Npm2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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24 records found for search term Npm2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598219160	CV3997840	single nucleotide variant	NM_001286680.2(NPM2):c.14G>C (p.Ser5Thr)	not specified [RCV005379299]	uncertain significance	8	22025262	22025262	Human		name
597685113	CV3566508	single nucleotide variant	NM_001286680.2(NPM2):c.70A>G (p.Ser24Gly)	not specified [RCV004838089]	uncertain significance	8	22025447	22025447	Human		name
597685134	CV3566510	single nucleotide variant	NM_001286680.2(NPM2):c.94T>C (p.Phe32Leu)	not specified [RCV004838091]	uncertain significance	8	22025471	22025471	Human		name
598219166	CV3997841	single nucleotide variant	NM_001286680.2(NPM2):c.59G>T (p.Gly20Val)	not specified [RCV005379300]	uncertain significance	8	22025436	22025436	Human		name
15165646	CV711443	single nucleotide variant	NM_001286680.2(NPM2):c.369A>C (p.Ala123=)	not provided [RCV000970996]	benign	8	22034113	22034113	Human		name
156126299	CV2234325	single nucleotide variant	NM_001286680.2(NPM2):c.278T>C (p.Met93Thr)	not specified [RCV004100559]	uncertain significance	8	22033137	22033137	Human		name
156314830	CV2253319	single nucleotide variant	NM_001286680.2(NPM2):c.269T>C (p.Met90Thr)	not specified [RCV004123152]	uncertain significance	8	22025771	22025771	Human		name
155939851	CV2378873	single nucleotide variant	NM_001286680.2(NPM2):c.154G>A (p.Gly52Arg)	not specified [RCV004231307]	uncertain significance	8	22025656	22025656	Human		name
155919623	CV2202683	single nucleotide variant	NM_001286680.2(NPM2):c.476G>T (p.Ser159Ile)	not specified [RCV004082931]	uncertain significance	8	22034220	22034220	Human		name
156401704	CV2217575	single nucleotide variant	NM_001286680.2(NPM2):c.523G>A (p.Val175Met)	not specified [RCV004090104]	uncertain significance	8	22034267	22034267	Human		name
155924538	CV2220339	single nucleotide variant	NM_001286680.2(NPM2):c.619G>A (p.Ala207Thr)	not specified [RCV004095758]	uncertain significance	8	22036656	22036656	Human		name
329377079	CV2456902	single nucleotide variant	NM_001286680.2(NPM2):c.466G>C (p.Glu156Gln)	not specified [RCV004270859]	uncertain significance	8	22034210	22034210	Human		name
401748134	CV2687691	single nucleotide variant	NM_001286680.2(NPM2):c.337G>A (p.Val113Met)	not specified [RCV004302686]	uncertain significance	8	22033196	22033196	Human		name
401745945	CV2695470	single nucleotide variant	NM_001286680.2(NPM2):c.572G>T (p.Ser191Ile)	not specified [RCV004305660]	uncertain significance	8	22036498	22036498	Human		name
401759150	CV2712439	single nucleotide variant	NM_001286680.2(NPM2):c.298C>T (p.Pro100Ser)	not specified [RCV004313902]	uncertain significance	8	22033157	22033157	Human		name
401873989	CV2757793	single nucleotide variant	NM_001286680.2(NPM2):c.457A>G (p.Ile153Val)	not specified [RCV004336940]	likely benign	8	22034201	22034201	Human		name
405692891	CV3352284	single nucleotide variant	NM_001286680.2(NPM2):c.320G>C (p.Arg107Pro)	not specified [RCV004491063]	uncertain significance	8	22033179	22033179	Human		name
405692893	CV3352285	single nucleotide variant	NM_001286680.2(NPM2):c.359G>A (p.Arg120His)	not specified [RCV004491064]	uncertain significance	8	22033218	22033218	Human		name
407498712	CV3465670	single nucleotide variant	NM_001286680.2(NPM2):c.614C>T (p.Ala205Val)	not specified [RCV004644101]	uncertain significance	8	22036651	22036651	Human		name
407498715	CV3465671	single nucleotide variant	NM_001286680.2(NPM2):c.557A>G (p.Glu186Gly)	not specified [RCV004644102]	uncertain significance	8	22034535	22034535	Human		name
597685122	CV3566509	single nucleotide variant	NM_001286680.2(NPM2):c.301C>T (p.Pro101Ser)	not specified [RCV004838090]	uncertain significance	8	22033160	22033160	Human		name
597685145	CV3566511	single nucleotide variant	NM_001286680.2(NPM2):c.343C>T (p.Leu115Phe)	not specified [RCV004838092]	uncertain significance	8	22033202	22033202	Human		name
598219151	CV3997838	single nucleotide variant	NM_001286680.2(NPM2):c.332G>A (p.Gly111Glu)	not specified [RCV005379298]	uncertain significance	8	22033191	22033191	Human		name
598264318	CV3997839	single nucleotide variant	NM_001286680.2(NPM2):c.391G>A (p.Glu131Lys)	not specified [RCV005387732]	uncertain significance	8	22034135	22034135	Human		name

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