Papln Variant Search Result - Rat Genome Database

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169 records found for search term Papln

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401934159	CV2810543	single nucleotide variant	NM_001365906.3(PAPLN):c.2987-3C>T	not provided [RCV003411044]	likely benign	14	73264585	73264585	Human		name
598128748	CV3886545	deletion	NM_001365906.3(PAPLN):c.2987-2_2987-1del	not provided [RCV005244205]	likely benign	14	73264586	73264587	Human		name
405759088	CV3364109	single nucleotide variant	NM_001365906.3(PAPLN):c.11T>C (p.Leu4Pro)	not specified [RCV004500310]	uncertain significance	14	73239789	73239789	Human		name
8627564	CV82708	single nucleotide variant	NM_173462.3(PAPLN):c.935C>T (p.Pro312Leu)	Malignant melanoma [RCV000062788]	not provided	14	73252697	73252697	Human		name
8635281	CV90503	single nucleotide variant	NM_173462.3(PAPLN):c.604C>T (p.Arg202Cys)	Malignant melanoma [RCV000070601]	not provided	14	73251678	73251678	Human		name
401934158	CV2810542	single nucleotide variant	NM_001365906.3(PAPLN):c.825G>A (p.Ser275=)	not provided [RCV003411043]	likely benign	14	73251818	73251818	Human		name
407518034	CV3466457	single nucleotide variant	NM_001365906.3(PAPLN):c.74A>G (p.Gln25Arg)	not specified [RCV004650863]	uncertain significance	14	73244663	73244663	Human		name
156272685	CV2323410	single nucleotide variant	NM_001365906.3(PAPLN):c.247G>T (p.Ala83Ser)	not specified [RCV004171804]	uncertain significance	14	73246088	73246088	Human		name
156347350	CV2382881	single nucleotide variant	NM_001365906.3(PAPLN):c.152G>A (p.Arg51His)	not specified [RCV004217480]	uncertain significance	14	73244741	73244741	Human		name
329360618	CV2439535	single nucleotide variant	NM_001365906.3(PAPLN):c.244G>A (p.Gly82Ser)	not specified [RCV004262471]	uncertain significance	14	73246085	73246085	Human		name
401756514	CV2687187	single nucleotide variant	NM_001365906.3(PAPLN):c.251G>A (p.Arg84Gln)	not specified [RCV004298136]	uncertain significance	14	73246092	73246092	Human		name
401874669	CV2759312	single nucleotide variant	NM_001365906.3(PAPLN):c.188G>A (p.Ser63Asn)	not specified [RCV004335898]	uncertain significance	14	73245653	73245653	Human		name
407518007	CV3466445	single nucleotide variant	NM_001365906.3(PAPLN):c.259C>T (p.Arg87Trp)	not specified [RCV004650854]	uncertain significance	14	73246100	73246100	Human		name
407518038	CV3466458	single nucleotide variant	NM_001365906.3(PAPLN):c.155C>T (p.Pro52Leu)	not specified [RCV004650864]	uncertain significance	14	73244744	73244744	Human		name
597717395	CV3571229	single nucleotide variant	NM_001365906.3(PAPLN):c.118C>T (p.Arg40Trp)	not specified [RCV004841527]	uncertain significance	14	73244707	73244707	Human		name
597717405	CV3571230	single nucleotide variant	NM_001365906.3(PAPLN):c.130G>C (p.Gly44Arg)	not specified [RCV004841528]	uncertain significance	14	73244719	73244719	Human		name
598259258	CV4005816	single nucleotide variant	NM_001365906.3(PAPLN):c.271T>C (p.Cys91Arg)	not specified [RCV005386449]	uncertain significance	14	73246112	73246112	Human		name
598259327	CV4005828	single nucleotide variant	NM_001365906.3(PAPLN):c.2355C>T (p.Gly785=)	not specified [RCV005386461]	likely benign	14	73262459	73262459	Human		name
156026996	CV2199245	single nucleotide variant	NM_001365906.3(PAPLN):c.572C>T (p.Ala191Val)	not specified [RCV004082605]	uncertain significance	14	73251013	73251013	Human		name
156115525	CV2221476	single nucleotide variant	NM_001365906.3(PAPLN):c.686G>A (p.Arg229His)	not specified [RCV004096757]	uncertain significance	14	73251679	73251679	Human		name
155927913	CV2366004	single nucleotide variant	NM_001365906.3(PAPLN):c.307C>T (p.Arg103Trp)	not specified [RCV004207605]	uncertain significance	14	73246148	73246148	Human		name
401728724	CV2673026	single nucleotide variant	NM_001365906.3(PAPLN):c.587G>A (p.Arg196Gln)	not specified [RCV004284021]	uncertain significance	14	73251028	73251028	Human		name
401738361	CV2676259	single nucleotide variant	NM_001365906.3(PAPLN):c.770G>A (p.Arg257Gln)	not specified [RCV004286298]	uncertain significance	14	73251763	73251763	Human		name
401756385	CV2733979	single nucleotide variant	NM_001365906.3(PAPLN):c.428C>T (p.Pro143Leu)	not specified [RCV004330541]	uncertain significance	14	73250077	73250077	Human		name
401870056	CV2765603	single nucleotide variant	NM_001365906.3(PAPLN):c.964G>A (p.Gly322Arg)	not specified [RCV004335616]	uncertain significance	14	73252138	73252138	Human		name
401934160	CV2810544	single nucleotide variant	NM_001365906.3(PAPLN):c.3153G>C (p.Arg1051=)	not provided [RCV003411045]	likely benign	14	73265397	73265397	Human		name
405759164	CV3364121	single nucleotide variant	NM_001365906.3(PAPLN):c.299A>T (p.Gln100Leu)	not specified [RCV004500322]	uncertain significance	14	73246140	73246140	Human		name
405759171	CV3364122	single nucleotide variant	NM_001365906.3(PAPLN):c.305G>A (p.Arg102Gln)	not specified [RCV004500323]	uncertain significance	14	73246146	73246146	Human		name
405759190	CV3364125	single nucleotide variant	NM_001365906.3(PAPLN):c.435G>C (p.Lys145Asn)	not specified [RCV004500326]	uncertain significance	14	73250084	73250084	Human		name
405759194	CV3364126	single nucleotide variant	NM_001365906.3(PAPLN):c.497C>T (p.Ser166Phe)	not specified [RCV004500327]	uncertain significance	14	73250938	73250938	Human		name
405759199	CV3364127	single nucleotide variant	NM_001365906.3(PAPLN):c.725C>T (p.Ala242Val)	not specified [RCV004500328]	uncertain significance	14	73251718	73251718	Human		name
405759204	CV3364128	single nucleotide variant	NM_001365906.3(PAPLN):c.731G>C (p.Arg244Pro)	not specified [RCV004500329]	uncertain significance	14	73251724	73251724	Human		name
405759209	CV3364129	single nucleotide variant	NM_001365906.3(PAPLN):c.769C>T (p.Arg257Trp)	not specified [RCV004500330]	uncertain significance	14	73251762	73251762	Human		name
405759214	CV3364130	single nucleotide variant	NM_001365906.3(PAPLN):c.800G>A (p.Arg267Gln)	not specified [RCV004500331]	uncertain significance	14	73251793	73251793	Human		name
405759219	CV3364131	single nucleotide variant	NM_001365906.3(PAPLN):c.812G>A (p.Arg271Gln)	not specified [RCV004500332]	uncertain significance	14	73251805	73251805	Human		name
405759221	CV3364132	single nucleotide variant	NM_001365906.3(PAPLN):c.979C>G (p.Arg327Gly)	not specified [RCV004500333]	uncertain significance	14	73252660	73252660	Human		name
407479470	CV3466443	single nucleotide variant	NM_001365906.3(PAPLN):c.839T>C (p.Ile280Thr)	not specified [RCV004664141]	uncertain significance	14	73251832	73251832	Human		name
407518004	CV3466444	single nucleotide variant	NM_001365906.3(PAPLN):c.730C>T (p.Arg244Trp)	not specified [RCV004650853]	uncertain significance	14	73251723	73251723	Human		name
407518026	CV3466454	single nucleotide variant	NM_001365906.3(PAPLN):c.704A>G (p.Asn235Ser)	not specified [RCV004650860]	uncertain significance	14	73251697	73251697	Human		name
407518044	CV3466461	single nucleotide variant	NM_001365906.3(PAPLN):c.766G>A (p.Glu256Lys)	not specified [RCV004650866]	uncertain significance	14	73251759	73251759	Human		name
597657844	CV3571227	single nucleotide variant	NM_001365906.3(PAPLN):c.841G>A (p.Glu281Lys)	not specified [RCV004827683]	uncertain significance	14	73251834	73251834	Human		name
597717507	CV3571243	single nucleotide variant	NM_001365906.3(PAPLN):c.308G>A (p.Arg103Gln)	not specified [RCV004841540]	uncertain significance	14	73246149	73246149	Human		name
597717574	CV3571252	single nucleotide variant	NM_001365906.3(PAPLN):c.931G>A (p.Gly311Ser)	not specified [RCV004841546]	uncertain significance	14	73252105	73252105	Human		name
598259251	CV4005815	single nucleotide variant	NM_001365906.3(PAPLN):c.452A>G (p.Asp151Gly)	not specified [RCV005386448]	uncertain significance	14	73250101	73250101	Human		name
598259263	CV4005817	single nucleotide variant	NM_001365906.3(PAPLN):c.302G>A (p.Gly101Glu)	not specified [RCV005386450]	uncertain significance	14	73246143	73246143	Human		name
598259268	CV4005818	single nucleotide variant	NM_001365906.3(PAPLN):c.790G>A (p.Ala264Thr)	not specified [RCV005386451]	uncertain significance	14	73251783	73251783	Human		name
598259321	CV4005827	single nucleotide variant	NM_001365906.3(PAPLN):c.835G>A (p.Val279Ile)	not specified [RCV005386460]	uncertain significance	14	73251828	73251828	Human		name
156188945	CV2205871	single nucleotide variant	NM_001365906.3(PAPLN):c.1159G>A (p.Val387Met)	not specified [RCV004078309]	uncertain significance	14	73253818	73253818	Human		name
156279678	CV2206292	single nucleotide variant	NM_001365906.3(PAPLN):c.2566G>A (p.Gly856Ser)	not specified [RCV004078637]	uncertain significance	14	73262670	73262670	Human		name
156150077	CV2213042	single nucleotide variant	NM_001365906.3(PAPLN):c.2750C>T (p.Ser917Leu)	not specified [RCV004091619]	uncertain significance	14	73263671	73263671	Human		name
156123427	CV2234022	single nucleotide variant	NM_001365906.3(PAPLN):c.1451G>A (p.Ser484Asn)	not specified [RCV004106141]	uncertain significance	14	73254661	73254661	Human		name
155974390	CV2235687	single nucleotide variant	NM_001365906.3(PAPLN):c.2945G>A (p.Arg982Gln)	not specified [RCV004111828]	uncertain significance	14	73264294	73264294	Human		name
156361615	CV2269279	single nucleotide variant	NM_001365906.3(PAPLN):c.2241C>G (p.Ser747Arg)	not specified [RCV004130427]	uncertain significance	14	73261290	73261290	Human		name
156365097	CV2272053	single nucleotide variant	NM_001365906.3(PAPLN):c.1514G>A (p.Arg505Gln)	not specified [RCV004124850]	uncertain significance	14	73254905	73254905	Human		name
156194361	CV2302078	single nucleotide variant	NM_001365906.3(PAPLN):c.1342G>A (p.Val448Ile)	not specified [RCV004158836]	uncertain significance	14	73254552	73254552	Human		name
156304496	CV2304794	single nucleotide variant	NM_001365906.3(PAPLN):c.2363A>G (p.His788Arg)	not specified [RCV004166935]	uncertain significance	14	73262467	73262467	Human		name
156150446	CV2307479	single nucleotide variant	NM_001365906.3(PAPLN):c.1336C>T (p.Arg446Trp)	not specified [RCV004166137]	uncertain significance	14	73254546	73254546	Human		name
156294462	CV2333276	single nucleotide variant	NM_001365906.3(PAPLN):c.1508G>C (p.Gly503Ala)	not specified [RCV004197025]	uncertain significance	14	73254899	73254899	Human		name
156080365	CV2337505	single nucleotide variant	NM_001365906.3(PAPLN):c.2317G>A (p.Val773Ile)	not specified [RCV004187938]	likely benign	14	73262421	73262421	Human		name
156065673	CV2346588	single nucleotide variant	NM_001365906.3(PAPLN):c.2918C>T (p.Ala973Val)	not specified [RCV004206498]	uncertain significance	14	73264267	73264267	Human		name
156145413	CV2358736	single nucleotide variant	NM_001365906.3(PAPLN):c.1330C>T (p.Arg444Trp)	not specified [RCV004209647]	uncertain significance	14	73254540	73254540	Human		name
155986088	CV2363597	single nucleotide variant	NM_001365906.3(PAPLN):c.2158C>T (p.Arg720Trp)	not specified [RCV004216552]	uncertain significance	14	73261207	73261207	Human		name
156252484	CV2369071	single nucleotide variant	NM_001365906.3(PAPLN):c.1864C>T (p.Arg622Trp)	not specified [RCV004207998]	uncertain significance	14	73259424	73259424	Human		name
156162305	CV2371684	single nucleotide variant	NM_001365906.3(PAPLN):c.2306G>A (p.Arg769His)	not specified [RCV004216922]	uncertain significance	14	73262410	73262410	Human		name
155933738	CV2372332	single nucleotide variant	NM_001365906.3(PAPLN):c.1042C>T (p.Arg348Trp)	not specified [RCV004217101]	uncertain significance	14	73252723	73252723	Human		name
156172414	CV2380819	single nucleotide variant	NM_001365906.3(PAPLN):c.2906A>G (p.Gln969Arg)	not specified [RCV004218379]	likely benign	14	73264255	73264255	Human		name
156042640	CV2381475	single nucleotide variant	NM_001365906.3(PAPLN):c.1401C>A (p.Asp467Glu)	not specified [RCV004229956]	uncertain significance	14	73254611	73254611	Human		name
156163287	CV2389558	single nucleotide variant	NM_001365906.3(PAPLN):c.1520G>A (p.Arg507Gln)	not specified [RCV004243627]	uncertain significance	14	73254911	73254911	Human		name
156007477	CV2392619	single nucleotide variant	NM_001365906.3(PAPLN):c.2656T>G (p.Ser886Ala)	not specified [RCV004245857]	uncertain significance	14	73262760	73262760	Human		name
329358029	CV2427919	single nucleotide variant	NM_001365906.3(PAPLN):c.1403G>A (p.Arg468Gln)	not specified [RCV004254307]	likely benign	14	73254613	73254613	Human		name
329386738	CV2428433	single nucleotide variant	NM_001365906.3(PAPLN):c.1865G>A (p.Arg622Gln)	not specified [RCV004253231]	likely benign	14	73259425	73259425	Human		name
329366046	CV2438037	single nucleotide variant	NM_001365906.3(PAPLN):c.2696C>T (p.Ala899Val)	not specified [RCV004263740]	likely benign	14	73262800	73262800	Human		name
329388538	CV2447621	single nucleotide variant	NM_001365906.3(PAPLN):c.1442C>G (p.Pro481Arg)	not specified [RCV004258424]	uncertain significance	14	73254652	73254652	Human		name
329360515	CV2458804	single nucleotide variant	NM_001365906.3(PAPLN):c.2419T>A (p.Ser807Thr)	not specified [RCV004270230]	uncertain significance	14	73262523	73262523	Human		name
329396895	CV2463609	single nucleotide variant	NM_001365906.3(PAPLN):c.1061C>G (p.Ser354Cys)	not specified [RCV004277407]	uncertain significance	14	73252742	73252742	Human		name
329397712	CV2463938	single nucleotide variant	NM_001365906.3(PAPLN):c.2356G>A (p.Gly786Ser)	not specified [RCV004280002]	uncertain significance	14	73262460	73262460	Human		name
329388750	CV2469549	single nucleotide variant	NM_001365906.3(PAPLN):c.1379C>T (p.Thr460Ile)	not specified [RCV004282989]	uncertain significance	14	73254589	73254589	Human		name
401739935	CV2684217	single nucleotide variant	NM_001365906.3(PAPLN):c.1918G>A (p.Asp640Asn)	not specified [RCV004288882]	uncertain significance	14	73259478	73259478	Human		name
401780610	CV2685564	single nucleotide variant	NM_001365906.3(PAPLN):c.1082C>T (p.Pro361Leu)	not specified [RCV004294575]	uncertain significance	14	73252763	73252763	Human		name
401732781	CV2705022	single nucleotide variant	NM_001365906.3(PAPLN):c.1613G>A (p.Cys538Tyr)	not specified [RCV004309943]	uncertain significance	14	73255004	73255004	Human		name
401761955	CV2713956	single nucleotide variant	NM_001365906.3(PAPLN):c.2186A>G (p.Asp729Gly)	not specified [RCV004315375]	uncertain significance	14	73261235	73261235	Human		name
401751775	CV2727138	single nucleotide variant	NM_001365906.3(PAPLN):c.1103C>T (p.Ala368Val)	not specified [RCV004325497]	uncertain significance	14	73253762	73253762	Human		name
401872320	CV2754340	single nucleotide variant	NM_001365906.3(PAPLN):c.2881G>A (p.Gly961Arg)	not specified [RCV004334516]	uncertain significance	14	73264230	73264230	Human		name
401860992	CV2758700	single nucleotide variant	NM_001365906.3(PAPLN):c.1868C>T (p.Ser623Leu)	not specified [RCV004337764]	uncertain significance	14	73259428	73259428	Human		name
401887502	CV2771977	single nucleotide variant	NM_001365906.3(PAPLN):c.1292C>T (p.Pro431Leu)	not specified [RCV004344665]	uncertain significance	14	73253951	73253951	Human		name
401858411	CV2774041	single nucleotide variant	NM_001365906.3(PAPLN):c.2254G>A (p.Val752Met)	not specified [RCV004345649]	uncertain significance	14	73262358	73262358	Human		name
405759061	CV3364104	single nucleotide variant	NM_001365906.3(PAPLN):c.1115C>T (p.Ala372Val)	not specified [RCV004500305]	uncertain significance	14	73253774	73253774	Human		name
405759066	CV3364105	single nucleotide variant	NM_001365906.3(PAPLN):c.1117C>T (p.Pro373Ser)	not specified [RCV004500306]	uncertain significance	14	73253776	73253776	Human		name
405759072	CV3364106	single nucleotide variant	NM_001365906.3(PAPLN):c.1149G>T (p.Gln383His)	not specified [RCV004500307]	uncertain significance	14	73253808	73253808	Human		name
405759076	CV3364107	single nucleotide variant	NM_001365906.3(PAPLN):c.1267C>G (p.Arg423Gly)	not specified [RCV004500308]	uncertain significance	14	73253926	73253926	Human		name
405759082	CV3364108	single nucleotide variant	NM_001365906.3(PAPLN):c.1271G>A (p.Cys424Tyr)	not specified [RCV004500309]	uncertain significance	14	73253930	73253930	Human		name
405759102	CV3364111	single nucleotide variant	NM_001365906.3(PAPLN):c.1668C>A (p.Asn556Lys)	not specified [RCV004500312]	uncertain significance	14	73259019	73259019	Human		name
405759108	CV3364112	single nucleotide variant	NM_001365906.3(PAPLN):c.2079G>A (p.Met693Ile)	not specified [RCV004500313]	uncertain significance	14	73260802	73260802	Human		name
405759115	CV3364113	single nucleotide variant	NM_001365906.3(PAPLN):c.2330G>A (p.Gly777Asp)	not specified [RCV004500314]	uncertain significance	14	73262434	73262434	Human		name
405759121	CV3364114	single nucleotide variant	NM_001365906.3(PAPLN):c.2387C>T (p.Ser796Leu)	not specified [RCV004500315]	uncertain significance	14	73262491	73262491	Human		name
405759128	CV3364115	single nucleotide variant	NM_001365906.3(PAPLN):c.2485G>A (p.Gly829Ser)	not specified [RCV004500316]	likely benign	14	73262589	73262589	Human		name
405759138	CV3364117	single nucleotide variant	NM_001365906.3(PAPLN):c.2722A>G (p.Arg908Gly)	not specified [RCV004500318]	uncertain significance	14	73262826	73262826	Human		name
405759151	CV3364119	single nucleotide variant	NM_001365906.3(PAPLN):c.2996T>C (p.Met999Thr)	not specified [RCV004500320]	uncertain significance	14	73264597	73264597	Human		name
405759226	CV3364133	single nucleotide variant	NM_001365906.3(PAPLN):c.1033C>T (p.Arg345Cys)	not specified [RCV004500334]	uncertain significance	14	73252714	73252714	Human		name
407518010	CV3466446	single nucleotide variant	NM_001365906.3(PAPLN):c.1928C>T (p.Thr643Met)	not specified [RCV004650855]	uncertain significance	14	73259488	73259488	Human		name
407479475	CV3466447	single nucleotide variant	NM_001365906.3(PAPLN):c.2441C>T (p.Pro814Leu)	not specified [RCV004664142]	uncertain significance	14	73262545	73262545	Human		name
407479479	CV3466448	single nucleotide variant	NM_001365906.3(PAPLN):c.1352G>A (p.Arg451Gln)	not specified [RCV004664143]	likely benign	14	73254562	73254562	Human		name
407518013	CV3466449	single nucleotide variant	NM_001365906.3(PAPLN):c.1795C>G (p.Gln599Glu)	not specified [RCV004650856]	uncertain significance	14	73259355	73259355	Human		name
407518016	CV3466450	single nucleotide variant	NM_001365906.3(PAPLN):c.2438G>A (p.Arg813His)	not specified [RCV004650857]	uncertain significance	14	73262542	73262542	Human		name
407479483	CV3466451	single nucleotide variant	NM_001365906.3(PAPLN):c.1678C>T (p.Pro560Ser)	not specified [RCV004664144]	likely benign	14	73259029	73259029	Human		name
407518019	CV3466452	single nucleotide variant	NM_001365906.3(PAPLN):c.2029C>T (p.His677Tyr)	not specified [RCV004650858]	uncertain significance	14	73260752	73260752	Human		name
407518022	CV3466453	single nucleotide variant	NM_001365906.3(PAPLN):c.2349G>T (p.Trp783Cys)	not specified [RCV004650859]	uncertain significance	14	73262453	73262453	Human		name
407518028	CV3466455	single nucleotide variant	NM_001365906.3(PAPLN):c.1732G>A (p.Ala578Thr)	not specified [RCV004650861]	uncertain significance	14	73259292	73259292	Human		name
407479487	CV3466459	single nucleotide variant	NM_001365906.3(PAPLN):c.1450A>C (p.Ser484Arg)	not specified [RCV004664145]	likely benign	14	73254660	73254660	Human		name
597717433	CV3571234	single nucleotide variant	NM_001365906.3(PAPLN):c.1385C>T (p.Ala462Val)	not specified [RCV004841531]	uncertain significance	14	73254595	73254595	Human		name
597717441	CV3571235	single nucleotide variant	NM_001365906.3(PAPLN):c.2635C>T (p.Pro879Ser)	not specified [RCV004841532]	uncertain significance	14	73262739	73262739	Human		name
597717458	CV3571237	single nucleotide variant	NM_001365906.3(PAPLN):c.1222G>A (p.Gly408Arg)	not specified [RCV004841534]	uncertain significance	14	73253881	73253881	Human		name
597717472	CV3571239	single nucleotide variant	NM_001365906.3(PAPLN):c.1058G>A (p.Arg353His)	not specified [RCV004841536]	uncertain significance	14	73252739	73252739	Human		name
597717480	CV3571240	single nucleotide variant	NM_001365906.3(PAPLN):c.1153C>T (p.Arg385Cys)	not specified [RCV004841537]	uncertain significance	14	73253812	73253812	Human		name
597717488	CV3571241	single nucleotide variant	NM_001365906.3(PAPLN):c.2089A>G (p.Arg697Gly)	not specified [RCV004841538]	uncertain significance	14	73260812	73260812	Human		name
597717498	CV3571242	single nucleotide variant	NM_001365906.3(PAPLN):c.1286C>T (p.Pro429Leu)	not specified [RCV004841539]	uncertain significance	14	73253945	73253945	Human		name
597657858	CV3571244	single nucleotide variant	NM_001365906.3(PAPLN):c.1231G>T (p.Gly411Trp)	not specified [RCV004827685]	uncertain significance	14	73253890	73253890	Human		name
597717518	CV3571245	single nucleotide variant	NM_001365906.3(PAPLN):c.2249A>T (p.Tyr750Phe)	not specified [RCV004841541]	uncertain significance	14	73262353	73262353	Human		name
597717529	CV3571247	single nucleotide variant	NM_001365906.3(PAPLN):c.2687G>T (p.Gly896Val)	not specified [RCV004841542]	uncertain significance	14	73262791	73262791	Human		name
597717550	CV3571250	single nucleotide variant	NM_001365906.3(PAPLN):c.2204C>T (p.Ala735Val)	not specified [RCV004841544]	uncertain significance	14	73261253	73261253	Human		name
597657872	CV3571253	single nucleotide variant	NM_001365906.3(PAPLN):c.1674G>C (p.Trp558Cys)	not specified [RCV004827687]	uncertain significance	14	73259025	73259025	Human		name
597717584	CV3571254	single nucleotide variant	NM_001365906.3(PAPLN):c.2408G>C (p.Ser803Thr)	not specified [RCV004841547]	uncertain significance	14	73262512	73262512	Human		name
597657878	CV3571255	single nucleotide variant	NM_001365906.3(PAPLN):c.1028G>A (p.Cys343Tyr)	not specified [RCV004827688]	uncertain significance	14	73252709	73252709	Human		name
597717594	CV3571256	single nucleotide variant	NM_001365906.3(PAPLN):c.2077A>G (p.Met693Val)	not specified [RCV004841548]	uncertain significance	14	73260800	73260800	Human		name
597717613	CV3571258	single nucleotide variant	NM_001365906.3(PAPLN):c.2366G>C (p.Gly789Ala)	not specified [RCV004841550]	uncertain significance	14	73262470	73262470	Human		name
597717626	CV3571259	single nucleotide variant	NM_001365906.3(PAPLN):c.2606C>T (p.Ala869Val)	not specified [RCV004841551]	uncertain significance	14	73262710	73262710	Human		name
597717645	CV3571261	single nucleotide variant	NM_001365906.3(PAPLN):c.2335T>G (p.Cys779Gly)	not specified [RCV004841553]	uncertain significance	14	73262439	73262439	Human		name
597717656	CV3571262	single nucleotide variant	NM_001365906.3(PAPLN):c.1340G>A (p.Ser447Asn)	not specified [RCV004841554]	uncertain significance	14	73254550	73254550	Human		name
597717671	CV3571263	single nucleotide variant	NM_001365906.3(PAPLN):c.2944C>T (p.Arg982Trp)	not specified [RCV004841555]	uncertain significance	14	73264293	73264293	Human		name
598259246	CV4005814	single nucleotide variant	NM_001365906.3(PAPLN):c.2618A>C (p.Gln873Pro)	not specified [RCV005386447]	uncertain significance	14	73262722	73262722	Human		name
598259281	CV4005820	single nucleotide variant	NM_001365906.3(PAPLN):c.1904A>G (p.His635Arg)	not specified [RCV005386453]	uncertain significance	14	73259464	73259464	Human		name
598259288	CV4005821	single nucleotide variant	NM_001365906.3(PAPLN):c.1537A>T (p.Ile513Phe)	not specified [RCV005386454]	uncertain significance	14	73254928	73254928	Human		name
598259293	CV4005822	single nucleotide variant	NM_001365906.3(PAPLN):c.1268G>T (p.Arg423Leu)	not specified [RCV005386455]	uncertain significance	14	73253927	73253927	Human		name
598259298	CV4005823	single nucleotide variant	NM_001365906.3(PAPLN):c.1312A>T (p.Ser438Cys)	not specified [RCV005386456]	uncertain significance	14	73254522	73254522	Human		name
598259304	CV4005824	single nucleotide variant	NM_001365906.3(PAPLN):c.1576A>G (p.Lys526Glu)	not specified [RCV005386457]	uncertain significance	14	73254967	73254967	Human		name
598259315	CV4005826	single nucleotide variant	NM_001365906.3(PAPLN):c.1166G>A (p.Cys389Tyr)	not specified [RCV005386459]	uncertain significance	14	73253825	73253825	Human		name
15198071	CV725789	single nucleotide variant	NM_001365906.3(PAPLN):c.2017G>A (p.Ala673Thr)	not provided [RCV000890248]	benign	14	73260740	73260740	Human		name
156057477	CV2239097	single nucleotide variant	NM_001365906.3(PAPLN):c.3638G>A (p.Arg1213His)	not specified [RCV004112099]	uncertain significance	14	73268694	73268694	Human		name
156088581	CV2259060	single nucleotide variant	NM_001365906.3(PAPLN):c.3578G>A (p.Arg1193Gln)	not specified [RCV004120324]	likely benign	14	73268634	73268634	Human		name
156112233	CV2261891	single nucleotide variant	NM_001365906.3(PAPLN):c.3518A>G (p.Gln1173Arg)	not specified [RCV004127942]	likely benign	14	73268574	73268574	Human		name
156257680	CV2264899	single nucleotide variant	NM_001365906.3(PAPLN):c.3241G>A (p.Gly1081Arg)	not specified [RCV004134647]	uncertain significance	14	73265485	73265485	Human		name
156072708	CV2267543	single nucleotide variant	NM_001365906.3(PAPLN):c.3752A>G (p.Gln1251Arg)	not specified [RCV004135962]	uncertain significance	14	73272579	73272579	Human		name
156056218	CV2269708	single nucleotide variant	NM_001365906.3(PAPLN):c.3824C>T (p.Pro1275Leu)	not specified [RCV004126695]	uncertain significance	14	73272651	73272651	Human		name
155969605	CV2335486	single nucleotide variant	NM_001365906.3(PAPLN):c.3826A>T (p.Ile1276Phe)	not specified [RCV004191656]	uncertain significance	14	73272653	73272653	Human		name
156080448	CV2337518	single nucleotide variant	NM_001365906.3(PAPLN):c.3738G>C (p.Leu1246Phe)	not specified [RCV004187948]	uncertain significance	14	73272565	73272565	Human		name
156083350	CV2342991	single nucleotide variant	NM_001365906.3(PAPLN):c.3196C>T (p.Arg1066Cys)	not specified [RCV004192594]	uncertain significance	14	73265440	73265440	Human		name
329377258	CV2435861	single nucleotide variant	NM_001365906.3(PAPLN):c.3449C>A (p.Ala1150Asp)	not specified [RCV004255096]	uncertain significance	14	73266780	73266780	Human		name
329364495	CV2447527	single nucleotide variant	NM_001365906.3(PAPLN):c.3359G>A (p.Arg1120Gln)	not specified [RCV004255888]	uncertain significance	14	73266596	73266596	Human		name
329396499	CV2462602	single nucleotide variant	NM_001365906.3(PAPLN):c.3619G>C (p.Gly1207Arg)	not specified [RCV004278548]	uncertain significance	14	73268675	73268675	Human		name
329382313	CV2465169	single nucleotide variant	NM_001365906.3(PAPLN):c.3025C>A (p.Arg1009Ser)	not specified [RCV004287214]	uncertain significance	14	73264626	73264626	Human		name
329394158	CV2472355	single nucleotide variant	NM_001365906.3(PAPLN):c.3275A>T (p.Gln1092Leu)	not specified [RCV004285238]	uncertain significance	14	73266512	73266512	Human		name
401727920	CV2678585	single nucleotide variant	NM_001365906.3(PAPLN):c.3449C>T (p.Ala1150Val)	not specified [RCV004292592]	uncertain significance	14	73266780	73266780	Human		name
401766066	CV2717993	single nucleotide variant	NM_001365906.3(PAPLN):c.3770A>G (p.Tyr1257Cys)	not specified [RCV004321938]	uncertain significance	14	73272597	73272597	Human		name
401865319	CV2778690	single nucleotide variant	NM_001365906.3(PAPLN):c.3059T>C (p.Phe1020Ser)	not specified [RCV004346607]	likely benign	14	73264660	73264660	Human		name
405759158	CV3364120	single nucleotide variant	NM_001365906.3(PAPLN):c.3002T>C (p.Val1001Ala)	not specified [RCV004500321]	uncertain significance	14	73264603	73264603	Human		name
405759176	CV3364123	single nucleotide variant	NM_001365906.3(PAPLN):c.3197G>A (p.Arg1066His)	not specified [RCV004500324]	uncertain significance	14	73265441	73265441	Human		name
405759182	CV3364124	single nucleotide variant	NM_001365906.3(PAPLN):c.3345C>G (p.Phe1115Leu)	not specified [RCV004500325]	uncertain significance	14	73266582	73266582	Human		name
407518041	CV3466460	single nucleotide variant	NM_001365906.3(PAPLN):c.3706G>A (p.Val1236Ile)	not specified [RCV004650865]	likely benign	14	73272533	73272533	Human		name
597717415	CV3571231	single nucleotide variant	NM_001365906.3(PAPLN):c.3446C>T (p.Thr1149Met)	not specified [RCV004841529]	uncertain significance	14	73266777	73266777	Human		name
597657850	CV3571232	single nucleotide variant	NM_001365906.3(PAPLN):c.3016G>A (p.Glu1006Lys)	not specified [RCV004827684]	uncertain significance	14	73264617	73264617	Human		name
597717425	CV3571233	single nucleotide variant	NM_001365906.3(PAPLN):c.3766G>A (p.Glu1256Lys)	not specified [RCV004841530]	uncertain significance	14	73272593	73272593	Human		name
597717449	CV3571236	single nucleotide variant	NM_001365906.3(PAPLN):c.3004C>G (p.Leu1002Val)	not specified [RCV004841533]	uncertain significance	14	73264605	73264605	Human		name
597657864	CV3571246	single nucleotide variant	NM_001365906.3(PAPLN):c.3136G>A (p.Asp1046Asn)	not specified [RCV004827686]	uncertain significance	14	73265380	73265380	Human		name
597717562	CV3571251	single nucleotide variant	NM_001365906.3(PAPLN):c.3137A>G (p.Asp1046Gly)	not specified [RCV004841545]	uncertain significance	14	73265381	73265381	Human		name
597717604	CV3571257	single nucleotide variant	NM_001365906.3(PAPLN):c.3821A>G (p.Gln1274Arg)	not specified [RCV004841549]	uncertain significance	14	73272648	73272648	Human		name
598259241	CV4005813	single nucleotide variant	NM_001365906.3(PAPLN):c.3197G>T (p.Arg1066Leu)	not specified [RCV005386446]	uncertain significance	14	73265441	73265441	Human		name
598259273	CV4005819	single nucleotide variant	NM_001365906.3(PAPLN):c.3610G>A (p.Ala1204Thr)	not specified [RCV005386452]	uncertain significance	14	73268666	73268666	Human		name
598259309	CV4005825	single nucleotide variant	NM_001365906.3(PAPLN):c.3646G>A (p.Glu1216Lys)	not specified [RCV005386458]	uncertain significance	14	73268702	73268702	Human		name
15121965	CV714228	single nucleotide variant	NM_001365906.3(PAPLN):c.3340G>A (p.Ala1114Thr)	not provided [RCV000962990]	benign	14	73266577	73266577	Human		name

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