Eri2 Variant Search Result - Rat Genome Database

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54 records found for search term Eri2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155974649	CV2269983	single nucleotide variant	NM_001142725.2(ERI2):c.5C>T (p.Ala2Val)	not specified [RCV004128975]	uncertain significance	16	20806426	20806426	Human		name
597647747	CV3668265	single nucleotide variant	NM_001142725.2(ERI2):c.44G>A (p.Arg15Lys)	not specified [RCV004910128]	uncertain significance	16	20803650	20803650	Human		name
597647754	CV3668266	single nucleotide variant	NM_001142725.2(ERI2):c.53T>C (p.Ile18Thr)	not specified [RCV004910129]	uncertain significance	16	20803641	20803641	Human		name
401751767	CV2672570	single nucleotide variant	NM_001142725.2(ERI2):c.251A>G (p.Gln84Arg)	not specified [RCV004287603]	uncertain significance	16	20802848	20802848	Human		name
401722277	CV2706448	single nucleotide variant	NM_001142725.2(ERI2):c.201C>G (p.Asn67Lys)	not specified [RCV004317268]	uncertain significance	16	20802898	20802898	Human		name
405741380	CV3259469	single nucleotide variant	NM_001142725.2(ERI2):c.262A>G (p.Ile88Val)	not specified [RCV004380607]	likely benign	16	20802837	20802837	Human		name
597647762	CV3668267	single nucleotide variant	NM_001142725.2(ERI2):c.209C>T (p.Thr70Ile)	not specified [RCV004910130]	uncertain significance	16	20802890	20802890	Human		name
597647768	CV3668268	single nucleotide variant	NM_001142725.2(ERI2):c.241G>A (p.Val81Ile)	not specified [RCV004910131]	uncertain significance	16	20802858	20802858	Human		name
156264039	CV2312045	single nucleotide variant	NM_001142725.2(ERI2):c.485A>C (p.Glu162Ala)	not specified [RCV004164976]	uncertain significance	16	20800378	20800378	Human		name
156074076	CV2321634	single nucleotide variant	NM_001142725.2(ERI2):c.475G>T (p.Val159Phe)	not specified [RCV004179648]	uncertain significance	16	20800388	20800388	Human		name
156154071	CV2374897	single nucleotide variant	NM_001142725.2(ERI2):c.652G>A (p.Asp218Asn)	not specified [RCV004227921]	uncertain significance	16	20799343	20799343	Human		name
405741387	CV3259470	single nucleotide variant	NM_001142725.2(ERI2):c.493T>C (p.Cys165Arg)	not specified [RCV004380608]	uncertain significance	16	20800370	20800370	Human		name
407480179	CV3442094	single nucleotide variant	NM_001142725.2(ERI2):c.554C>A (p.Thr185Asn)	not specified [RCV004617970]	uncertain significance	16	20800309	20800309	Human		name
407480190	CV3442096	single nucleotide variant	NM_001142725.2(ERI2):c.539T>C (p.Ile180Thr)	not specified [RCV004617972]	uncertain significance	16	20800324	20800324	Human		name
407480197	CV3442097	single nucleotide variant	NM_001142725.2(ERI2):c.870T>A (p.His290Gln)	not specified [RCV004617973]	uncertain significance	16	20798930	20798930	Human		name
597647708	CV3668259	single nucleotide variant	NM_001142725.2(ERI2):c.734T>G (p.Val245Gly)	not specified [RCV004910123]	uncertain significance	16	20799066	20799066	Human		name
597748345	CV3668261	single nucleotide variant	NM_001142725.2(ERI2):c.565T>C (p.Phe189Leu)	not specified [RCV004923084]	uncertain significance	16	20800035	20800035	Human		name
597647724	CV3668262	single nucleotide variant	NM_001142725.2(ERI2):c.527T>C (p.Leu176Ser)	not specified [RCV004910125]	uncertain significance	16	20800336	20800336	Human		name
597647732	CV3668263	single nucleotide variant	NM_001142725.2(ERI2):c.478T>G (p.Cys160Gly)	not specified [RCV004910126]	uncertain significance	16	20800385	20800385	Human		name
597647787	CV3668271	single nucleotide variant	NM_001142725.2(ERI2):c.421G>A (p.Ala141Thr)	not specified [RCV004910134]	likely benign	16	20801242	20801242	Human		name
598181217	CV3961955	single nucleotide variant	NM_001142725.2(ERI2):c.533C>A (p.Ser178Tyr)	not specified [RCV005332885]	uncertain significance	16	20800330	20800330	Human		name
598181226	CV3961957	single nucleotide variant	NM_001142725.2(ERI2):c.304G>T (p.Ala102Ser)	not specified [RCV005332887]	uncertain significance	16	20801359	20801359	Human		name
156151347	CV2197900	single nucleotide variant	NM_001142725.2(ERI2):c.1157C>T (p.Thr386Ile)	not specified [RCV004077124]	uncertain significance	16	20798643	20798643	Human		name
156166990	CV2270456	single nucleotide variant	NM_001142725.2(ERI2):c.1108G>C (p.Ala370Pro)	not specified [RCV004137423]	uncertain significance	16	20798692	20798692	Human		name
156201378	CV2290574	single nucleotide variant	NM_001142725.2(ERI2):c.1426T>G (p.Tyr476Asp)	not specified [RCV004149120]	uncertain significance	16	20798374	20798374	Human		name
156003464	CV2295670	single nucleotide variant	NM_001142725.2(ERI2):c.1865G>A (p.Cys622Tyr)	not specified [RCV004149826]	uncertain significance	16	20797935	20797935	Human		name
156198447	CV2312921	single nucleotide variant	NM_001142725.2(ERI2):c.1526T>G (p.Phe509Cys)	not specified [RCV004159433]	uncertain significance	16	20798274	20798274	Human		name
156127350	CV2351186	single nucleotide variant	NM_001142725.2(ERI2):c.1873G>A (p.Gly625Arg)	not specified [RCV004214035]	uncertain significance	16	20797927	20797927	Human		name
329385539	CV2432176	single nucleotide variant	NM_001142725.2(ERI2):c.1150G>C (p.Val384Leu)	not specified [RCV004249319]	uncertain significance	16	20798650	20798650	Human		name
401717831	CV2704035	single nucleotide variant	NM_001142725.2(ERI2):c.1153C>G (p.Pro385Ala)	not specified [RCV004308920]	uncertain significance	16	20798647	20798647	Human		name
401899945	CV2765774	single nucleotide variant	NM_001142725.2(ERI2):c.1940G>C (p.Arg647Thr)	not specified [RCV004335774]	uncertain significance	16	20797860	20797860	Human		name
405741323	CV3259461	single nucleotide variant	NM_001142725.2(ERI2):c.1267G>A (p.Val423Ile)	not specified [RCV004380599]	likely benign	16	20798533	20798533	Human		name
405741327	CV3259462	single nucleotide variant	NM_001142725.2(ERI2):c.1548G>A (p.Met516Ile)	not specified [RCV004380600]	uncertain significance	16	20798252	20798252	Human		name
405741337	CV3259463	single nucleotide variant	NM_001142725.2(ERI2):c.1582C>T (p.Leu528Phe)	not specified [RCV004380601]	uncertain significance	16	20798218	20798218	Human		name
405741344	CV3259464	single nucleotide variant	NM_001142725.2(ERI2):c.1690C>G (p.Pro564Ala)	not specified [RCV004380602]	uncertain significance	16	20798110	20798110	Human		name
405741353	CV3259465	single nucleotide variant	NM_001142725.2(ERI2):c.1715G>A (p.Arg572His)	not specified [RCV004380603]	likely benign	16	20798085	20798085	Human		name
405741360	CV3259466	single nucleotide variant	NM_001142725.2(ERI2):c.1766G>C (p.Ser589Thr)	not specified [RCV004380604]	uncertain significance	16	20798034	20798034	Human		name
405741368	CV3259467	single nucleotide variant	NM_001142725.2(ERI2):c.1912A>C (p.Lys638Gln)	not specified [RCV004380605]	uncertain significance	16	20797888	20797888	Human		name
405741377	CV3259468	single nucleotide variant	NM_001142725.2(ERI2):c.1976G>T (p.Gly659Val)	not specified [RCV004380606]	uncertain significance	16	20797824	20797824	Human		name
407480173	CV3442093	single nucleotide variant	NM_001142725.2(ERI2):c.1483G>C (p.Asp495His)	not specified [RCV004617969]	uncertain significance	16	20798317	20798317	Human		name
407480185	CV3442095	single nucleotide variant	NM_001142725.2(ERI2):c.1142C>A (p.Ser381Tyr)	not specified [RCV004617971]	uncertain significance	16	20798658	20798658	Human		name
407480200	CV3442098	single nucleotide variant	NM_001142725.2(ERI2):c.1562T>C (p.Val521Ala)	not specified [RCV004617974]	uncertain significance	16	20798238	20798238	Human		name
407480206	CV3442099	single nucleotide variant	NM_001142725.2(ERI2):c.2012G>T (p.Cys671Phe)	not specified [RCV004617975]	uncertain significance	16	20797788	20797788	Human		name
597647715	CV3668260	single nucleotide variant	NM_001142725.2(ERI2):c.1168G>T (p.Val390Phe)	not specified [RCV004910124]	uncertain significance	16	20798632	20798632	Human		name
597647741	CV3668264	single nucleotide variant	NM_001142725.2(ERI2):c.1793A>G (p.Lys598Arg)	not specified [RCV004910127]	uncertain significance	16	20798007	20798007	Human		name
597647780	CV3668270	single nucleotide variant	NM_001142725.2(ERI2):c.1420A>G (p.Ile474Val)	not specified [RCV004910133]	likely benign	16	20798380	20798380	Human		name
597647794	CV3668272	single nucleotide variant	NM_001142725.2(ERI2):c.1714C>T (p.Arg572Cys)	not specified [RCV004910135]	uncertain significance	16	20798086	20798086	Human		name
598181180	CV3961948	single nucleotide variant	NM_001142725.2(ERI2):c.1064A>G (p.Lys355Arg)	not specified [RCV005332878]	uncertain significance	16	20798736	20798736	Human		name
598181185	CV3961949	single nucleotide variant	NM_001142725.2(ERI2):c.1834G>A (p.Gly612Arg)	not specified [RCV005332879]	uncertain significance	16	20797966	20797966	Human		name
598181190	CV3961950	single nucleotide variant	NM_001142725.2(ERI2):c.1898G>A (p.Cys633Tyr)	not specified [RCV005332880]	uncertain significance	16	20797902	20797902	Human		name
598181195	CV3961951	single nucleotide variant	NM_001142725.2(ERI2):c.1688C>G (p.Ser563Cys)	not specified [RCV005332881]	uncertain significance	16	20798112	20798112	Human		name
598181206	CV3961953	single nucleotide variant	NM_001142725.2(ERI2):c.1124C>T (p.Ser375Leu)	not specified [RCV005332883]	uncertain significance	16	20798676	20798676	Human		name
598181211	CV3961954	single nucleotide variant	NM_001142725.2(ERI2):c.1942G>A (p.Ala648Thr)	not specified [RCV005332884]	uncertain significance	16	20797858	20797858	Human		name
598181221	CV3961956	single nucleotide variant	NM_001142725.2(ERI2):c.1976G>A (p.Gly659Glu)	not specified [RCV005332886]	uncertain significance	16	20797824	20797824	Human		name

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