Ipo4 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

123 records found for search term Ipo4

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156226187	CV2401086	single nucleotide variant	NM_024658.4(IPO4):c.31C>T (p.Arg11Trp)	not specified [RCV004245657]	uncertain significance	14	24188757	24188757	Human		name
405794099	CV3264472	single nucleotide variant	NM_024658.4(IPO4):c.82C>T (p.Leu28Phe)	not specified [RCV004400749]	uncertain significance	14	24188626	24188626	Human		name
597785469	CV3680337	single nucleotide variant	NM_024658.4(IPO4):c.55G>A (p.Glu19Lys)	not specified [RCV004931966]	uncertain significance	14	24188733	24188733	Human		name
15157319	CV714089	single nucleotide variant	NM_024658.4(IPO4):c.58C>T (p.Arg20Cys)	not provided [RCV000969286]	benign	14	24188730	24188730	Human		name
156316404	CV2250904	single nucleotide variant	NM_024658.4(IPO4):c.221C>T (p.Ala74Val)	not specified [RCV004123487]	uncertain significance	14	24188359	24188359	Human		name
155919894	CV2279496	single nucleotide variant	NM_024658.4(IPO4):c.244T>A (p.Ser82Thr)	not specified [RCV004142017]	uncertain significance	14	24188250	24188250	Human		name
156272621	CV2308835	single nucleotide variant	NM_024658.4(IPO4):c.133C>A (p.Leu45Ile)	not specified [RCV004169139]	uncertain significance	14	24188575	24188575	Human		name
401891456	CV2779133	single nucleotide variant	NM_024658.4(IPO4):c.227A>C (p.Gln76Pro)	not specified [RCV004349051]	uncertain significance	14	24188353	24188353	Human		name
401910358	CV2810316	single nucleotide variant	NM_024658.4(IPO4):c.2046G>A (p.Glu682=)	not provided [RCV003424990]	likely benign	14	24183607	24183607	Human		name
401910359	CV2810317	single nucleotide variant	NM_024658.4(IPO4):c.1545G>A (p.Leu515=)	not provided [RCV003424991]	likely benign	14	24184741	24184741	Human		name
405794064	CV3264460	single nucleotide variant	NM_024658.4(IPO4):c.140C>T (p.Ser47Leu)	not specified [RCV004400737]	uncertain significance	14	24188568	24188568	Human		name
405794079	CV3264465	single nucleotide variant	NM_024658.4(IPO4):c.209G>A (p.Arg70Gln)	not specified [RCV004400742]	uncertain significance	14	24188371	24188371	Human		name
407523033	CV3455133	single nucleotide variant	NM_024658.4(IPO4):c.148G>A (p.Asp50Asn)	not specified [RCV004630929]	uncertain significance	14	24188560	24188560	Human		name
598194091	CV3968992	single nucleotide variant	NM_024658.4(IPO4):c.131T>C (p.Leu44Pro)	not specified [RCV005354775]	uncertain significance	14	24188577	24188577	Human		name
15193721	CV725635	single nucleotide variant	NM_024658.4(IPO4):c.1908C>T (p.Asp636=)	not provided [RCV000889025]	benign	14	24183860	24183860	Human		name
156093760	CV2300246	single nucleotide variant	NM_024658.4(IPO4):c.566C>T (p.Pro189Leu)	not specified [RCV004153211]	uncertain significance	14	24187422	24187422	Human		name
155954755	CV2302240	single nucleotide variant	NM_024658.4(IPO4):c.388C>T (p.Pro130Ser)	not specified [RCV004159231]	uncertain significance	14	24187687	24187687	Human		name
155964811	CV2330498	single nucleotide variant	NM_024658.4(IPO4):c.983C>T (p.Thr328Ile)	not specified [RCV004181063]	uncertain significance	14	24186309	24186309	Human		name
156303683	CV2359415	single nucleotide variant	NM_024658.4(IPO4):c.510G>C (p.Glu170Asp)	not specified [RCV004214738]	uncertain significance	14	24187478	24187478	Human		name
156063064	CV2380443	single nucleotide variant	NM_024658.4(IPO4):c.715A>C (p.Ile239Leu)	not specified [RCV004218043]	uncertain significance	14	24186919	24186919	Human		name
329376343	CV2438159	single nucleotide variant	NM_024658.4(IPO4):c.342G>T (p.Glu114Asp)	not specified [RCV004256936]	uncertain significance	14	24187733	24187733	Human		name
329363689	CV2446039	single nucleotide variant	NM_024658.4(IPO4):c.326G>A (p.Arg109Gln)	not specified [RCV004270610]	uncertain significance	14	24187749	24187749	Human		name
401890072	CV2763622	single nucleotide variant	NM_024658.4(IPO4):c.655G>A (p.Ala219Thr)	not specified [RCV004343129]	uncertain significance	14	24186979	24186979	Human		name
405794091	CV3264469	single nucleotide variant	NM_024658.4(IPO4):c.467A>G (p.His156Arg)	not specified [RCV004400746]	uncertain significance	14	24187521	24187521	Human		name
405794094	CV3264470	single nucleotide variant	NM_024658.4(IPO4):c.545G>A (p.Arg182His)	not specified [RCV004400747]	uncertain significance	14	24187443	24187443	Human		name
405794097	CV3264471	single nucleotide variant	NM_024658.4(IPO4):c.722C>G (p.Pro241Arg)	not specified [RCV004400748]	uncertain significance	14	24186912	24186912	Human		name
407523047	CV3455138	single nucleotide variant	NM_024658.4(IPO4):c.947A>T (p.Glu316Val)	not specified [RCV004630934]	uncertain significance	14	24186345	24186345	Human		name
597785460	CV3680335	single nucleotide variant	NM_024658.4(IPO4):c.515G>T (p.Gly172Val)	not specified [RCV004931964]	uncertain significance	14	24187473	24187473	Human		name
597785473	CV3680338	single nucleotide variant	NM_024658.4(IPO4):c.680C>A (p.Ala227Asp)	not specified [RCV004931967]	uncertain significance	14	24186954	24186954	Human		name
597785476	CV3680339	single nucleotide variant	NM_024658.4(IPO4):c.767A>G (p.Asn256Ser)	not specified [RCV004931968]	uncertain significance	14	24186781	24186781	Human		name
598194016	CV3968977	single nucleotide variant	NM_024658.4(IPO4):c.473G>A (p.Arg158Gln)	not specified [RCV005354762]	uncertain significance	14	24187515	24187515	Human		name
598194022	CV3968978	single nucleotide variant	NM_024658.4(IPO4):c.512T>C (p.Val171Ala)	not specified [RCV005354763]	uncertain significance	14	24187476	24187476	Human		name
598194027	CV3968979	single nucleotide variant	NM_024658.4(IPO4):c.880A>G (p.Thr294Ala)	not specified [RCV005354764]	uncertain significance	14	24186412	24186412	Human		name
598221627	CV3968986	single nucleotide variant	NM_024658.4(IPO4):c.517T>G (p.Ser173Ala)	not specified [RCV005340620]	uncertain significance	14	24187471	24187471	Human		name
598194116	CV3968996	single nucleotide variant	NM_024658.4(IPO4):c.605T>G (p.Leu202Trp)	not specified [RCV005354778]	uncertain significance	14	24187134	24187134	Human		name
156232853	CV2196318	single nucleotide variant	NM_024658.4(IPO4):c.1541C>T (p.Ser514Leu)	not specified [RCV004072496]	uncertain significance	14	24184745	24184745	Human		name
156231747	CV2199685	single nucleotide variant	NM_024658.4(IPO4):c.2591G>C (p.Cys864Ser)	not specified [RCV004072421]	uncertain significance	14	24182285	24182285	Human		name
156373146	CV2204833	single nucleotide variant	NM_024658.4(IPO4):c.1723G>A (p.Asp575Asn)	not specified [RCV004075086]	likely benign	14	24184332	24184332	Human		name
156152894	CV2209403	single nucleotide variant	NM_024658.4(IPO4):c.2411T>C (p.Leu804Pro)	not specified [RCV004093567]	uncertain significance	14	24182986	24182986	Human		name
156077466	CV2230289	single nucleotide variant	NM_024658.4(IPO4):c.2072T>G (p.Phe691Cys)	not specified [RCV004099902]	uncertain significance	14	24183505	24183505	Human		name
156299027	CV2248584	single nucleotide variant	NM_024658.4(IPO4):c.1082T>C (p.Leu361Ser)	not specified [RCV004121776]	uncertain significance	14	24185948	24185948	Human		name
155948246	CV2272045	single nucleotide variant	NM_024658.4(IPO4):c.1255G>A (p.Gly419Ser)	not specified [RCV004124845]	uncertain significance	14	24185482	24185482	Human		name
156126746	CV2283737	single nucleotide variant	NM_024658.4(IPO4):c.2641A>G (p.Thr881Ala)	not specified [RCV004142258]	uncertain significance	14	24182121	24182121	Human		name
156043097	CV2311023	single nucleotide variant	NM_024658.4(IPO4):c.2413C>G (p.Gln805Glu)	not specified [RCV004164041]	uncertain significance	14	24182984	24182984	Human		name
156088079	CV2337102	single nucleotide variant	NM_024658.4(IPO4):c.1088G>A (p.Ser363Asn)	not specified [RCV004192865]	uncertain significance	14	24185942	24185942	Human		name
155975223	CV2341519	single nucleotide variant	NM_024658.4(IPO4):c.2249G>A (p.Arg750Gln)	not specified [RCV004188911]	uncertain significance	14	24183148	24183148	Human		name
156063393	CV2349586	single nucleotide variant	NM_024658.4(IPO4):c.2041G>C (p.Gly681Arg)	not specified [RCV004204010]	uncertain significance	14	24183612	24183612	Human		name
156100705	CV2351628	single nucleotide variant	NM_024658.4(IPO4):c.2254G>A (p.Val752Met)	not specified [RCV004195344]	uncertain significance	14	24183143	24183143	Human		name
155988710	CV2355144	single nucleotide variant	NM_024658.4(IPO4):c.2782G>A (p.Glu928Lys)	not specified [RCV004198534]	uncertain significance	14	24181980	24181980	Human		name
156268081	CV2371934	single nucleotide variant	NM_024658.4(IPO4):c.1682C>T (p.Pro561Leu)	not specified [RCV004221617]	uncertain significance	14	24184373	24184373	Human		name
156389474	CV2373917	single nucleotide variant	NM_024658.4(IPO4):c.2569G>A (p.Gly857Ser)	not specified [RCV004224848]	uncertain significance	14	24182307	24182307	Human		name
156172034	CV2380771	single nucleotide variant	NM_024658.4(IPO4):c.2152C>T (p.His718Tyr)	not specified [RCV004218335]	uncertain significance	14	24183325	24183325	Human		name
156038500	CV2390192	single nucleotide variant	NM_024658.4(IPO4):c.1231C>T (p.Arg411Cys)	not specified [RCV004240575]	uncertain significance	14	24185506	24185506	Human		name
156246980	CV2396854	single nucleotide variant	NM_024658.4(IPO4):c.1829C>T (p.Thr610Met)	not specified [RCV004233982]	uncertain significance	14	24184038	24184038	Human		name
329381841	CV2424238	single nucleotide variant	NM_024658.4(IPO4):c.1191G>T (p.Gln397His)	not specified [RCV004250359]	uncertain significance	14	24185546	24185546	Human		name
329399246	CV2436466	single nucleotide variant	NM_024658.4(IPO4):c.2547C>G (p.Asp849Glu)	not specified [RCV004251846]	uncertain significance	14	24182329	24182329	Human		name
329360717	CV2439633	single nucleotide variant	NM_024658.4(IPO4):c.2191G>A (p.Ala731Thr)	not specified [RCV004255650]	uncertain significance	14	24183286	24183286	Human		name
329372135	CV2442994	single nucleotide variant	NM_024658.4(IPO4):c.2007C>G (p.Phe669Leu)	not specified [RCV004253586]	uncertain significance	14	24183646	24183646	Human		name
401741405	CV2681312	single nucleotide variant	NM_024658.4(IPO4):c.1805C>T (p.Ala602Val)	not specified [RCV004289436]	uncertain significance	14	24184062	24184062	Human		name
401771829	CV2693539	single nucleotide variant	NM_024658.4(IPO4):c.2083A>G (p.Met695Val)	not specified [RCV004297522]	uncertain significance	14	24183494	24183494	Human		name
401746660	CV2694901	single nucleotide variant	NM_024658.4(IPO4):c.2736C>G (p.Asp912Glu)	not specified [RCV004300968]	uncertain significance	14	24182026	24182026	Human		name
401723161	CV2703634	single nucleotide variant	NM_024658.4(IPO4):c.2288G>A (p.Arg763Gln)	not specified [RCV004317796]	uncertain significance	14	24183109	24183109	Human		name
401763019	CV2710410	single nucleotide variant	NM_024658.4(IPO4):c.1033C>T (p.Pro345Ser)	not specified [RCV004317568]	uncertain significance	14	24186155	24186155	Human		name
401762293	CV2714088	single nucleotide variant	NM_024658.4(IPO4):c.2590T>C (p.Cys864Arg)	not specified [RCV004315485]	uncertain significance	14	24182286	24182286	Human		name
401773308	CV2716522	single nucleotide variant	NM_024658.4(IPO4):c.1507G>A (p.Ala503Thr)	not specified [RCV004327606]	uncertain significance	14	24184882	24184882	Human		name
401725165	CV2725726	single nucleotide variant	NM_024658.4(IPO4):c.1489A>G (p.Lys497Glu)	not specified [RCV004322418]	uncertain significance	14	24184900	24184900	Human		name
401877614	CV2761225	single nucleotide variant	NM_024658.4(IPO4):c.2395G>A (p.Val799Met)	not specified [RCV004341103]	likely benign	14	24183002	24183002	Human		name
401884345	CV2761678	single nucleotide variant	NM_024658.4(IPO4):c.1220C>T (p.Ser407Leu)	not specified [RCV004337296]	uncertain significance	14	24185517	24185517	Human		name
401893060	CV2762788	single nucleotide variant	NM_024658.4(IPO4):c.2293C>T (p.Arg765Cys)	not specified [RCV004340340]	uncertain significance	14	24183104	24183104	Human		name
401891860	CV2779516	single nucleotide variant	NM_024658.4(IPO4):c.1966G>A (p.Asp656Asn)	not specified [RCV004351138]	uncertain significance	14	24183802	24183802	Human		name
401872500	CV2779697	single nucleotide variant	NM_024658.4(IPO4):c.1882G>A (p.Gly628Arg)	not specified [RCV004351386]	uncertain significance	14	24183886	24183886	Human		name
405794052	CV3264456	single nucleotide variant	NM_024658.4(IPO4):c.1039G>C (p.Glu347Gln)	not specified [RCV004400733]	uncertain significance	14	24186149	24186149	Human		name
405794055	CV3264457	single nucleotide variant	NM_024658.4(IPO4):c.1183C>A (p.Leu395Met)	not specified [RCV004400734]	uncertain significance	14	24185554	24185554	Human		name
405794058	CV3264458	single nucleotide variant	NM_024658.4(IPO4):c.1205G>T (p.Gly402Val)	not specified [RCV004400735]	uncertain significance	14	24185532	24185532	Human		name
405794061	CV3264459	single nucleotide variant	NM_024658.4(IPO4):c.1250C>T (p.Ala417Val)	not specified [RCV004400736]	uncertain significance	14	24185487	24185487	Human		name
405794067	CV3264461	single nucleotide variant	NM_024658.4(IPO4):c.1549C>T (p.Pro517Ser)	not specified [RCV004400738]	uncertain significance	14	24184737	24184737	Human		name
405794070	CV3264462	single nucleotide variant	NM_024658.4(IPO4):c.1858G>A (p.Glu620Lys)	not specified [RCV004400739]	uncertain significance	14	24184009	24184009	Human		name
405794073	CV3264463	single nucleotide variant	NM_024658.4(IPO4):c.1996G>C (p.Glu666Gln)	not specified [RCV004400740]	uncertain significance	14	24183657	24183657	Human		name
405794076	CV3264464	single nucleotide variant	NM_024658.4(IPO4):c.2038G>A (p.Val680Met)	not specified [RCV004400741]	uncertain significance	14	24183615	24183615	Human		name
405794082	CV3264466	single nucleotide variant	NM_024658.4(IPO4):c.2131C>G (p.Leu711Val)	not specified [RCV004400743]	uncertain significance	14	24183346	24183346	Human		name
405794085	CV3264467	single nucleotide variant	NM_024658.4(IPO4):c.2858G>A (p.Arg953Gln)	not specified [RCV004400744]	uncertain significance	14	24181793	24181793	Human		name
407523036	CV3455134	single nucleotide variant	NM_024658.4(IPO4):c.1580G>A (p.Arg527Gln)	not specified [RCV004630930]	uncertain significance	14	24184706	24184706	Human		name
407523042	CV3455136	single nucleotide variant	NM_024658.4(IPO4):c.1283A>G (p.His428Arg)	not specified [RCV004630932]	uncertain significance	14	24185308	24185308	Human		name
407523045	CV3455137	single nucleotide variant	NM_024658.4(IPO4):c.2873G>A (p.Arg958His)	not specified [RCV004630933]	uncertain significance	14	24181778	24181778	Human		name
407523050	CV3455139	single nucleotide variant	NM_024658.4(IPO4):c.1751G>A (p.Arg584His)	not specified [RCV004630935]	uncertain significance	14	24184304	24184304	Human		name
407523053	CV3455140	single nucleotide variant	NM_024658.4(IPO4):c.2854G>A (p.Glu952Lys)	not specified [RCV004630936]	uncertain significance	14	24181797	24181797	Human		name
407523056	CV3455141	single nucleotide variant	NM_024658.4(IPO4):c.2699T>C (p.Leu900Pro)	not specified [RCV004630937]	uncertain significance	14	24182063	24182063	Human		name
597785403	CV3680320	single nucleotide variant	NM_024658.4(IPO4):c.1988A>G (p.Tyr663Cys)	not specified [RCV004931949]	uncertain significance	14	24183665	24183665	Human		name
597785405	CV3680321	single nucleotide variant	NM_024658.4(IPO4):c.2338C>T (p.Arg780Cys)	not specified [RCV004931950]	uncertain significance	14	24183059	24183059	Human		name
597785409	CV3680322	single nucleotide variant	NM_024658.4(IPO4):c.2951C>T (p.Ala984Val)	not specified [RCV004931951]	uncertain significance	14	24181607	24181607	Human		name
597785413	CV3680323	single nucleotide variant	NM_024658.4(IPO4):c.1305G>C (p.Glu435Asp)	not specified [RCV004931952]	uncertain significance	14	24185286	24185286	Human		name
597785417	CV3680324	single nucleotide variant	NM_024658.4(IPO4):c.1022C>T (p.Ala341Val)	not specified [RCV004931953]	uncertain significance	14	24186166	24186166	Human		name
597785427	CV3680326	single nucleotide variant	NM_024658.4(IPO4):c.2851C>T (p.Arg951Trp)	not specified [RCV004931955]	uncertain significance	14	24181800	24181800	Human		name
597785430	CV3680327	single nucleotide variant	NM_024658.4(IPO4):c.2872C>T (p.Arg958Cys)	not specified [RCV004931956]	uncertain significance	14	24181779	24181779	Human		name
597785433	CV3680328	single nucleotide variant	NM_024658.4(IPO4):c.2041G>A (p.Gly681Arg)	not specified [RCV004931957]	uncertain significance	14	24183612	24183612	Human		name
597785437	CV3680329	single nucleotide variant	NM_024658.4(IPO4):c.2195G>C (p.Cys732Ser)	not specified [RCV004931958]	uncertain significance	14	24183282	24183282	Human		name
597785440	CV3680330	single nucleotide variant	NM_024658.4(IPO4):c.2485G>A (p.Ala829Thr)	not specified [RCV004931959]	uncertain significance	14	24182391	24182391	Human		name
597785444	CV3680331	single nucleotide variant	NM_024658.4(IPO4):c.2254G>T (p.Val752Leu)	not specified [RCV004931960]	uncertain significance	14	24183143	24183143	Human		name
597785448	CV3680332	single nucleotide variant	NM_024658.4(IPO4):c.2423C>T (p.Thr808Ile)	not specified [RCV004931961]	uncertain significance	14	24182841	24182841	Human		name
597785452	CV3680333	single nucleotide variant	NM_024658.4(IPO4):c.2425G>T (p.Ala809Ser)	not specified [RCV004931962]	uncertain significance	14	24182839	24182839	Human		name
597785457	CV3680334	single nucleotide variant	NM_024658.4(IPO4):c.2509G>C (p.Glu837Gln)	not specified [RCV004931963]	uncertain significance	14	24182367	24182367	Human		name
597785464	CV3680336	single nucleotide variant	NM_024658.4(IPO4):c.1443G>A (p.Met481Ile)	not specified [RCV004931965]	uncertain significance	14	24184946	24184946	Human		name
598193998	CV3968974	single nucleotide variant	NM_024658.4(IPO4):c.2695C>T (p.Arg899Trp)	not specified [RCV005354759]	uncertain significance	14	24182067	24182067	Human		name
598194004	CV3968975	single nucleotide variant	NM_024658.4(IPO4):c.2932G>A (p.Glu978Lys)	not specified [RCV005354760]	uncertain significance	14	24181719	24181719	Human		name
598194010	CV3968976	single nucleotide variant	NM_024658.4(IPO4):c.1090G>A (p.Glu364Lys)	not specified [RCV005354761]	uncertain significance	14	24185940	24185940	Human		name
598194043	CV3968983	single nucleotide variant	NM_024658.4(IPO4):c.1061T>C (p.Met354Thr)	not specified [RCV005354767]	uncertain significance	14	24185969	24185969	Human		name
598194049	CV3968984	single nucleotide variant	NM_024658.4(IPO4):c.1295A>G (p.Tyr432Cys)	not specified [RCV005354768]	uncertain significance	14	24185296	24185296	Human		name
598194055	CV3968985	single nucleotide variant	NM_024658.4(IPO4):c.2983T>G (p.Leu995Val)	not specified [RCV005354769]	uncertain significance	14	24181575	24181575	Human		name
598194060	CV3968987	single nucleotide variant	NM_024658.4(IPO4):c.2484C>A (p.Asp828Glu)	not specified [RCV005354770]	uncertain significance	14	24182392	24182392	Human		name
598194065	CV3968988	single nucleotide variant	NM_024658.4(IPO4):c.1079C>T (p.Ala360Val)	not specified [RCV005354771]	uncertain significance	14	24185951	24185951	Human		name
598194072	CV3968989	single nucleotide variant	NM_024658.4(IPO4):c.1908C>A (p.Asp636Glu)	not specified [RCV005354772]	uncertain significance	14	24183860	24183860	Human		name
598194085	CV3968991	single nucleotide variant	NM_024658.4(IPO4):c.2434G>C (p.Asp812His)	not specified [RCV005354774]	uncertain significance	14	24182830	24182830	Human		name
598221634	CV3968994	single nucleotide variant	NM_024658.4(IPO4):c.1291A>C (p.Ser431Arg)	not specified [RCV005340621]	uncertain significance	14	24185300	24185300	Human		name
598194108	CV3968995	single nucleotide variant	NM_024658.4(IPO4):c.1657C>G (p.Arg553Gly)	not specified [RCV005354777]	uncertain significance	14	24184398	24184398	Human		name
15199994	CV702840	single nucleotide variant	NM_024658.4(IPO4):c.1480C>A (p.Pro494Thr)	not provided [RCV000957202]	benign	14	24184909	24184909	Human		name
156193314	CV2214019	single nucleotide variant	NM_024658.4(IPO4):c.3002T>C (p.Ile1001Thr)	not specified [RCV004084065]	uncertain significance	14	24181556	24181556	Human		name
155924989	CV2358247	single nucleotide variant	NM_024658.4(IPO4):c.3229G>A (p.Val1077Ile)	not specified [RCV004212036]	uncertain significance	14	24180459	24180459	Human		name
401887566	CV2772017	single nucleotide variant	NM_024658.4(IPO4):c.3208A>G (p.Lys1070Glu)	not specified [RCV004344695]	uncertain significance	14	24180480	24180480	Human		name
405794088	CV3264468	single nucleotide variant	NM_024658.4(IPO4):c.3149T>C (p.Phe1050Ser)	not specified [RCV004400745]	uncertain significance	14	24180539	24180539	Human		name
407523039	CV3455135	single nucleotide variant	NM_024658.4(IPO4):c.3161A>T (p.Gln1054Leu)	not specified [RCV004630931]	uncertain significance	14	24180527	24180527	Human		name
597785481	CV3680340	single nucleotide variant	NM_024658.4(IPO4):c.3131T>C (p.Leu1044Pro)	not specified [RCV004931969]	uncertain significance	14	24180557	24180557	Human		name
598194039	CV3968982	single nucleotide variant	NM_024658.4(IPO4):c.3026A>T (p.Tyr1009Phe)	not specified [RCV005354766]	uncertain significance	14	24181532	24181532	Human		name
598194099	CV3968993	single nucleotide variant	NM_024658.4(IPO4):c.3056T>A (p.Val1019Glu)	not specified [RCV005354776]	uncertain significance	14	24180748	24180748	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message