCV002634934]\|not specified [RCV005382441]	uncertain significance	4	168878264	168878264	Human	2	name
156390209	CV1996177	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13019G>A	Pancreatic adenocarcinoma [RCV002654302]	likely benign	4	168877903	168877903	Human	2	name
156014824	CV2013461	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12799G>A	Pancreatic adenocarcinoma [RCV002735084]	uncertain significance	4	168878123	168878123	Human	2	name
155950559	CV2013959	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12809C>T	Pancreatic adenocarcinoma [RCV002685998]	likely benign	4	168878113	168878113	Human	2	name
156209488	CV2036774	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12572G>A	Pancreatic adenocarcinoma [RCV002790187]	likely benign	4	168878350	168878350	Human	2	name
156208282	CV2040426	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12860G>A	Pancreatic adenocarcinoma [RCV002790143]\|not specified [RCV005382476]	likely benign	4	168878062	168878062	Human	2	name
156275326	CV2056172	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12656C>T	Pancreatic adenocarcinoma [RCV002806803]	likely benign	4	168878266	168878266	Human	2	name
156093256	CV2106278	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12730G>A	Pancreatic adenocarcinoma [RCV002952444]	uncertain significance	4	168878192	168878192	Human	2	name
156004435	CV2106962	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13017C>T	Pancreatic adenocarcinoma [RCV002947946]	uncertain significance	4	168877905	168877905	Human	2	name
156198564	CV2113811	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12679C>G	Pancreatic adenocarcinoma [RCV002957296]\|not specified [RCV005382498]	uncertain significance	4	168878243	168878243	Human	2	name
156296627	CV2119269	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12688C>T	Pancreatic adenocarcinoma [RCV002961948]\|not specified [RCV004827919]	uncertain significance	4	168878234	168878234	Human	2	name
10405757	CV212358	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12953C>T	Pancreatic adenocarcinoma [RCV000197834]\|Pancreatic cancer, susceptibility to, 1 [RCV003316096]\|not provided [RCV004717084]\|not specified [RCV004837752]	benign\|likely benign	4	168877969	168877969	Human	3	name
10405619	CV212359	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12937C>T	Pancreatic adenocarcinoma [RCV000196326]	uncertain significance	4	168877985	168877985	Human	2	name
10405593	CV212360	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12908G>A	PALLD-related disorder [RCV003947653]\|Pancreatic adenocarcinoma [RCV000196136]	pathogenic\|benign\|likely benign	4	168878014	168878014	Human	3	name , alternate_id
10405766	CV212361	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12907G>A	Pancreatic adenocarcinoma [RCV000197950]\|not specified [RCV005384673]	likely benign\|uncertain significance	4	168878015	168878015	Human	2	name
10405959	CV212362	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12800C>T	Pancreatic adenocarcinoma [RCV000199978]\|Pancreatic cancer, susceptibility to, 1 [RCV003316105]\|not specified [RCV004827763]	likely benign	4	168878122	168878122	Human	3	name
10405660	CV212363	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12764G>C	Pancreatic adenocarcinoma [RCV000196732]\|not provided [RCV001795323]\|not specified [RCV001795324]	benign\|likely benign	4	168878158	168878158	Human	2	name
10405797	CV212364	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12758G>C	Pancreatic adenocarcinoma [RCV000198297]\|not provided [RCV004715761]\|not specified [RCV001795325]	benign\|likely benign	4	168878164	168878164	Human	2	name
10406011	CV212365	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12755A>C	PALLD-related disorder [RCV003927853]\|Pancreatic adenocarcinoma [RCV000200513]\|not provided [RCV004717085]	pathogenic\|likely pathogenic\|benign\|likely benign	4	168878167	168878167	Human	3	name , alternate_id
10405535	CV212366	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12718C>T	Pancreatic adenocarcinoma [RCV000195528]\|not specified [RCV004020468]	likely benign\|uncertain significance	4	168878204	168878204	Human	2	name
10405638	CV212367	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12704A>G	Pancreatic adenocarcinoma [RCV002515457]	likely benign	4	168878218	168878218	Human	2	name
10405556	CV212368	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12530C>T	Pancreatic adenocarcinoma [RCV001086219]\|Pancreatic cancer, susceptibility to, 1 [RCV003316095]\|not specified [RCV004837751]	likely pathogenic\|benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	4	168878392	168878392	Human	3	name
156124154	CV2124809	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12844C>G	Pancreatic adenocarcinoma [RCV002953617]	uncertain significance	4	168878078	168878078	Human	2	name
156005559	CV2127371	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12816C>T	Pancreatic adenocarcinoma [RCV002948002]	uncertain significance	4	168878106	168878106	Human	2	name
156093001	CV2135639	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12637C>A	Pancreatic adenocarcinoma [RCV003001902]\|not specified [RCV005399052]	uncertain significance	4	168878285	168878285	Human	2	name
155949748	CV2158823	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12918A>T	Pancreatic adenocarcinoma [RCV003014783]	uncertain significance	4	168878004	168878004	Human	2	name
10767193	CV221435	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13016C>T	Pancreatic adenocarcinoma [RCV000204304]\|not specified [RCV004827764]	benign\|likely benign	4	168877906	168877906	Human	2	name
10768160	CV221436	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12990C>T	Pancreatic adenocarcinoma [RCV000205931]	uncertain significance	4	168877932	168877932	Human	2	name
10767598	CV221437	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12941G>A	Pancreatic adenocarcinoma [RCV001436211]\|not specified [RCV004837758]	likely benign	4	168877981	168877981	Human	2	name
10767827	CV221438	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12913A>C	Pancreatic adenocarcinoma [RCV000205380]\|not specified [RCV004837756]	uncertain significance	4	168878009	168878009	Human	2	name
10768630	CV221439	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12777C>T	PALLD-related disorder [RCV003417739]\|Pancreatic adenocarcinoma [RCV000206720]\|not specified [RCV004837754]	uncertain significance	4	168878145	168878145	Human	3	name , alternate_id
10767179	CV221442	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12736A>C	Pancreatic adenocarcinoma [RCV001516271]	benign	4	168878186	168878186	Human	2	name
10768320	CV221443	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12692A>C	Pancreatic adenocarcinoma [RCV000206208]	likely benign	4	168878230	168878230	Human	2	name
10766994	CV221444	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12683G>A	Pancreatic adenocarcinoma [RCV001453315]\|not specified [RCV005384677]	likely benign	4	168878239	168878239	Human	2	name
10768473	CV221445	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12566C>T	Pancreatic adenocarcinoma [RCV001466188]\|not specified [RCV004837755]	likely benign	4	168878356	168878356	Human	2	name
11345815	CV239343	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12748G>C	Pancreatic adenocarcinoma [RCV000226381]\|not specified [RCV004827766]	uncertain significance	4	168878174	168878174	Human	2	name
11351615	CV239344	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12637C>G	Pancreatic adenocarcinoma [RCV000229224]	uncertain significance	4	168878285	168878285	Human	2	name
11352059	CV239345	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12556C>T	PALLD-related disorder [RCV003977653]\|Pancreatic adenocarcinoma [RCV001434441]	likely benign	4	168878366	168878366	Human	3	name , alternate_id
11351391	CV239346	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12535A>C	Pancreatic adenocarcinoma [RCV000227055]\|not specified [RCV004837759]	uncertain significance	4	168878387	168878387	Human	2	name
329390696	CV2440343	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12861C>A	not specified [RCV004262820]	uncertain significance	4	168878061	168878061	Human		name
401895696	CV2771488	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12976A>C	not specified [RCV004348528]	uncertain significance	4	168877946	168877946	Human		name
401936280	CV2803069	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13020T>C	PALLD-related disorder [RCV003414283]	uncertain significance	4	168877902	168877902	Human		name , trait , alternate_id
405150212	CV2869612	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12597C>G	Pancreatic adenocarcinoma [RCV003585585]	uncertain significance	4	168878325	168878325	Human	2	name
405149867	CV2875267	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12677G>A	Pancreatic adenocarcinoma [RCV003585555]\|not specified [RCV004827971]	likely benign	4	168878245	168878245	Human	2	name
405149958	CV2875752	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12935C>A	PALLD-related disorder [RCV003980980]\|Pancreatic adenocarcinoma [RCV003585563]\|not specified [RCV005392628]	likely benign	4	168877987	168877987	Human	3	name , alternate_id
405150481	CV2884721	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12823G>A	Pancreatic adenocarcinoma [RCV003585608]\|not specified [RCV005392630]	uncertain significance	4	168878099	168878099	Human	2	name
405139909	CV2885575	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12934G>A	Pancreatic adenocarcinoma [RCV003584034]\|not specified [RCV004369195]	uncertain significance	4	168877988	168877988	Human	2	name
405140113	CV2886110	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12725C>T	Pancreatic adenocarcinoma [RCV003584055]	likely benign	4	168878197	168878197	Human	2	name
405140718	CV2886640	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12822C>A	Pancreatic adenocarcinoma [RCV003584087]\|not specified [RCV004837905]	uncertain significance	4	168878100	168878100	Human	2	name
405139893	CV2888665	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12823G>C	Pancreatic adenocarcinoma [RCV003584032]	uncertain significance	4	168878099	168878099	Human	2	name
405140002	CV2888789	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12792C>T	Pancreatic adenocarcinoma [RCV003584043]\|not specified [RCV005387196]	uncertain significance	4	168878130	168878130	Human	2	name
405150413	CV2890995	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12993A>T	Pancreatic adenocarcinoma [RCV003585602]	uncertain significance	4	168877929	168877929	Human	2	name
405139875	CV2892172	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12873C>T	Pancreatic adenocarcinoma [RCV003584030]\|not specified [RCV005387194]	uncertain significance	4	168878049	168878049	Human	2	name
405139983	CV2892519	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12848C>G	Pancreatic adenocarcinoma [RCV003584041]	uncertain significance	4	168878074	168878074	Human	2	name
405141376	CV2896439	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12515C>T	Pancreatic adenocarcinoma [RCV003584155]	likely benign	4	168878407	168878407	Human	2	name
405142254	CV2909824	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12678C>T	Pancreatic adenocarcinoma [RCV003584270]\|not specified [RCV004369413]	uncertain significance	4	168878244	168878244	Human	2	name
405142807	CV2919721	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13004C>T	Pancreatic adenocarcinoma [RCV003584233]	likely benign	4	168877918	168877918	Human	2	name
405144012	CV2931116	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12723C>A	Pancreatic adenocarcinoma [RCV003584328]	uncertain significance	4	168878199	168878199	Human	2	name
405248325	CV2938197	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12947C>T	Pancreatic adenocarcinoma [RCV003746740]\|not specified [RCV005392652]	likely benign	4	168877975	168877975	Human	2	name
405246501	CV3009632	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12550C>A	Pancreatic adenocarcinoma [RCV003746017]	uncertain significance	4	168878372	168878372	Human	2	name
405246666	CV3010679	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12549T>C	Pancreatic adenocarcinoma [RCV003746070]	uncertain significance	4	168878373	168878373	Human	2	name
405246567	CV3016474	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12627A>C	Pancreatic adenocarcinoma [RCV003746038]	uncertain significance	4	168878295	168878295	Human	2	name
405246786	CV3021404	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12761C>T	Pancreatic adenocarcinoma [RCV003746118]	likely benign	4	168878161	168878161	Human	2	name
405247179	CV3027397	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12764G>T	Pancreatic adenocarcinoma [RCV003746246]	likely benign	4	168878158	168878158	Human	2	name
405247170	CV3030615	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12640A>G	Pancreatic adenocarcinoma [RCV003746242]	uncertain significance	4	168878282	168878282	Human	2	name
405247280	CV3040407	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12911G>T	Pancreatic adenocarcinoma [RCV003746274]	likely benign	4	168878011	168878011	Human	2	name
405250410	CV3062365	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12909C>G	Pancreatic adenocarcinoma [RCV003747515]	uncertain significance	4	168878013	168878013	Human	2	name
405250445	CV3062490	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12847G>A	Pancreatic adenocarcinoma [RCV003747531]	uncertain significance	4	168878075	168878075	Human	2	name
405250403	CV3065417	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12985G>A	Pancreatic adenocarcinoma [RCV003747512]\|not specified [RCV004827996]	uncertain significance	4	168877937	168877937	Human	2	name
405250529	CV3070364	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12554G>C	Pancreatic adenocarcinoma [RCV003747568]\|not specified [RCV005392689]	likely benign	4	168878368	168878368	Human	2	name
405088681	CV3122249	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12766C>T	Pancreatic adenocarcinoma [RCV003811004]\|not specified [RCV005387266]	uncertain significance	4	168878156	168878156	Human	2	name
405199832	CV3128860	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12761C>A	Pancreatic adenocarcinoma [RCV003821903]	likely benign	4	168878161	168878161	Human	2	name
405062084	CV3129621	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12901A>C	Pancreatic adenocarcinoma [RCV003832890]\|not specified [RCV005387272]	uncertain significance	4	168878021	168878021	Human	2	name
405065917	CV3140001	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12821G>A	Pancreatic adenocarcinoma [RCV003833156]	likely benign	4	168878101	168878101	Human	2	name
405159089	CV3159854	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12684C>T	Pancreatic adenocarcinoma [RCV003856925]\|not specified [RCV005387280]	uncertain significance	4	168878238	168878238	Human	2	name
405240096	CV3166096	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12985G>C	Pancreatic adenocarcinoma [RCV003867108]\|not specified [RCV004837926]	uncertain significance	4	168877937	168877937	Human	2	name
402518919	CV3175308	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12811G>A	Pancreatic adenocarcinoma [RCV003879591]\|not specified [RCV005387290]	uncertain significance	4	168878111	168878111	Human	2	name
402509237	CV3182069	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12553G>A	Pancreatic adenocarcinoma [RCV003878722]\|not specified [RCV004369619]	uncertain significance	4	168878369	168878369	Human	2	name
402488939	CV3182250	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13006G>A	Pancreatic adenocarcinoma [RCV003876736]	uncertain significance	4	168877916	168877916	Human	2	name
405757247	CV3367712	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12912C>T	not specified [RCV004500032]	uncertain significance	4	168878010	168878010	Human		name
405757275	CV3367716	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12853C>G	not specified [RCV004500036]	uncertain significance	4	168878069	168878069	Human		name
405757329	CV3367723	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12941G>C	not specified [RCV004500043]	uncertain significance	4	168877981	168877981	Human		name
597715619	CV3574898	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12626C>T	not specified [RCV004841351]	likely benign	4	168878296	168878296	Human		name
597715628	CV3574900	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12573C>T	not specified [RCV004841352]	uncertain significance	4	168878349	168878349	Human		name
597715649	CV3574903	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12930C>T	Pancreatic adenocarcinoma [RCV005061506]\|not specified [RCV004841354]	uncertain significance	4	168877992	168877992	Human	2	name
597715659	CV3574904	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13003C>T	not specified [RCV004841355]	uncertain significance	4	168877919	168877919	Human		name
597715692	CV3574908	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12776G>A	not specified [RCV004841358]	likely benign	4	168878146	168878146	Human		name
597657552	CV3574910	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12930C>A	not specified [RCV004827643]	uncertain significance	4	168877992	168877992	Human		name
597715714	CV3574911	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12891C>T	not specified [RCV004841360]	uncertain significance	4	168878031	168878031	Human		name
597657559	CV3574912	duplication	NM_001166108.2(PALLD):c.1965-12765dup	not specified [RCV004827644]	uncertain significance	4	168878152	168878153	Human		name
597715726	CV3574913	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12863G>A	not specified [RCV004841361]	likely benign	4	168878059	168878059	Human		name
597657567	CV3574914	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12542G>A	not specified [RCV004827645]	likely benign	4	168878380	168878380	Human		name
597715738	CV3574915	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12789G>T	not specified [RCV004841362]	uncertain significance	4	168878133	168878133	Human		name
597715746	CV3574916	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12900G>T	not specified [RCV004841363]	uncertain significance	4	168878022	168878022	Human		name
597715785	CV3574921	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12746C>G	not specified [RCV004841367]	likely benign	4	168878176	168878176	Human		name
597715802	CV3574924	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12983C>G	not specified [RCV004841369]	likely benign	4	168877939	168877939	Human		name
597715812	CV3574925	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12865C>A	not specified [RCV004841370]	uncertain significance	4	168878057	168878057	Human		name
597715824	CV3574927	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12888C>T	not specified [RCV004841371]	uncertain significance	4	168878034	168878034	Human		name
597657594	CV3574928	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12643G>A	not specified [RCV004827649]	uncertain significance	4	168878279	168878279	Human		name
597715835	CV3574929	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12772T>A	not specified [RCV004841372]	uncertain significance	4	168878150	168878150	Human		name
597715844	CV3574930	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12554G>T	not specified [RCV004841373]	likely benign	4	168878368	168878368	Human		name
597715866	CV3574932	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12549T>A	not specified [RCV004841375]	uncertain significance	4	168878373	168878373	Human		name
597715878	CV3574933	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12544A>C	not specified [RCV004841376]	uncertain significance	4	168878378	168878378	Human		name
597715889	CV3574934	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12572G>C	not specified [RCV004841377]	likely benign	4	168878350	168878350	Human		name
597715902	CV3574935	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12783C>T	not specified [RCV004841378]	uncertain significance	4	168878139	168878139	Human		name
597715910	CV3574936	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12538G>A	not specified [RCV004841379]	uncertain significance	4	168878384	168878384	Human		name
597715920	CV3574937	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12618C>T	not specified [RCV004841380]	uncertain significance	4	168878304	168878304	Human		name
597715943	CV3574941	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12712G>A	not specified [RCV004841382]	uncertain significance	4	168878210	168878210	Human		name
597657617	CV3574943	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12585C>T	not specified [RCV004827652]	uncertain significance	4	168878337	168878337	Human		name
597715964	CV3574944	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12604C>T	not specified [RCV004841384]	uncertain significance	4	168878318	168878318	Human		name
597715973	CV3574945	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12858C>A	not specified [RCV004841385]	uncertain significance	4	168878064	168878064	Human		name
597715984	CV3574946	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12645C>T	not specified [RCV004841386]	uncertain significance	4	168878277	168878277	Human		name
597846288	CV3736438	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12620G>T	Pancreatic adenocarcinoma [RCV005060016]	uncertain significance	4	168878302	168878302	Human	2	name
597920624	CV3738101	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12835G>A	Pancreatic adenocarcinoma [RCV005074700]	uncertain significance	4	168878087	168878087	Human	2	name
597879775	CV3744454	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12753C>T	Pancreatic adenocarcinoma [RCV005069668]	uncertain significance	4	168878169	168878169	Human	2	name
597930220	CV3745818	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12881C>G	Pancreatic adenocarcinoma [RCV005075803]	likely benign	4	168878041	168878041	Human	2	name
597970219	CV3750177	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12528C>T	Pancreatic adenocarcinoma [RCV005084118]	uncertain significance	4	168878394	168878394	Human	2	name
597864447	CV3767047	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12513C>T	Pancreatic adenocarcinoma [RCV005106569]	likely benign	4	168878409	168878409	Human	2	name
597900772	CV3771277	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12965C>G	Pancreatic adenocarcinoma [RCV005112242]\|not specified [RCV005392968]	likely benign	4	168877957	168877957	Human	2	name
597966575	CV3794263	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12945C>T	Pancreatic adenocarcinoma [RCV005140439]	uncertain significance	4	168877977	168877977	Human	2	name
597974622	CV3802283	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12993A>G	Pancreatic adenocarcinoma [RCV005144060]	uncertain significance	4	168877929	168877929	Human	2	name
597877079	CV3813341	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12707C>T	Pancreatic adenocarcinoma [RCV005149277]	likely benign	4	168878215	168878215	Human	2	name
597849752	CV3824499	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12713C>G	Pancreatic adenocarcinoma [RCV005173538]	uncertain significance	4	168878209	168878209	Human	2	name
597869385	CV3835167	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12571G>A	Pancreatic adenocarcinoma [RCV005176343]\|not specified [RCV005392990]	uncertain significance	4	168878351	168878351	Human	2	name
597871819	CV3835769	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12969C>T	Pancreatic adenocarcinoma [RCV005176760]	uncertain significance	4	168877953	168877953	Human	2	name
597873078	CV3836235	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12720T>A	Pancreatic adenocarcinoma [RCV005177032]\|not specified [RCV005387382]	uncertain significance	4	168878202	168878202	Human	2	name
597867861	CV3838799	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12915G>A	Pancreatic adenocarcinoma [RCV005176095]	uncertain significance	4	168878007	168878007	Human	2	name
597888601	CV3839456	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13021C>T	Pancreatic adenocarcinoma [RCV005179348]	likely benign	4	168877901	168877901	Human	2	name
597888607	CV3839457	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12533C>A	Pancreatic adenocarcinoma [RCV005179349]	likely benign	4	168878389	168878389	Human	2	name
597953760	CV3844258	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12856A>C	Pancreatic adenocarcinoma [RCV005190930]	likely benign	4	168878066	168878066	Human	2	name
597937536	CV3862721	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13018G>A	Pancreatic adenocarcinoma [RCV005207993]\|not specified [RCV005387395]	uncertain significance	4	168877904	168877904	Human	2	name
12888532	CV393886	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12832C>A	Pancreatic adenocarcinoma [RCV000471084]	uncertain significance	4	168878090	168878090	Human	2	name
12892148	CV393890	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12673C>T	Pancreatic adenocarcinoma [RCV000458107]	uncertain significance	4	168878249	168878249	Human	2	name
12888340	CV394142	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12575G>A	Pancreatic adenocarcinoma [RCV000470692]\|not specified [RCV004837764]	likely benign	4	168878347	168878347	Human	2	name
12884837	CV394309	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12828C>T	Pancreatic adenocarcinoma [RCV000464208]\|not specified [RCV005384725]	uncertain significance	4	168878094	168878094	Human	2	name
12881825	CV394310	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12737C>T	Pancreatic adenocarcinoma [RCV000458524]\|not specified [RCV005384729]	likely benign	4	168878185	168878185	Human	2	name
598258205	CV4005564	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12893C>G	not specified [RCV005386228]	uncertain significance	4	168878029	168878029	Human		name
598258212	CV4005566	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12758G>A	not specified [RCV005386230]	likely benign	4	168878164	168878164	Human		name
598258218	CV4005568	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12829C>T	not specified [RCV005386232]	uncertain significance	4	168878093	168878093	Human		name
598258222	CV4005569	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12750C>T	not specified [RCV005386233]	uncertain significance	4	168878172	168878172	Human		name
598258233	CV4005572	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12886A>G	not specified [RCV005386236]	uncertain significance	4	168878036	168878036	Human		name
598258238	CV4005573	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12574C>G	not specified [RCV005386237]	uncertain significance	4	168878348	168878348	Human		name
598258243	CV4005574	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12630G>C	not specified [RCV005386238]	uncertain significance	4	168878292	168878292	Human		name
598258249	CV4005576	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12751C>T	not specified [RCV005386239]	uncertain significance	4	168878171	168878171	Human		name
598258263	CV4005580	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12529G>A	not specified [RCV005386242]	uncertain significance	4	168878393	168878393	Human		name
598258268	CV4005581	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12970G>A	not specified [RCV005386243]	uncertain significance	4	168877952	168877952	Human		name
598258279	CV4005583	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12609C>T	not specified [RCV005386245]	uncertain significance	4	168878313	168878313	Human		name
598258284	CV4005584	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12854G>T	not specified [RCV005386246]	uncertain significance	4	168878068	168878068	Human		name
598258289	CV4005585	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12934G>C	not specified [RCV005386247]	uncertain significance	4	168877988	168877988	Human		name
598258292	CV4005586	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12532C>G	not specified [RCV005386248]	uncertain significance	4	168878390	168878390	Human		name
598258300	CV4005588	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12560C>T	not specified [RCV005386250]	likely benign	4	168878362	168878362	Human		name
598184815	CV4005589	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12740C>T	not specified [RCV005395509]	likely benign	4	168878182	168878182	Human		name
598258303	CV4005590	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12734G>C	not specified [RCV005386251]	likely benign	4	168878188	168878188	Human		name
598184821	CV4005591	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12561A>G	not specified [RCV005395510]	likely benign	4	168878361	168878361	Human		name
598258308	CV4005592	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12682C>T	not specified [RCV005386252]	likely benign	4	168878240	168878240	Human		name
598258314	CV4005593	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12624G>A	not specified [RCV005386253]	uncertain significance	4	168878298	168878298	Human		name
598258329	CV4005596	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12649T>C	not specified [RCV005386256]	uncertain significance	4	168878273	168878273	Human		name
598258337	CV4005599	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12929C>A	not specified [RCV005386258]	likely benign	4	168877993	168877993	Human		name
598258348	CV4005602	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12764G>A	not specified [RCV005386260]	likely benign	4	168878158	168878158	Human		name
598258353	CV4005603	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12540G>C	not specified [RCV005386261]	uncertain significance	4	168878382	168878382	Human		name
598258359	CV4005604	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13007C>A	not specified [RCV005386262]	likely benign	4	168877915	168877915	Human		name
598258388	CV4005610	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12722G>A	not specified [RCV005386269]	likely benign	4	168878200	168878200	Human		name
598258393	CV4005611	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12692A>G	not specified [RCV005386270]	likely benign	4	168878230	168878230	Human		name
598258404	CV4005613	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12843G>A	not specified [RCV005386272]	uncertain significance	4	168878079	168878079	Human		name
598258410	CV4005615	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12728C>T	not specified [RCV005386274]	likely benign	4	168878194	168878194	Human		name
598184836	CV4005619	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12965C>T	not specified [RCV005395513]	likely benign	4	168877957	168877957	Human		name
598258439	CV4005622	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12653C>G	not specified [RCV005386280]	uncertain significance	4	168878269	168878269	Human		name
598258461	CV4005627	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12800C>G	not specified [RCV005386285]	likely benign	4	168878122	168878122	Human		name
598258476	CV4005630	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12556C>G	not specified [RCV005386288]	uncertain significance	4	168878366	168878366	Human		name
598258493	CV4005634	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12961A>C	not specified [RCV005386292]	uncertain significance	4	168877961	168877961	Human		name
598258497	CV4005635	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12911G>A	not specified [RCV005386293]	likely benign	4	168878011	168878011	Human		name
598258516	CV4005639	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12958C>G	not specified [RCV005386297]	uncertain significance	4	168877964	168877964	Human		name
598184842	CV4005642	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13011G>A	not specified [RCV005395514]	uncertain significance	4	168877911	168877911	Human		name
598258556	CV4005647	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12533C>G	not specified [RCV005386304]	likely benign	4	168878389	168878389	Human		name
598258576	CV4005652	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12747T>G	not specified [RCV005386308]	uncertain significance	4	168878175	168878175	Human		name
598258585	CV4005654	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12844C>T	not specified [RCV005386310]	uncertain significance	4	168878078	168878078	Human		name
598258590	CV4005655	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12984G>A	not specified [RCV005386311]	uncertain significance	4	168877938	168877938	Human		name
598258600	CV4005657	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12855G>A	not specified [RCV005386313]	likely benign	4	168878067	168878067	Human		name
598258607	CV4005659	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12689A>G	not specified [RCV005386315]	likely benign	4	168878233	168878233	Human		name
598258624	CV4005663	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12623C>G	not specified [RCV005386318]	uncertain significance	4	168878299	168878299	Human		name
598258633	CV4005665	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12933G>A	not specified [RCV005386320]	uncertain significance	4	168877989	168877989	Human		name
598258639	CV4005666	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12564T>C	not specified [RCV005386321]	uncertain significance	4	168878358	168878358	Human		name
598258647	CV4005668	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12824C>T	not specified [RCV005386323]	likely benign	4	168878098	168878098	Human		name
598258652	CV4005669	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12532C>T	not specified [RCV005386324]	uncertain significance	4	168878390	168878390	Human		name
598184858	CV4005671	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12956G>C	not specified [RCV005395517]	uncertain significance	4	168877966	168877966	Human		name
598258664	CV4005673	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12945C>G	not specified [RCV005386326]	uncertain significance	4	168877977	168877977	Human		name
598258670	CV4005674	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12636G>T	not specified [RCV005386327]	uncertain significance	4	168878286	168878286	Human		name
598258677	CV4005675	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12948C>T	not specified [RCV005386328]	uncertain significance	4	168877974	168877974	Human		name
598258689	CV4005678	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12989C>T	not specified [RCV005386331]	likely benign	4	168877933	168877933	Human		name
598184871	CV4005679	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12619A>C	not specified [RCV005395519]	uncertain significance	4	168878303	168878303	Human		name
598184877	CV4005681	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13013C>T	not specified [RCV005395520]	likely benign	4	168877909	168877909	Human		name
598258711	CV4005683	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12898C>T	not specified [RCV005386334]	uncertain significance	4	168878024	168878024	Human		name
598258733	CV4005686	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12803G>C	not specified [RCV005386337]	uncertain significance	4	168878119	168878119	Human		name
598258738	CV4005687	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12562A>T	not specified [RCV005386338]	uncertain significance	4	168878360	168878360	Human		name
598258743	CV4005688	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12729C>T	not specified [RCV005386339]	uncertain significance	4	168878193	168878193	Human		name
598258758	CV4005691	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12894G>A	not specified [RCV005386343]	uncertain significance	4	168878028	168878028	Human		name
598258763	CV4005692	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12558C>G	not specified [RCV005386344]	uncertain significance	4	168878364	168878364	Human		name
617153280	CV4021186	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12606T>C	not provided [RCV005428939]	uncertain significance	4	168878316	168878316	Human		name
617149581	CV4021360	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12595C>T	not provided [RCV005425329]	likely benign	4	168878327	168878327	Human		name
13491880	CV453031	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12857G>A	Pancreatic adenocarcinoma [RCV001408157]\|not specified [RCV005384772]	likely benign	4	168878065	168878065	Human	2	name
13491912	CV453038	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12805G>C	Pancreatic adenocarcinoma [RCV000534561]	uncertain significance	4	168878117	168878117	Human	2	name
13481780	CV453322	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12803G>A	Pancreatic adenocarcinoma [RCV000551583]\|not specified [RCV005384773]	likely benign	4	168878119	168878119	Human	2	name
13489632	CV453417	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12880C>T	Pancreatic adenocarcinoma [RCV000533020]	uncertain significance	4	168878042	168878042	Human	2	name
13500913	CV453419	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12519C>G	Pancreatic adenocarcinoma [RCV000540708]	likely benign	4	168878403	168878403	Human	2	name
13479240	CV453820	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12569G>A	PALLD-related disorder [RCV003952886]\|Pancreatic adenocarcinoma [RCV000527996]\|not specified [RCV004837768]	likely benign\|uncertain significance	4	168878353	168878353	Human	3	name , alternate_id
13625503	CV519804	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12896C>T	Pancreatic adenocarcinoma [RCV000653483]\|not specified [RCV004827781]	likely benign	4	168878026	168878026	Human	2	name
13625502	CV519808	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12641C>T	Pancreatic adenocarcinoma [RCV000653482]\|not specified [RCV005384808]	likely benign	4	168878281	168878281	Human	2	name
13625504	CV519833	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12605C>T	Pancreatic adenocarcinoma [RCV000653484]	likely benign	4	168878317	168878317	Human	2	name
13625451	CV520107	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12889T>C	Pancreatic adenocarcinoma [RCV000653473]\|not specified [RCV004837771]	uncertain significance	4	168878033	168878033	Human	2	name
13625450	CV520111	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12870T>C	Pancreatic adenocarcinoma [RCV000653472]\|not specified [RCV005384806]	uncertain significance	4	168878052	168878052	Human	2	name
13812054	CV559627	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12990C>A	Pancreatic adenocarcinoma [RCV000703452]	uncertain significance	4	168877932	168877932	Human	2	name
13813548	CV559629	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12552G>C	Pancreatic adenocarcinoma [RCV000704436]	uncertain significance	4	168878370	168878370	Human	2	name
13807901	CV559784	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12771C>T	Pancreatic adenocarcinoma [RCV000701385]	uncertain significance	4	168878151	168878151	Human	2	name
13803128	CV563575	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12705C>T	Pancreatic adenocarcinoma [RCV000698890]\|not specified [RCV005384824]	uncertain significance	4	168878217	168878217	Human	2	name
14735253	CV632077	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12837C>G	Pancreatic adenocarcinoma [RCV000819502]\|not specified [RCV004029007]	uncertain significance	4	168878085	168878085	Human	2	name
14709929	CV632078	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12597C>A	Pancreatic adenocarcinoma [RCV000792995]	uncertain significance	4	168878325	168878325	Human	2	name
14704989	CV632079	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12573C>G	Pancreatic adenocarcinoma [RCV000807967]\|not specified [RCV004837776]	uncertain significance	4	168878349	168878349	Human	2	name
15115736	CV683628	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13022G>A	Pancreatic adenocarcinoma [RCV001467902]	likely benign	4	168877900	168877900	Human	2	name
15139602	CV686508	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13001C>G	Pancreatic adenocarcinoma [RCV001480406]	likely benign	4	168877921	168877921	Human	2	name
15158174	CV686509	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12898C>A	PALLD-related disorder [RCV004751764]\|Pancreatic adenocarcinoma [RCV000868586]\|not specified [RCV004027730]	likely benign\|uncertain significance	4	168878024	168878024	Human	3	name , alternate_id
15101024	CV686510	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12817C>T	PALLD-related disorder [RCV003975420]\|Pancreatic adenocarcinoma [RCV000870169]\|not specified [RCV004027771]	likely benign\|uncertain significance	4	168878105	168878105	Human	3	name , alternate_id
15102893	CV686511	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12599C>T	Pancreatic adenocarcinoma [RCV001410318]	likely benign	4	168878323	168878323	Human	2	name
15101845	CV686512	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12592C>T	Pancreatic adenocarcinoma [RCV001479045]\|not specified [RCV005384885]	likely benign	4	168878330	168878330	Human	2	name
15140072	CV691527	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12944G>C	Pancreatic adenocarcinoma [RCV001446548]	likely benign	4	168877978	168877978	Human	2	name
15136152	CV691528	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12866C>T	Pancreatic adenocarcinoma [RCV001410813]	likely benign	4	168878056	168878056	Human	2	name
15108162	CV691529	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12686G>A	Pancreatic adenocarcinoma [RCV000871643]	likely benign	4	168878236	168878236	Human	2	name
15120399	CV691530	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12617G>A	Pancreatic adenocarcinoma [RCV000874054]\|not specified [RCV004837777]	likely benign	4	168878305	168878305	Human	2	name
15164123	CV709230	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12587C>T	Pancreatic adenocarcinoma [RCV001396643]\|not specified [RCV005392599]	likely benign	4	168878335	168878335	Human	2	name
26897397	CV828942	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12987C>T	Pancreatic adenocarcinoma [RCV001070284]	uncertain significance	4	168877935	168877935	Human	2	name
26892003	CV828943	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12769C>A	Pancreatic adenocarcinoma [RCV001046721]	uncertain significance	4	168878153	168878153	Human	2	name
38484542	CV923460	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12850T>G	Pancreatic adenocarcinoma [RCV001219479]	uncertain significance	4	168878072	168878072	Human	2	name
38494276	CV923461	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12702T>G	Pancreatic adenocarcinoma [RCV001224851]	uncertain significance	4	168878220	168878220	Human	2	name
38481937	CV932247	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12879C>T	Pancreatic adenocarcinoma [RCV001207053]\|not specified [RCV004827796]	uncertain significance	4	168878043	168878043	Human	2	name
38474948	CV943892	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12924C>T	Pancreatic adenocarcinoma [RCV001232412]\|not specified [RCV004033164]	uncertain significance	4	168877998	168877998	Human	2	name
38495442	CV943893	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12918A>G	Pancreatic adenocarcinoma [RCV001225721]\|not specified [RCV004837790]	uncertain significance	4	168878004	168878004	Human	2	name
38473665	CV943894	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12903C>G	Pancreatic adenocarcinoma [RCV001231892]\|not specified [RCV004837792]	uncertain significance	4	168878019	168878019	Human	2	name
38467474	CV943895	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12749G>A	Pancreatic adenocarcinoma [RCV001230436]	likely benign\|uncertain significance	4	168878173	168878173	Human	2	name
38466405	CV943896	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12699C>T	Pancreatic adenocarcinoma [RCV001230276]\|not specified [RCV004032696]	uncertain significance	4	168878223	168878223	Human	2	name
126765438	CV990014	single nucleotide variant	NM_001166108.2(PALLD):c.1965-13026G>A	Pancreatic adenocarcinoma [RCV001301488]	uncertain significance	4	168877896	168877896	Human	2	name
126756431	CV990015	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12964C>T	Pancreatic adenocarcinoma [RCV001308110]	uncertain significance	4	168877958	168877958	Human	2	name
126753089	CV990018	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12724C>T	Pancreatic adenocarcinoma [RCV001307335]	uncertain significance	4	168878198	168878198	Human	2	name
126753805	CV990019	single nucleotide variant	NM_001166108.2(PALLD):c.1965-12544A>G	Pancreatic adenocarcinoma [RCV001307477]\|not specified [RCV005394924]	uncertain significance	4	168878378	168878378	Human	2	name
155727054	CV1822402	single nucleotide variant	NM_001166108.2(PALLD):c.6A>G (p.Ser2=)	not specified [RCV004055120]	likely benign	4	168511510	168511510	Human		name
155727060	CV1822404	single nucleotide variant	NM_001166108.2(PALLD):c.6A>T (p.Ser2=)	not specified [RCV004055121]	likely benign	4	168511510	168511510	Human		name
10405626	CV212342	deletion	NM_001166110.1(PALLD):c.640-?_960+?del	Pancreatic adenocarcinoma [RCV000196373]	pathogenic\|likely pathogenic\|uncertain significance				Human	2	name
11654075	CV292764	duplication	NM_001166108.2(PALLD):c.1011_1014dup	Carcinoma of pancreas [RCV000315023]	uncertain significance	4	168927189	168927190	Human	1	name
11632706	CV297667	deletion	NM_001166108.2(PALLD):c.2155_2156del	Carcinoma of pancreas [RCV000278358]\|not provided [RCV004695784]	uncertain significance	4	168928327	168928328	Human	1	name
155720446	CV1835787	single nucleotide variant	NM_001166108.2(PALLD):c.12C>T (p.Thr4=)	not specified [RCV004058244]	likely benign	4	168511516	168511516	Human		name
155719405	CV1837362	single nucleotide variant	NM_001166108.2(PALLD):c.15C>G (p.Ser5=)	not specified [RCV004057411]	likely benign	4	168511519	168511519	Human		name
329364507	CV2425763	single nucleotide variant	NM_001166108.2(PALLD):c.15C>T (p.Ser5=)	not specified [RCV004243163]	likely benign	4	168511519	168511519	Human		name
11633576	CV292728	single nucleotide variant	NM_001166108.2(PALLD):c.18C>T (p.Ser6=)	Pancreatic adenocarcinoma [RCV002520224]\|Pancreatic cancer, susceptibility to, 1 [RCV000348927]\|not provided [RCV000874570]\|not specified [RCV004021943]	benign	4	168511522	168511522	Human	3	name
405708502	CV3384221	single nucleotide variant	NM_001166108.2(PALLD):c.27C>G (p.Ser9=)	not specified [RCV004521958]	likely benign	4	168511531	168511531	Human		name
126756696	CV1025739	microsatellite	NM_001166108.2(PALLD):c.1965-12701GCC[6]	Pancreatic adenocarcinoma [RCV001339353]\|not specified [RCV005385044]	uncertain significance	4	168878220	168878221	Human		name
127316727	CV1154707	microsatellite	NM_001166108.2(PALLD):c.1965-12701GCC[4]	Pancreatic adenocarcinoma [RCV001520676]	benign	4	168878220	168878221	Human		name
155734347	CV1802285	single nucleotide variant	NM_001166108.2(PALLD):c.48C>T (p.Asp16=)	not specified [RCV004050184]	likely benign	4	168511552	168511552	Human		name
155704199	CV1810646	single nucleotide variant	NM_001166108.2(PALLD):c.57A>G (p.Glu19=)	not specified [RCV004054107]	likely benign	4	168511561	168511561	Human		name
155699038	CV1813327	single nucleotide variant	NM_001166108.2(PALLD):c.75C>T (p.Asp25=)	not specified [RCV004056440]	likely benign	4	168511579	168511579	Human		name
155689690	CV1814526	single nucleotide variant	NM_001166108.2(PALLD):c.87C>A (p.Gly29=)	not specified [RCV004056722]	likely benign	4	168511591	168511591	Human		name
155727046	CV1822397	single nucleotide variant	NM_001166108.2(PALLD):c.69T>C (p.Asn23=)	not specified [RCV004055117]	likely benign	4	168511573	168511573	Human		name
155744712	CV1824368	single nucleotide variant	NM_001166108.2(PALLD):c.84G>A (p.Pro28=)	not specified [RCV004056198]	likely benign	4	168511588	168511588	Human		name
329363579	CV2425745	single nucleotide variant	NM_001166108.2(PALLD):c.78C>T (p.Phe26=)	not specified [RCV004243145]	likely benign	4	168511582	168511582	Human		name
329389982	CV2465675	single nucleotide variant	NM_001166108.2(PALLD):c.63C>T (p.Ser21=)	not specified [RCV004281500]	likely benign	4	168511567	168511567	Human		name
597715103	CV3574834	single nucleotide variant	NM_001166108.2(PALLD):c.42C>G (p.Leu14=)	not specified [RCV004841303]	likely benign	4	168511546	168511546	Human		name
597715408	CV3574874	single nucleotide variant	NM_001166108.2(PALLD):c.81C>T (p.Phe27=)	not specified [RCV004841332]	likely benign	4	168511585	168511585	Human		name
597956967	CV3800381	microsatellite	NM_001166108.2(PALLD):c.1965-12581GCC[4]	Pancreatic adenocarcinoma [RCV005137473]	uncertain significance	4	168878340	168878341	Human		name
12881396	CV394313	microsatellite	NM_001166108.2(PALLD):c.1965-12688CCG[3]	PALLD-related disorder [RCV003960102]\|Pancreatic adenocarcinoma [RCV000457761]\|not provided [RCV001637047]\|not specified [RCV004837763]	benign	4	168878233	168878234	Human		name , alternate_id
13493567	CV453418	microsatellite	NM_001166108.2(PALLD):c.1965-12694CCA[3]	Pancreatic adenocarcinoma [RCV000535774]\|not provided [RCV001613380]\|not specified [RCV001358463]	benign	4	168878227	168878228	Human		name
15105839	CV695220	microsatellite	NM_001166108.2(PALLD):c.2101-6_2101-4del	Pancreatic adenocarcinoma [RCV002539100]	likely benign	4	168894570	168894572	Human		name
15115161	CV759287	duplication	NM_001166108.2(PALLD):c.3358+7_3358+8dup	Pancreatic adenocarcinoma [RCV001414878]	likely benign	4	168925084	168925085	Human	2	name
28882133	CV890391	single nucleotide variant	NM_001166108.2(PALLD):c.8G>T (p.Gly3Val)	PALLD-related disorder [RCV003938516]\|Pancreatic cancer, susceptibility to, 1 [RCV001149845]\|not specified [RCV004032775]	benign\|likely benign	4	168511512	168511512	Human	1	name , alternate_id
38456247	CV943897	microsatellite	NM_001166108.2(PALLD):c.1965-12581GCC[2]	Pancreatic adenocarcinoma [RCV001228288]	uncertain significance	4	168878341	168878343	Human		name
126726090	CV990016	microsatellite	NM_001166108.2(PALLD):c.1965-12785CTC[2]	Pancreatic adenocarcinoma [RCV001302783]	uncertain significance	4	168878137	168878139	Human		name
155667337	CV1789441	single nucleotide variant	NM_001166108.2(PALLD):c.114G>A (p.Glu38=)	not specified [RCV004049596]	likely benign	4	168511618	168511618	Human		name
155732811	CV1826500	single nucleotide variant	NM_001166108.2(PALLD):c.135G>A (p.Leu45=)	not specified [RCV004058834]	likely benign	4	168511639	168511639	Human		name
155689114	CV1826642	single nucleotide variant	NM_001166108.2(PALLD):c.141G>C (p.Arg47=)	not specified [RCV004057234]	likely benign	4	168511645	168511645	Human		name
155719082	CV1827880	single nucleotide variant	NM_001166108.2(PALLD):c.159C>G (p.Ser53=)	not specified [RCV004057399]	likely benign	4	168511663	168511663	Human		name
155719115	CV1827886	single nucleotide variant	NM_001166108.2(PALLD):c.159C>T (p.Ser53=)	PALLD-related disorder [RCV003896171]\|not specified [RCV004057400]	likely benign	4	168511663	168511663	Human	1	name , alternate_id
155738008	CV1831852	single nucleotide variant	NM_001166108.2(PALLD):c.180G>A (p.Ser60=)	not specified [RCV004059316]	likely benign	4	168511684	168511684	Human		name
155709665	CV1832697	single nucleotide variant	NM_001166108.2(PALLD):c.138C>T (p.Ala46=)	not specified [RCV004057076]	likely benign	4	168511642	168511642	Human		name
155720324	CV1835767	single nucleotide variant	NM_001166108.2(PALLD):c.129T>C (p.Leu43=)	not specified [RCV004058241]	likely benign	4	168511633	168511633	Human		name
155745139	CV1838025	single nucleotide variant	NM_001166108.2(PALLD):c.168A>G (p.Glu56=)	not specified [RCV004059923]	likely benign	4	168511672	168511672	Human		name
155703325	CV1838433	single nucleotide variant	NM_001166108.2(PALLD):c.105C>T (p.Ser35=)	not specified [RCV004061394]	likely benign	4	168511609	168511609	Human		name
155720888	CV1840599	single nucleotide variant	NM_001166108.2(PALLD):c.216T>G (p.Pro72=)	not specified [RCV004061105]	likely benign	4	168511720	168511720	Human		name
155705628	CV1841095	single nucleotide variant	NM_001166108.2(PALLD):c.108G>A (p.Gln36=)	not specified [RCV004062528]	likely benign	4	168511612	168511612	Human		name
155685973	CV1841332	single nucleotide variant	NM_001166108.2(PALLD):c.237T>G (p.Pro79=)	not specified [RCV004063357]	likely benign	4	168511741	168511741	Human		name
155726347	CV1841601	single nucleotide variant	NM_001166108.2(PALLD):c.23A>T (p.Glu8Val)	not specified [RCV004063404]	uncertain significance	4	168511527	168511527	Human		name
155678307	CV1841819	single nucleotide variant	NM_001166108.2(PALLD):c.24G>C (p.Glu8Asp)	not specified [RCV004062017]	likely benign	4	168511528	168511528	Human		name
155733476	CV1842629	single nucleotide variant	NM_001166108.2(PALLD):c.189G>A (p.Glu63=)	not specified [RCV004060755]	likely benign	4	168511693	168511693	Human		name
155716694	CV1844742	single nucleotide variant	NM_001166108.2(PALLD):c.234T>C (p.His78=)	not specified [RCV004063246]	likely benign	4	168511738	168511738	Human		name
155669435	CV1845624	single nucleotide variant	NM_001166108.2(PALLD):c.258G>A (p.Leu86=)	not specified [RCV004062846]	likely benign	4	168511762	168511762	Human		name
155668407	CV1846595	single nucleotide variant	NM_001166108.2(PALLD):c.201T>A (p.Ile67=)	not specified [RCV004059517]	likely benign	4	168511705	168511705	Human		name
155748130	CV1846835	single nucleotide variant	NM_001166108.2(PALLD):c.210T>C (p.Thr70=)	not specified [RCV004060364]	likely benign	4	168511714	168511714	Human		name
155714726	CV1849254	single nucleotide variant	NM_001166108.2(PALLD):c.270C>T (p.Ala90=)	not specified [RCV004063718]	likely benign	4	168511774	168511774	Human		name
155689324	CV1850521	single nucleotide variant	NM_001166108.2(PALLD):c.219A>C (p.Ala73=)	not specified [RCV004061201]	likely benign	4	168511723	168511723	Human		name
155689859	CV1850600	single nucleotide variant	NM_001166108.2(PALLD):c.21T>A (p.His7Gln)	not specified [RCV004061215]	uncertain significance	4	168511525	168511525	Human		name
155726850	CV1851217	single nucleotide variant	NM_001166108.2(PALLD):c.240C>T (p.Ser80=)	not specified [RCV004063439]	likely benign	4	168511744	168511744	Human		name
155678600	CV1851705	single nucleotide variant	NM_001166108.2(PALLD):c.252C>T (p.Thr84=)	not specified [RCV004062109]	likely benign	4	168511756	168511756	Human		name
155703775	CV1852402	single nucleotide variant	NM_001166108.2(PALLD):c.267C>T (p.His89=)	not specified [RCV004063623]	likely benign	4	168511771	168511771	Human		name
155680037	CV1853148	single nucleotide variant	NM_001166108.2(PALLD):c.276G>A (p.Arg92=)	not specified [RCV004064176]	likely benign	4	168511780	168511780	Human		name
155678891	CV1854077	single nucleotide variant	NM_001166108.2(PALLD):c.273G>A (p.Ser91=)	not specified [RCV004064071]	likely benign	4	168511777	168511777	Human		name
155666058	CV1855508	single nucleotide variant	NM_001166108.2(PALLD):c.285G>A (p.Gln95=)	not specified [RCV004062443]	likely benign	4	168511789	168511789	Human		name
329364444	CV2425725	single nucleotide variant	NM_001166108.2(PALLD):c.180G>C (p.Ser60=)	not specified [RCV004243125]	likely benign	4	168511684	168511684	Human		name
329363570	CV2425737	single nucleotide variant	NM_001166108.2(PALLD):c.11C>T (p.Thr4Ile)	not specified [RCV004243137]	uncertain significance	4	168511515	168511515	Human		name
329358409	CV2432278	single nucleotide variant	NM_001166108.2(PALLD):c.153C>T (p.Ala51=)	not specified [RCV004247319]	likely benign	4	168511657	168511657	Human		name
329390005	CV2465687	single nucleotide variant	NM_001166108.2(PALLD):c.14C>A (p.Ser5Tyr)	not specified [RCV004281512]	uncertain significance	4	168511518	168511518	Human		name
401765682	CV2724442	single nucleotide variant	NM_001166108.2(PALLD):c.216T>C (p.Pro72=)	not specified [RCV004331282]	likely benign	4	168511720	168511720	Human		name
401765736	CV2724463	single nucleotide variant	NM_001166108.2(PALLD):c.147C>T (p.Ala49=)	not specified [RCV004331303]	likely benign	4	168511651	168511651	Human		name
401886187	CV2790343	single nucleotide variant	NM_001166108.2(PALLD):c.256T>C (p.Leu86=)	not specified [RCV004364372]	likely benign	4	168511760	168511760	Human		name
11632897	CV292731	single nucleotide variant	NM_001166108.2(PALLD):c.186G>A (p.Lys62=)	Pancreatic adenocarcinoma [RCV002520225]\|Pancreatic cancer, susceptibility to, 1 [RCV000295176]\|not provided [RCV000874562]\|not specified [RCV000454887]	benign	4	168511690	168511690	Human	3	name
11633012	CV294120	insertion	NM_001166108.2(PALLD):c.1786_1787insATT	Carcinoma of pancreas [RCV000303576]	uncertain significance	4	168927966	168927967	Human	1	name
405257389	CV3194337	single nucleotide variant	NM_001166108.2(PALLD):c.159C>A (p.Ser53=)	PALLD-related disorder [RCV003892236]	likely benign	4	168511663	168511663	Human		name , trait , alternate_id
405757253	CV3367713	single nucleotide variant	NM_001166108.2(PALLD):c.14C>T (p.Ser5Phe)	not specified [RCV004500033]	uncertain significance	4	168511518	168511518	Human		name
405707361	CV3384169	single nucleotide variant	NM_001166108.2(PALLD):c.138C>A (p.Ala46=)	not specified [RCV004521913]	likely benign	4	168511642	168511642	Human		name
405707368	CV3384170	single nucleotide variant	NM_001166108.2(PALLD):c.139C>A (p.Arg47=)	not specified [RCV004521914]	likely benign	4	168511643	168511643	Human		name
405707525	CV3384195	single nucleotide variant	NM_001166108.2(PALLD):c.195G>T (p.Ser65=)	not specified [RCV004521937]	likely benign	4	168511699	168511699	Human		name
405708452	CV3384228	single nucleotide variant	NM_001166108.2(PALLD):c.288T>C (p.Asp96=)	not specified [RCV004521965]	likely benign	4	168511792	168511792	Human		name
407517735	CV3470209	single nucleotide variant	NM_001166108.2(PALLD):c.213T>C (p.Ser71=)	not specified [RCV004650763]	likely benign	4	168511717	168511717	Human		name
597696121	CV3574772	single nucleotide variant	NM_001166108.2(PALLD):c.216T>A (p.Pro72=)	not specified [RCV004839196]	likely benign	4	168511720	168511720	Human		name
597696586	CV3574810	single nucleotide variant	NM_001166108.2(PALLD):c.207T>C (p.Ser69=)	not specified [RCV004839227]	likely benign	4	168511711	168511711	Human		name
597657379	CV3574813	single nucleotide variant	NM_001166108.2(PALLD):c.111A>G (p.Glu37=)	not specified [RCV004827619]	likely benign	4	168511615	168511615	Human		name
597715190	CV3574845	single nucleotide variant	NM_001166108.2(PALLD):c.24G>T (p.Glu8Asp)	not specified [RCV004841311]	likely benign	4	168511528	168511528	Human		name
597715427	CV3574877	single nucleotide variant	NM_001166108.2(PALLD):c.123G>A (p.Lys41=)	not specified [RCV004841334]	likely benign	4	168511627	168511627	Human		name
28882142	CV890393	single nucleotide variant	NM_001166108.2(PALLD):c.195G>A (p.Ser65=)	Pancreatic cancer, susceptibility to, 1 [RCV001149847]\|not provided [RCV003438682]\|not specified [RCV004032776]	benign\|likely benign	4	168511699	168511699	Human	1	name
28882151	CV890394	single nucleotide variant	NM_001166108.2(PALLD):c.222C>T (p.Ser74=)	Pancreatic cancer, susceptibility to, 1 [RCV001149848]\|not specified [RCV004032777]	likely benign\|uncertain significance	4	168511726	168511726	Human	1	name
150475993	CV1279167	deletion	NM_001166108.2(PALLD):c.-82-107_-82-106del	not provided [RCV001713920]	benign	4	168511316	168511317	Human		name
152145337	CV1543264	deletion	NM_001166108.2(PALLD):c.2101-11_2101-10del	Pancreatic adenocarcinoma [RCV002178638]	likely benign	4	168894568	168894569	Human	2	name
155732324	CV1785714	single nucleotide variant	NM_001166108.2(PALLD):c.336T>C (p.Ser112=)	not specified [RCV004047856]	likely benign	4	168511840	168511840	Human		name
155686722	CV1787265	single nucleotide variant	NM_001166108.2(PALLD):c.390G>A (p.Arg130=)	not specified [RCV004050380]	likely benign	4	168511894	168511894	Human		name
155704292	CV1787568	single nucleotide variant	NM_001166108.2(PALLD):c.408C>T (p.Ser136=)	not specified [RCV004051300]	likely benign	4	168511912	168511912	Human		name
155701216	CV1788255	single nucleotide variant	NM_001166108.2(PALLD):c.318A>G (p.Ala106=)	not specified [RCV004048878]	likely benign	4	168511822	168511822	Human		name
155667823	CV1789529	single nucleotide variant	NM_001166108.2(PALLD):c.366T>C (p.Pro122=)	not specified [RCV004049624]	likely benign	4	168511870	168511870	Human		name
155696234	CV1790659	single nucleotide variant	NM_001166108.2(PALLD):c.405G>A (p.Arg135=)	not specified [RCV004051232]	likely benign	4	168511909	168511909	Human		name
155741473	CV1790813	single nucleotide variant	NM_001166108.2(PALLD):c.417G>A (p.Lys139=)	not specified [RCV004051845]	likely benign	4	168511921	168511921	Human		name
155726503	CV1791081	single nucleotide variant	NM_001166108.2(PALLD):c.420T>G (p.Ala140=)	not specified [RCV004051899]	likely benign	4	168511924	168511924	Human		name
155721206	CV1793399	single nucleotide variant	NM_001166108.2(PALLD):c.37T>C (p.Ser13Pro)	not specified [RCV004048115]	uncertain significance	4	168511541	168511541	Human		name
155685617	CV1793402	single nucleotide variant	NM_001166108.2(PALLD):c.37T>G (p.Ser13Ala)	not specified [RCV004048118]	uncertain significance	4	168511541	168511541	Human		name
155686056	CV1793588	single nucleotide variant	NM_001166108.2(PALLD):c.381G>A (p.Leu127=)	not specified [RCV004048152]	likely benign	4	168511885	168511885	Human		name
155695576	CV1793860	single nucleotide variant	NM_001166108.2(PALLD):c.399C>T (p.Tyr133=)	not specified [RCV004050564]	likely benign	4	168511903	168511903	Human		name
155739222	CV1794231	single nucleotide variant	NM_001166108.2(PALLD):c.432T>G (p.Gly144=)	not specified [RCV004050006]	likely benign	4	168511936	168511936	Human		name
155739858	CV1794429	single nucleotide variant	NM_001166108.2(PALLD):c.435A>G (p.Ala145=)	not specified [RCV004050052]	likely benign	4	168511939	168511939	Human		name
155717558	CV1795744	single nucleotide variant	NM_001166108.2(PALLD):c.342T>C (p.Ser114=)	not specified [RCV004048515]	likely benign	4	168511846	168511846	Human		name
155695382	CV1795955	single nucleotide variant	NM_001166108.2(PALLD):c.357G>A (p.Lys119=)	not specified [RCV004049171]	likely benign	4	168511861	168511861	Human		name
155696229	CV1797125	single nucleotide variant	NM_001166108.2(PALLD):c.396C>T (p.Ser132=)	not specified [RCV004050502]	likely benign	4	168511900	168511900	Human		name
155741004	CV1797462	single nucleotide variant	NM_001166108.2(PALLD):c.414A>G (p.Arg138=)	not specified [RCV004051774]	likely benign	4	168511918	168511918	Human		name
155727801	CV1798175	single nucleotide variant	NM_001166108.2(PALLD):c.444C>T (p.Pro148=)	not specified [RCV004050719]	likely benign	4	168511948	168511948	Human		name
155707503	CV1798663	single nucleotide variant	NM_001166108.2(PALLD):c.468G>A (p.Thr156=)	not specified [RCV004051985]	likely benign	4	168511972	168511972	Human		name
155734691	CV1799069	single nucleotide variant	NM_001166108.2(PALLD):c.492C>T (p.Pro164=)	not specified [RCV004050238]	likely benign	4	168511996	168511996	Human		name
155726034	CV1799627	single nucleotide variant	NM_001166108.2(PALLD):c.51G>T (p.Met17Ile)	not specified [RCV004051689]	uncertain significance	4	168511555	168511555	Human		name
155672443	CV1801031	single nucleotide variant	NM_001166108.2(PALLD):c.627T>C (p.Asn209=)	not specified [RCV004053481]	likely benign	4	168512131	168512131	Human		name
155683446	CV1801380	single nucleotide variant	NM_001166108.2(PALLD):c.633G>A (p.Pro211=)	not specified [RCV004053862]	likely benign	4	168512137	168512137	Human		name
155733450	CV1802055	single nucleotide variant	NM_001166108.2(PALLD):c.486T>C (p.Gly162=)	not specified [RCV004050131]	likely benign	4	168511990	168511990	Human		name
155734256	CV1802243	single nucleotide variant	NM_001166108.2(PALLD):c.489C>G (p.Gly163=)	not specified [RCV004050174]	likely benign	4	168511993	168511993	Human		name
155713363	CV1802442	single nucleotide variant	NM_001166108.2(PALLD):c.510C>T (p.Asp170=)	not specified [RCV004051026]	likely benign	4	168512014	168512014	Human		name
155745269	CV1802743	single nucleotide variant	NM_001166108.2(PALLD):c.534G>A (p.Glu178=)	not specified [RCV004052439]	likely benign	4	168512038	168512038	Human		name
155688258	CV1803821	single nucleotide variant	NM_001166108.2(PALLD):c.594G>A (p.Ser198=)	PALLD-related disorder [RCV003933758]\|not specified [RCV004052483]	likely benign	4	168512098	168512098	Human	1	name , alternate_id
155665600	CV1804149	single nucleotide variant	NM_001166108.2(PALLD):c.621T>C (p.Pro207=)	not specified [RCV004053413]	likely benign	4	168512125	168512125	Human		name
155744883	CV1806359	single nucleotide variant	NM_001166108.2(PALLD):c.531G>A (p.Glu177=)	not specified [RCV004052391]	likely benign	4	168512035	168512035	Human		name
155676444	CV1806524	single nucleotide variant	NM_001166108.2(PALLD):c.555C>A (p.Ala185=)	not specified [RCV004053231]	likely benign	4	168512059	168512059	Human		name
155676499	CV1806533	single nucleotide variant	NM_001166108.2(PALLD):c.555C>T (p.Ala185=)	not specified [RCV004053233]	likely benign	4	168512059	168512059	Human		name
155681093	CV1807617	single nucleotide variant	NM_001166108.2(PALLD):c.615G>A (p.Leu205=)	not specified [RCV004053337]	likely benign	4	168512119	168512119	Human		name
155711899	CV1807915	single nucleotide variant	NM_001166108.2(PALLD):c.643C>T (p.Leu215=)	not specified [RCV004053991]	likely benign	4	168512147	168512147	Human		name
155712845	CV1808028	single nucleotide variant	NM_001166108.2(PALLD):c.645G>A (p.Leu215=)	not specified [RCV004054013]	likely benign	4	168512149	168512149	Human		name
155719300	CV1809099	single nucleotide variant	NM_001166108.2(PALLD):c.477A>G (p.Gln159=)	not specified [RCV004052108]	likely benign	4	168511981	168511981	Human		name
155740507	CV1809433	single nucleotide variant	NM_001166108.2(PALLD):c.49A>C (p.Met17Leu)	not specified [RCV004050865]	uncertain significance	4	168511553	168511553	Human		name
155740516	CV1809437	single nucleotide variant	NM_001166108.2(PALLD):c.49A>G (p.Met17Val)	not specified [RCV004050866]	likely benign	4	168511553	168511553	Human		name
155715436	CV1812223	single nucleotide variant	NM_001166108.2(PALLD):c.68A>G (p.Asn23Ser)	not specified [RCV004052940]	uncertain significance	4	168511572	168511572	Human		name
155680921	CV1812747	single nucleotide variant	NM_001166108.2(PALLD):c.723T>C (p.His241=)	not specified [RCV004055802]	likely benign	4	168512227	168512227	Human		name
155728747	CV1813028	single nucleotide variant	NM_001166108.2(PALLD):c.729C>T (p.Tyr243=)	not specified [RCV004055854]	likely benign	4	168512233	168512233	Human		name
155707630	CV1813479	single nucleotide variant	NM_001166108.2(PALLD):c.762C>T (p.Asn254=)	not specified [RCV004056476]	likely benign	4	168512266	168512266	Human		name
155747474	CV1813697	single nucleotide variant	NM_001166108.2(PALLD):c.795C>G (p.Leu265=)	not provided [RCV003434478]\|not specified [RCV004054809]	likely benign	4	168512299	168512299	Human		name
155730216	CV1814132	single nucleotide variant	NM_001166108.2(PALLD):c.834G>A (p.Arg278=)	not specified [RCV004056066]	likely benign	4	168512338	168512338	Human		name
155689193	CV1814431	single nucleotide variant	NM_001166108.2(PALLD):c.876T>C (p.Cys292=)	not specified [RCV004056700]	likely benign	4	168512380	168512380	Human		name
155682075	CV1814799	single nucleotide variant	NM_001166108.2(PALLD):c.921A>G (p.Glu307=)	not specified [RCV004055603]	likely benign	4	168668202	168668202	Human		name
155682705	CV1814898	single nucleotide variant	NM_001166108.2(PALLD):c.924G>A (p.Gly308=)	not specified [RCV004055633]	likely benign	4	168668205	168668205	Human		name
155706694	CV1815278	single nucleotide variant	NM_001166108.2(PALLD):c.684G>A (p.Gly228=)	not specified [RCV004052879]	likely benign	4	168512188	168512188	Human		name
155714962	CV1815424	single nucleotide variant	NM_001166108.2(PALLD):c.687G>A (p.Glu229=)	not specified [RCV004052907]	likely benign	4	168512191	168512191	Human		name
155741651	CV1816460	single nucleotide variant	NM_001166108.2(PALLD):c.783C>T (p.Pro261=)	not specified [RCV004054722]	likely benign	4	168512287	168512287	Human		name
155742725	CV1816934	single nucleotide variant	NM_001166108.2(PALLD):c.822C>A (p.Ile274=)	PALLD-related disorder [RCV003943383]\|not specified [RCV004055557]	likely benign	4	168512326	168512326	Human	1	name , alternate_id
155722280	CV1817529	single nucleotide variant	NM_001166108.2(PALLD):c.870G>A (p.Leu290=)	not specified [RCV004056657]	likely benign	4	168512374	168512374	Human		name
155688465	CV1817628	single nucleotide variant	NM_001166108.2(PALLD):c.873G>A (p.Glu291=)	not specified [RCV004056675]	likely benign	4	168512377	168512377	Human		name
155668582	CV1818206	single nucleotide variant	NM_001166108.2(PALLD):c.960C>T (p.His320=)	not specified [RCV004056951]	likely benign	4	168668241	168668241	Human		name
155677035	CV1818789	single nucleotide variant	NM_001166108.2(PALLD):c.67A>G (p.Asn23Asp)	not specified [RCV004052820]	uncertain significance	4	168511571	168511571	Human		name
155669999	CV1819082	single nucleotide variant	NM_001166108.2(PALLD):c.708C>T (p.Ser236=)	not specified [RCV004055231]	likely benign	4	168512212	168512212	Human		name
155708583	CV1819279	single nucleotide variant	NM_001166108.2(PALLD):c.711T>G (p.Pro237=)	not specified [RCV004055278]	likely benign	4	168512215	168512215	Human		name
155718331	CV1819352	single nucleotide variant	NM_001166108.2(PALLD):c.738C>T (p.Asn246=)	not specified [RCV004055967]	likely benign	4	168512242	168512242	Human		name
155737590	CV1820008	single nucleotide variant	NM_001166108.2(PALLD):c.777A>T (p.Pro259=)	not specified [RCV004054671]	likely benign	4	168512281	168512281	Human		name
155697772	CV1820514	single nucleotide variant	NM_001166108.2(PALLD):c.819C>T (p.Phe273=)	not specified [RCV004055531]	likely benign	4	168512323	168512323	Human		name
155714451	CV1820802	single nucleotide variant	NM_001166108.2(PALLD):c.858C>T (p.Ser286=)	not specified [RCV004056529]	likely benign	4	168512362	168512362	Human		name
155715013	CV1820913	single nucleotide variant	NM_001166108.2(PALLD):c.861A>G (p.Arg287=)	not specified [RCV004056556]	likely benign	4	168512365	168512365	Human		name
155691503	CV1821381	single nucleotide variant	NM_001166108.2(PALLD):c.945T>A (p.Pro315=)	not specified [RCV004056831]	likely benign	4	168668226	168668226	Human		name
155668060	CV1821864	single nucleotide variant	NM_001166108.2(PALLD):c.666C>T (p.Ser222=)	not specified [RCV004054532]	likely benign	4	168512170	168512170	Human		name
155708189	CV1822578	single nucleotide variant	NM_001166108.2(PALLD):c.702C>G (p.Val234=)	not specified [RCV004055161]	likely benign	4	168512206	168512206	Human		name
155666330	CV1823621	single nucleotide variant	NM_001166108.2(PALLD):c.801C>T (p.Phe267=)	not specified [RCV004055384]	likely benign	4	168512305	168512305	Human		name
155699652	CV1824705	single nucleotide variant	NM_001166108.2(PALLD):c.894C>G (p.Pro298=)	not specified [RCV004054886]	likely benign	4	168512398	168512398	Human		name
155699670	CV1824710	single nucleotide variant	NM_001166108.2(PALLD):c.894C>T (p.Pro298=)	not specified [RCV004054888]	likely benign	4	168512398	168512398	Human		name
155684405	CV1824870	single nucleotide variant	NM_001166108.2(PALLD):c.933G>A (p.Leu311=)	not specified [RCV004055698]	likely benign	4	168668214	168668214	Human		name
155684597	CV1824943	single nucleotide variant	NM_001166108.2(PALLD):c.936C>T (p.His312=)	not specified [RCV004055711]	likely benign	4	168668217	168668217	Human		name
155672954	CV1825442	single nucleotide variant	NM_001166108.2(PALLD):c.972G>A (p.Gly324=)	not specified [RCV004057558]	likely benign	4	168668253	168668253	Human		name
155703359	CV1825626	single nucleotide variant	NM_001166108.2(PALLD):c.978C>G (p.Leu326=)	not specified [RCV004057605]	likely benign	4	168668259	168668259	Human		name
155730210	CV1825752	single nucleotide variant	NM_001166108.2(PALLD):c.996A>G (p.Ala332=)	not specified [RCV004057726]	likely benign	4	168668277	168668277	Human		name
155730857	CV1825857	single nucleotide variant	NM_001166108.2(PALLD):c.999G>A (p.Glu333=)	not specified [RCV004057748]	likely benign	4	168668280	168668280	Human		name
155675052	CV1828888	single nucleotide variant	NM_001166108.2(PALLD):c.987G>T (p.Leu329=)	not specified [RCV004057674]	likely benign	4	168668268	168668268	Human		name
155729085	CV1828982	single nucleotide variant	NM_001166108.2(PALLD):c.990C>T (p.Ile330=)	not specified [RCV004057698]	likely benign	4	168668271	168668271	Human		name
155698490	CV1855071	single nucleotide variant	NM_001166108.2(PALLD):c.306C>T (p.Val102=)	not specified [RCV004066430]	likely benign	4	168511810	168511810	Human		name
329358114	CV2422342	single nucleotide variant	NM_001166108.2(PALLD):c.535C>T (p.Leu179=)	not specified [RCV004247294]	likely benign	4	168512039	168512039	Human		name
329383548	CV2422348	single nucleotide variant	NM_001166108.2(PALLD):c.918T>C (p.Cys306=)	PALLD-related disorder [RCV003900976]\|not specified [RCV004247295]	likely benign	4	168668199	168668199	Human	1	name , alternate_id
329383650	CV2422435	single nucleotide variant	NM_001166108.2(PALLD):c.441T>A (p.Thr147=)	not specified [RCV004247308]	likely benign	4	168511945	168511945	Human		name
329383666	CV2422442	single nucleotide variant	NM_001166108.2(PALLD):c.942T>A (p.Thr314=)	not specified [RCV004247309]	likely benign	4	168668223	168668223	Human		name
329364429	CV2425717	single nucleotide variant	NM_001166108.2(PALLD):c.798C>T (p.His266=)	not specified [RCV004243117]	likely benign	4	168512302	168512302	Human		name
329364431	CV2425718	single nucleotide variant	NM_001166108.2(PALLD):c.95C>G (p.Ala32Gly)	not specified [RCV004243118]	uncertain significance	4	168511599	168511599	Human		name
329364474	CV2425740	single nucleotide variant	NM_001166108.2(PALLD):c.699G>A (p.Glu233=)	not specified [RCV004243140]	likely benign	4	168512203	168512203	Human		name
329364513	CV2425767	single nucleotide variant	NM_001166108.2(PALLD):c.942T>G (p.Thr314=)	not specified [RCV004243167]	likely benign	4	168668223	168668223	Human		name
329364524	CV2425775	single nucleotide variant	NM_001166108.2(PALLD):c.594G>C (p.Ser198=)	not specified [RCV004243175]	likely benign	4	168512098	168512098	Human		name
329364531	CV2425780	single nucleotide variant	NM_001166108.2(PALLD):c.456A>G (p.Val152=)	not specified [RCV004243180]	likely benign	4	168511960	168511960	Human		name
329358345	CV2432241	single nucleotide variant	NM_001166108.2(PALLD):c.993A>T (p.Ile331=)	not specified [RCV004247315]	likely benign	4	168668274	168668274	Human		name
329383806	CV2432307	single nucleotide variant	NM_001166108.2(PALLD):c.50T>C (p.Met17Thr)	not specified [RCV004247323]	uncertain significance	4	168511554	168511554	Human		name
329389957	CV2465662	single nucleotide variant	NM_001166108.2(PALLD):c.759C>T (p.His253=)	not specified [RCV004281487]	likely benign	4	168512263	168512263	Human		name
329389962	CV2465665	single nucleotide variant	NM_001166108.2(PALLD):c.855G>C (p.Gly285=)	not specified [RCV004281490]	likely benign	4	168512359	168512359	Human		name
401775151	CV2724003	single nucleotide variant	NM_001166108.2(PALLD):c.972G>T (p.Gly324=)	not specified [RCV004326150]	likely benign	4	168668253	168668253	Human		name
401765708	CV2724452	single nucleotide variant	NM_001166108.2(PALLD):c.38C>A (p.Ser13Tyr)	not specified [RCV004331292]	uncertain significance	4	168511542	168511542	Human		name
401765754	CV2724470	single nucleotide variant	NM_001166108.2(PALLD):c.945T>C (p.Pro315=)	not specified [RCV004331310]	likely benign	4	168668226	168668226	Human		name
401868746	CV2787550	single nucleotide variant	NM_001166108.2(PALLD):c.978C>T (p.Leu326=)	not specified [RCV004366321]	likely benign	4	168668259	168668259	Human		name
401886199	CV2790347	single nucleotide variant	NM_001166108.2(PALLD):c.456A>C (p.Val152=)	not specified [RCV004364374]	likely benign	4	168511960	168511960	Human		name
11634002	CV292729	single nucleotide variant	NM_001166108.2(PALLD):c.65A>G (p.Lys22Arg)	Pancreatic cancer, susceptibility to, 1 [RCV000389359]\|not specified [RCV004021944]	benign\|likely benign\|uncertain significance	4	168511569	168511569	Human	1	name
11634060	CV292738	single nucleotide variant	NM_001166108.2(PALLD):c.366T>G (p.Pro122=)	Pancreatic cancer, susceptibility to, 1 [RCV000394421]\|not specified [RCV004021946]	likely benign	4	168511870	168511870	Human	1	name
11632998	CV297625	single nucleotide variant	NM_001166108.2(PALLD):c.678C>T (p.Asp226=)	Pancreatic adenocarcinoma [RCV002523467]\|Pancreatic cancer, susceptibility to, 1 [RCV000305338]\|not provided [RCV000874563]\|not specified [RCV000454895]	benign	4	168512182	168512182	Human	3	name
11633039	CV297634	single nucleotide variant	NM_001166108.2(PALLD):c.789C>T (p.Ser263=)	Pancreatic cancer, susceptibility to, 1 [RCV000306330]\|not provided [RCV000874572]\|not specified [RCV004021948]	benign	4	168512293	168512293	Human	1	name
405134230	CV3163963	deletion	NM_001166108.2(PALLD):c.3225-16_3225-15del	Pancreatic adenocarcinoma [RCV003854951]	likely benign	4	168924928	168924929	Human	2	name
405278830	CV3212698	single nucleotide variant	NM_001166108.2(PALLD):c.822C>T (p.Ile274=)	PALLD-related disorder [RCV003954724]\|not specified [RCV004369860]	likely benign	4	168512326	168512326	Human	1	name , alternate_id
405757340	CV3367724	single nucleotide variant	NM_001166108.2(PALLD):c.91T>C (p.Ser31Pro)	not specified [RCV004500044]	uncertain significance	4	168511595	168511595	Human		name
405707638	CV3384245	single nucleotide variant	NM_001166108.2(PALLD):c.351T>G (p.Val117=)	not specified [RCV004521978]	likely benign	4	168511855	168511855	Human		name
405707647	CV3384246	single nucleotide variant	NM_001166108.2(PALLD):c.366T>A (p.Pro122=)	not specified [RCV004521979]	likely benign	4	168511870	168511870	Human		name
405707677	CV3384251	single nucleotide variant	NM_001166108.2(PALLD):c.438A>G (p.Lys146=)	not specified [RCV004521983]	likely benign	4	168511942	168511942	Human		name
405707703	CV3384255	single nucleotide variant	NM_001166108.2(PALLD):c.48C>A (p.Asp16Glu)	not specified [RCV004521987]	uncertain significance	4	168511552	168511552	Human		name
405707727	CV3384258	single nucleotide variant	NM_001166108.2(PALLD):c.504G>A (p.Leu168=)	not specified [RCV004521990]	likely benign	4	168512008	168512008	Human		name
405707748	CV3384261	single nucleotide variant	NM_001166108.2(PALLD):c.564A>G (p.Pro188=)	not specified [RCV004521993]	likely benign	4	168512068	168512068	Human		name
405707763	CV3384263	single nucleotide variant	NM_001166108.2(PALLD):c.579A>G (p.Pro193=)	not specified [RCV004521995]	likely benign	4	168512083	168512083	Human		name
405707776	CV3384265	single nucleotide variant	NM_001166108.2(PALLD):c.582T>C (p.Asn194=)	not specified [RCV004521997]	likely benign	4	168512086	168512086	Human		name
405707783	CV3384266	single nucleotide variant	NM_001166108.2(PALLD):c.615G>C (p.Leu205=)	not specified [RCV004521998]	likely benign	4	168512119	168512119	Human		name
405707834	CV3384273	single nucleotide variant	NM_001166108.2(PALLD):c.765C>G (p.Arg255=)	not specified [RCV004522005]	likely benign	4	168512269	168512269	Human		name
405707876	CV3384281	single nucleotide variant	NM_001166108.2(PALLD):c.954A>G (p.Gln318=)	not specified [RCV004522011]	likely benign	4	168668235	168668235	Human		name
405707889	CV3384283	single nucleotide variant	NM_001166108.2(PALLD):c.984C>T (p.Thr328=)	not specified [RCV004522013]	likely benign	4	168668265	168668265	Human		name
407479095	CV3470190	single nucleotide variant	NM_001166108.2(PALLD):c.83C>A (p.Pro28Gln)	not specified [RCV004664052]	uncertain significance	4	168511587	168511587	Human		name
407517729	CV3470207	single nucleotide variant	NM_001166108.2(PALLD):c.711T>C (p.Pro237=)	not specified [RCV004650761]	likely benign	4	168512215	168512215	Human		name
407479136	CV3470212	single nucleotide variant	NM_001166108.2(PALLD):c.68A>C (p.Asn23Thr)	not specified [RCV004664061]	uncertain significance	4	168511572	168511572	Human		name
407479185	CV3470233	single nucleotide variant	NM_001166108.2(PALLD):c.79T>C (p.Phe27Leu)	not specified [RCV004664073]	uncertain significance	4	168511583	168511583	Human		name
407479194	CV3470235	single nucleotide variant	NM_001166108.2(PALLD):c.486T>A (p.Gly162=)	not specified [RCV004664075]	likely benign	4	168511990	168511990	Human		name
407479234	CV3470248	single nucleotide variant	NM_001166108.2(PALLD):c.423A>G (p.Glu141=)	not specified [RCV004664084]	likely benign	4	168511927	168511927	Human		name
407479274	CV3470270	single nucleotide variant	NM_001166108.2(PALLD):c.744C>T (p.Asp248=)	not specified [RCV004664093]	likely benign	4	168512248	168512248	Human		name
407517837	CV3470279	single nucleotide variant	NM_001166108.2(PALLD):c.561G>A (p.Lys187=)	not specified [RCV004650798]	likely benign	4	168512065	168512065	Human		name
407479282	CV3470282	single nucleotide variant	NM_001166108.2(PALLD):c.640C>T (p.Leu214=)	not specified [RCV004664095]	likely benign	4	168512144	168512144	Human		name
597657318	CV3574756	single nucleotide variant	NM_001166108.2(PALLD):c.363A>G (p.Lys121=)	not specified [RCV004827610]	likely benign	4	168511867	168511867	Human		name
597695998	CV3574757	single nucleotide variant	NM_001166108.2(PALLD):c.981T>C (p.His327=)	not specified [RCV004839182]	likely benign	4	168668262	168668262	Human		name
597657324	CV3574759	single nucleotide variant	NM_001166108.2(PALLD):c.639C>T (p.Ala213=)	not specified [RCV004827611]	likely benign	4	168512143	168512143	Human		name
597696386	CV3574783	single nucleotide variant	NM_001166108.2(PALLD):c.82C>T (p.Pro28Ser)	not specified [RCV004839204]	uncertain significance	4	168511586	168511586	Human		name
597657359	CV3574794	single nucleotide variant	NM_001166108.2(PALLD):c.474T>C (p.His158=)	not specified [RCV004827616]	likely benign	4	168511978	168511978	Human		name
597715144	CV3574838	single nucleotide variant	NM_001166108.2(PALLD):c.987G>C (p.Leu329=)	not specified [RCV004841307]	likely benign	4	168668268	168668268	Human		name
597657425	CV3574841	single nucleotide variant	NM_001166108.2(PALLD):c.612C>T (p.Tyr204=)	not specified [RCV004827625]	likely benign	4	168512116	168512116	Human		name
597715311	CV3574861	single nucleotide variant	NM_001166108.2(PALLD):c.339C>T (p.Ile113=)	not specified [RCV004841323]	likely benign	4	168511843	168511843	Human		name
597715334	CV3574863	single nucleotide variant	NM_001166108.2(PALLD):c.489C>T (p.Gly163=)	not specified [RCV004841325]	likely benign	4	168511993	168511993	Human		name
597715355	CV3574868	single nucleotide variant	NM_001166108.2(PALLD):c.360G>A (p.Arg120=)	not specified [RCV004841327]	likely benign	4	168511864	168511864	Human		name
597715365	CV3574869	single nucleotide variant	NM_001166108.2(PALLD):c.77T>A (p.Phe26Tyr)	not specified [RCV004841328]	uncertain significance	4	168511581	168511581	Human		name
597715397	CV3574873	single nucleotide variant	NM_001166108.2(PALLD):c.924G>C (p.Gly308=)	not specified [RCV004841331]	likely benign	4	168668205	168668205	Human		name
597715573	CV3574892	single nucleotide variant	NM_001166108.2(PALLD):c.810A>G (p.Ala270=)	not specified [RCV004841347]	likely benign	4	168512314	168512314	Human		name
597743108	CV3721374	single nucleotide variant	NM_001166108.2(PALLD):c.34G>A (p.Asp12Asn)	Pancreatic cancer, susceptibility to, 1 [RCV005039054]	uncertain significance	4	168511538	168511538	Human	1	name
597654854	CV3721377	single nucleotide variant	NM_001166108.2(PALLD):c.855G>T (p.Gly285=)	Pancreatic cancer, susceptibility to, 1 [RCV005027301]	uncertain significance	4	168512359	168512359	Human	1	name
28870769	CV890396	single nucleotide variant	NM_001166108.2(PALLD):c.453C>T (p.Asn151=)	PALLD-related disorder [RCV003938503]\|Pancreatic cancer, susceptibility to, 1 [RCV001145509]\|not specified [RCV004032738]	benign\|likely benign	4	168511957	168511957	Human	1	name , alternate_id
28875016	CV890401	single nucleotide variant	NM_001166108.2(PALLD):c.639C>A (p.Ala213=)	Pancreatic cancer, susceptibility to, 1 [RCV001147461]	uncertain significance	4	168512143	168512143	Human	1	name
126910105	CV1037451	single nucleotide variant	NM_001166108.2(PALLD):c.260G>C (p.Gly87Ala)	not provided [RCV001354367]	uncertain significance	4	168511764	168511764	Human		name
127231426	CV1071538	single nucleotide variant	NM_001166108.2(PALLD):c.1986T>C (p.Ser662=)	Pancreatic adenocarcinoma [RCV001413105]\|not specified [RCV004038101]	likely benign	4	168890943	168890943	Human	2	name
127257279	CV1071539	single nucleotide variant	NM_001166108.2(PALLD):c.2007C>T (p.Ser669=)	Pancreatic adenocarcinoma [RCV001401418]\|not specified [RCV004037822]	likely benign	4	168890964	168890964	Human	2	name
127230826	CV1071540	single nucleotide variant	NM_001166108.2(PALLD):c.2625C>T (p.Gly875=)	Pancreatic adenocarcinoma [RCV001412747]\|not specified [RCV004038096]	likely benign	4	168913929	168913929	Human	2	name
127244283	CV1093135	single nucleotide variant	NM_001166108.2(PALLD):c.2133A>G (p.Arg711=)	Pancreatic adenocarcinoma [RCV001434992]\|not specified [RCV005385095]	likely benign	4	168894611	168894611	Human	2	name
127240281	CV1093136	single nucleotide variant	NM_001166108.2(PALLD):c.2268C>T (p.Ser756=)	Pancreatic adenocarcinoma [RCV001423285]\|not specified [RCV004038210]	likely benign	4	168898510	168898510	Human	2	name
127236434	CV1093137	single nucleotide variant	NM_001166108.2(PALLD):c.2688G>T (p.Arg896=)	Pancreatic adenocarcinoma [RCV001422508]\|not specified [RCV004038202]	likely benign	4	168913992	168913992	Human	2	name
127269166	CV1093139	single nucleotide variant	NM_001166108.2(PALLD):c.2922C>T (p.His974=)	Pancreatic adenocarcinoma [RCV001430207]\|not specified [RCV004038282]	likely benign	4	168921605	168921605	Human	2	name
127246663	CV1093140	single nucleotide variant	NM_001166108.2(PALLD):c.2988C>T (p.Ala996=)	Pancreatic adenocarcinoma [RCV001435470]\|not specified [RCV004038337]	likely benign	4	168921671	168921671	Human	2	name
127313512	CV1114685	single nucleotide variant	NM_001166108.2(PALLD):c.2169T>A (p.Ile723=)	Pancreatic adenocarcinoma [RCV001457478]	likely benign	4	168894647	168894647	Human	2	name
127334125	CV1114686	single nucleotide variant	NM_001166108.2(PALLD):c.2550C>G (p.Thr850=)	Pancreatic adenocarcinoma [RCV001473402]	likely benign	4	168903834	168903834	Human	2	name
127333308	CV1114688	single nucleotide variant	NM_001166108.2(PALLD):c.2862A>G (p.Leu954=)	Pancreatic adenocarcinoma [RCV001472820]\|not specified [RCV004037133]	likely benign	4	168921545	168921545	Human	2	name
127310568	CV1114689	single nucleotide variant	NM_001166108.2(PALLD):c.2901C>T (p.Pro967=)	Pancreatic adenocarcinoma [RCV001463895]\|not specified [RCV004038626]	likely benign	4	168921584	168921584	Human	2	name
127302555	CV1114690	single nucleotide variant	NM_001166108.2(PALLD):c.2916T>C (p.Ser972=)	Pancreatic adenocarcinoma [RCV001461667]	likely benign	4	168921599	168921599	Human	2	name
127314510	CV1114691	single nucleotide variant	NM_001166108.2(PALLD):c.2961C>T (p.Ile987=)	Pancreatic adenocarcinoma [RCV001457711]	likely benign	4	168921644	168921644	Human	2	name
127290462	CV1135586	single nucleotide variant	NM_001166108.2(PALLD):c.2319T>C (p.Pro773=)	Pancreatic adenocarcinoma [RCV001495981]\|not specified [RCV004037357]	likely benign	4	168898561	168898561	Human	2	name
127335797	CV1135587	single nucleotide variant	NM_001166108.2(PALLD):c.2586T>C (p.Asp862=)	Pancreatic adenocarcinoma [RCV001491725]\|not specified [RCV004037317]	likely benign	4	168903870	168903870	Human	2	name
151853974	CV1510982	single nucleotide variant	NM_001166108.2(PALLD):c.2901C>G (p.Pro967=)	Pancreatic adenocarcinoma [RCV001979299]	likely benign\|uncertain significance	4	168921584	168921584	Human	2	name
152071122	CV1570218	single nucleotide variant	NM_001166108.2(PALLD):c.2466G>A (p.Lys822=)	Pancreatic adenocarcinoma [RCV002191797]\|not specified [RCV004047132]	likely benign	4	168898708	168898708	Human	2	name
152141114	CV1571421	single nucleotide variant	NM_001166108.2(PALLD):c.2904A>G (p.Val968=)	Pancreatic adenocarcinoma [RCV002138188]\|not specified [RCV004046596]	likely benign	4	168921587	168921587	Human	2	name
152107879	CV1579633	single nucleotide variant	NM_001166108.2(PALLD):c.2085G>T (p.Leu695=)	Pancreatic adenocarcinoma [RCV002173956]\|not specified [RCV004047036]	likely benign	4	168891042	168891042	Human	2	name
152062877	CV1587659	single nucleotide variant	NM_001166108.2(PALLD):c.2148C>T (p.Asp716=)	Pancreatic adenocarcinoma [RCV002090473]\|not specified [RCV004045736]	likely benign	4	168894626	168894626	Human	2	name
152149983	CV1625648	single nucleotide variant	NM_001166108.2(PALLD):c.2382A>G (p.Pro794=)	Pancreatic adenocarcinoma [RCV002139371]\|not specified [RCV004046351]	likely benign	4	168898624	168898624	Human	2	name
152139682	CV1638274	single nucleotide variant	NM_001166108.2(PALLD):c.2874T>C (p.Asp958=)	Pancreatic adenocarcinoma [RCV002177890]\|not specified [RCV004045072]	likely benign	4	168921557	168921557	Human	2	name
152094360	CV1648372	single nucleotide variant	NM_001166108.2(PALLD):c.2745A>G (p.Gly915=)	Pancreatic adenocarcinoma [RCV002114502]\|not specified [RCV004046523]	likely benign	4	168915922	168915922	Human	2	name
152073677	CV1660399	single nucleotide variant	NM_001166108.2(PALLD):c.2517T>C (p.Asp839=)	Pancreatic adenocarcinoma [RCV002169620]\|not specified [RCV004044989]	likely benign	4	168903801	168903801	Human	2	name
153305137	CV1687545	single nucleotide variant	NM_001166108.2(PALLD):c.232C>T (p.His78Tyr)	not provided [RCV002263366]\|not specified [RCV004047433]	likely benign\|uncertain significance	4	168511736	168511736	Human		name
155265450	CV1695586	single nucleotide variant	NM_001166108.2(PALLD):c.296C>A (p.Ser99Ter)	Pancreatic cancer, susceptibility to, 1 [RCV002280318]	likely benign	4	168511800	168511800	Human	1	name
155718876	CV1788709	single nucleotide variant	NM_001166108.2(PALLD):c.1011C>T (p.Asp337=)	not specified [RCV004047767]	likely benign	4	168668292	168668292	Human		name
155704150	CV1810636	single nucleotide variant	NM_001166108.2(PALLD):c.120C>A (p.Asn40Lys)	not specified [RCV004054100]	uncertain significance	4	168511624	168511624	Human		name
155665269	CV1813804	single nucleotide variant	NM_001166108.2(PALLD):c.1254G>A (p.Val418=)	not specified [RCV004055343]	likely benign	4	168683097	168683097	Human		name
155709282	CV1815715	single nucleotide variant	NM_001166108.2(PALLD):c.1239A>C (p.Pro413=)	not specified [RCV004055324]	likely benign	4	168683082	168683082	Human		name
155691431	CV1825234	single nucleotide variant	NM_001166108.2(PALLD):c.1278A>G (p.Ser426=)	not specified [RCV004056813]	likely benign	4	168685502	168685502	Human		name
155678217	CV1826345	single nucleotide variant	NM_001166108.2(PALLD):c.1353C>T (p.Ala451=)	not specified [RCV004058802]	likely benign	4	168690620	168690620	Human		name
155688918	CV1826613	single nucleotide variant	NM_001166108.2(PALLD):c.1419G>A (p.Gln473=)	not specified [RCV004057226]	likely benign	4	168690686	168690686	Human		name
155690178	CV1826792	single nucleotide variant	NM_001166108.2(PALLD):c.1035G>A (p.Leu345=)	not specified [RCV004057262]	likely benign	4	168668316	168668316	Human		name
155684632	CV1827071	single nucleotide variant	NM_001166108.2(PALLD):c.149T>C (p.Ile50Thr)	not specified [RCV004058537]	uncertain significance	4	168511653	168511653	Human		name
155684817	CV1827127	single nucleotide variant	NM_001166108.2(PALLD):c.1500T>G (p.Pro500=)	not specified [RCV004058547]	likely benign	4	168691291	168691291	Human		name
155685190	CV1827250	single nucleotide variant	NM_001166108.2(PALLD):c.1509T>C (p.Ile503=)	not specified [RCV004058579]	likely benign	4	168709035	168709035	Human		name
155691984	CV1827385	single nucleotide variant	NM_001166108.2(PALLD):c.1041G>A (p.Thr347=)	not specified [RCV004058615]	likely benign	4	168668322	168668322	Human		name
155692065	CV1827399	single nucleotide variant	NM_001166108.2(PALLD):c.1515C>G (p.Thr505=)	not specified [RCV004058620]	likely benign	4	168709041	168709041	Human		name
155692208	CV1827425	single nucleotide variant	NM_001166108.2(PALLD):c.1516C>T (p.Leu506=)	not specified [RCV004058628]	likely benign	4	168709042	168709042	Human		name
155718396	CV1827760	single nucleotide variant	NM_001166108.2(PALLD):c.1593C>T (p.Thr531=)	not specified [RCV004057374]	likely benign	4	168709119	168709119	Human		name
155700460	CV1828447	single nucleotide variant	NM_001166108.2(PALLD):c.1743A>G (p.Pro581=)	not specified [RCV004061238]	likely benign	4	168711702	168711702	Human		name
155700864	CV1828519	single nucleotide variant	NM_001166108.2(PALLD):c.1746T>A (p.Ser582=)	not specified [RCV004061257]	likely benign	4	168711705	168711705	Human		name
155700872	CV1828520	single nucleotide variant	NM_001166108.2(PALLD):c.1746T>C (p.Ser582=)	not specified [RCV004061258]	likely benign	4	168711705	168711705	Human		name
155701492	CV1828675	single nucleotide variant	NM_001166108.2(PALLD):c.1059C>T (p.Asp353=)	not specified [RCV004061310]	likely benign	4	168668340	168668340	Human		name
155676608	CV1829383	single nucleotide variant	NM_001166108.2(PALLD):c.1338A>G (p.Glu446=)	not specified [RCV004058710]	likely benign	4	168690605	168690605	Human		name
155676735	CV1829405	single nucleotide variant	NM_001166108.2(PALLD):c.1339C>T (p.Leu447=)	not specified [RCV004058718]	likely benign	4	168690606	168690606	Human		name
155681416	CV1829685	single nucleotide variant	NM_001166108.2(PALLD):c.1404C>G (p.Pro468=)	not specified [RCV004057154]	likely benign	4	168690671	168690671	Human		name
155682430	CV1829839	single nucleotide variant	NM_001166108.2(PALLD):c.1410G>T (p.Leu470=)	not specified [RCV004057182]	likely benign	4	168690677	168690677	Human		name
155683800	CV1830291	single nucleotide variant	NM_001166108.2(PALLD):c.1491A>T (p.Thr497=)	not specified [RCV004058499]	likely benign	4	168691282	168691282	Human		name
155684198	CV1830365	single nucleotide variant	NM_001166108.2(PALLD):c.1494T>C (p.Ala498=)	not specified [RCV004058513]	likely benign	4	168691285	168691285	Human		name
155719717	CV1830625	single nucleotide variant	NM_001166108.2(PALLD):c.1569A>G (p.Ala523=)	not specified [RCV004059176]	likely benign	4	168709095	168709095	Human		name
155704163	CV1831113	single nucleotide variant	NM_001166108.2(PALLD):c.164C>A (p.Thr55Lys)	Pancreatic cancer, susceptibility to, 1 [RCV005032262]\|not specified [RCV004059714]	uncertain significance	4	168511668	168511668	Human	1	name
155669432	CV1832158	single nucleotide variant	NM_001166108.2(PALLD):c.1311C>T (p.Ala437=)	not specified [RCV004058316]	likely benign	4	168685535	168685535	Human		name
155670834	CV1832441	single nucleotide variant	NM_001166108.2(PALLD):c.1323T>C (p.Pro441=)	not specified [RCV004058381]	likely benign	4	168685547	168685547	Human		name
155709551	CV1832679	single nucleotide variant	NM_001166108.2(PALLD):c.1389G>C (p.Arg463=)	not specified [RCV004057072]	likely benign	4	168690656	168690656	Human		name
155680204	CV1832828	single nucleotide variant	NM_001166108.2(PALLD):c.1395T>C (p.Arg465=)	not specified [RCV004057106]	likely benign	4	168690662	168690662	Human		name
155680647	CV1832925	single nucleotide variant	NM_001166108.2(PALLD):c.139C>T (p.Arg47Trp)	not specified [RCV004057129]	uncertain significance	4	168511643	168511643	Human		name
155711375	CV1833187	single nucleotide variant	NM_001166108.2(PALLD):c.1468C>T (p.Leu490=)	not specified [RCV004057994]	likely benign	4	168690735	168690735	Human		name
155708190	CV1833553	single nucleotide variant	NM_001166108.2(PALLD):c.1548A>G (p.Ala516=)	not specified [RCV004059047]	likely benign	4	168709074	168709074	Human		name
155718268	CV1833767	single nucleotide variant	NM_001166108.2(PALLD):c.1557T>C (p.Phe519=)	not specified [RCV004059102]	likely benign	4	168709083	168709083	Human		name
155703084	CV1834200	single nucleotide variant	NM_001166108.2(PALLD):c.1050C>T (p.Ser350=)	PALLD-related disorder [RCV003943394]\|not specified [RCV004058104]	likely benign	4	168668331	168668331	Human	1	name , alternate_id
155721953	CV1834652	single nucleotide variant	NM_001166108.2(PALLD):c.1719C>G (p.Ser573=)	PALLD-related disorder [RCV003971289]\|not specified [RCV004060605]	likely benign	4	168711678	168711678	Human	1	name , alternate_id
155719312	CV1835605	single nucleotide variant	NM_001166108.2(PALLD):c.1293T>C (p.Pro431=)	not specified [RCV004058211]	likely benign	4	168685517	168685517	Human		name
155699445	CV1836526	single nucleotide variant	NM_001166108.2(PALLD):c.143G>C (p.Arg48Thr)	not specified [RCV004057854]	uncertain significance	4	168511647	168511647	Human		name
155699673	CV1836583	single nucleotide variant	NM_001166108.2(PALLD):c.1443C>A (p.Ile481=)	not specified [RCV004057869]	likely benign	4	168690710	168690710	Human		name
155701227	CV1836870	single nucleotide variant	NM_001166108.2(PALLD):c.1455A>G (p.Pro485=)	not specified [RCV004057928]	likely benign	4	168690722	168690722	Human		name
155692913	CV1836982	single nucleotide variant	NM_001166108.2(PALLD):c.1521T>A (p.Val507=)	not specified [RCV004058657]	likely benign	4	168709047	168709047	Human		name
155706630	CV1837220	single nucleotide variant	NM_001166108.2(PALLD):c.1533T>G (p.Thr511=)	not specified [RCV004058978]	likely benign	4	168709059	168709059	Human		name
155706792	CV1837255	single nucleotide variant	NM_001166108.2(PALLD):c.1536C>T (p.Phe512=)	not specified [RCV004058987]	likely benign	4	168709062	168709062	Human		name
155702392	CV1838292	single nucleotide variant	NM_001166108.2(PALLD):c.1764C>T (p.Asn588=)	not specified [RCV004061353]	likely benign	4	168711723	168711723	Human		name
155703114	CV1838399	single nucleotide variant	NM_001166108.2(PALLD):c.176A>C (p.Asp59Ala)	not specified [RCV004061381]	uncertain significance	4	168511680	168511680	Human		name
155703152	CV1838407	single nucleotide variant	NM_001166108.2(PALLD):c.176A>T (p.Asp59Val)	not specified [RCV004061384]	uncertain significance	4	168511680	168511680	Human		name
155701697	CV1839081	single nucleotide variant	NM_001166108.2(PALLD):c.1758G>A (p.Gln586=)	not specified [RCV004061324]	likely benign	4	168711717	168711717	Human		name
155682352	CV1839783	single nucleotide variant	NM_001166108.2(PALLD):c.1071T>C (p.Ala357=)	not specified [RCV004061608]	likely benign	4	168668352	168668352	Human		name
155677798	CV1840075	single nucleotide variant	NM_001166108.2(PALLD):c.2064T>G (p.Leu688=)	not specified [RCV004059691]	likely benign	4	168891021	168891021	Human		name
155678133	CV1840154	single nucleotide variant	NM_001166108.2(PALLD):c.206G>C (p.Ser69Thr)	not specified [RCV004059700]	uncertain significance	4	168511710	168511710	Human		name
155678238	CV1840184	single nucleotide variant	NM_001166108.2(PALLD):c.2070C>T (p.Phe690=)	not specified [RCV004059706]	likely benign	4	168891027	168891027	Human		name
155678362	CV1840227	single nucleotide variant	NM_001166108.2(PALLD):c.2073G>A (p.Lys691=)	not specified [RCV004060232]	likely benign	4	168891030	168891030	Human		name
155684370	CV1840381	single nucleotide variant	NM_001166108.2(PALLD):c.2082C>T (p.Leu694=)	not specified [RCV004060267]	likely benign	4	168891039	168891039	Human		name
155684421	CV1840394	single nucleotide variant	NM_001166108.2(PALLD):c.2083C>T (p.Leu695=)	not specified [RCV004060272]	likely benign	4	168891040	168891040	Human		name
155705935	CV1841192	single nucleotide variant	NM_001166108.2(PALLD):c.2334T>C (p.Gly778=)	not specified [RCV004062545]	likely benign	4	168898576	168898576	Human		name
155686178	CV1841392	single nucleotide variant	NM_001166108.2(PALLD):c.2436T>C (p.Thr812=)	not specified [RCV004063368]	likely benign	4	168898678	168898678	Human		name
155663731	CV1841925	single nucleotide variant	NM_001166108.2(PALLD):c.2559C>G (p.Leu853=)	not specified [RCV004062044]	likely benign	4	168903843	168903843	Human		name
155663743	CV1841946	single nucleotide variant	NM_001166108.2(PALLD):c.250A>G (p.Thr84Ala)	not specified [RCV004062053]	uncertain significance	4	168511754	168511754	Human		name
155678453	CV1842093	single nucleotide variant	NM_001166108.2(PALLD):c.251C>A (p.Thr84Asn)	Hereditary cancer-predisposing syndrome [RCV002455668]\|Inborn genetic diseases [RCV003101919]	uncertain significance	4	168511755	168511755	Human	2	name
155693627	CV1842225	single nucleotide variant	NM_001166108.2(PALLD):c.2671A>C (p.Arg891=)	not specified [RCV004062967]	likely benign	4	168913975	168913975	Human		name
155669732	CV1842376	single nucleotide variant	NM_001166108.2(PALLD):c.2685C>G (p.Pro895=)	not specified [RCV004063008]	likely benign	4	168913989	168913989	Human		name
155674628	CV1843137	single nucleotide variant	NM_001166108.2(PALLD):c.194C>T (p.Ser65Leu)	not specified [RCV004061473]	uncertain significance	4	168511698	168511698	Human		name
155675080	CV1843210	single nucleotide variant	NM_001166108.2(PALLD):c.1953C>T (p.Ala651=)	not specified [RCV004061501]	likely benign	4	168711912	168711912	Human		name
155675358	CV1843250	single nucleotide variant	NM_001166108.2(PALLD):c.1956A>G (p.Lys652=)	not specified [RCV004061511]	likely benign	4	168711915	168711915	Human		name
155670281	CV1843482	single nucleotide variant	NM_001166108.2(PALLD):c.2037T>C (p.Ala679=)	not specified [RCV004059587]	likely benign	4	168890994	168890994	Human		name
155670878	CV1843609	single nucleotide variant	NM_001166108.2(PALLD):c.2046A>G (p.Gln682=)	not specified [RCV004059622]	likely benign	4	168891003	168891003	Human		name
155676912	CV1843741	single nucleotide variant	NM_001166108.2(PALLD):c.2052G>C (p.Leu684=)	not specified [RCV004059652]	likely benign	4	168891009	168891009	Human		name
155671447	CV1844289	single nucleotide variant	NM_001166108.2(PALLD):c.2289T>C (p.Ser763=)	not specified [RCV004061869]	likely benign	4	168898531	168898531	Human		name
155699886	CV1844303	single nucleotide variant	NM_001166108.2(PALLD):c.223C>A (p.Leu75Ile)	not specified [RCV004061874]	uncertain significance	4	168511727	168511727	Human		name
155699917	CV1844313	single nucleotide variant	NM_001166108.2(PALLD):c.223C>T (p.Leu75Phe)	not specified [RCV004061878]	likely benign	4	168511727	168511727	Human		name
155694850	CV1844494	single nucleotide variant	NM_001166108.2(PALLD):c.2302A>C (p.Arg768=)	not specified [RCV004061912]	likely benign	4	168898544	168898544	Human		name
155695672	CV1844681	single nucleotide variant	NM_001166108.2(PALLD):c.2311A>C (p.Arg771=)	not specified [RCV004061950]	likely benign	4	168898553	168898553	Human		name
155685663	CV1845061	single nucleotide variant	NM_001166108.2(PALLD):c.2424A>G (p.Gly808=)	not specified [RCV004063326]	likely benign	4	168898666	168898666	Human		name
155678141	CV1845229	single nucleotide variant	NM_001166108.2(PALLD):c.2523C>T (p.Tyr841=)	not specified [RCV004063933]	likely benign	4	168903807	168903807	Human		name
155696597	CV1845327	single nucleotide variant	NM_001166108.2(PALLD):c.247G>A (p.Glu83Lys)	not specified [RCV004063960]	uncertain significance	4	168511751	168511751	Human		name
155669349	CV1845589	single nucleotide variant	NM_001166108.2(PALLD):c.2640T>C (p.Thr880=)	not specified [RCV004062839]	likely benign	4	168913944	168913944	Human		name
155692200	CV1845630	single nucleotide variant	NM_001166108.2(PALLD):c.258G>T (p.Leu86Phe)	not specified [RCV004062848]	uncertain significance	4	168511762	168511762	Human		name
155692351	CV1845671	single nucleotide variant	NM_001166108.2(PALLD):c.2644C>A (p.Arg882=)	Pancreatic adenocarcinoma [RCV005098210]\|not specified [RCV004062856]	likely benign	4	168913948	168913948	Human	2	name
155671677	CV1845923	single nucleotide variant	NM_001166108.2(PALLD):c.2661T>C (p.Ala887=)	not specified [RCV004062929]	likely benign	4	168913965	168913965	Human		name
155668663	CV1846634	single nucleotide variant	NM_001166108.2(PALLD):c.2022A>G (p.Gln674=)	not specified [RCV004059527]	likely benign	4	168890979	168890979	Human		name
155669088	CV1846695	single nucleotide variant	NM_001166108.2(PALLD):c.2025C>T (p.Gly675=)	not specified [RCV004059540]	likely benign	4	168890982	168890982	Human		name
155698804	CV1847372	single nucleotide variant	NM_001166108.2(PALLD):c.2271T>C (p.Cys757=)	not specified [RCV004061804]	likely benign	4	168898513	168898513	Human		name
155699547	CV1847577	single nucleotide variant	NM_001166108.2(PALLD):c.2283C>T (p.Leu761=)	not specified [RCV004061839]	likely benign	4	168898525	168898525	Human		name
155715398	CV1847663	single nucleotide variant	NM_001166108.2(PALLD):c.2370T>C (p.Asn790=)	Pancreatic adenocarcinoma [RCV003585272]\|not specified [RCV004062675]	likely benign	4	168898612	168898612	Human	2	name
155685213	CV1847771	single nucleotide variant	NM_001166108.2(PALLD):c.1092C>T (p.Ala364=)	not specified [RCV004062696]	likely benign	4	168681336	168681336	Human		name
155685387	CV1847958	single nucleotide variant	NM_001166108.2(PALLD):c.233A>G (p.His78Arg)	not specified [RCV004062733]	uncertain significance	4	168511737	168511737	Human		name
155677306	CV1848166	single nucleotide variant	NM_001166108.2(PALLD):c.2493G>A (p.Gly831=)	not specified [RCV004063830]	likely benign	4	168903777	168903777	Human		name
155691257	CV1848697	single nucleotide variant	NM_001166108.2(PALLD):c.2619T>C (p.Pro873=)	not specified [RCV004062765]	likely benign	4	168903903	168903903	Human		name
155672202	CV1849232	single nucleotide variant	NM_001166108.2(PALLD):c.1110C>T (p.Asp370=)	not specified [RCV004063716]	likely benign	4	168681354	168681354	Human		name
155684936	CV1850836	single nucleotide variant	NM_001166108.2(PALLD):c.2346G>A (p.Gln782=)	not specified [RCV004062589]	likely benign	4	168898588	168898588	Human		name
155706763	CV1851014	single nucleotide variant	NM_001166108.2(PALLD):c.2355T>C (p.Asp785=)	not specified [RCV004062629]	likely benign	4	168898597	168898597	Human		name
155703750	CV1852396	single nucleotide variant	NM_001166108.2(PALLD):c.267C>A (p.His89Gln)	not specified [RCV004063622]	likely benign	4	168511771	168511771	Human		name
155702040	CV1852959	single nucleotide variant	NM_001166108.2(PALLD):c.264A>C (p.Glu88Asp)	Hereditary cancer-predisposing syndrome [RCV002428675]\|Inborn genetic diseases [RCV003164552]\|Pancreatic cancer, susceptibility to, 1 [RCV005397428]	uncertain significance	4	168511768	168511768	Human	3	name
155679457	CV1852984	single nucleotide variant	NM_001166108.2(PALLD):c.2808T>C (p.Asp936=)	not specified [RCV004064130]	likely benign	4	168915985	168915985	Human		name
155679783	CV1853078	single nucleotide variant	NM_001166108.2(PALLD):c.2814T>A (p.Thr938=)	Pancreatic adenocarcinoma [RCV003102192]\|not specified [RCV004064155]	likely benign	4	168915991	168915991	Human	2	name
155679787	CV1853079	single nucleotide variant	NM_001166108.2(PALLD):c.2814T>C (p.Thr938=)	not specified [RCV004064156]	likely benign	4	168915991	168915991	Human		name
155680433	CV1853229	single nucleotide variant	NM_001166108.2(PALLD):c.2829A>G (p.Lys943=)	not specified [RCV004064192]	likely benign	4	168916006	168916006	Human		name
155685871	CV1853293	single nucleotide variant	NM_001166108.2(PALLD):c.2832C>T (p.Leu944=)	not specified [RCV004064205]	likely benign	4	168916009	168916009	Human		name
155686155	CV1853381	single nucleotide variant	NM_001166108.2(PALLD):c.278G>A (p.Arg93Lys)	not specified [RCV004064225]	uncertain significance	4	168511782	168511782	Human		name
155683058	CV1853488	single nucleotide variant	NM_001166108.2(PALLD):c.2988C>G (p.Ala996=)	not specified [RCV004063196]	likely benign	4	168921671	168921671	Human		name
155687562	CV1853663	single nucleotide variant	NM_001166108.2(PALLD):c.294G>T (p.Arg98Ser)	not specified [RCV004065328]	uncertain significance	4	168511798	168511798	Human		name
155715631	CV1853909	single nucleotide variant	NM_001166108.2(PALLD):c.2778C>T (p.Phe926=)	not specified [RCV004064024]	likely benign	4	168915955	168915955	Human		name
155672343	CV1853951	single nucleotide variant	NM_001166108.2(PALLD):c.2781A>G (p.Arg927=)	not specified [RCV004064030]	likely benign	4	168915958	168915958	Human		name
155672718	CV1854041	single nucleotide variant	NM_001166108.2(PALLD):c.2790C>T (p.Phe930=)	not specified [RCV004064059]	likely benign	4	168915967	168915967	Human		name
155679002	CV1854111	single nucleotide variant	NM_001166108.2(PALLD):c.2793G>A (p.Leu931=)	not specified [RCV004064085]	likely benign	4	168915970	168915970	Human		name
155679336	CV1854233	single nucleotide variant	NM_001166108.2(PALLD):c.2802T>C (p.Pro934=)	not specified [RCV004064110]	likely benign	4	168915979	168915979	Human		name
155676122	CV1854375	single nucleotide variant	NM_001166108.2(PALLD):c.2952C>T (p.His984=)	not specified [RCV004063105]	likely benign	4	168921635	168921635	Human		name
155680725	CV1854410	single nucleotide variant	NM_001166108.2(PALLD):c.2955T>G (p.Ser985=)	not specified [RCV004063113]	likely benign	4	168921638	168921638	Human		name
155675020	CV1855866	single nucleotide variant	NM_001166108.2(PALLD):c.288T>G (p.Asp96Glu)	not specified [RCV004063063]	uncertain significance	4	168511792	168511792	Human		name
155675220	CV1855896	single nucleotide variant	NM_001166108.2(PALLD):c.2943C>T (p.Asn981=)	Pancreatic adenocarcinoma [RCV003102843]\|not specified [RCV004063071]	likely benign	4	168921626	168921626	Human	2	name
155675391	CV1855919	single nucleotide variant	NM_001166108.2(PALLD):c.2946G>A (p.Gly982=)	not specified [RCV004063077]	likely benign	4	168921629	168921629	Human		name
10406018	CV212374	single nucleotide variant	NM_001166108.2(PALLD):c.2532A>G (p.Gln844=)	Pancreatic adenocarcinoma [RCV000200565]\|not specified [RCV004020465]	likely benign\|uncertain significance	4	168903816	168903816	Human	2	name
10405964	CV212375	single nucleotide variant	NM_001166108.2(PALLD):c.2541C>T (p.Leu847=)	Pancreatic adenocarcinoma [RCV001424160]\|not specified [RCV004020450]	likely benign	4	168903825	168903825	Human	2	name
10405919	CV212379	single nucleotide variant	NM_001166108.2(PALLD):c.2784T>C (p.Pro928=)	PALLD-related disorder [RCV003955200]\|Pancreatic adenocarcinoma [RCV000199612]\|Pancreatic cancer, susceptibility to, 1 [RCV000369325]\|not specified [RCV004020441]	likely pathogenic\|benign\|likely benign	4	168915961	168915961	Human	3	name , alternate_id
10767069	CV221440	microsatellite	NM_001166108.2(PALLD):c.1965-12771CGCCCC[3]	PALLD-related disorder [RCV003927875]\|Pancreatic adenocarcinoma [RCV000204114]\|not specified [RCV004837757]	benign\|likely benign\|uncertain significance	4	168878150	168878151	Human		name , alternate_id
10768121	CV221448	single nucleotide variant	NM_001166108.2(PALLD):c.2130T>C (p.Arg710=)	Pancreatic adenocarcinoma [RCV000205872]\|not specified [RCV004020536]	likely benign	4	168894608	168894608	Human	2	name
11633209	CV294087	single nucleotide variant	NM_001166108.2(PALLD):c.1386C>T (p.Cys462=)	Pancreatic cancer, susceptibility to, 1 [RCV000319577]\|not specified [RCV004021952]	likely benign\|uncertain significance	4	168690653	168690653	Human	1	name
11633465	CV294105	single nucleotide variant	NM_001166108.2(PALLD):c.1527T>G (p.Ala509=)	PALLD-related disorder [RCV003983027]\|Pancreatic cancer, susceptibility to, 1 [RCV000339615]\|not provided [RCV000874587]\|not specified [RCV004021954]	benign	4	168709053	168709053	Human	1	name , alternate_id
11633120	CV297542	single nucleotide variant	NM_001166108.2(PALLD):c.2679A>G (p.Arg893=)	Pancreatic adenocarcinoma [RCV000860256]\|Pancreatic cancer, susceptibility to, 1 [RCV000312336]\|not provided [RCV001691995]\|not specified [RCV004021955]	benign	4	168913983	168913983	Human	3	name
11632707	CV297636	single nucleotide variant	NM_001166108.2(PALLD):c.1347C>T (p.Asn449=)	PALLD-related disorder [RCV003972470]\|Pancreatic cancer, susceptibility to, 1 [RCV000278588]\|not provided [RCV001613146]\|not specified [RCV004021951]	benign	4	168690614	168690614	Human	1	name , alternate_id
11657930	CV297638	single nucleotide variant	NM_001166108.2(PALLD):c.1926C>G (p.Pro642=)	Pancreatic cancer, susceptibility to, 1 [RCV000345422]	uncertain significance	4	168711885	168711885	Human	1	name
12887195	CV393891	single nucleotide variant	NM_001166108.2(PALLD):c.2976G>A (p.Thr992=)	PALLD-related disorder [RCV003972797]\|Pancreatic adenocarcinoma [RCV000468633]\|not specified [RCV004023020]	likely benign	4	168921659	168921659	Human	3	name , alternate_id
12891935	CV393898	single nucleotide variant	NM_001166108.2(PALLD):c.2112C>T (p.Tyr704=)	Pancreatic adenocarcinoma [RCV001472301]\|Pancreatic cancer, susceptibility to, 1 [RCV003316620]\|not specified [RCV004023021]	likely benign	4	168894590	168894590	Human	3	name
12892426	CV394145	single nucleotide variant	NM_001166108.2(PALLD):c.2598T>C (p.Tyr866=)	Pancreatic adenocarcinoma [RCV000469577]\|not specified [RCV004023022]	likely benign	4	168903882	168903882	Human	2	name
13625457	CV519838	single nucleotide variant	NM_001166108.2(PALLD):c.2100G>C (p.Pro700=)	Pancreatic adenocarcinoma [RCV000653479]	uncertain significance	4	168891057	168891057	Human	2	name
15137927	CV686513	single nucleotide variant	NM_001166108.2(PALLD):c.2892T>C (p.Asp964=)	Pancreatic adenocarcinoma [RCV000864749]\|not specified [RCV004027630]	benign\|likely benign	4	168921575	168921575	Human	2	name
15131537	CV691531	single nucleotide variant	NM_001166108.2(PALLD):c.2175G>A (p.Glu725=)	Pancreatic adenocarcinoma [RCV001395305]\|not specified [RCV004027870]	likely benign	4	168894653	168894653	Human	2	name
15189454	CV720833	single nucleotide variant	NM_001166108.2(PALLD):c.2304G>A (p.Arg768=)	Pancreatic adenocarcinoma [RCV000887824]\|not specified [RCV004028366]	likely benign	4	168898546	168898546	Human	2	name
127298377	CV1114693	single nucleotide variant	NM_001166108.2(PALLD):c.3243C>T (p.His1081=)	PALLD-related disorder [RCV003938814]\|Pancreatic adenocarcinoma [RCV001453291]\|not specified [RCV004038520]	likely benign	4	168924963	168924963	Human	3	alternate_id
8658520	CV133551	single nucleotide variant	NM_001166108.2(PALLD):c.1040C>T (p.Thr347Met)	PALLD-related disorder [RCV004751271]\|Pancreatic cancer, susceptibility to, 1 [RCV000330846]\|not provided [RCV000116038]	benign\|likely benign\|uncertain significance	4	168668321	168668321	Human	1	alternate_id
8658522	CV133553	single nucleotide variant	NM_001166108.2(PALLD):c.1289G>A (p.Arg430Gln)	PALLD-related disorder [RCV003905104]\|Pancreatic cancer, susceptibility to, 1 [RCV000373110]\|not provided [RCV000116040]	benign\|likely benign\|uncertain significance	4	168685513	168685513	Human	1	alternate_id
8658523	CV133554	single nucleotide variant	NM_001166108.2(PALLD):c.1394G>A (p.Arg465His)	PALLD-related disorder [RCV003915129]\|Pancreatic cancer, susceptibility to, 1 [RCV000374192]\|not provided [RCV000116041]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	4	168690661	168690661	Human	1	alternate_id
8658526	CV133557	single nucleotide variant	NM_001166108.2(PALLD):c.1873G>A (p.Gly625Ser)	PALLD-related disorder [RCV003407504]\|not provided [RCV000116044]\|not specified [RCV004019616]	uncertain significance	4	168711832	168711832	Human	1	alternate_id
8658537	CV133568	single nucleotide variant	NM_001166108.2(PALLD):c.539C>T (p.Thr180Ile)	PALLD-related disorder [RCV003905105]\|Pancreatic cancer, susceptibility to, 1 [RCV000400101]\|not provided [RCV000116055]\|not specified [RCV004019620]	likely benign\|uncertain significance	4	168512043	168512043	Human	1	alternate_id
8658539	CV133570	single nucleotide variant	NM_001166108.2(PALLD):c.731A>G (p.Gln244Arg)	PALLD-related disorder [RCV003905106]\|Pancreatic cancer, susceptibility to, 1 [RCV000359984]\|not provided [RCV000116057]	benign\|likely benign\|uncertain significance	4	168512235	168512235	Human	1	alternate_id
8658540	CV133571	single nucleotide variant	NM_001166108.2(PALLD):c.764G>A (p.Arg255His)	PALLD-related disorder [RCV003925120]\|Pancreatic cancer, susceptibility to, 1 [RCV000401033]\|not provided [RCV001356526]\|not specified [RCV000116058]	benign\|likely benign	4	168512268	168512268	Human	1	alternate_id
8658541	CV133572	single nucleotide variant	NM_001166108.2(PALLD):c.909A>T (p.Arg303Ser)	PALLD-related disorder [RCV003952560]\|Pancreatic cancer, susceptibility to, 1 [RCV000271106]\|not provided [RCV000116059]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	4	168668190	168668190	Human	1	alternate_id
8689785	CV139712	single nucleotide variant	NM_001166108.2(PALLD):c.3297T>C (p.Tyr1099=)	PALLD-related disorder [RCV003952631]\|Pancreatic adenocarcinoma [RCV000123166]\|Pancreatic cancer, susceptibility to, 1 [RCV000319186]\|not provided [RCV002055381]\|not specified [RCV000194244]	benign\|likely benign	4	168925017	168925017	Human	3	alternate_id
151886558	CV1437783	single nucleotide variant	NM_001166108.2(PALLD):c.1975A>G (p.Lys659Glu)	PALLD-related disorder [RCV004752095]\|Pancreatic adenocarcinoma [RCV001887591]\|not specified [RCV004041624]	uncertain significance	4	168890932	168890932	Human	3	alternate_id
155694766	CV1788915	single nucleotide variant	NM_001166108.2(PALLD):c.1139C>T (p.Ala380Val)	PALLD-related disorder [RCV004731265]\|not specified [RCV004047817]	uncertain significance	4	168681383	168681383	Human	1	alternate_id
155673290	CV1792327	single nucleotide variant	NM_001166108.2(PALLD):c.3365G>A (p.Arg1122Gln)	PALLD-related disorder [RCV003960997]\|not specified [RCV004049532]	likely benign	4	168925239	168925239	Human	1	alternate_id
155707210	CV1798583	single nucleotide variant	NM_001166108.2(PALLD):c.467C>T (p.Thr156Met)	PALLD-related disorder [RCV003943367]\|Pancreatic cancer, susceptibility to, 1 [RCV005032242]\|not specified [RCV004051966]	likely benign	4	168511971	168511971	Human	1	alternate_id
9834684	CV180161	single nucleotide variant	NM_001166108.2(PALLD):c.3256C>T (p.Leu1086=)	PALLD-related disorder [RCV003965182]\|Pancreatic adenocarcinoma [RCV000204944]\|Pancreatic cancer, susceptibility to, 1 [RCV000261555]\|not specified [RCV000160878]	benign\|likely benign	4	168924976	168924976	Human	3	alternate_id
155721391	CV1817227	single nucleotide variant	NM_001166108.2(PALLD):c.862G>A (p.Val288Ile)	PALLD-related disorder [RCV003408255]\|not specified [RCV004056571]	uncertain significance	4	168512366	168512366	Human	1	alternate_id
155674072	CV1820352	single nucleotide variant	NM_001166108.2(PALLD):c.815G>A (p.Arg272Gln)	PALLD-related disorder [RCV003933769]\|Pancreatic cancer, susceptibility to, 1 [RCV005025809]\|not specified [RCV004055502]	likely benign\|uncertain significance	4	168512319	168512319	Human	1	alternate_id
155730899	CV1825863	single nucleotide variant	NM_001166108.2(PALLD):c.999G>T (p.Glu333Asp)	PALLD-related disorder [RCV003971275]\|not specified [RCV004057752]	benign\|uncertain significance	4	168668280	168668280	Human	1	alternate_id
155681614	CV1829715	single nucleotide variant	NM_001166108.2(PALLD):c.1406C>T (p.Pro469Leu)	PALLD-related disorder [RCV004750736]\|not specified [RCV004057159]	uncertain significance	4	168690673	168690673	Human	1	alternate_id
155693192	CV1837032	single nucleotide variant	NM_001166108.2(PALLD):c.1524C>T (p.Ile508=)	PALLD-related disorder [RCV003933775]\|not provided [RCV005424909]\|not specified [RCV004058672]	likely benign	4	168709050	168709050	Human	1	name , alternate_id
155723947	CV1837957	single nucleotide variant	NM_001166108.2(PALLD):c.1686T>C (p.Phe562=)	PALLD-related disorder [RCV003943395]\|not specified [RCV004059907]	likely benign	4	168711645	168711645	Human	1	alternate_id
155725483	CV1844947	single nucleotide variant	NM_001166108.2(PALLD):c.1094G>C (p.Ser365Thr)	PALLD-related disorder [RCV003403827]\|not specified [RCV004063300]	uncertain significance	4	168681338	168681338	Human	1	alternate_id
155927114	CV2365875	single nucleotide variant	NM_001166108.2(PALLD):c.2225T>C (p.Val742Ala)	PALLD-related disorder [RCV003963775]\|not specified [RCV004214404]	likely benign\|uncertain significance	4	168896574	168896574	Human	1	alternate_id
329383708	CV2432239	single nucleotide variant	NM_001166108.2(PALLD):c.1051G>A (p.Gly351Ser)	PALLD-related disorder [RCV003946454]\|not specified [RCV004247314]	uncertain significance	4	168668332	168668332	Human	1	alternate_id
329383798	CV2432301	single nucleotide variant	NM_001166108.2(PALLD):c.1427G>A (p.Arg476Gln)	PALLD-related disorder [RCV003420588]\|not specified [RCV004247322]	uncertain significance	4	168690694	168690694	Human	1	alternate_id
329389953	CV2465660	single nucleotide variant	NM_001166108.2(PALLD):c.3214G>A (p.Asp1072Asn)	PALLD-related disorder [RCV003396952]\|not specified [RCV004281485]	uncertain significance	4	168924410	168924410	Human	1	alternate_id
401744843	CV2688243	single nucleotide variant	NM_001166108.2(PALLD):c.1541A>G (p.Glu514Gly)	PALLD-related disorder [RCV003395739]\|not specified [RCV004298927]	uncertain significance	4	168709067	168709067	Human	1	alternate_id
401938010	CV2797385	single nucleotide variant	NM_001166108.2(PALLD):c.3221T>G (p.Val1074Gly)	PALLD-related disorder [RCV003417110]\|not specified [RCV005382636]	uncertain significance	4	168924417	168924417	Human	1	alternate_id
401926633	CV2798697	single nucleotide variant	NM_001166108.2(PALLD):c.1141G>A (p.Gly381Arg)	PALLD-related disorder [RCV003405999]	uncertain significance	4	168681385	168681385	Human		trait , alternate_id
11633394	CV294085	single nucleotide variant	NM_001166108.2(PALLD):c.365C>T (p.Pro122Leu)	PALLD-related disorder [RCV003902342]\|Pancreatic cancer, susceptibility to, 1 [RCV000336218]\|not provided [RCV000998316]\|not specified [RCV004021945]	benign\|likely benign\|uncertain significance	4	168511869	168511869	Human	1	alternate_id
405288719	CV3193750	single nucleotide variant	NM_001166108.2(PALLD):c.1479A>T (p.Lys493Asn)	PALLD-related disorder [RCV003982756]\|not specified [RCV004369921]	uncertain significance	4	168691270	168691270	Human	1	alternate_id
405280064	CV3200242	single nucleotide variant	NM_001166108.2(PALLD):c.2242G>C (p.Gly748Arg)	PALLD-related disorder [RCV003977159]	uncertain significance	4	168896591	168896591	Human		trait , alternate_id
405268997	CV3201237	single nucleotide variant	NM_001166108.2(PALLD):c.1680A>T (p.Gln560His)	PALLD-related disorder [RCV003899343]	uncertain significance	4	168711639	168711639	Human		trait , alternate_id
405274694	CV3209092	single nucleotide variant	NM_001166108.2(PALLD):c.1301C>T (p.Thr434Ile)	PALLD-related disorder [RCV003951841]	uncertain significance	4	168685525	168685525	Human		trait , alternate_id
408383357	CV3503862	single nucleotide variant	NM_001166108.2(PALLD):c.1935G>T (p.Glu645Asp)	PALLD-related disorder [RCV004730589]	uncertain significance	4	168711894	168711894	Human		trait , alternate_id
408377441	CV3507229	single nucleotide variant	NM_001166108.2(PALLD):c.408C>A (p.Ser136Arg)	PALLD-related disorder [RCV004750978]	uncertain significance	4	168511912	168511912	Human		trait , alternate_id
13809047	CV561967	single nucleotide variant	NM_001166108.2(PALLD):c.2749G>A (p.Glu917Lys)	Hereditary cancer-predisposing syndrome [RCV002424594]\|Inborn genetic diseases [RCV002547116]\|PALLD-related disorder [RCV003420218]\|Pancreatic adenocarcinoma [RCV000687569]	uncertain significance	4	168915926	168915926	Human	5	alternate_id
26897462	CV828949	single nucleotide variant	NM_001166108.2(PALLD):c.2801C>T (p.Pro934Leu)	PALLD-related disorder [RCV003405249]\|Pancreatic adenocarcinoma [RCV001048556]\|not specified [RCV004031514]	uncertain significance	4	168915978	168915978	Human	3	alternate_id
13625453	CV520114	indel	NM_001166108.2(PALLD):c.1965-12772delinsCCGCCCC	Pancreatic adenocarcinoma [RCV000653475]	uncertain significance	4	168878150	168878150	Human		name
126771869	CV1025735	duplication	NM_001166108.2(PALLD):c.1965-13028_1965-13016dup	Pancreatic adenocarcinoma [RCV001345294]	uncertain significance	4	168877893	168877894	Human	2	name
151830793	CV1343499	deletion	NM_001166108.2(PALLD):c.1965-12802_1965-12797del	Pancreatic adenocarcinoma [RCV001920469]	uncertain significance	4	168878117	168878122	Human	2	name
151728395	CV1388626	deletion	NM_001166108.2(PALLD):c.1965-12821_1965-12807del	Pancreatic adenocarcinoma [RCV001966859]	uncertain significance	4	168878098	168878112	Human	2	name
8689782	CV139709	deletion	NM_001166108.2(PALLD):c.1965-12905_1965-12891del	Pancreatic adenocarcinoma [RCV000123163]	uncertain significance	4	168878016	168878030	Human	2	name
151869520	CV1516783	deletion	NM_001166108.2(PALLD):c.1965-12766_1965-12737del	Pancreatic adenocarcinoma [RCV001981117]	uncertain significance	4	168878153	168878182	Human	2	name
156440867	CV1940596	deletion	NM_001166108.2(PALLD):c.1965-12693_1965-12682del	Pancreatic adenocarcinoma [RCV003110910]	uncertain significance	4	168878222	168878233	Human	2	name
156354332	CV1962261	inversion	NM_001166108.2(PALLD):c.1965-12626_1965-12625inv	Pancreatic adenocarcinoma [RCV002581284]	uncertain significance	4	168878296	168878297	Human		name
155932684	CV2067419	duplication	NM_001166108.2(PALLD):c.1965-12582_1965-12577dup	Pancreatic adenocarcinoma [RCV002838857]	uncertain significance	4	168878336	168878337	Human	2	name
10768445	CV221441	duplication	NM_001166108.2(PALLD):c.1965-12758_1965-12753dup	Pancreatic adenocarcinoma [RCV000206416]	uncertain significance	4	168878161	168878162	Human	2	name
405249248	CV2966680	deletion	NM_001166108.2(PALLD):c.1965-12790_1965-12764del	Pancreatic adenocarcinoma [RCV003747036]	uncertain significance	4	168878127	168878153	Human	2	name
405249866	CV2996540	deletion	NM_001166108.2(PALLD):c.1965-12982_1965-12839del	Pancreatic adenocarcinoma [RCV003747307]	uncertain significance	4	168877939	168878082	Human	2	name
402484541	CV3171191	deletion	NM_001166108.2(PALLD):c.1965-12822_1965-12811del	Pancreatic adenocarcinoma [RCV003876218]\|not specified [RCV005387286]	uncertain significance	4	168878092	168878103	Human	2	name
597966138	CV3751507	duplication	NM_001166108.2(PALLD):c.1965-12822_1965-12811dup	Pancreatic adenocarcinoma [RCV005082876]	uncertain significance	4	168878091	168878092	Human	2	name
597951255	CV3847133	duplication	NM_001166108.2(PALLD):c.1965-12773_1965-12768dup	Pancreatic adenocarcinoma [RCV005190305]	uncertain significance	4	168878143	168878144	Human	2	name
13498220	CV453041	microsatellite	NM_001166108.2(PALLD):c.1965-12761_1965-12756del	Pancreatic adenocarcinoma [RCV000527878]\|not specified [RCV005384774]	uncertain significance	4	168878151	168878156	Human		name
13625459	CV520122	duplication	NM_001166108.2(PALLD):c.1965-12692_1965-12681dup	Pancreatic adenocarcinoma [RCV000653481]	uncertain significance	4	168878229	168878230	Human	2	name
26899228	CV828944	deletion	NM_001166108.2(PALLD):c.1965-12698_1965-12690del	Pancreatic adenocarcinoma [RCV001034939]	uncertain significance	4	168878222	168878230	Human	2	name
126733670	CV990013	inversion	NM_001166108.2(PALLD):c.1964+44317_1964+44318inv	Pancreatic adenocarcinoma [RCV001294785]	uncertain significance	4	168756240	168756241	Human		name
126736310	CV990017	deletion	NM_001166108.2(PALLD):c.1965-12758_1965-12753del	Pancreatic adenocarcinoma [RCV001295205]\|not specified [RCV005385017]	uncertain significance	4	168878162	168878167	Human	2	name
150492955	CV1281536	insertion	NM_001166108.2(PALLD):c.1965-12240_1965-12239insTG	not provided [RCV001716910]	benign	4	168878682	168878683	Human		name
156412685	CV1886844	insertion	NM_001166108.2(PALLD):c.1965-12693_1965-12692insCCC	Pancreatic adenocarcinoma [RCV003072995]	benign	4	168878227	168878228	Human	2	name
597888774	CV3859554	indel	NM_001166108.2(PALLD):c.1965-12625_1965-12624delinsGC	Pancreatic adenocarcinoma [RCV005200210]	uncertain significance	4	168878297	168878298	Human		name
598258324	CV4005595	indel	NM_001166108.2(PALLD):c.1965-12773_1965-12772delinsCC	not specified [RCV005386255]	likely benign	4	168878149	168878150	Human		name
151748647	CV1430217	microsatellite	NM_001166108.2(PALLD):c.1965-12764_1965-12763insTCCCCG	Pancreatic adenocarcinoma [RCV002006621]	uncertain significance	4	168878153	168878154	Human		name
598184852	CV4005662	indel	NM_001166108.2(PALLD):c.1965-12625_1965-12623delinsGGG	not specified [RCV005395516]	likely benign	4	168878297	168878299	Human		name
155717837	CV1792679	single nucleotide variant	NM_001166108.2(PALLD):c.1143A>T (p.Gly381=)	not specified [RCV004048605]	likely benign	4	168681387	168681387	Human		name

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