Iglon5 Variant Search Result - Rat Genome Database

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46 records found for search term Iglon5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155914913	CV2242868	single nucleotide variant	NM_001101372.3(IGLON5):c.7C>A (p.Pro3Thr)	not specified [RCV004107459]	uncertain significance	19	51311854	51311854	Human		name
155973599	CV2334457	single nucleotide variant	NM_001101372.3(IGLON5):c.7C>G (p.Pro3Ala)	not specified [RCV004188428]	uncertain significance	19	51311854	51311854	Human		name
156041286	CV2342127	single nucleotide variant	NM_001101372.3(IGLON5):c.8C>A (p.Pro3His)	not specified [RCV004191720]	uncertain significance	19	51311855	51311855	Human		name
401742930	CV2697902	single nucleotide variant	NM_001101372.3(IGLON5):c.5C>T (p.Pro2Leu)	not specified [RCV004300611]	uncertain significance	19	51311852	51311852	Human		name
405799777	CV3274517	single nucleotide variant	NM_001101372.3(IGLON5):c.4C>G (p.Pro2Ala)	not specified [RCV004402655]	uncertain significance	19	51311851	51311851	Human		name
405799791	CV3274522	single nucleotide variant	NM_001101372.3(IGLON5):c.8C>T (p.Pro3Leu)	not specified [RCV004402660]	uncertain significance	19	51311855	51311855	Human		name
598207027	CV3975800	single nucleotide variant	NM_001101372.3(IGLON5):c.7C>T (p.Pro3Ser)	not specified [RCV005337902]	uncertain significance	19	51311854	51311854	Human		name
156389146	CV2229960	single nucleotide variant	NM_001101372.3(IGLON5):c.11C>G (p.Pro4Arg)	not specified [RCV004105494]	uncertain significance	19	51311858	51311858	Human		name
156115771	CV2349327	single nucleotide variant	NM_001101372.3(IGLON5):c.10C>G (p.Pro4Ala)	not specified [RCV004199270]	uncertain significance	19	51311857	51311857	Human		name
597792198	CV3689874	single nucleotide variant	NM_001101372.3(IGLON5):c.10C>A (p.Pro4Thr)	not specified [RCV004933767]	uncertain significance	19	51311857	51311857	Human		name
597792222	CV3689882	single nucleotide variant	NM_001101372.3(IGLON5):c.159C>T (p.Ser53=)	not specified [RCV004933775]	likely benign	19	51323662	51323662	Human		name
598269457	CV3975798	single nucleotide variant	NM_001101372.3(IGLON5):c.17C>T (p.Pro6Leu)	not specified [RCV005349899]	uncertain significance	19	51311864	51311864	Human		name
155933748	CV2372333	single nucleotide variant	NM_001101372.3(IGLON5):c.89C>G (p.Ser30Cys)	not specified [RCV004217102]	uncertain significance	19	51322073	51322073	Human		name
155930860	CV2399736	single nucleotide variant	NM_001101372.3(IGLON5):c.47C>T (p.Ala16Val)	not specified [RCV004245554]	uncertain significance	19	51311894	51311894	Human		name
405799774	CV3274516	single nucleotide variant	NM_001101372.3(IGLON5):c.31C>T (p.Arg11Trp)	not specified [RCV004402654]	uncertain significance	19	51311878	51311878	Human		name
598269462	CV3975801	single nucleotide variant	NM_001101372.3(IGLON5):c.41C>T (p.Ala14Val)	not specified [RCV005349900]	uncertain significance	19	51311888	51311888	Human		name
156269672	CV2315029	single nucleotide variant	NM_001101372.3(IGLON5):c.223G>A (p.Gly75Ser)	not specified [RCV004164943]	uncertain significance	19	51323726	51323726	Human		name
401780880	CV2681803	single nucleotide variant	NM_001101372.3(IGLON5):c.185G>A (p.Arg62His)	not specified [RCV004296805]	uncertain significance	19	51323688	51323688	Human		name
405799770	CV3274515	single nucleotide variant	NM_001101372.3(IGLON5):c.118G>A (p.Asp40Asn)	not specified [RCV004402653]	uncertain significance	19	51322102	51322102	Human		name
407511132	CV3440831	single nucleotide variant	NM_001101372.3(IGLON5):c.210C>A (p.Asn70Lys)	not specified [RCV004626364]	uncertain significance	19	51323713	51323713	Human		name
597792195	CV3689873	single nucleotide variant	NM_001101372.3(IGLON5):c.251G>A (p.Arg84Gln)	not specified [RCV004933766]	uncertain significance	19	51323754	51323754	Human		name
597792207	CV3689877	single nucleotide variant	NM_001101372.3(IGLON5):c.248C>T (p.Pro83Leu)	not specified [RCV004933770]	uncertain significance	19	51323751	51323751	Human		name
597792219	CV3689881	single nucleotide variant	NM_001101372.3(IGLON5):c.232C>T (p.Arg78Cys)	not specified [RCV004933774]	uncertain significance	19	51323735	51323735	Human		name
155935103	CV2225493	single nucleotide variant	NM_001101372.3(IGLON5):c.773G>A (p.Ser258Asn)	not specified [RCV004100886]	uncertain significance	19	51327737	51327737	Human		name
156017082	CV2266619	single nucleotide variant	NM_001101372.3(IGLON5):c.416C>T (p.Ser139Leu)	not specified [RCV004131163]	uncertain significance	19	51325370	51325370	Human		name
155927129	CV2285064	single nucleotide variant	NM_001101372.3(IGLON5):c.774C>G (p.Ser258Arg)	not specified [RCV004145302]	uncertain significance	19	51327738	51327738	Human		name
155905170	CV2285874	single nucleotide variant	NM_001101372.3(IGLON5):c.372G>C (p.Gln124His)	not specified [RCV004143810]	uncertain significance	19	51323875	51323875	Human		name
155905465	CV2286010	single nucleotide variant	NM_001101372.3(IGLON5):c.446A>G (p.Asn149Ser)	not specified [RCV004143919]	uncertain significance	19	51325400	51325400	Human		name
155932892	CV2299989	single nucleotide variant	NM_001101372.3(IGLON5):c.454C>G (p.Leu152Val)	not specified [RCV004151205]	uncertain significance	19	51325408	51325408	Human		name
156192213	CV2301871	single nucleotide variant	NM_001101372.3(IGLON5):c.571G>A (p.Gly191Arg)	not specified [RCV004156662]	uncertain significance	19	51326823	51326823	Human		name
156297985	CV2310574	single nucleotide variant	NM_001101372.3(IGLON5):c.806C>A (p.Thr269Lys)	not specified [RCV004163591]	uncertain significance	19	51327770	51327770	Human		name
155919364	CV2360237	single nucleotide variant	NM_001101372.3(IGLON5):c.643A>T (p.Asn215Tyr)	not specified [RCV004208584]	uncertain significance	19	51326895	51326895	Human		name
401764866	CV2701475	single nucleotide variant	NM_001101372.3(IGLON5):c.939G>T (p.Glu313Asp)	not specified [RCV004312144]	uncertain significance	19	51328687	51328687	Human		name
401760020	CV2701839	single nucleotide variant	NM_001101372.3(IGLON5):c.983C>T (p.Ala328Val)	not specified [RCV004307804]	uncertain significance	19	51328731	51328731	Human		name
401772604	CV2712818	single nucleotide variant	NM_001101372.3(IGLON5):c.313G>A (p.Gly105Ser)	not specified [RCV004314240]	uncertain significance	19	51323816	51323816	Human		name
401874256	CV2773717	single nucleotide variant	NM_001101372.3(IGLON5):c.326T>C (p.Leu109Pro)	not specified [RCV004356395]	uncertain significance	19	51323829	51323829	Human		name
405799779	CV3274518	single nucleotide variant	NM_001101372.3(IGLON5):c.667G>C (p.Val223Leu)	not specified [RCV004402656]	uncertain significance	19	51327100	51327100	Human		name
405799786	CV3274520	single nucleotide variant	NM_001101372.3(IGLON5):c.725C>T (p.Ala242Val)	not specified [RCV004402658]	uncertain significance	19	51327158	51327158	Human		name
405799789	CV3274521	single nucleotide variant	NM_001101372.3(IGLON5):c.869C>A (p.Thr290Lys)	not specified [RCV004402659]	uncertain significance	19	51327833	51327833	Human		name
407515140	CV3440830	single nucleotide variant	NM_001101372.3(IGLON5):c.914G>C (p.Arg305Pro)	not specified [RCV004627810]	uncertain significance	19	51327878	51327878	Human		name
407515144	CV3440832	single nucleotide variant	NM_001101372.3(IGLON5):c.428C>T (p.Thr143Met)	not specified [RCV004627811]	uncertain significance	19	51325382	51325382	Human		name
597792210	CV3689878	single nucleotide variant	NM_001101372.3(IGLON5):c.910A>G (p.Met304Val)	not specified [RCV004933771]	uncertain significance	19	51327874	51327874	Human		name
597792213	CV3689879	single nucleotide variant	NM_001101372.3(IGLON5):c.664G>C (p.Asp222His)	not specified [RCV004933772]	uncertain significance	19	51327097	51327097	Human		name
597792216	CV3689880	single nucleotide variant	NM_001101372.3(IGLON5):c.931T>C (p.Ser311Pro)	not specified [RCV004933773]	uncertain significance	19	51328679	51328679	Human		name
598207020	CV3975799	single nucleotide variant	NM_001101372.3(IGLON5):c.509G>A (p.Arg170Gln)	not specified [RCV005337901]	uncertain significance	19	51325463	51325463	Human		name
598269467	CV3975802	single nucleotide variant	NM_001101372.3(IGLON5):c.453C>A (p.Asn151Lys)	not specified [RCV005349901]	uncertain significance	19	51325407	51325407	Human		name

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