Alpi Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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84 records found for search term Alpi

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405257937	CV3207967	single nucleotide variant	NM_001631.5(ALPI):c.-7C>G	ALPI-related disorder [RCV003941435]	likely benign	2	232456193	232456193	Human		name , trait , alternate_id
405277115	CV3198759	single nucleotide variant	NM_001631.5(ALPI):c.857-7C>T	ALPI-related disorder [RCV003904083]	likely benign	2	232457991	232457991	Human		name , trait , alternate_id
405293890	CV3214631	single nucleotide variant	NM_001631.5(ALPI):c.783+8G>A	ALPI-related disorder [RCV003932289]	benign	2	232457707	232457707	Human		name , trait , alternate_id
404984377	CV2849363	single nucleotide variant	NM_001631.5(ALPI):c.991+33C>T	not specified [RCV003489235]	benign	2	232458165	232458165	Human		name
404982042	CV2848976	single nucleotide variant	NM_001631.5(ALPI):c.1183+59T>C	not specified [RCV003488848]	benign	2	232458467	232458467	Human		name
405806602	CV3268619	single nucleotide variant	NM_001631.5(ALPI):c.20T>C (p.Leu7Pro)	ALPI-related disorder [RCV004750463]\|not specified [RCV004406133]	uncertain significance	2	232456219	232456219	Human		name , trait , alternate_id
408376765	CV3516276	single nucleotide variant	NM_001631.5(ALPI):c.153C>T (p.Val51=)	ALPI-related disorder [RCV004749449]	likely benign	2	232456434	232456434	Human		name , trait , alternate_id
596929824	CV3538616	single nucleotide variant	NM_001631.5(ALPI):c.26T>C (p.Leu9Pro)	not provided [RCV004792085]	uncertain significance	2	232456225	232456225	Human		name
405283534	CV3191752	single nucleotide variant	NM_001631.5(ALPI):c.58G>A (p.Val20Ile)	ALPI-related disorder [RCV003921852]	benign	2	232456257	232456257	Human		name , trait , alternate_id
405272477	CV3199348	single nucleotide variant	NM_001631.5(ALPI):c.98G>T (p.Arg33Leu)	ALPI-related disorder [RCV003914296]	benign	2	232456379	232456379	Human		name , trait , alternate_id
405258180	CV3208272	single nucleotide variant	NM_001631.5(ALPI):c.870C>T (p.Pro290=)	ALPI-related disorder [RCV003941703]	benign	2	232458011	232458011	Human		name , trait , alternate_id
405290129	CV3214036	single nucleotide variant	NM_001631.5(ALPI):c.660C>T (p.Gly220=)	ALPI-related disorder [RCV003926879]	likely benign	2	232457576	232457576	Human	1	name , trait , alternate_id
405290129	CV3214036	single nucleotide variant	NM_001631.5(ALPI):c.660C>T (p.Gly220=)	ALPI-related disorder [RCV003926879]	likely benign	2	232457576	232457577	Human	1	name , trait , alternate_id
405290189	CV3214139	single nucleotide variant	NM_001631.5(ALPI):c.522G>A (p.Ser174=)	ALPI-related disorder [RCV003926974]	likely benign	2	232457196	232457196	Human		name , trait , alternate_id
405289907	CV3218894	single nucleotide variant	NM_001631.5(ALPI):c.744C>T (p.Asp248=)	ALPI-related disorder [RCV003962011]	likely benign	2	232457660	232457660	Human		name , trait , alternate_id
405278106	CV3221702	single nucleotide variant	NM_001631.5(ALPI):c.333C>T (p.Ser111=)	ALPI-related disorder [RCV003976302]	benign	2	232456931	232456931	Human		name , trait , alternate_id
405867914	CV3396649	single nucleotide variant	NM_001631.5(ALPI):c.83C>T (p.Pro28Leu)	Inflammatory bowel disease [RCV004560521]	uncertain significance	2	232456364	232456364	Human	2	name
156289375	CV2309687	single nucleotide variant	NM_001631.5(ALPI):c.290C>G (p.Ala97Gly)	not specified [RCV004160823]	uncertain significance	2	232456685	232456685	Human		name
156084183	CV2330836	single nucleotide variant	NM_001631.5(ALPI):c.200C>T (p.Thr67Met)	not specified [RCV004185892]	uncertain significance	2	232456595	232456595	Human		name
155990671	CV2372083	single nucleotide variant	NM_001631.5(ALPI):c.296C>A (p.Ser99Tyr)	not specified [RCV004221746]	uncertain significance	2	232456691	232456691	Human		name
401737691	CV2718176	single nucleotide variant	NM_001631.5(ALPI):c.133C>A (p.Leu45Met)	not specified [RCV004315875]	uncertain significance	2	232456414	232456414	Human		name
405279801	CV3191480	single nucleotide variant	NM_001631.5(ALPI):c.1065C>T (p.Asp355=)	ALPI-related disorder [RCV003919632]	benign	2	232458290	232458290	Human		name , trait , alternate_id
405286444	CV3192834	single nucleotide variant	NM_001631.5(ALPI):c.1050G>A (p.Ala350=)	ALPI-related disorder [RCV003981561]	likely benign	2	232458275	232458275	Human		name , trait , alternate_id
405291494	CV3205722	single nucleotide variant	NM_001631.5(ALPI):c.1488G>A (p.Ala496=)	ALPI-related disorder [RCV003963863]	likely benign	2	232459047	232459047	Human		name , trait , alternate_id
405291751	CV3206094	single nucleotide variant	NM_001631.5(ALPI):c.274C>T (p.Arg92Cys)	ALPI-related disorder [RCV003964173]\|not provided [RCV004790648]	benign\|uncertain significance	2	232456669	232456669	Human		name , trait , alternate_id
405293148	CV3207236	single nucleotide variant	NM_001631.5(ALPI):c.1122C>T (p.Thr374=)	ALPI-related disorder [RCV003931634]	likely benign	2	232458347	232458347	Human		name , trait , alternate_id
405258058	CV3208132	single nucleotide variant	NM_001631.5(ALPI):c.1332G>A (p.Val444=)	ALPI-related disorder [RCV003941578]	likely benign	2	232458891	232458891	Human		name , trait , alternate_id
405295371	CV3209381	single nucleotide variant	NM_001631.5(ALPI):c.1185G>A (p.Gly395=)	ALPI-related disorder [RCV003937256]	likely benign	2	232458633	232458633	Human		name , trait , alternate_id
405290065	CV3214046	single nucleotide variant	NM_001631.5(ALPI):c.1095C>T (p.Ser365=)	ALPI-related disorder [RCV003926888]\|not specified [RCV005407286]	likely benign	2	232458320	232458320	Human		name , trait , alternate_id
405283449	CV3217153	single nucleotide variant	NM_001631.5(ALPI):c.1023T>C (p.Gly341=)	ALPI-related disorder [RCV003979261]	benign	2	232458248	232458248	Human		name , trait , alternate_id
407523839	CV3455800	single nucleotide variant	NM_001631.5(ALPI):c.280C>T (p.Pro94Ser)	not specified [RCV004631197]	uncertain significance	2	232456675	232456675	Human		name
598124819	CV3885414	single nucleotide variant	NM_001631.5(ALPI):c.1269C>T (p.Gly423=)	not specified [RCV005239991]	uncertain significance	2	232458717	232458717	Human		name
155804226	CV1866656	single nucleotide variant	NM_001631.5(ALPI):c.895C>T (p.Arg299Ter)	not provided [RCV002481207]	uncertain significance	2	232458036	232458036	Human		name
156254698	CV2203289	single nucleotide variant	NM_001631.5(ALPI):c.361G>A (p.Gly121Arg)	not specified [RCV004071323]	uncertain significance	2	232456959	232456959	Human		name
156239767	CV2217354	single nucleotide variant	NM_001631.5(ALPI):c.529G>A (p.Gly177Ser)	not specified [RCV004087790]	uncertain significance	2	232457203	232457203	Human		name
156386510	CV2228235	single nucleotide variant	NM_001631.5(ALPI):c.371C>T (p.Ala124Val)	not specified [RCV004097969]	uncertain significance	2	232456969	232456969	Human		name
156207467	CV2250043	single nucleotide variant	NM_001631.5(ALPI):c.676A>G (p.Met226Val)	not specified [RCV004116871]	uncertain significance	2	232457592	232457592	Human		name
156015214	CV2269839	single nucleotide variant	NM_001631.5(ALPI):c.931A>G (p.Thr311Ala)	not specified [RCV004127074]	uncertain significance	2	232458072	232458072	Human		name
155956392	CV2281917	single nucleotide variant	NM_001631.5(ALPI):c.592C>T (p.Arg198Cys)	not specified [RCV004138693]	uncertain significance	2	232457266	232457266	Human		name
156091320	CV2302648	single nucleotide variant	NM_001631.5(ALPI):c.869C>T (p.Pro290Leu)	not specified [RCV004162595]	uncertain significance	2	232458010	232458010	Human		name
156149466	CV2377408	single nucleotide variant	NM_001631.5(ALPI):c.967C>T (p.Arg323Cys)	not specified [RCV004225583]	uncertain significance	2	232458108	232458108	Human		name
156172428	CV2380821	single nucleotide variant	NM_001631.5(ALPI):c.425C>T (p.Thr142Met)	not specified [RCV004218380]	uncertain significance	2	232457023	232457023	Human		name
156096651	CV2399108	single nucleotide variant	NM_001631.5(ALPI):c.824C>T (p.Ala275Val)	not specified [RCV004246543]	uncertain significance	2	232457835	232457835	Human		name
329375470	CV2468628	single nucleotide variant	NM_001631.5(ALPI):c.994G>A (p.Gly332Ser)	not specified [RCV004278183]	uncertain significance	2	232458219	232458219	Human		name
401728885	CV2673079	single nucleotide variant	NM_001631.5(ALPI):c.577A>G (p.Met193Val)	not specified [RCV004284066]	uncertain significance	2	232457251	232457251	Human		name
401760294	CV2718788	single nucleotide variant	NM_001631.5(ALPI):c.986T>C (p.Val329Ala)	not specified [RCV004328534]	uncertain significance	2	232458127	232458127	Human		name
401900014	CV2780180	single nucleotide variant	NM_001631.5(ALPI):c.797T>C (p.Val266Ala)	not specified [RCV004355828]	uncertain significance	2	232457808	232457808	Human		name
401912218	CV2795970	single nucleotide variant	NM_001631.5(ALPI):c.487G>A (p.Gly163Arg)	ALPI-related disorder [RCV003399706]	uncertain significance	2	232457161	232457161	Human		name , trait , alternate_id
405272455	CV3199341	single nucleotide variant	NM_001631.5(ALPI):c.620C>T (p.Thr207Ile)	ALPI-related disorder [RCV003914290]	benign	2	232457294	232457294	Human		name , trait , alternate_id
405276005	CV3199554	single nucleotide variant	NM_001631.5(ALPI):c.431G>A (p.Arg144His)	ALPI-related disorder [RCV003916950]	benign	2	232457029	232457029	Human		name , trait , alternate_id
405290240	CV3214152	single nucleotide variant	NM_001631.5(ALPI):c.438T>A (p.Asn146Lys)	ALPI-related disorder [RCV003926985]	benign	2	232457036	232457036	Human		name , trait , alternate_id
405806633	CV3268635	single nucleotide variant	NM_001631.5(ALPI):c.512A>G (p.Gln171Arg)	not specified [RCV004406149]	uncertain significance	2	232457186	232457186	Human		name
405806869	CV3268650	single nucleotide variant	NM_001631.5(ALPI):c.593G>T (p.Arg198Leu)	not specified [RCV004406164]	likely benign	2	232457267	232457267	Human		name
405806728	CV3268662	single nucleotide variant	NM_001631.5(ALPI):c.805C>T (p.Arg269Cys)	not specified [RCV004406176]	uncertain significance	2	232457816	232457816	Human		name
405867919	CV3396660	single nucleotide variant	NM_001631.5(ALPI):c.406C>T (p.Arg136Cys)	Inflammatory bowel disease [RCV004560532]	uncertain significance	2	232457004	232457004	Human	2	name
407523733	CV3455758	single nucleotide variant	NM_001631.5(ALPI):c.416A>C (p.Gln139Pro)	not specified [RCV004631164]	uncertain significance	2	232457014	232457014	Human		name
407495717	CV3455769	single nucleotide variant	NM_001631.5(ALPI):c.925G>A (p.Glu309Lys)	not specified [RCV004621659]	uncertain significance	2	232458066	232458066	Human		name
407523813	CV3455789	single nucleotide variant	NM_001631.5(ALPI):c.396T>G (p.Ser132Arg)	not specified [RCV004631187]	uncertain significance	2	232456994	232456994	Human		name
408376836	CV3516521	single nucleotide variant	NM_001631.5(ALPI):c.517G>A (p.Ala173Thr)	ALPI-related disorder [RCV004749971]	uncertain significance	2	232457191	232457191	Human		name , trait , alternate_id
596929988	CV3538617	single nucleotide variant	NM_001631.5(ALPI):c.461G>A (p.Arg154Gln)	not provided [RCV004792086]	uncertain significance	2	232457059	232457059	Human		name
597792515	CV3689997	single nucleotide variant	NM_001631.5(ALPI):c.371C>G (p.Ala124Gly)	not specified [RCV004933869]	uncertain significance	2	232456969	232456969	Human		name
597792546	CV3690007	single nucleotide variant	NM_001631.5(ALPI):c.806G>A (p.Arg269His)	not specified [RCV004933879]	uncertain significance	2	232457817	232457817	Human		name
598124985	CV3885513	single nucleotide variant	NM_001631.5(ALPI):c.940G>A (p.Ala314Thr)	not specified [RCV005240091]	uncertain significance	2	232458081	232458081	Human		name
598191664	CV3971707	single nucleotide variant	NM_001631.5(ALPI):c.388G>A (p.Gly130Ser)	not specified [RCV005354324]	uncertain significance	2	232456986	232456986	Human		name
598191675	CV3971711	single nucleotide variant	NM_001631.5(ALPI):c.466A>G (p.Lys156Glu)	not specified [RCV005354326]	uncertain significance	2	232457064	232457064	Human		name
598191686	CV3971713	single nucleotide variant	NM_001631.5(ALPI):c.476G>A (p.Gly159Glu)	not specified [RCV005354328]	uncertain significance	2	232457150	232457150	Human		name
151353329	CV1326419	single nucleotide variant	NM_001631.5(ALPI):c.1315C>T (p.Gln439Ter)	not provided [RCV001816294]	likely pathogenic	2	232458874	232458874	Human		name
156078799	CV2230383	single nucleotide variant	NM_001631.5(ALPI):c.1330G>C (p.Val444Leu)	not specified [RCV004099976]	uncertain significance	2	232458889	232458889	Human		name
156333688	CV2336033	single nucleotide variant	NM_001631.5(ALPI):c.1347G>C (p.Glu449Asp)	ALPI-related disorder [RCV003946389]\|not specified [RCV004189638]	likely benign\|uncertain significance	2	232458906	232458906	Human		name , trait , alternate_id
155982600	CV2337174	single nucleotide variant	NM_001631.5(ALPI):c.1164G>T (p.Leu388Phe)	not specified [RCV004192932]	likely benign	2	232458389	232458389	Human		name
156106376	CV2370895	single nucleotide variant	NM_001631.5(ALPI):c.1498T>C (p.Cys500Arg)	not specified [RCV004218629]	uncertain significance	2	232459057	232459057	Human		name
329397534	CV2456274	single nucleotide variant	NM_001631.5(ALPI):c.1056G>A (p.Met352Ile)	not specified [RCV004275448]	uncertain significance	2	232458281	232458281	Human		name
329359601	CV2461566	single nucleotide variant	NM_001631.5(ALPI):c.1238G>A (p.Gly413Asp)	not specified [RCV004269750]	uncertain significance	2	232458686	232458686	Human		name
329398560	CV2471554	single nucleotide variant	NM_001631.5(ALPI):c.1201G>T (p.Ala401Ser)	not specified [RCV004286860]	uncertain significance	2	232458649	232458649	Human		name
401728745	CV2673033	single nucleotide variant	NM_001631.5(ALPI):c.1306C>G (p.Pro436Ala)	not specified [RCV004284026]	uncertain significance	2	232458865	232458865	Human		name
405806501	CV3268591	single nucleotide variant	NM_001631.5(ALPI):c.1003G>A (p.Asp335Asn)	not specified [RCV004406105]	uncertain significance	2	232458228	232458228	Human		name
405806562	CV3268599	single nucleotide variant	NM_001631.5(ALPI):c.1226C>A (p.Ser409Tyr)	not specified [RCV004406113]	uncertain significance	2	232458674	232458674	Human		name
407523790	CV3455780	single nucleotide variant	NM_001631.5(ALPI):c.1015C>G (p.His339Asp)	not specified [RCV004631180]	uncertain significance	2	232458240	232458240	Human		name
408375536	CV3509729	single nucleotide variant	NM_001631.5(ALPI):c.1528G>T (p.Ala510Ser)	ALPI-related disorder [RCV004748123]	uncertain significance	2	232459087	232459087	Human		name , trait , alternate_id
597792410	CV3689988	single nucleotide variant	NM_001631.5(ALPI):c.1021G>T (p.Gly341Cys)	not specified [RCV004933860]	uncertain significance	2	232458246	232458246	Human		name
597792577	CV3690017	single nucleotide variant	NM_001631.5(ALPI):c.1184G>A (p.Gly395Glu)	not specified [RCV004933889]	uncertain significance	2	232458632	232458632	Human		name
597792609	CV3690027	single nucleotide variant	NM_001631.5(ALPI):c.1287T>A (p.Asn429Lys)	not specified [RCV004933899]	uncertain significance	2	232458735	232458735	Human		name
597792632	CV3690034	single nucleotide variant	NM_001631.5(ALPI):c.1270G>A (p.Val424Met)	not specified [RCV004933906]	uncertain significance	2	232458718	232458718	Human		name
598191681	CV3971712	single nucleotide variant	NM_001631.5(ALPI):c.1478G>A (p.Cys493Tyr)	not specified [RCV005354327]	uncertain significance	2	232459037	232459037	Human		name

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