Rpusd2 Variant Search Result - Rat Genome Database

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56 records found for search term Rpusd2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156076404	CV2291509	single nucleotide variant	NM_152260.3(RPUSD2):c.20G>A (p.Gly7Glu)	not specified [RCV004155818]	uncertain significance	15	40569357	40569357	Human		name
401748063	CV2699993	single nucleotide variant	NM_152260.3(RPUSD2):c.23G>T (p.Trp8Leu)	not specified [RCV004310425]	uncertain significance	15	40569360	40569360	Human		name
597786440	CV3604438	single nucleotide variant	NM_152260.3(RPUSD2):c.38G>A (p.Gly13Glu)	not specified [RCV004854980]	uncertain significance	15	40569375	40569375	Human		name
156163489	CV2305507	single nucleotide variant	NM_152260.3(RPUSD2):c.175G>C (p.Ala59Pro)	not specified [RCV004165218]	uncertain significance	15	40569512	40569512	Human		name
156104804	CV2361047	single nucleotide variant	NM_152260.3(RPUSD2):c.287C>T (p.Pro96Leu)	not specified [RCV004216243]	uncertain significance	15	40569624	40569624	Human		name
329352221	CV2452145	single nucleotide variant	NM_152260.3(RPUSD2):c.265C>T (p.Pro89Ser)	not specified [RCV004278860]	uncertain significance	15	40569602	40569602	Human		name
405739920	CV3316509	single nucleotide variant	NM_152260.3(RPUSD2):c.185A>C (p.Asp62Ala)	not specified [RCV004452220]	uncertain significance	15	40569522	40569522	Human		name
405739931	CV3316510	single nucleotide variant	NM_152260.3(RPUSD2):c.286C>T (p.Pro96Ser)	not specified [RCV004452221]	uncertain significance	15	40569623	40569623	Human		name
407488337	CV3476281	single nucleotide variant	NM_152260.3(RPUSD2):c.162G>C (p.Gln54His)	not specified [RCV004665851]	uncertain significance	15	40569499	40569499	Human		name
598221890	CV3903102	single nucleotide variant	NM_152260.3(RPUSD2):c.242C>G (p.Pro81Arg)	not specified [RCV005272541]	uncertain significance	15	40569579	40569579	Human		name
155925074	CV2220429	single nucleotide variant	NM_152260.3(RPUSD2):c.955G>C (p.Val319Leu)	not specified [RCV004095831]	uncertain significance	15	40573578	40573578	Human		name
155982233	CV2244175	single nucleotide variant	NM_152260.3(RPUSD2):c.383T>G (p.Phe128Cys)	not specified [RCV004108624]	uncertain significance	15	40569720	40569720	Human		name
156007720	CV2288338	single nucleotide variant	NM_152260.3(RPUSD2):c.919G>A (p.Val307Met)	not specified [RCV004150108]	uncertain significance	15	40573542	40573542	Human		name
156285709	CV2289092	single nucleotide variant	NM_152260.3(RPUSD2):c.730C>G (p.His244Asp)	not specified [RCV004150031]	uncertain significance	15	40571727	40571727	Human		name
155902092	CV2301381	single nucleotide variant	NM_152260.3(RPUSD2):c.769A>G (p.Ile257Val)	not specified [RCV004160534]	uncertain significance	15	40571766	40571766	Human		name
156245249	CV2313334	single nucleotide variant	NM_152260.3(RPUSD2):c.304C>T (p.Arg102Trp)	not specified [RCV004163364]	uncertain significance	15	40569641	40569641	Human		name
155911918	CV2313412	single nucleotide variant	NM_152260.3(RPUSD2):c.883G>A (p.Glu295Lys)	not specified [RCV004163733]	uncertain significance	15	40571880	40571880	Human		name
156109081	CV2313923	single nucleotide variant	NM_152260.3(RPUSD2):c.928G>A (p.Val310Met)	not specified [RCV004164231]	uncertain significance	15	40573551	40573551	Human		name
156194507	CV2350815	single nucleotide variant	NM_152260.3(RPUSD2):c.923G>C (p.Cys308Ser)	not specified [RCV004207143]	uncertain significance	15	40573546	40573546	Human		name
401877588	CV2790222	single nucleotide variant	NM_152260.3(RPUSD2):c.716C>T (p.Ser239Phe)	not specified [RCV004364135]	uncertain significance	15	40571713	40571713	Human		name
405739937	CV3316511	single nucleotide variant	NM_152260.3(RPUSD2):c.302A>T (p.Lys101Met)	not specified [RCV004452222]	uncertain significance	15	40569639	40569639	Human		name
405739943	CV3316512	single nucleotide variant	NM_152260.3(RPUSD2):c.337C>T (p.Pro113Ser)	not specified [RCV004452223]	uncertain significance	15	40569674	40569674	Human		name
405739947	CV3316513	single nucleotide variant	NM_152260.3(RPUSD2):c.358G>A (p.Gly120Arg)	not specified [RCV004452224]	uncertain significance	15	40569695	40569695	Human		name
405739953	CV3316514	single nucleotide variant	NM_152260.3(RPUSD2):c.467G>T (p.Arg156Leu)	not specified [RCV004452225]	uncertain significance	15	40569804	40569804	Human		name
405739961	CV3316515	single nucleotide variant	NM_152260.3(RPUSD2):c.671G>A (p.Arg224His)	not specified [RCV004452226]	uncertain significance	15	40571668	40571668	Human		name
405739968	CV3316516	single nucleotide variant	NM_152260.3(RPUSD2):c.835G>C (p.Gly279Arg)	not specified [RCV004452227]	uncertain significance	15	40571832	40571832	Human		name
407488324	CV3476279	single nucleotide variant	NM_152260.3(RPUSD2):c.742C>T (p.Arg248Cys)	not specified [RCV004665849]	uncertain significance	15	40571739	40571739	Human		name
407513842	CV3476283	single nucleotide variant	NM_152260.3(RPUSD2):c.550G>A (p.Ala184Thr)	not specified [RCV004674267]	uncertain significance	15	40569887	40569887	Human		name
597786432	CV3604433	single nucleotide variant	NM_152260.3(RPUSD2):c.721A>G (p.Ile241Val)	not specified [RCV004854978]	uncertain significance	15	40571718	40571718	Human		name
597786444	CV3604439	single nucleotide variant	NM_152260.3(RPUSD2):c.940T>C (p.Phe314Leu)	not specified [RCV004854981]	uncertain significance	15	40573563	40573563	Human		name
598221887	CV3903103	single nucleotide variant	NM_152260.3(RPUSD2):c.425T>G (p.Val142Gly)	not specified [RCV005272542]	uncertain significance	15	40569762	40569762	Human		name
8627631	CV82775	single nucleotide variant	NM_152260.2(RPUSD2):c.814C>T (p.Arg272Trp)	Malignant melanoma [RCV000062855]	not provided	15	40571811	40571811	Human		name
155975420	CV2211279	single nucleotide variant	NM_152260.3(RPUSD2):c.1064G>A (p.Gly355Asp)	not specified [RCV004090213]	uncertain significance	15	40573687	40573687	Human		name
156328727	CV2216253	single nucleotide variant	NM_152260.3(RPUSD2):c.1364A>C (p.Glu455Ala)	not specified [RCV004097202]	uncertain significance	15	40573987	40573987	Human		name
156084146	CV2289665	single nucleotide variant	NM_152260.3(RPUSD2):c.1051C>G (p.Leu351Val)	not specified [RCV004148577]	uncertain significance	15	40573674	40573674	Human		name
155941635	CV2300891	single nucleotide variant	NM_152260.3(RPUSD2):c.1018C>T (p.Arg340Trp)	not specified [RCV004158090]	uncertain significance	15	40573641	40573641	Human		name
329370588	CV2435599	single nucleotide variant	NM_152260.3(RPUSD2):c.1019G>A (p.Arg340Gln)	not specified [RCV004254850]	likely benign	15	40573642	40573642	Human		name
329394551	CV2469929	single nucleotide variant	NM_152260.3(RPUSD2):c.1220C>A (p.Thr407Lys)	not specified [RCV004285392]	uncertain significance	15	40573843	40573843	Human		name
401737622	CV2679928	single nucleotide variant	NM_152260.3(RPUSD2):c.1582T>G (p.Phe528Val)	not specified [RCV004284210]	uncertain significance	15	40574205	40574205	Human		name
401876919	CV2767763	single nucleotide variant	NM_152260.3(RPUSD2):c.1517G>A (p.Arg506Gln)	not specified [RCV004345890]	uncertain significance	15	40574140	40574140	Human		name
405739892	CV3316505	single nucleotide variant	NM_152260.3(RPUSD2):c.1186C>T (p.Pro396Ser)	not specified [RCV004452216]	uncertain significance	15	40573809	40573809	Human		name
405739899	CV3316506	single nucleotide variant	NM_152260.3(RPUSD2):c.1285G>A (p.Asp429Asn)	not specified [RCV004452217]	uncertain significance	15	40573908	40573908	Human		name
405739906	CV3316507	single nucleotide variant	NM_152260.3(RPUSD2):c.1411G>A (p.Ala471Thr)	not specified [RCV004452218]	uncertain significance	15	40574034	40574034	Human		name
405739914	CV3316508	single nucleotide variant	NM_152260.3(RPUSD2):c.1489C>T (p.Pro497Ser)	not specified [RCV004452219]	likely benign	15	40574112	40574112	Human		name
407488332	CV3476280	single nucleotide variant	NM_152260.3(RPUSD2):c.1436C>G (p.Ala479Gly)	not specified [RCV004665850]	uncertain significance	15	40574059	40574059	Human		name
407488345	CV3476282	single nucleotide variant	NM_152260.3(RPUSD2):c.1027C>A (p.Pro343Thr)	not specified [RCV004665852]	uncertain significance	15	40573650	40573650	Human		name
597786413	CV3604427	single nucleotide variant	NM_152260.3(RPUSD2):c.1063G>A (p.Gly355Ser)	not specified [RCV004854973]	uncertain significance	15	40573686	40573686	Human		name
597786417	CV3604428	single nucleotide variant	NM_152260.3(RPUSD2):c.1543G>C (p.Val515Leu)	not specified [RCV004854974]	uncertain significance	15	40574166	40574166	Human		name
597786421	CV3604429	single nucleotide variant	NM_152260.3(RPUSD2):c.1193G>A (p.Arg398Gln)	not specified [RCV004854975]	uncertain significance	15	40573816	40573816	Human		name
597786425	CV3604430	single nucleotide variant	NM_152260.3(RPUSD2):c.1472T>G (p.Met491Arg)	not specified [RCV004854976]	uncertain significance	15	40574095	40574095	Human		name
597786428	CV3604431	single nucleotide variant	NM_152260.3(RPUSD2):c.1082G>A (p.Arg361Gln)	not specified [RCV004854977]	uncertain significance	15	40573705	40573705	Human		name
597710344	CV3604432	single nucleotide variant	NM_152260.3(RPUSD2):c.1328C>T (p.Thr443Met)	not specified [RCV004860946]	uncertain significance	15	40573951	40573951	Human		name
597710350	CV3604434	single nucleotide variant	NM_152260.3(RPUSD2):c.1415C>T (p.Pro472Leu)	not specified [RCV004860947]	uncertain significance	15	40574038	40574038	Human		name
597710360	CV3604436	single nucleotide variant	NM_152260.3(RPUSD2):c.1028C>T (p.Pro343Leu)	not specified [RCV004860948]	uncertain significance	15	40573651	40573651	Human		name
597786436	CV3604437	single nucleotide variant	NM_152260.3(RPUSD2):c.1466A>G (p.Asp489Gly)	not specified [RCV004854979]	uncertain significance	15	40574089	40574089	Human		name
598221902	CV3903100	single nucleotide variant	NM_152260.3(RPUSD2):c.1399G>A (p.Val467Ile)	not specified [RCV005272539]	uncertain significance	15	40574022	40574022	Human		name

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