Mphosph9 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 Mphosph9

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156190386	CV2384981	single nucleotide variant	NM_022782.4(MPHOSPH9):c.649G>A (p.Glu217Lys)	not specified [RCV004226208]	uncertain significance	12	123221595	123221595	Human		name
401773146	CV2698110	single nucleotide variant	NM_022782.4(MPHOSPH9):c.965A>G (p.Asn322Ser)	not specified [RCV004302900]	likely benign	12	123218407	123218407	Human		name
405709252	CV3359252	single nucleotide variant	NM_022782.4(MPHOSPH9):c.698C>T (p.Ala233Val)	not specified [RCV004493599]	likely benign	12	123221546	123221546	Human		name
405709421	CV3359274	single nucleotide variant	NM_022782.4(MPHOSPH9):c.748A>G (p.Ile250Val)	not specified [RCV004493621]	uncertain significance	12	123221496	123221496	Human		name
405709500	CV3359285	single nucleotide variant	NM_022782.4(MPHOSPH9):c.985C>G (p.Pro329Ala)	not specified [RCV004493632]	uncertain significance	12	123218387	123218387	Human		name
405708833	CV3362725	single nucleotide variant	NM_022782.4(MPHOSPH9):c.608G>C (p.Cys203Ser)	not specified [RCV004493540]	uncertain significance	12	123221636	123221636	Human		name
597661211	CV3564074	single nucleotide variant	NM_022782.4(MPHOSPH9):c.818A>T (p.His273Leu)	not specified [RCV004828481]	uncertain significance	12	123221426	123221426	Human		name
598168275	CV3982467	single nucleotide variant	NM_022782.4(MPHOSPH9):c.517A>G (p.Thr173Ala)	not specified [RCV005369675]	uncertain significance	12	123221727	123221727	Human		name
598168266	CV3986409	single nucleotide variant	NM_022782.4(MPHOSPH9):c.541A>C (p.Met181Leu)	not specified [RCV005369673]	uncertain significance	12	123221703	123221703	Human		name
598201557	CV3986410	single nucleotide variant	NM_022782.4(MPHOSPH9):c.602C>A (p.Thr201Asn)	not specified [RCV005376052]	uncertain significance	12	123221642	123221642	Human		name
598201561	CV3986411	single nucleotide variant	NM_022782.4(MPHOSPH9):c.811T>A (p.Phe271Ile)	not specified [RCV005376053]	uncertain significance	12	123221433	123221433	Human		name
155917839	CV2199134	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2476G>A (p.Val826Ile)	not specified [RCV004080529]	uncertain significance	12	123166770	123166770	Human		name
156061838	CV2203392	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2843G>A (p.Arg948Lys)	not specified [RCV004072619]	uncertain significance	12	123164015	123164015	Human		name
156259101	CV2204709	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2513A>G (p.Tyr838Cys)	not specified [RCV004081811]	uncertain significance	12	123166733	123166733	Human		name
156139560	CV2212088	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1454C>G (p.Ser485Cys)	not specified [RCV004088997]	uncertain significance	12	123202951	123202951	Human		name
156381571	CV2215059	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1538C>T (p.Thr513Ile)	not specified [RCV004084828]	uncertain significance	12	123202867	123202867	Human		name
156135490	CV2256905	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2722T>C (p.Phe908Leu)	not specified [RCV004121106]	uncertain significance	12	123165347	123165347	Human		name
155978155	CV2266488	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2024T>G (p.Val675Gly)	not specified [RCV004131057]	uncertain significance	12	123198248	123198248	Human		name
156280815	CV2295061	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1549C>T (p.Pro517Ser)	not specified [RCV004156178]	uncertain significance	12	123202856	123202856	Human		name
156088980	CV2295552	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1352A>G (p.Lys451Arg)	not specified [RCV004160647]	uncertain significance	12	123203053	123203053	Human		name
155930157	CV2299765	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2249G>A (p.Gly750Glu)	not specified [RCV004148923]	uncertain significance	12	123181203	123181203	Human		name
156100581	CV2313415	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1198A>G (p.Asn400Asp)	not specified [RCV004163736]	uncertain significance	12	123203372	123203372	Human		name
156176589	CV2327112	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1585G>A (p.Glu529Lys)	not specified [RCV004178682]	uncertain significance	12	123202820	123202820	Human		name
156077322	CV2331872	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1699C>A (p.Gln567Lys)	not specified [RCV004186528]	uncertain significance	12	123202706	123202706	Human		name
156064739	CV2340785	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2714G>A (p.Gly905Glu)	not specified [RCV004188145]	likely benign	12	123165355	123165355	Human		name
156182450	CV2353157	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1027G>C (p.Ala343Pro)	not specified [RCV004203630]	uncertain significance	12	123214804	123214804	Human		name
156109091	CV2355453	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2948A>G (p.Tyr983Cys)	not specified [RCV004205304]	uncertain significance	12	123163095	123163095	Human		name
155925642	CV2365619	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2084G>A (p.Arg695Gln)	not specified [RCV004214185]	uncertain significance	12	123194543	123194543	Human		name
156262315	CV2376956	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1641C>G (p.Ile547Met)	not specified [RCV004229644]	uncertain significance	12	123202764	123202764	Human		name
155937714	CV2380072	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2066C>A (p.Ser689Tyr)	not specified [RCV004222199]	uncertain significance	12	123194561	123194561	Human		name
156082991	CV2394879	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1120A>G (p.Met374Val)	not specified [RCV004234536]	uncertain significance	12	123210130	123210130	Human		name
329370543	CV2435638	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2812C>G (p.Pro938Ala)	not specified [RCV004254882]	uncertain significance	12	123164046	123164046	Human		name
329390752	CV2437217	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2232G>A (p.Met744Ile)	not specified [RCV004256108]	uncertain significance	12	123194395	123194395	Human		name
329392790	CV2439186	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1202C>G (p.Thr401Ser)	not specified [RCV004266462]	uncertain significance	12	123203368	123203368	Human		name
329396689	CV2455709	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1509A>C (p.Leu503Phe)	not specified [RCV004279009]	uncertain significance	12	123202896	123202896	Human		name
401721184	CV2673629	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1979G>A (p.Arg660His)	not specified [RCV004282364]	uncertain significance	12	123198293	123198293	Human		name
401723588	CV2675008	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1024C>T (p.Arg342Cys)	not specified [RCV004296312]	uncertain significance	12	123214807	123214807	Human		name
401727780	CV2678441	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1630A>G (p.Ser544Gly)	not specified [RCV004292461]	uncertain significance	12	123202775	123202775	Human		name
401737782	CV2679977	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1454C>A (p.Ser485Tyr)	not specified [RCV004284252]	uncertain significance	12	123202951	123202951	Human		name
401740086	CV2684261	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2807G>A (p.Arg936His)	not specified [RCV004288921]	uncertain significance	12	123164051	123164051	Human		name
401750460	CV2696059	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2516C>A (p.Ser839Tyr)	not specified [RCV004310128]	uncertain significance	12	123166730	123166730	Human		name
401776857	CV2721498	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2818A>G (p.Lys940Glu)	not specified [RCV004316015]	uncertain significance	12	123164040	123164040	Human		name
401877270	CV2764569	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1645G>T (p.Val549Phe)	not provided [RCV004696487]\|not specified [RCV004339124]	uncertain significance	12	123202760	123202760	Human		name
401866480	CV2782856	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2209C>G (p.Gln737Glu)	not specified [RCV004361664]	likely benign	12	123194418	123194418	Human		name
401897491	CV2787097	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1020T>G (p.His340Gln)	not specified [RCV004366201]	uncertain significance	12	123214811	123214811	Human		name
401896781	CV2788776	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1742T>G (p.Ile581Ser)	not specified [RCV004361239]	uncertain significance	12	123202663	123202663	Human		name
401893020	CV2791977	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2831A>G (p.Gln944Arg)	not specified [RCV004359397]	uncertain significance	12	123164027	123164027	Human		name
405709553	CV3359293	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1175C>T (p.Thr392Ile)	not specified [RCV004493640]	uncertain significance	12	123210075	123210075	Human		name
405709619	CV3359303	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1435G>A (p.Val479Ile)	not specified [RCV004493650]	uncertain significance	12	123202970	123202970	Human		name
405709631	CV3359305	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1438C>A (p.Leu480Ile)	not specified [RCV004493652]	uncertain significance	12	123202967	123202967	Human		name
405708644	CV3362697	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1576T>C (p.Phe526Leu)	not specified [RCV004493512]	uncertain significance	12	123202829	123202829	Human		name
405708679	CV3362702	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1584C>A (p.Asn528Lys)	not specified [RCV004493517]	uncertain significance	12	123202821	123202821	Human		name
405708785	CV3362718	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1814G>A (p.Arg605Gln)	not specified [RCV004493533]	uncertain significance	12	123202287	123202287	Human		name
405708882	CV3362732	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2042G>A (p.Arg681His)	not specified [RCV004493547]	uncertain significance	12	123194585	123194585	Human		name
405708921	CV3362738	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2102C>A (p.Thr701Lys)	not specified [RCV004493553]	uncertain significance	12	123194525	123194525	Human		name
405708950	CV3362742	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2135G>A (p.Arg712Gln)	not specified [RCV004493557]	uncertain significance	12	123194492	123194492	Human		name
405709070	CV3362759	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2417G>A (p.Arg806His)	not specified [RCV004493574]	uncertain significance	12	123176727	123176727	Human		name
407518997	CV3453976	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1037T>G (p.Leu346Arg)	not specified [RCV004629084]	uncertain significance	12	123214794	123214794	Human		name
407518999	CV3453977	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1223C>T (p.Pro408Leu)	not specified [RCV004629085]	uncertain significance	12	123203347	123203347	Human		name
407496248	CV3453978	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1010C>T (p.Ala337Val)	not specified [RCV004643429]	uncertain significance	12	123214821	123214821	Human		name
407496252	CV3453979	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2306C>T (p.Thr769Ile)	not specified [RCV004643430]	uncertain significance	12	123179974	123179974	Human		name
407496255	CV3453981	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2627G>C (p.Gly876Ala)	not specified [RCV004643431]	uncertain significance	12	123165442	123165442	Human		name
407496257	CV3453982	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1049A>G (p.Asp350Gly)	not specified [RCV004643432]	uncertain significance	12	123214782	123214782	Human		name
407496261	CV3453983	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2932C>G (p.Pro978Ala)	not specified [RCV004643433]	uncertain significance	12	123163111	123163111	Human		name
407496265	CV3453984	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1058C>A (p.Pro353Gln)	not specified [RCV004643434]	uncertain significance	12	123214773	123214773	Human		name
407519003	CV3453985	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2510A>G (p.Glu837Gly)	not specified [RCV004629087]	uncertain significance	12	123166736	123166736	Human		name
597661174	CV3564068	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2041C>T (p.Arg681Cys)	not specified [RCV004828477]	uncertain significance	12	123194586	123194586	Human		name
597661183	CV3564069	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1154C>T (p.Thr385Met)	not specified [RCV004828478]	uncertain significance	12	123210096	123210096	Human		name
597661192	CV3564070	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2725A>G (p.Lys909Glu)	not specified [RCV004828479]	uncertain significance	12	123165344	123165344	Human		name
597661200	CV3564073	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2078A>G (p.Gln693Arg)	not specified [RCV004828480]	uncertain significance	12	123194549	123194549	Human		name
597661228	CV3564076	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2294C>A (p.Ala765Glu)	not specified [RCV004828483]	uncertain significance	12	123179986	123179986	Human		name
597637252	CV3564077	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1805A>G (p.Lys602Arg)	not specified [RCV004824712]	uncertain significance	12	123202296	123202296	Human		name
597661235	CV3564078	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2168C>G (p.Ala723Gly)	not specified [RCV004828484]	uncertain significance	12	123194459	123194459	Human		name
597661246	CV3564079	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1382C>T (p.Pro461Leu)	not specified [RCV004828485]	uncertain significance	12	123203023	123203023	Human		name
597637257	CV3564080	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1726A>G (p.Ser576Gly)	not specified [RCV004824713]	uncertain significance	12	123202679	123202679	Human		name
597661263	CV3564082	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1806G>C (p.Lys602Asn)	not specified [RCV004828487]	uncertain significance	12	123202295	123202295	Human		name
597661271	CV3564083	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2075T>C (p.Leu692Ser)	not specified [RCV004828488]	uncertain significance	12	123194552	123194552	Human		name
597661282	CV3564084	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2888A>G (p.Asn963Ser)	not specified [RCV004828489]	likely benign	12	123163970	123163970	Human		name
597661298	CV3564086	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2581T>G (p.Cys861Gly)	not specified [RCV004828491]	uncertain significance	12	123166665	123166665	Human		name
597661308	CV3564087	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2406G>A (p.Met802Ile)	not specified [RCV004828492]	uncertain significance	12	123176738	123176738	Human		name
598201570	CV3982465	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2393A>C (p.Glu798Ala)	not specified [RCV005376055]	uncertain significance	12	123176751	123176751	Human		name
598168271	CV3982466	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1226C>T (p.Ser409Leu)	not specified [RCV005369674]	uncertain significance	12	123203344	123203344	Human		name
598168291	CV3982471	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1484A>C (p.Gln495Pro)	not specified [RCV005369678]	uncertain significance	12	123202921	123202921	Human		name
598201577	CV3982472	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2449C>T (p.Arg817Cys)	not specified [RCV005376057]	uncertain significance	12	123176695	123176695	Human		name
598168296	CV3982473	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2776C>T (p.Arg926Trp)	not specified [RCV005369679]	uncertain significance	12	123164082	123164082	Human		name
598168304	CV3982475	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2385G>C (p.Lys795Asn)	not specified [RCV005369680]	uncertain significance	12	123176759	123176759	Human		name
598201585	CV3982476	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2275C>T (p.His759Tyr)	not specified [RCV005376059]	uncertain significance	12	123181177	123181177	Human		name
598168311	CV3982477	single nucleotide variant	NM_022782.4(MPHOSPH9):c.2543C>T (p.Thr848Ile)	not specified [RCV005369681]	uncertain significance	12	123166703	123166703	Human		name
598201552	CV3986408	single nucleotide variant	NM_022782.4(MPHOSPH9):c.1586A>G (p.Glu529Gly)	not specified [RCV005376051]	uncertain significance	12	123202819	123202819	Human		name
8634554	CV89774	single nucleotide variant	NM_022782.3(MPHOSPH9):c.1609C>T (p.Pro537Ser)	Malignant melanoma [RCV000069871]	not provided	12	123202796	123202796	Human		name
156281139	CV2224343	single nucleotide variant	NM_022782.4(MPHOSPH9):c.3506T>C (p.Met1169Thr)	not specified [RCV004097689]	uncertain significance	12	123156853	123156853	Human		name
156177923	CV2230456	single nucleotide variant	NM_022782.4(MPHOSPH9):c.3055G>C (p.Asp1019His)	not specified [RCV004097434]	uncertain significance	12	123162193	123162193	Human		name
156129365	CV2238528	single nucleotide variant	NM_022782.4(MPHOSPH9):c.3185G>T (p.Cys1062Phe)	not specified [RCV004107146]	uncertain significance	12	123161332	123161332	Human		name
156193478	CV2325835	single nucleotide variant	NM_022782.4(MPHOSPH9):c.3196G>A (p.Val1066Met)	not specified [RCV004173713]	uncertain significance	12	123161321	123161321	Human		name
401742671	CV2715289	single nucleotide variant	NM_022782.4(MPHOSPH9):c.3160G>T (p.Asp1054Tyr)	not specified [RCV004324627]	uncertain significance	12	123161357	123161357	Human		name
401752012	CV2723088	single nucleotide variant	NM_022782.4(MPHOSPH9):c.3194C>T (p.Pro1065Leu)	not specified [RCV004327563]	likely benign	12	123161323	123161323	Human		name
401778832	CV2732915	single nucleotide variant	NM_022782.4(MPHOSPH9):c.3061G>A (p.Val1021Ile)	not specified [RCV004331094]	uncertain significance	12	123162187	123162187	Human		name
401870695	CV2792476	single nucleotide variant	NM_022782.4(MPHOSPH9):c.3532C>T (p.Arg1178Cys)	not specified [RCV004363217]	uncertain significance	12	123156827	123156827	Human		name
405709336	CV3359263	single nucleotide variant	NM_022782.4(MPHOSPH9):c.3160G>A (p.Asp1054Asn)	not specified [RCV004493610]	uncertain significance	12	123161357	123161357	Human		name
597637246	CV3564072	single nucleotide variant	NM_022782.4(MPHOSPH9):c.3533G>A (p.Arg1178His)	not specified [RCV004824711]	uncertain significance	12	123156826	123156826	Human		name
597661220	CV3564075	single nucleotide variant	NM_022782.4(MPHOSPH9):c.3125A>T (p.Asp1042Val)	not specified [RCV004828482]	uncertain significance	12	123162123	123162123	Human		name
597661254	CV3564081	single nucleotide variant	NM_022782.4(MPHOSPH9):c.3347G>A (p.Arg1116Gln)	not specified [RCV004828486]	uncertain significance	12	123161170	123161170	Human		name
597661290	CV3564085	single nucleotide variant	NM_022782.4(MPHOSPH9):c.3343G>C (p.Glu1115Gln)	not specified [RCV004828490]	uncertain significance	12	123161174	123161174	Human		name
598201574	CV3982468	single nucleotide variant	NM_022782.4(MPHOSPH9):c.3385G>A (p.Glu1129Lys)	not specified [RCV005376056]	uncertain significance	12	123160846	123160846	Human		name
598201581	CV3982474	single nucleotide variant	NM_022782.4(MPHOSPH9):c.3032T>C (p.Phe1011Ser)	not specified [RCV005376058]	uncertain significance	12	123162216	123162216	Human		name
598201565	CV3986412	single nucleotide variant	NM_022782.4(MPHOSPH9):c.3253G>C (p.Val1085Leu)	not specified [RCV005376054]	uncertain significance	12	123161264	123161264	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)

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