Cpne5 Variant Search Result - Rat Genome Database

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48 records found for search term Cpne5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15111869	CV730426	single nucleotide variant	NM_020939.2(CPNE5):c.288-8C>T	not provided [RCV000894354]	benign	6	36798502	36798502	Human		name
15185179	CV777565	single nucleotide variant	NM_020939.2(CPNE5):c.1201-9G>A	not provided [RCV000952904]	benign	6	36745524	36745524	Human		name
15180673	CV779260	microsatellite	NM_020939.2(CPNE5):c.405-13TC[3]	not provided [RCV000974209]	benign	6	36794655	36794656	Human		name
407457182	CV3419663	single nucleotide variant	NM_020939.2(CPNE5):c.91T>C (p.Cys31Arg)	not specified [RCV004611057]	uncertain significance	6	36839287	36839287	Human		name
15185183	CV699567	single nucleotide variant	NM_020939.2(CPNE5):c.708G>A (p.Val236=)	not provided [RCV000952905]	benign	6	36774990	36774990	Human		name
15157741	CV699568	single nucleotide variant	NM_020939.2(CPNE5):c.510G>A (p.Glu170=)	not provided [RCV000946940]	benign	6	36792051	36792051	Human		name
156054485	CV2326509	single nucleotide variant	NM_020939.2(CPNE5):c.229G>A (p.Val77Met)	not specified [RCV004183065]	uncertain significance	6	36800025	36800025	Human		name
401856488	CV2764818	single nucleotide variant	NM_020939.2(CPNE5):c.242T>G (p.Ile81Ser)	not specified [RCV004334921]	uncertain significance	6	36800012	36800012	Human		name
405696957	CV3245626	single nucleotide variant	NM_020939.2(CPNE5):c.277C>T (p.Arg93Cys)	not specified [RCV004374550]	uncertain significance	6	36799977	36799977	Human		name
597651754	CV3651162	single nucleotide variant	NM_020939.2(CPNE5):c.130G>A (p.Asp44Asn)	not specified [RCV004910630]	uncertain significance	6	36823064	36823064	Human		name
15151193	CV710485	single nucleotide variant	NM_020939.2(CPNE5):c.1758G>T (p.Ala586=)	not provided [RCV000968087]	benign	6	36742292	36742292	Human		name
156076428	CV2248335	single nucleotide variant	NM_020939.2(CPNE5):c.446T>C (p.Met149Thr)	not specified [RCV004119492]	uncertain significance	6	36794608	36794608	Human		name
156001856	CV2257900	single nucleotide variant	NM_020939.2(CPNE5):c.553G>A (p.Ala185Thr)	not specified [RCV004129725]	uncertain significance	6	36778933	36778933	Human		name
155904287	CV2298778	single nucleotide variant	NM_020939.2(CPNE5):c.883A>G (p.Lys295Glu)	not specified [RCV004156335]	uncertain significance	6	36756271	36756271	Human		name
156340630	CV2368293	single nucleotide variant	NM_020939.2(CPNE5):c.983A>G (p.Asn328Ser)	not specified [RCV004219076]	uncertain significance	6	36748256	36748256	Human		name
156056596	CV2396257	single nucleotide variant	NM_020939.2(CPNE5):c.827G>A (p.Arg276His)	not specified [RCV004240209]	uncertain significance	6	36762945	36762945	Human		name
401739044	CV2676425	single nucleotide variant	NM_020939.2(CPNE5):c.740C>A (p.Thr247Asn)	not specified [RCV004286445]	uncertain significance	6	36765374	36765374	Human		name
401898522	CV2787981	single nucleotide variant	NM_020939.2(CPNE5):c.593A>G (p.Asp198Gly)	not specified [RCV004358637]	uncertain significance	6	36778893	36778893	Human		name
405696961	CV3245627	single nucleotide variant	NM_020939.2(CPNE5):c.382A>T (p.Ser128Cys)	not specified [RCV004374551]	uncertain significance	6	36798187	36798187	Human		name
405696969	CV3245628	single nucleotide variant	NM_020939.2(CPNE5):c.385C>T (p.Arg129Cys)	not specified [RCV004374552]	uncertain significance	6	36798184	36798184	Human		name
405696975	CV3245629	single nucleotide variant	NM_020939.2(CPNE5):c.733G>A (p.Asp245Asn)	not specified [RCV004374553]	uncertain significance	6	36774965	36774965	Human		name
407457178	CV3419661	single nucleotide variant	NM_020939.2(CPNE5):c.538A>G (p.Thr180Ala)	not specified [RCV004611055]	uncertain significance	6	36778948	36778948	Human		name
407457181	CV3419662	single nucleotide variant	NM_020939.2(CPNE5):c.727G>A (p.Asp243Asn)	not specified [RCV004611056]	uncertain significance	6	36774971	36774971	Human		name
407457186	CV3419664	single nucleotide variant	NM_020939.2(CPNE5):c.364A>G (p.Ile122Val)	not specified [RCV004611058]	uncertain significance	6	36798205	36798205	Human		name
597651765	CV3651163	single nucleotide variant	NM_020939.2(CPNE5):c.984C>G (p.Asn328Lys)	not specified [RCV004910631]	uncertain significance	6	36748255	36748255	Human		name
597773981	CV3651164	single nucleotide variant	NM_020939.2(CPNE5):c.406A>T (p.Ile136Leu)	not specified [RCV004897629]	uncertain significance	6	36794648	36794648	Human		name
598246623	CV3945295	single nucleotide variant	NM_020939.2(CPNE5):c.442C>G (p.Pro148Ala)	not specified [RCV005322346]	uncertain significance	6	36794612	36794612	Human		name
598246637	CV3945297	single nucleotide variant	NM_020939.2(CPNE5):c.473C>T (p.Pro158Leu)	not specified [RCV005322348]	uncertain significance	6	36792088	36792088	Human		name
598246642	CV3945298	single nucleotide variant	NM_020939.2(CPNE5):c.662T>G (p.Met221Arg)	not specified [RCV005322349]	uncertain significance	6	36775036	36775036	Human		name
156378380	CV2207705	single nucleotide variant	NM_020939.2(CPNE5):c.1697G>A (p.Arg566His)	not specified [RCV004084153]	uncertain significance	6	36742353	36742353	Human		name
155977359	CV2246831	single nucleotide variant	NM_020939.2(CPNE5):c.1730C>T (p.Ser577Leu)	not specified [RCV004112647]	uncertain significance	6	36742320	36742320	Human		name
156169030	CV2276686	single nucleotide variant	NM_020939.2(CPNE5):c.1488C>A (p.Asp496Glu)	not specified [RCV004146486]	uncertain significance	6	36744269	36744269	Human		name
156074068	CV2294715	single nucleotide variant	NM_020939.2(CPNE5):c.1298A>G (p.Asn433Ser)	not specified [RCV004161957]	uncertain significance	6	36745418	36745418	Human		name
156297480	CV2328907	single nucleotide variant	NM_020939.2(CPNE5):c.1726C>T (p.Pro576Ser)	not specified [RCV004180213]	uncertain significance	6	36742324	36742324	Human		name
156307811	CV2369824	single nucleotide variant	NM_020939.2(CPNE5):c.1744C>T (p.Arg582Cys)	not specified [RCV004208299]	uncertain significance	6	36742306	36742306	Human		name
329384778	CV2435196	single nucleotide variant	NM_020939.2(CPNE5):c.1270C>T (p.Arg424Cys)	not specified [RCV004252833]	uncertain significance	6	36745446	36745446	Human		name
329359624	CV2461577	single nucleotide variant	NM_020939.2(CPNE5):c.1760C>A (p.Ser587Tyr)	not specified [RCV004269759]	uncertain significance	6	36742290	36742290	Human		name
401766145	CV2679584	single nucleotide variant	NM_020939.2(CPNE5):c.1261C>T (p.Arg421Cys)	not specified [RCV004282066]	uncertain significance	6	36745455	36745455	Human		name
401857475	CV2760184	single nucleotide variant	NM_020939.2(CPNE5):c.1513G>A (p.Asp505Asn)	not specified [RCV004347361]	uncertain significance	6	36743739	36743739	Human		name
401886598	CV2780431	single nucleotide variant	NM_020939.2(CPNE5):c.1544C>A (p.Ala515Asp)	not specified [RCV004357819]	uncertain significance	6	36743708	36743708	Human		name
405696950	CV3245624	single nucleotide variant	NM_020939.2(CPNE5):c.1271G>A (p.Arg424His)	not specified [RCV004374548]	uncertain significance	6	36745445	36745445	Human		name
405696952	CV3245625	single nucleotide variant	NM_020939.2(CPNE5):c.1748C>T (p.Thr583Met)	not specified [RCV004374549]	uncertain significance	6	36742302	36742302	Human		name
407457174	CV3419660	single nucleotide variant	NM_020939.2(CPNE5):c.1397C>T (p.Ser466Leu)	not specified [RCV004611054]	uncertain significance	6	36745082	36745082	Human		name
597651737	CV3651160	single nucleotide variant	NM_020939.2(CPNE5):c.1519C>T (p.Arg507Trp)	not specified [RCV004910628]	uncertain significance	6	36743733	36743733	Human		name
597651744	CV3651161	single nucleotide variant	NM_020939.2(CPNE5):c.1231G>A (p.Gly411Ser)	not specified [RCV004910629]	uncertain significance	6	36745485	36745485	Human		name
598246617	CV3945294	single nucleotide variant	NM_020939.2(CPNE5):c.1636G>A (p.Val546Met)	not specified [RCV005322345]	uncertain significance	6	36742414	36742414	Human		name
598246630	CV3945296	single nucleotide variant	NM_020939.2(CPNE5):c.1592G>A (p.Arg531His)	not specified [RCV005322347]	uncertain significance	6	36742458	36742458	Human		name
15181294	CV710486	single nucleotide variant	NM_020939.2(CPNE5):c.1332T>G (p.Asn444Lys)	not provided [RCV000974357]	benign	6	36745147	36745147	Human		name

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