Prr5l Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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43 records found for search term Prr5l

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8652935	CV129510	single nucleotide variant	NM_001160167.1(PRR5L):c.-125-6601A>G	Lung cancer [RCV000109997]	uncertain significance	11	36394396	36394396	Human		name
15199052	CV701751	single nucleotide variant	NM_001160167.2(PRR5L):c.8G>A (p.Arg3His)	not provided [RCV000956932]	benign	11	36401129	36401129	Human		name
405653677	CV3379927	single nucleotide variant	NM_001160167.2(PRR5L):c.16G>A (p.Ala6Thr)	not specified [RCV004510367]	uncertain significance	11	36401137	36401137	Human		name
15193880	CV724421	single nucleotide variant	NM_001160167.2(PRR5L):c.234C>T (p.Asn78=)	not provided [RCV000889066]	benign	11	36403367	36403367	Human		name
405653683	CV3379930	single nucleotide variant	NM_001160167.2(PRR5L):c.45G>T (p.Lys15Asn)	not specified [RCV004510370]	uncertain significance	11	36401166	36401166	Human		name
405653687	CV3379932	single nucleotide variant	NM_001160167.2(PRR5L):c.723C>T (p.His241=)	not specified [RCV004510372]	likely benign	11	36462352	36462352	Human		name
407466288	CV3461369	single nucleotide variant	NM_001160167.2(PRR5L):c.31G>T (p.Val11Phe)	not specified [RCV004660435]	uncertain significance	11	36401152	36401152	Human		name
15174902	CV712813	single nucleotide variant	NM_001160167.2(PRR5L):c.891G>A (p.Ser297=)	not provided [RCV000972820]	benign	11	36462520	36462520	Human		name
15174906	CV712814	single nucleotide variant	NM_001160167.2(PRR5L):c.936G>T (p.Leu312=)	not provided [RCV000972821]	benign	11	36462565	36462565	Human		name
156253931	CV2193166	single nucleotide variant	NM_001160167.2(PRR5L):c.122C>A (p.Ala41Asp)	not specified [RCV004071162]	uncertain significance	11	36401243	36401243	Human		name
401749228	CV2694592	single nucleotide variant	NM_001160167.2(PRR5L):c.124C>T (p.Arg42Trp)	not specified [RCV004298712]	uncertain significance	11	36401245	36401245	Human		name
405653679	CV3379928	single nucleotide variant	NM_001160167.2(PRR5L):c.217G>A (p.Glu73Lys)	not specified [RCV004510368]	uncertain significance	11	36403350	36403350	Human		name
598160403	CV3901520	single nucleotide variant	NM_001160167.2(PRR5L):c.166G>A (p.Val56Ile)	not specified [RCV005260974]	uncertain significance	11	36403299	36403299	Human		name
150448912	CV1215041	single nucleotide variant	NM_001160167.2(PRR5L):c.415A>G (p.Thr139Ala)	not provided [RCV001611630]	benign	11	36437447	36437447	Human	9	name
150448912	CV1215041	single nucleotide variant	NM_001160167.2(PRR5L):c.415A>G (p.Thr139Ala)	not provided [RCV001611630]	benign	11	36437447	36437448	Human	9	name
155915625	CV2200433	single nucleotide variant	NM_001160167.2(PRR5L):c.362G>T (p.Arg121Leu)	not specified [RCV004076749]	uncertain significance	11	36437394	36437394	Human		name
155967608	CV2329942	single nucleotide variant	NM_001160167.2(PRR5L):c.947C>A (p.Ala316Asp)	not specified [RCV004183396]	uncertain significance	11	36462576	36462576	Human		name
329358730	CV2425351	single nucleotide variant	NM_001160167.2(PRR5L):c.679G>C (p.Asp227His)	not specified [RCV004251013]	uncertain significance	11	36451302	36451302	Human		name
329383151	CV2441913	single nucleotide variant	NM_001160167.2(PRR5L):c.667G>A (p.Gly223Ser)	not specified [RCV004262094]	uncertain significance	11	36451290	36451290	Human		name
401761212	CV2689066	single nucleotide variant	NM_001160167.2(PRR5L):c.766C>T (p.Pro256Ser)	not specified [RCV004305837]	uncertain significance	11	36462395	36462395	Human		name
401771209	CV2726399	single nucleotide variant	NM_001160167.2(PRR5L):c.997C>A (p.His333Asn)	not specified [RCV004328613]	uncertain significance	11	36462626	36462626	Human		name
401861575	CV2756355	single nucleotide variant	NM_001160167.2(PRR5L):c.701C>T (p.Thr234Met)	not specified [RCV004342901]	uncertain significance	11	36451324	36451324	Human		name
401870527	CV2762847	single nucleotide variant	NM_001160167.2(PRR5L):c.719G>A (p.Arg240Gln)	not specified [RCV004340393]	uncertain significance	11	36462348	36462348	Human		name
405653681	CV3379929	single nucleotide variant	NM_001160167.2(PRR5L):c.307G>A (p.Ala103Thr)	not specified [RCV004510369]	uncertain significance	11	36431865	36431865	Human		name
405653685	CV3379931	single nucleotide variant	NM_001160167.2(PRR5L):c.508G>A (p.Val170Met)	not specified [RCV004510371]	uncertain significance	11	36446363	36446363	Human		name
405653689	CV3379933	single nucleotide variant	NM_001160167.2(PRR5L):c.784C>T (p.Arg262Trp)	not specified [RCV004510373]	uncertain significance	11	36462413	36462413	Human		name
405653691	CV3379934	single nucleotide variant	NM_001160167.2(PRR5L):c.889T>G (p.Ser297Ala)	not specified [RCV004510374]	uncertain significance	11	36462518	36462518	Human		name
405653694	CV3379935	single nucleotide variant	NM_001160167.2(PRR5L):c.938G>T (p.Gly313Val)	not specified [RCV004510375]	uncertain significance	11	36462567	36462567	Human		name
407466293	CV3461370	single nucleotide variant	NM_001160167.2(PRR5L):c.833A>C (p.Glu278Ala)	not specified [RCV004660436]	uncertain significance	11	36462462	36462462	Human		name
597760845	CV3584667	single nucleotide variant	NM_001160167.2(PRR5L):c.364A>G (p.Ile122Val)	not specified [RCV004849020]	uncertain significance	11	36437396	36437396	Human		name
597760855	CV3584669	single nucleotide variant	NM_001160167.2(PRR5L):c.992C>T (p.Pro331Leu)	not specified [RCV004849022]	uncertain significance	11	36462621	36462621	Human		name
597760860	CV3584670	single nucleotide variant	NM_001160167.2(PRR5L):c.859G>C (p.Val287Leu)	not specified [RCV004849023]	uncertain significance	11	36462488	36462488	Human		name
598249865	CV3901516	single nucleotide variant	NM_001160167.2(PRR5L):c.911T>G (p.Met304Arg)	not specified [RCV005258988]	uncertain significance	11	36462540	36462540	Human		name
598160387	CV3901517	single nucleotide variant	NM_001160167.2(PRR5L):c.718C>T (p.Arg240Trp)	not specified [RCV005260971]	uncertain significance	11	36462347	36462347	Human		name
598160393	CV3901518	single nucleotide variant	NM_001160167.2(PRR5L):c.776C>T (p.Ala259Val)	not specified [RCV005260972]	uncertain significance	11	36462405	36462405	Human		name
156143718	CV2200109	single nucleotide variant	NM_001160167.2(PRR5L):c.1024A>G (p.Ile342Val)	not specified [RCV004069683]	uncertain significance	11	36462653	36462653	Human		name
156183434	CV2327968	single nucleotide variant	NM_001160167.2(PRR5L):c.1042G>A (p.Gly348Arg)	not specified [RCV004179283]	uncertain significance	11	36462671	36462671	Human		name
156170579	CV2337451	single nucleotide variant	NM_001160167.2(PRR5L):c.1000C>T (p.Arg334Trp)	not specified [RCV004187889]	uncertain significance	11	36462629	36462629	Human		name
401780502	CV2716804	single nucleotide variant	NM_001160167.2(PRR5L):c.1054G>A (p.Gly352Arg)	not specified [RCV004329624]	uncertain significance	11	36462683	36462683	Human		name
401898943	CV2792143	single nucleotide variant	NM_001160167.2(PRR5L):c.1091G>A (p.Cys364Tyr)	not specified [RCV004361361]	uncertain significance	11	36462720	36462720	Human		name
407513759	CV3461372	single nucleotide variant	NM_001160167.2(PRR5L):c.1037C>T (p.Pro346Leu)	not specified [RCV004648940]	uncertain significance	11	36462666	36462666	Human		name
407466304	CV3461373	single nucleotide variant	NM_001160167.2(PRR5L):c.1088A>G (p.Asn363Ser)	not specified [RCV004660438]	uncertain significance	11	36462717	36462717	Human		name
597760850	CV3584668	single nucleotide variant	NM_001160167.2(PRR5L):c.1001G>A (p.Arg334Gln)	not specified [RCV004849021]	uncertain significance	11	36462630	36462630	Human		name

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