Anpep Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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106 records found for search term Anpep

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15168533	CV779980	single nucleotide variant	NM_001150.3(ANPEP):c.614+9C>T	not provided [RCV000971634]	benign	15	89805961	89805961	Human		name
15147690	CV779728	single nucleotide variant	NM_001150.3(ANPEP):c.1437+8C>G	not provided [RCV000967390]	benign	15	89803639	89803639	Human		name
15147649	CV779975	single nucleotide variant	NM_001150.3(ANPEP):c.1437+9C>G	not provided [RCV000967381]	benign	15	89803638	89803638	Human		name
15164785	CV760246	single nucleotide variant	NM_001150.3(ANPEP):c.1437+10G>A	not provided [RCV000926467]	benign	15	89803637	89803637	Human		name
597636241	CV3561948	single nucleotide variant	NM_001150.3(ANPEP):c.23C>T (p.Ser8Phe)	not specified [RCV004831319]	uncertain significance	15	89806561	89806561	Human		name
15193888	CV703413	single nucleotide variant	NM_001150.3(ANPEP):c.192C>A (p.Thr64=)	not provided [RCV000955497]	benign\|likely benign	15	89806392	89806392	Human		name
150504039	CV1212603	single nucleotide variant	NM_001150.3(ANPEP):c.954G>T (p.Leu318=)	not provided [RCV001595478]	benign	15	89804561	89804561	Human		name
150449927	CV1275737	single nucleotide variant	NM_001150.3(ANPEP):c.963G>A (p.Thr321=)	not provided [RCV001708192]	benign	15	89804552	89804552	Human		name
155988919	CV2355184	single nucleotide variant	NM_001150.3(ANPEP):c.67G>A (p.Val23Met)	not specified [RCV004198565]	uncertain significance	15	89806517	89806517	Human		name
407489776	CV3451056	single nucleotide variant	NM_001150.3(ANPEP):c.82G>T (p.Ala28Ser)	not specified [RCV004641535]	uncertain significance	15	89806502	89806502	Human		name
15111273	CV714685	single nucleotide variant	NM_001150.3(ANPEP):c.298C>T (p.Leu100=)	not provided [RCV000961073]	benign\|likely benign	15	89806286	89806286	Human		name
15102238	CV770414	single nucleotide variant	NM_001150.3(ANPEP):c.894C>G (p.Val298=)	not provided [RCV000936952]	likely benign	15	89805081	89805081	Human		name
156238768	CV2235843	single nucleotide variant	NM_001150.3(ANPEP):c.182C>T (p.Ser61Leu)	not specified [RCV004111959]	likely benign	15	89806402	89806402	Human		name
156006744	CV2299608	single nucleotide variant	NM_001150.3(ANPEP):c.263C>T (p.Thr88Met)	not specified [RCV004154928]	uncertain significance	15	89806321	89806321	Human		name
156077453	CV2331881	single nucleotide variant	NM_001150.3(ANPEP):c.121G>A (p.Ala41Thr)	not specified [RCV004186536]	uncertain significance	15	89806463	89806463	Human		name
156332605	CV2339809	single nucleotide variant	NM_001150.3(ANPEP):c.157G>A (p.Ala53Thr)	not specified [RCV004196500]	likely benign	15	89806427	89806427	Human		name
329358769	CV2425369	single nucleotide variant	NM_001150.3(ANPEP):c.152C>T (p.Pro51Leu)	not specified [RCV004251030]	uncertain significance	15	89806432	89806432	Human		name
329371018	CV2431842	single nucleotide variant	NM_001150.3(ANPEP):c.218G>A (p.Arg73His)	not specified [RCV004254983]	uncertain significance	15	89806366	89806366	Human		name
329372054	CV2442866	single nucleotide variant	NM_001150.3(ANPEP):c.247G>T (p.Asp83Tyr)	not specified [RCV004253475]	uncertain significance	15	89806337	89806337	Human		name
401775116	CV2696223	single nucleotide variant	NM_001150.3(ANPEP):c.236C>T (p.Thr79Met)	not specified [RCV004310265]	uncertain significance	15	89806348	89806348	Human		name
407526457	CV3454985	single nucleotide variant	NM_001150.3(ANPEP):c.262A>T (p.Thr88Ser)	not specified [RCV004654820]	uncertain significance	15	89806322	89806322	Human		name
597667159	CV3561862	single nucleotide variant	NM_001150.3(ANPEP):c.272C>T (p.Pro91Leu)	not specified [RCV004829210]	uncertain significance	15	89806312	89806312	Human		name
15099070	CV703412	single nucleotide variant	NM_001150.3(ANPEP):c.1839C>T (p.Ser613=)	not provided [RCV000958696]	benign	15	89799540	89799540	Human		name
15110978	CV714684	single nucleotide variant	NM_001150.3(ANPEP):c.2310G>A (p.Glu770=)	not provided [RCV000961013]	benign	15	89792502	89792502	Human		name
15111164	CV726338	single nucleotide variant	NM_001150.3(ANPEP):c.2433C>T (p.Phe811=)	not provided [RCV000894217]	benign	15	89792255	89792255	Human		name
15110409	CV726339	single nucleotide variant	NM_001150.3(ANPEP):c.2013C>G (p.Ala671=)	not provided [RCV000894057]	benign	15	89797719	89797719	Human		name
15166153	CV754779	single nucleotide variant	NM_001150.3(ANPEP):c.2808C>T (p.Ala936=)	not provided [RCV000926800]	likely benign	15	89785445	89785445	Human		name
15115195	CV754780	single nucleotide variant	NM_001150.3(ANPEP):c.1431C>T (p.Tyr477=)	not provided [RCV000917413]	likely benign	15	89803653	89803653	Human		name
15144576	CV754781	single nucleotide variant	NM_001150.3(ANPEP):c.1245C>A (p.Ser415=)	not provided [RCV000922391]	likely benign	15	89803937	89803937	Human		name
8627724	CV82868	single nucleotide variant	NM_001150.2(ANPEP):c.2415G>A (p.Gly805=)	Malignant melanoma [RCV000062948]	not provided	15	89792273	89792273	Human		name
150470488	CV1269854	single nucleotide variant	NM_001150.3(ANPEP):c.932C>T (p.Ala311Val)	not provided [RCV001695141]	benign	15	89804583	89804583	Human	4	name
150470488	CV1269854	single nucleotide variant	NM_001150.3(ANPEP):c.932C>T (p.Ala311Val)	not provided [RCV001695141]	benign	15	89804583	89804584	Human	4	name
156044063	CV2342364	single nucleotide variant	NM_001150.3(ANPEP):c.992A>G (p.His331Arg)	not specified [RCV004191930]	uncertain significance	15	89804523	89804523	Human		name
156071899	CV2353271	single nucleotide variant	NM_001150.3(ANPEP):c.958G>A (p.Val320Met)	not specified [RCV004205749]	uncertain significance	15	89804557	89804557	Human		name
156382860	CV2362972	single nucleotide variant	NM_001150.3(ANPEP):c.325G>A (p.Val109Ile)	not specified [RCV004211117]	uncertain significance	15	89806259	89806259	Human		name
156092676	CV2381923	single nucleotide variant	NM_001150.3(ANPEP):c.769C>A (p.Pro257Thr)	not specified [RCV004225861]	uncertain significance	15	89805206	89805206	Human		name
329375902	CV2431660	single nucleotide variant	NM_001150.3(ANPEP):c.366C>G (p.Ile122Met)	not specified [RCV004248830]	uncertain significance	15	89806218	89806218	Human		name
401728791	CV2673048	single nucleotide variant	NM_001150.3(ANPEP):c.837G>C (p.Leu279Phe)	not specified [RCV004284037]	uncertain significance	15	89805138	89805138	Human		name
401730351	CV2680145	single nucleotide variant	NM_001150.3(ANPEP):c.902G>A (p.Arg301Gln)	not specified [RCV004286629]	uncertain significance	15	89804613	89804613	Human		name
401723779	CV2684864	single nucleotide variant	NM_001150.3(ANPEP):c.307T>C (p.Phe103Leu)	not specified [RCV004296370]	uncertain significance	15	89806277	89806277	Human		name
401728876	CV2693887	single nucleotide variant	NM_001150.3(ANPEP):c.656A>T (p.Lys219Met)	not specified [RCV004300187]	uncertain significance	15	89805422	89805422	Human		name
401743652	CV2696838	single nucleotide variant	NM_001150.3(ANPEP):c.946T>C (p.Tyr316His)	not specified [RCV004290805]	uncertain significance	15	89804569	89804569	Human		name
401767706	CV2727251	single nucleotide variant	NM_001150.3(ANPEP):c.760C>G (p.Pro254Ala)	not specified [RCV004327369]	uncertain significance	15	89805215	89805215	Human		name
405696101	CV3282609	single nucleotide variant	NM_001150.3(ANPEP):c.941G>A (p.Gly314Asp)	not specified [RCV004424570]	uncertain significance	15	89804574	89804574	Human		name
407489669	CV3454943	single nucleotide variant	NM_001150.3(ANPEP):c.943G>A (p.Asp315Asn)	not specified [RCV004641513]	uncertain significance	15	89804572	89804572	Human		name
407526404	CV3454954	single nucleotide variant	NM_001150.3(ANPEP):c.929C>T (p.Ala310Val)	not specified [RCV004654801]	uncertain significance	15	89804586	89804586	Human		name
407489731	CV3454975	single nucleotide variant	NM_001150.3(ANPEP):c.317C>T (p.Ser106Phe)	not specified [RCV004641525]	uncertain significance	15	89806267	89806267	Human		name
597667187	CV3561902	single nucleotide variant	NM_001150.3(ANPEP):c.868G>A (p.Val290Met)	not specified [RCV004829239]	uncertain significance	15	89805107	89805107	Human		name
597636252	CV3561967	single nucleotide variant	NM_001150.3(ANPEP):c.365T>C (p.Ile122Thr)	not specified [RCV004831321]	uncertain significance	15	89806219	89806219	Human		name
597636346	CV3561986	single nucleotide variant	NM_001150.3(ANPEP):c.424G>A (p.Val142Met)	not specified [RCV004831340]	uncertain significance	15	89806160	89806160	Human		name
597636379	CV3561995	single nucleotide variant	NM_001150.3(ANPEP):c.439C>G (p.Pro147Ala)	not specified [RCV004831346]	likely benign	15	89806145	89806145	Human		name
597636384	CV3562000	single nucleotide variant	NM_001150.3(ANPEP):c.442C>A (p.Pro148Thr)	not specified [RCV004831347]	uncertain significance	15	89806142	89806142	Human		name
598263449	CV3986449	single nucleotide variant	NM_001150.3(ANPEP):c.956A>C (p.Asn319Thr)	not specified [RCV005387455]	uncertain significance	15	89804559	89804559	Human		name
598227368	CV3990067	single nucleotide variant	NM_001150.3(ANPEP):c.715C>T (p.His239Tyr)	not specified [RCV005380715]	uncertain significance	15	89805363	89805363	Human		name
15192622	CV726341	single nucleotide variant	NM_001150.3(ANPEP):c.772C>A (p.Leu258Ile)	ANPEP-related disorder [RCV003940613]\|not provided [RCV000888713]	likely benign	15	89805203	89805203	Human		name , trait , alternate_id
156380281	CV2208085	single nucleotide variant	NM_001150.3(ANPEP):c.1249G>A (p.Val417Met)	not specified [RCV004086772]	uncertain significance	15	89803933	89803933	Human		name
156330691	CV2210680	single nucleotide variant	NM_001150.3(ANPEP):c.1394C>A (p.Pro465Gln)	not specified [RCV004083821]	uncertain significance	15	89803690	89803690	Human		name
156197303	CV2241609	single nucleotide variant	NM_001150.3(ANPEP):c.2092G>A (p.Ala698Thr)	not specified [RCV004104494]	uncertain significance	15	89797640	89797640	Human		name
156154085	CV2266051	single nucleotide variant	NM_001150.3(ANPEP):c.2801C>A (p.Thr934Asn)	not specified [RCV004126865]	uncertain significance	15	89785452	89785452	Human		name
156172529	CV2293349	single nucleotide variant	NM_001150.3(ANPEP):c.2612T>C (p.Ile871Thr)	not specified [RCV004150829]	uncertain significance	15	89791010	89791010	Human		name
155962935	CV2308213	single nucleotide variant	NM_001150.3(ANPEP):c.2310G>C (p.Glu770Asp)	not specified [RCV004164714]	uncertain significance	15	89792502	89792502	Human		name
155921324	CV2350648	single nucleotide variant	NM_001150.3(ANPEP):c.2455G>A (p.Ala819Thr)	not specified [RCV004204986]	uncertain significance	15	89792233	89792233	Human		name
156062519	CV2351421	single nucleotide variant	NM_001150.3(ANPEP):c.1483G>A (p.Val495Ile)	not specified [RCV004193109]	uncertain significance	15	89803462	89803462	Human		name
156137435	CV2357436	single nucleotide variant	NM_001150.3(ANPEP):c.2320G>A (p.Gly774Ser)	not specified [RCV004200312]	uncertain significance	15	89792492	89792492	Human		name
156071972	CV2365355	single nucleotide variant	NM_001150.3(ANPEP):c.1984A>G (p.Ile662Val)	not specified [RCV004209440]	uncertain significance	15	89799285	89799285	Human		name
156050502	CV2367515	single nucleotide variant	NM_001150.3(ANPEP):c.1304T>G (p.Met435Arg)	not specified [RCV004211450]	uncertain significance	15	89803780	89803780	Human		name
329385613	CV2432139	single nucleotide variant	NM_001150.3(ANPEP):c.2257G>A (p.Glu753Lys)	not specified [RCV004249285]	uncertain significance	15	89792555	89792555	Human		name
329370815	CV2461818	single nucleotide variant	NM_001150.3(ANPEP):c.1649C>T (p.Pro550Leu)	not specified [RCV004271738]	uncertain significance	15	89801528	89801528	Human		name
401728427	CV2672927	single nucleotide variant	NM_001150.3(ANPEP):c.1322A>G (p.Tyr441Cys)	not specified [RCV004283930]	uncertain significance	15	89803762	89803762	Human		name
401737985	CV2676089	single nucleotide variant	NM_001150.3(ANPEP):c.1880C>T (p.Thr627Met)	not specified [RCV004284315]	uncertain significance	15	89799499	89799499	Human		name
401719360	CV2679508	single nucleotide variant	NM_001150.3(ANPEP):c.1088G>A (p.Arg363Gln)	not specified [RCV004287812]	uncertain significance	15	89804344	89804344	Human		name
401782252	CV2719252	single nucleotide variant	NM_001150.3(ANPEP):c.1899C>G (p.Asn633Lys)	not specified [RCV004324900]	uncertain significance	15	89799480	89799480	Human		name
401893783	CV2759818	single nucleotide variant	NM_001150.3(ANPEP):c.1128C>A (p.Ser376Arg)	not specified [RCV004343254]	uncertain significance	15	89804304	89804304	Human		name
405279318	CV3206918	single nucleotide variant	NM_001150.3(ANPEP):c.1858G>C (p.Val620Leu)	ANPEP-related disorder [RCV003919476]	likely benign	15	89799521	89799521	Human	1	name , trait , alternate_id
405279318	CV3206918	single nucleotide variant	NM_001150.3(ANPEP):c.1858G>C (p.Val620Leu)	ANPEP-related disorder [RCV003919476]	likely benign	15	89799521	89799522	Human	1	name , trait , alternate_id
405696039	CV3282598	single nucleotide variant	NM_001150.3(ANPEP):c.1069T>G (p.Trp357Gly)	not specified [RCV004424559]	uncertain significance	15	89804363	89804363	Human		name
405696042	CV3282599	single nucleotide variant	NM_001150.3(ANPEP):c.1354T>C (p.Ser452Pro)	not specified [RCV004424560]	uncertain significance	15	89803730	89803730	Human		name
405696049	CV3282600	single nucleotide variant	NM_001150.3(ANPEP):c.1482C>A (p.Asp494Glu)	not specified [RCV004424561]	uncertain significance	15	89803463	89803463	Human		name
405696054	CV3282601	single nucleotide variant	NM_001150.3(ANPEP):c.1708C>G (p.Pro570Ala)	not specified [RCV004424562]	uncertain significance	15	89801469	89801469	Human		name
405696060	CV3282602	single nucleotide variant	NM_001150.3(ANPEP):c.1772T>A (p.Ile591Asn)	not specified [RCV004424563]	uncertain significance	15	89801158	89801158	Human		name
405696065	CV3282603	single nucleotide variant	NM_001150.3(ANPEP):c.1906G>A (p.Glu636Lys)	not specified [RCV004424564]	uncertain significance	15	89799473	89799473	Human		name
405696072	CV3282604	single nucleotide variant	NM_001150.3(ANPEP):c.2194C>A (p.His732Asn)	not specified [RCV004424565]	uncertain significance	15	89793090	89793090	Human		name
405696078	CV3282605	single nucleotide variant	NM_001150.3(ANPEP):c.2638G>C (p.Val880Leu)	not specified [RCV004424566]	uncertain significance	15	89790984	89790984	Human		name
405696085	CV3282606	single nucleotide variant	NM_001150.3(ANPEP):c.2668G>T (p.Asp890Tyr)	not specified [RCV004424567]	uncertain significance	15	89790954	89790954	Human		name
405696090	CV3282607	single nucleotide variant	NM_001150.3(ANPEP):c.2791G>A (p.Gly931Ser)	not specified [RCV004424568]	uncertain significance	15	89785462	89785462	Human		name
405696097	CV3282608	single nucleotide variant	NM_001150.3(ANPEP):c.2807C>G (p.Ala936Gly)	not specified [RCV004424569]	uncertain significance	15	89785446	89785446	Human		name
407526430	CV3454965	single nucleotide variant	NM_001150.3(ANPEP):c.1379C>T (p.Ser460Leu)	not specified [RCV004654810]	uncertain significance	15	89803705	89803705	Human		name
407489758	CV3454996	single nucleotide variant	NM_001150.3(ANPEP):c.2369C>G (p.Pro790Arg)	not specified [RCV004641531]	uncertain significance	15	89792319	89792319	Human		name
597667031	CV3561880	single nucleotide variant	NM_001150.3(ANPEP):c.1582C>T (p.Arg528Trp)	not specified [RCV004829228]	uncertain significance	15	89801595	89801595	Human		name
597666769	CV3561889	single nucleotide variant	NM_001150.3(ANPEP):c.1919G>A (p.Arg640Lys)	not specified [RCV004829237]	likely benign	15	89799460	89799460	Human		name
597666774	CV3561892	single nucleotide variant	NM_001150.3(ANPEP):c.1775G>A (p.Arg592Lys)	not specified [RCV004829238]	likely benign	15	89801155	89801155	Human		name
597666820	CV3561910	single nucleotide variant	NM_001150.3(ANPEP):c.2267C>T (p.Ala756Val)	not specified [RCV004829244]	uncertain significance	15	89792545	89792545	Human		name
597636164	CV3561920	single nucleotide variant	NM_001150.3(ANPEP):c.1681C>G (p.Leu561Val)	not specified [RCV004831304]	uncertain significance	15	89801496	89801496	Human		name
597636224	CV3561931	single nucleotide variant	NM_001150.3(ANPEP):c.1970A>G (p.Asn657Ser)	not specified [RCV004831315]	uncertain significance	15	89799299	89799299	Human		name
597636233	CV3561941	single nucleotide variant	NM_001150.3(ANPEP):c.2551C>T (p.Pro851Ser)	not specified [RCV004831317]	uncertain significance	15	89791071	89791071	Human		name
597636237	CV3561947	single nucleotide variant	NM_001150.3(ANPEP):c.1708C>T (p.Pro570Ser)	not specified [RCV004831318]	uncertain significance	15	89801469	89801469	Human		name
597636246	CV3561958	single nucleotide variant	NM_001150.3(ANPEP):c.1299C>G (p.Asp433Glu)	not specified [RCV004831320]	uncertain significance	15	89803785	89803785	Human		name
597636293	CV3561975	single nucleotide variant	NM_001150.3(ANPEP):c.2411G>C (p.Gly804Ala)	not specified [RCV004831329]	uncertain significance	15	89792277	89792277	Human		name
597636389	CV3562004	single nucleotide variant	NM_001150.3(ANPEP):c.1570G>T (p.Ala524Ser)	not specified [RCV004831348]	uncertain significance	15	89801607	89801607	Human		name
598263401	CV3986418	single nucleotide variant	NM_001150.3(ANPEP):c.2723G>A (p.Arg908Gln)	not specified [RCV005387442]	uncertain significance	15	89790488	89790488	Human		name
598227458	CV3986429	single nucleotide variant	NM_001150.3(ANPEP):c.1219C>G (p.Leu407Val)	not specified [RCV005380728]	uncertain significance	15	89803963	89803963	Human		name
598227492	CV3986438	single nucleotide variant	NM_001150.3(ANPEP):c.1012C>A (p.Leu338Ile)	not specified [RCV005380733]	uncertain significance	15	89804503	89804503	Human		name
598263460	CV3986457	single nucleotide variant	NM_001150.3(ANPEP):c.1883G>A (p.Gly628Asp)	not specified [RCV005387458]	uncertain significance	15	89799496	89799496	Human		name
598263383	CV3990060	single nucleotide variant	NM_001150.3(ANPEP):c.2564G>A (p.Arg855Gln)	not specified [RCV005387436]	uncertain significance	15	89791058	89791058	Human		name
15192619	CV726340	single nucleotide variant	NM_001150.3(ANPEP):c.1265C>G (p.Ala422Gly)	ANPEP-related disorder [RCV003930733]\|not provided [RCV000888712]	likely benign	15	89803917	89803917	Human		name , trait , alternate_id
8635632	CV90854	single nucleotide variant	NM_001150.2(ANPEP):c.1252G>A (p.Glu418Lys)	Malignant melanoma [RCV000070952]	not provided	15	89803930	89803930	Human		name

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