Mpnd Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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66 records found for search term Mpnd

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155980998	CV2336985	single nucleotide variant	NM_001300862.2(MPND):c.92A>C (p.Glu31Ala)	not specified [RCV004192756]	uncertain significance	19	4343792	4343792	Human		name
156013014	CV2359004	single nucleotide variant	NM_001300862.2(MPND):c.69C>G (p.Asp23Glu)	not specified [RCV004212331]	uncertain significance	19	4343769	4343769	Human		name
405711225	CV3359534	single nucleotide variant	NM_001300862.2(MPND):c.38C>T (p.Ala13Val)	not specified [RCV004493882]	uncertain significance	19	4343738	4343738	Human		name
405711242	CV3359536	single nucleotide variant	NM_001300862.2(MPND):c.41G>A (p.Gly14Asp)	not specified [RCV004493884]	uncertain significance	19	4343741	4343741	Human		name
598201597	CV3982489	single nucleotide variant	NM_001300862.2(MPND):c.61G>A (p.Asp21Asn)	not specified [RCV005376062]	uncertain significance	19	4343761	4343761	Human		name
155959691	CV2193985	single nucleotide variant	NM_001300862.2(MPND):c.272G>A (p.Gly91Glu)	not specified [RCV004074710]	uncertain significance	19	4343972	4343972	Human		name
156157480	CV2235295	single nucleotide variant	NM_001300862.2(MPND):c.104C>T (p.Ala35Val)	not specified [RCV004107332]	uncertain significance	19	4343804	4343804	Human		name
401719031	CV2679392	single nucleotide variant	NM_001300862.2(MPND):c.145G>C (p.Val49Leu)	not specified [RCV004285921]	uncertain significance	19	4343845	4343845	Human		name
401775199	CV2692292	single nucleotide variant	NM_001300862.2(MPND):c.251C>A (p.Ala84Glu)	not specified [RCV004310287]	uncertain significance	19	4343951	4343951	Human		name
155918989	CV2279331	single nucleotide variant	NM_001300862.2(MPND):c.686G>T (p.Arg229Leu)	not specified [RCV004139847]	uncertain significance	19	4354066	4354066	Human		name
156264799	CV2289954	single nucleotide variant	NM_001300862.2(MPND):c.806C>T (p.Pro269Leu)	not specified [RCV004150604]	uncertain significance	19	4354380	4354380	Human		name
156048213	CV2319222	single nucleotide variant	NM_001300862.2(MPND):c.987C>G (p.Ile329Met)	not specified [RCV004178271]	uncertain significance	19	4355164	4355164	Human		name
156383196	CV2361450	single nucleotide variant	NM_001300862.2(MPND):c.778T>A (p.Ser260Thr)	not specified [RCV004221091]	uncertain significance	19	4354352	4354352	Human		name
155989348	CV2371931	single nucleotide variant	NM_001300862.2(MPND):c.370C>T (p.Pro124Ser)	not specified [RCV004221614]	uncertain significance	19	4345820	4345820	Human		name
156096801	CV2399128	single nucleotide variant	NM_001300862.2(MPND):c.629C>A (p.Pro210Gln)	not specified [RCV004246562]	uncertain significance	19	4352994	4352994	Human		name
329376064	CV2437953	single nucleotide variant	NM_001300862.2(MPND):c.490C>T (p.Arg164Trp)	not specified [RCV004263672]	uncertain significance	19	4345940	4345940	Human		name
329362336	CV2444615	single nucleotide variant	NM_001300862.2(MPND):c.716G>A (p.Arg239His)	not specified [RCV004256836]	uncertain significance	19	4354096	4354096	Human		name
329391193	CV2447871	single nucleotide variant	NM_001300862.2(MPND):c.491G>A (p.Arg164Gln)	not specified [RCV004260687]	uncertain significance	19	4345941	4345941	Human		name
329358438	CV2450318	single nucleotide variant	NM_001300862.2(MPND):c.581A>G (p.Glu194Gly)	not specified [RCV004271407]	uncertain significance	19	4352946	4352946	Human		name
401769638	CV2689866	single nucleotide variant	NM_001300862.2(MPND):c.961G>A (p.Gly321Arg)	not specified [RCV004297764]	uncertain significance	19	4355138	4355138	Human		name
401861245	CV2769613	single nucleotide variant	NM_001300862.2(MPND):c.693C>G (p.Asp231Glu)	not specified [RCV004351256]	likely benign	19	4354073	4354073	Human		name
401877725	CV2779923	single nucleotide variant	NM_001300862.2(MPND):c.373A>T (p.Ser125Cys)	not specified [RCV004353530]	uncertain significance	19	4345823	4345823	Human		name
401866624	CV2782897	single nucleotide variant	NM_001300862.2(MPND):c.487C>T (p.Leu163Phe)	not specified [RCV004361700]	uncertain significance	19	4345937	4345937	Human		name
405711121	CV3359519	single nucleotide variant	NM_001300862.2(MPND):c.313G>A (p.Asp105Asn)	not specified [RCV004493867]	uncertain significance	19	4345763	4345763	Human		name
405711160	CV3359525	single nucleotide variant	NM_001300862.2(MPND):c.332G>A (p.Arg111Lys)	not specified [RCV004493873]	uncertain significance	19	4345782	4345782	Human		name
405711267	CV3359539	single nucleotide variant	NM_001300862.2(MPND):c.428G>A (p.Cys143Tyr)	not specified [RCV004493887]	uncertain significance	19	4345878	4345878	Human		name
405726985	CV3359574	single nucleotide variant	NM_001300862.2(MPND):c.832G>A (p.Val278Met)	not specified [RCV004495906]	uncertain significance	19	4354406	4354406	Human		name
405727031	CV3359580	single nucleotide variant	NM_001300862.2(MPND):c.844C>G (p.Leu282Val)	not specified [RCV004495912]	uncertain significance	19	4354418	4354418	Human		name
405727056	CV3359583	single nucleotide variant	NM_001300862.2(MPND):c.928G>A (p.Val310Met)	not specified [RCV004495915]	uncertain significance	19	4355105	4355105	Human		name
405727113	CV3359590	single nucleotide variant	NM_001300862.2(MPND):c.958C>T (p.Leu320Phe)	not specified [RCV004495922]	uncertain significance	19	4355135	4355135	Human		name
405727177	CV3359597	single nucleotide variant	NM_001300862.2(MPND):c.988G>A (p.Glu330Lys)	not specified [RCV004495929]	uncertain significance	19	4355165	4355165	Human		name
407496278	CV3453990	single nucleotide variant	NM_001300862.2(MPND):c.589G>A (p.Val197Ile)	not specified [RCV004643438]	uncertain significance	19	4352954	4352954	Human		name
407496281	CV3453991	single nucleotide variant	NM_001300862.2(MPND):c.895G>T (p.Gly299Cys)	not specified [RCV004643439]	uncertain significance	19	4354997	4354997	Human		name
407496284	CV3453992	single nucleotide variant	NM_001300862.2(MPND):c.526G>T (p.Asp176Tyr)	not specified [RCV004643440]	uncertain significance	19	4345976	4345976	Human		name
407496288	CV3453993	single nucleotide variant	NM_001300862.2(MPND):c.812A>G (p.Asn271Ser)	not specified [RCV004643441]	uncertain significance	19	4354386	4354386	Human		name
407496291	CV3453994	single nucleotide variant	NM_001300862.2(MPND):c.739G>A (p.Asp247Asn)	not specified [RCV004643442]	uncertain significance	19	4354119	4354119	Human		name
597637263	CV3564098	single nucleotide variant	NM_001300862.2(MPND):c.622C>T (p.Arg208Trp)	not specified [RCV004824714]	uncertain significance	19	4352987	4352987	Human		name
597661335	CV3564100	single nucleotide variant	NM_001300862.2(MPND):c.955C>T (p.Arg319Trp)	not specified [RCV004828495]	uncertain significance	19	4355132	4355132	Human		name
597661342	CV3564101	single nucleotide variant	NM_001300862.2(MPND):c.392G>A (p.Cys131Tyr)	not specified [RCV004828496]	uncertain significance	19	4345842	4345842	Human		name
597661351	CV3564102	single nucleotide variant	NM_001300862.2(MPND):c.862C>G (p.Leu288Val)	not specified [RCV004828497]	uncertain significance	19	4354964	4354964	Human		name
597661359	CV3564103	single nucleotide variant	NM_001300862.2(MPND):c.869G>A (p.Arg290Gln)	not specified [RCV004828498]	uncertain significance	19	4354971	4354971	Human		name
597661367	CV3564104	single nucleotide variant	NM_001300862.2(MPND):c.422C>T (p.Ser141Leu)	not specified [RCV004828499]	uncertain significance	19	4345872	4345872	Human		name
597661375	CV3564106	single nucleotide variant	NM_001300862.2(MPND):c.496C>T (p.His166Tyr)	not specified [RCV004828500]	uncertain significance	19	4345946	4345946	Human		name
597637271	CV3564107	single nucleotide variant	NM_001300862.2(MPND):c.473A>G (p.Tyr158Cys)	not specified [RCV004824716]	uncertain significance	19	4345923	4345923	Human		name
598168339	CV3982485	single nucleotide variant	NM_001300862.2(MPND):c.962G>A (p.Gly321Glu)	not specified [RCV005369688]	uncertain significance	19	4355139	4355139	Human		name
598201593	CV3982486	single nucleotide variant	NM_001300862.2(MPND):c.953G>T (p.Ser318Ile)	not specified [RCV005376061]	uncertain significance	19	4355130	4355130	Human		name
598168344	CV3982487	single nucleotide variant	NM_001300862.2(MPND):c.704G>A (p.Arg235Gln)	not specified [RCV005369689]	uncertain significance	19	4354084	4354084	Human		name
598201604	CV3982491	single nucleotide variant	NM_001300862.2(MPND):c.389A>C (p.His130Pro)	not specified [RCV005376064]	uncertain significance	19	4345839	4345839	Human		name
155972700	CV2224400	single nucleotide variant	NM_001300862.2(MPND):c.1124G>A (p.Gly375Asp)	not specified [RCV004098009]	uncertain significance	19	4357380	4357380	Human		name
156112051	CV2228367	single nucleotide variant	NM_001300862.2(MPND):c.1208C>T (p.Ser403Leu)	not specified [RCV004098349]	uncertain significance	19	4357557	4357557	Human		name
156151441	CV2307556	single nucleotide variant	NM_001300862.2(MPND):c.1153G>C (p.Ala385Pro)	not specified [RCV004166196]	uncertain significance	19	4357409	4357409	Human		name
156053107	CV2333270	single nucleotide variant	NM_001300862.2(MPND):c.1483G>A (p.Gly495Ser)	not specified [RCV004197019]	likely benign	19	4359979	4359979	Human		name
156064541	CV2349839	single nucleotide variant	NM_001300862.2(MPND):c.1455C>A (p.Ser485Arg)	not specified [RCV004206262]	uncertain significance	19	4359951	4359951	Human		name
401741931	CV2697660	single nucleotide variant	NM_001300862.2(MPND):c.1439C>T (p.Thr480Met)	not specified [RCV004300404]	uncertain significance	19	4359935	4359935	Human		name
401725493	CV2721798	single nucleotide variant	NM_001300862.2(MPND):c.1482C>G (p.Cys494Trp)	not specified [RCV004326316]	uncertain significance	19	4359978	4359978	Human		name
401879232	CV2758238	single nucleotide variant	NM_001300862.2(MPND):c.1379A>G (p.Glu460Gly)	not specified [RCV004341601]	uncertain significance	19	4359215	4359215	Human		name
401879234	CV2758239	single nucleotide variant	NM_001300862.2(MPND):c.1380A>T (p.Glu460Asp)	not specified [RCV004341602]	uncertain significance	19	4359216	4359216	Human		name
401879238	CV2758240	single nucleotide variant	NM_001300862.2(MPND):c.1381C>T (p.Pro461Ser)	not specified [RCV004341603]	uncertain significance	19	4359217	4359217	Human		name
405710785	CV3359471	single nucleotide variant	NM_001300862.2(MPND):c.1018C>T (p.Arg340Trp)	not specified [RCV004493819]	uncertain significance	19	4357274	4357274	Human		name
405710824	CV3359477	single nucleotide variant	NM_001300862.2(MPND):c.1097A>G (p.Gln366Arg)	not specified [RCV004493825]	uncertain significance	19	4357353	4357353	Human		name
405710859	CV3359482	single nucleotide variant	NM_001300862.2(MPND):c.1153G>A (p.Ala385Thr)	not specified [RCV004493830]	uncertain significance	19	4357409	4357409	Human		name
405710970	CV3359497	single nucleotide variant	NM_001300862.2(MPND):c.1465G>A (p.Val489Ile)	not specified [RCV004493845]	uncertain significance	19	4359961	4359961	Human		name
405710988	CV3359500	single nucleotide variant	NM_001300862.2(MPND):c.1481G>A (p.Cys494Tyr)	not specified [RCV004493848]	likely benign	19	4359977	4359977	Human		name
597637266	CV3564105	single nucleotide variant	NM_001300862.2(MPND):c.1130G>A (p.Ser377Asn)	not specified [RCV004824715]	uncertain significance	19	4357386	4357386	Human		name
598168349	CV3982488	single nucleotide variant	NM_001300862.2(MPND):c.1345T>C (p.Tyr449His)	not specified [RCV005369690]	uncertain significance	19	4359181	4359181	Human		name
598201600	CV3982490	single nucleotide variant	NM_001300862.2(MPND):c.1150C>T (p.Leu384Phe)	not specified [RCV005376063]	uncertain significance	19	4357406	4357406	Human		name

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