Rinl Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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59 records found for search term Rinl

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15202739	CV778539	single nucleotide variant	NM_001195833.2(RINL):c.451+10G>A	not provided [RCV000958016]	benign	19	38871637	38871637	Human		name
156098101	CV2206996	single nucleotide variant	NM_001195833.2(RINL):c.17A>C (p.Asp6Ala)	not specified [RCV004085616]	uncertain significance	19	38876726	38876726	Human		name
401910507	CV2808621	single nucleotide variant	NM_001195833.2(RINL):c.180G>A (p.Ala60=)	not provided [RCV003425139]	likely benign	19	38876361	38876361	Human		name
598228360	CV3899096	single nucleotide variant	NM_001195833.2(RINL):c.10C>T (p.Pro4Ser)	not specified [RCV005274088]	uncertain significance	19	38876733	38876733	Human		name
156147768	CV2307294	single nucleotide variant	NM_001195833.2(RINL):c.71A>G (p.Asn24Ser)	not specified [RCV004165989]	uncertain significance	19	38876470	38876470	Human		name
156179420	CV2327662	single nucleotide variant	NM_001195833.2(RINL):c.89C>T (p.Pro30Leu)	not specified [RCV004177241]	uncertain significance	19	38876452	38876452	Human		name
401752008	CV2682667	single nucleotide variant	NM_001195833.2(RINL):c.67G>A (p.Val23Met)	not specified [RCV004281649]	uncertain significance	19	38876474	38876474	Human		name
156113988	CV2224999	single nucleotide variant	NM_001195833.2(RINL):c.181G>A (p.Glu61Lys)	not specified [RCV004094836]	likely benign	19	38876360	38876360	Human		name
156338862	CV2225000	single nucleotide variant	NM_001195833.2(RINL):c.182A>C (p.Glu61Ala)	not specified [RCV004094837]	uncertain significance	19	38876359	38876359	Human		name
156032711	CV2259663	single nucleotide variant	NM_001195833.2(RINL):c.197T>A (p.Leu66Gln)	not specified [RCV004116696]	uncertain significance	19	38876344	38876344	Human		name
401722537	CV2677022	single nucleotide variant	NM_001195833.2(RINL):c.277G>A (p.Glu93Lys)	not specified [RCV004293623]	uncertain significance	19	38873922	38873922	Human		name
401937231	CV2808620	single nucleotide variant	NM_001195833.2(RINL):c.1164G>A (p.Gly388=)	not provided [RCV003415228]	likely benign	19	38870121	38870121	Human		name
405737127	CV3319802	single nucleotide variant	NM_001195833.2(RINL):c.190G>C (p.Val64Leu)	not specified [RCV004451813]	likely benign	19	38876351	38876351	Human		name
405737135	CV3319803	single nucleotide variant	NM_001195833.2(RINL):c.224C>T (p.Thr75Ile)	not specified [RCV004451814]	likely benign	19	38873975	38873975	Human		name
405737141	CV3319804	single nucleotide variant	NM_001195833.2(RINL):c.236C>T (p.Pro79Leu)	not specified [RCV004451815]	uncertain significance	19	38873963	38873963	Human		name
597776905	CV3583489	single nucleotide variant	NM_001195833.2(RINL):c.188T>C (p.Leu63Pro)	not specified [RCV004852647]	uncertain significance	19	38876353	38876353	Human		name
598228332	CV3899092	single nucleotide variant	NM_001195833.2(RINL):c.178G>T (p.Ala60Ser)	not specified [RCV005274084]	uncertain significance	19	38876363	38876363	Human		name
156321219	CV2197534	single nucleotide variant	NM_001195833.2(RINL):c.820G>A (p.Val274Met)	not specified [RCV004081258]	uncertain significance	19	38870774	38870774	Human		name
156044555	CV2215937	single nucleotide variant	NM_001195833.2(RINL):c.647C>T (p.Pro216Leu)	not specified [RCV004097014]	uncertain significance	19	38870947	38870947	Human		name
155925589	CV2230469	single nucleotide variant	NM_001195833.2(RINL):c.559C>T (p.Pro187Ser)	not provided [RCV004695400]\|not specified [RCV004097445]	uncertain significance	19	38871120	38871120	Human		name
156294760	CV2302985	single nucleotide variant	NM_001195833.2(RINL):c.625G>T (p.Gly209Trp)	not specified [RCV004156782]	uncertain significance	19	38870969	38870969	Human		name
156334616	CV2333410	single nucleotide variant	NM_001195833.2(RINL):c.593A>G (p.His198Arg)	not specified [RCV004190117]	uncertain significance	19	38871086	38871086	Human		name
156220252	CV2345011	single nucleotide variant	NM_001195833.2(RINL):c.932C>T (p.Thr311Ile)	not specified [RCV004193299]	likely benign	19	38870662	38870662	Human		name
156179045	CV2355980	single nucleotide variant	NM_001195833.2(RINL):c.766G>C (p.Glu256Gln)	not specified [RCV004201359]	uncertain significance	19	38870828	38870828	Human		name
156154634	CV2369527	single nucleotide variant	NM_001195833.2(RINL):c.526G>A (p.Glu176Lys)	not specified [RCV004210461]	uncertain significance	19	38871153	38871153	Human		name
155902551	CV2386263	single nucleotide variant	NM_001195833.2(RINL):c.409C>T (p.Leu137Phe)	not specified [RCV004228614]	uncertain significance	19	38871689	38871689	Human		name
401751659	CV2706624	single nucleotide variant	NM_001195833.2(RINL):c.881G>A (p.Gly294Glu)	not specified [RCV004319206]	uncertain significance	19	38870713	38870713	Human		name
405737148	CV3319805	single nucleotide variant	NM_001195833.2(RINL):c.323T>A (p.Leu108Gln)	not specified [RCV004451816]	uncertain significance	19	38871861	38871861	Human		name
405737155	CV3319806	single nucleotide variant	NM_001195833.2(RINL):c.383G>C (p.Ser128Thr)	not specified [RCV004451817]	uncertain significance	19	38871801	38871801	Human		name
405737160	CV3319807	single nucleotide variant	NM_001195833.2(RINL):c.415C>T (p.Pro139Ser)	not specified [RCV004451818]	uncertain significance	19	38871683	38871683	Human		name
405737167	CV3319808	single nucleotide variant	NM_001195833.2(RINL):c.745G>A (p.Asp249Asn)	not specified [RCV004451819]	uncertain significance	19	38870849	38870849	Human		name
407475168	CV3483196	single nucleotide variant	NM_001195833.2(RINL):c.550G>A (p.Glu184Lys)	not specified [RCV004663179]	uncertain significance	19	38871129	38871129	Human		name
597789053	CV3583480	single nucleotide variant	NM_001195833.2(RINL):c.854T>C (p.Ile285Thr)	not specified [RCV004855654]	uncertain significance	19	38870740	38870740	Human		name
597789059	CV3583486	single nucleotide variant	NM_001195833.2(RINL):c.516G>C (p.Gln172His)	not specified [RCV004855656]	uncertain significance	19	38871163	38871163	Human		name
597789063	CV3583487	single nucleotide variant	NM_001195833.2(RINL):c.913G>A (p.Asp305Asn)	not specified [RCV004855657]	uncertain significance	19	38870681	38870681	Human		name
597789075	CV3583491	single nucleotide variant	NM_001195833.2(RINL):c.609G>C (p.Arg203Ser)	not specified [RCV004855660]	uncertain significance	19	38870985	38870985	Human		name
598228351	CV3899095	single nucleotide variant	NM_001195833.2(RINL):c.622C>T (p.His208Tyr)	not specified [RCV005274087]	uncertain significance	19	38870972	38870972	Human		name
155924988	CV2211696	single nucleotide variant	NM_001195833.2(RINL):c.1225C>G (p.Arg409Gly)	not specified [RCV004084582]	uncertain significance	19	38870060	38870060	Human		name
156052752	CV2246348	single nucleotide variant	NM_001195833.2(RINL):c.1111C>A (p.Pro371Thr)	not specified [RCV004107790]	uncertain significance	19	38870174	38870174	Human		name
156265684	CV2299260	single nucleotide variant	NM_001195833.2(RINL):c.1381G>C (p.Glu461Gln)	not specified [RCV004152589]	uncertain significance	19	38869666	38869666	Human		name
156043433	CV2342313	single nucleotide variant	NM_001195833.2(RINL):c.1151G>A (p.Arg384Gln)	not specified [RCV004191880]	uncertain significance	19	38870134	38870134	Human		name
156148222	CV2358072	single nucleotide variant	NM_001195833.2(RINL):c.1406T>C (p.Ile469Thr)	not specified [RCV004211883]	uncertain significance	19	38869641	38869641	Human		name
156264729	CV2364393	single nucleotide variant	NM_001195833.2(RINL):c.1078G>A (p.Ala360Thr)	not specified [RCV004223605]	uncertain significance	19	38870207	38870207	Human		name
401727483	CV2681052	single nucleotide variant	NM_001195833.2(RINL):c.1051C>A (p.Gln351Lys)	not specified [RCV004296114]	uncertain significance	19	38870234	38870234	Human		name
401758770	CV2694269	single nucleotide variant	NM_001195833.2(RINL):c.1663T>C (p.Trp555Arg)	not specified [RCV004304470]	uncertain significance	19	38869142	38869142	Human		name
405269291	CV3187279	single nucleotide variant	NM_001195833.2(RINL):c.1327C>G (p.Arg443Gly)	not provided [RCV003887363]	uncertain significance	19	38869958	38869958	Human		name
405737105	CV3319799	single nucleotide variant	NM_001195833.2(RINL):c.1112C>T (p.Pro371Leu)	not specified [RCV004451810]	uncertain significance	19	38870173	38870173	Human		name
405737112	CV3319800	single nucleotide variant	NM_001195833.2(RINL):c.1156G>A (p.Gly386Arg)	not specified [RCV004451811]	uncertain significance	19	38870129	38870129	Human		name
407508351	CV3483195	single nucleotide variant	NM_001195833.2(RINL):c.1691G>A (p.Ser564Asn)	not specified [RCV004672011]	likely benign	19	38869114	38869114	Human		name
597776888	CV3583481	single nucleotide variant	NM_001195833.2(RINL):c.1586A>G (p.His529Arg)	not specified [RCV004852643]	likely benign	19	38869299	38869299	Human		name
597776892	CV3583482	single nucleotide variant	NM_001195833.2(RINL):c.1615A>G (p.Arg539Gly)	not specified [RCV004852644]	likely benign	19	38869270	38869270	Human		name
597776896	CV3583483	single nucleotide variant	NM_001195833.2(RINL):c.1157G>C (p.Gly386Ala)	not specified [RCV004852645]	uncertain significance	19	38870128	38870128	Human		name
597776900	CV3583484	single nucleotide variant	NM_001195833.2(RINL):c.1546G>C (p.Ala516Pro)	not specified [RCV004852646]	uncertain significance	19	38869339	38869339	Human		name
597789067	CV3583488	single nucleotide variant	NM_001195833.2(RINL):c.1544G>A (p.Arg515His)	not specified [RCV004855658]	uncertain significance	19	38869341	38869341	Human		name
597789071	CV3583490	single nucleotide variant	NM_001195833.2(RINL):c.1121G>A (p.Arg374Gln)	not specified [RCV004855659]	uncertain significance	19	38870164	38870164	Human		name
598228315	CV3899090	single nucleotide variant	NM_001195833.2(RINL):c.1207G>T (p.Ala403Ser)	not specified [RCV005274082]	uncertain significance	19	38870078	38870078	Human		name
598228324	CV3899091	single nucleotide variant	NM_001195833.2(RINL):c.1330G>A (p.Gly444Ser)	not specified [RCV005274083]	uncertain significance	19	38869955	38869955	Human		name
598228344	CV3899094	single nucleotide variant	NM_001195833.2(RINL):c.1190C>G (p.Pro397Arg)	not specified [RCV005274086]	uncertain significance	19	38870095	38870095	Human		name
598228369	CV3899097	single nucleotide variant	NM_001195833.2(RINL):c.1402G>T (p.Asp468Tyr)	not specified [RCV005274089]	uncertain significance	19	38869645	38869645	Human		name

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