Apoo Variant Search Result - Rat Genome Database

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42 records found for search term Apoo

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150449140	CV1253646	single nucleotide variant	NM_024122.5(APOO):c.117+16T>C	not provided [RCV001667574]	benign	X	23880829	23880829	Human		name
401918792	CV2821362	single nucleotide variant	NM_024122.5(APOO):c.147A>G (p.Gln49=)	not provided [RCV003430453]	likely benign	X	23879005	23879005	Human		name
407525026	CV3460914	single nucleotide variant	NM_024122.5(APOO):c.25G>C (p.Val9Leu)	not specified [RCV004653887]	uncertain significance	X	23880937	23880937	Human		name
405277778	CV3196052	single nucleotide variant	NM_024122.5(APOO):c.486T>C (p.Ser162=)	APOO-related disorder [RCV003904572]	likely benign	X	23856377	23856377	Human		name , trait , alternate_id
405291732	CV3206026	single nucleotide variant	NM_024122.5(APOO):c.43A>T (p.Ser15Cys)	APOO-related disorder [RCV003964115]	likely benign	X	23880919	23880919	Human		name , trait , alternate_id
598164529	CV4005909	single nucleotide variant	NM_024122.5(APOO):c.56T>C (p.Phe19Ser)	not specified [RCV005391171]	uncertain significance	X	23880906	23880906	Human		name
598164575	CV4005918	single nucleotide variant	NM_024122.5(APOO):c.76A>G (p.Lys26Glu)	not specified [RCV005391178]	uncertain significance	X	23880886	23880886	Human		name
598164594	CV4005922	single nucleotide variant	NM_024122.5(APOO):c.73C>G (p.Pro25Ala)	not specified [RCV005391182]	uncertain significance	X	23880889	23880889	Human		name
156086712	CV2205751	single nucleotide variant	NM_024122.5(APOO):c.133G>T (p.Val45Phe)	not specified [RCV004075801]	uncertain significance	X	23879019	23879019	Human		name
156184511	CV2292239	single nucleotide variant	NM_024122.5(APOO):c.224C>A (p.Thr75Lys)	not specified [RCV004148280]	uncertain significance	X	23878928	23878928	Human		name
401918795	CV2821363	single nucleotide variant	NM_024122.5(APOO):c.103G>A (p.Val35Met)	not provided [RCV003430454]\|not specified [RCV004364639]	likely benign\|uncertain significance	X	23880859	23880859	Human		name
597740221	CV3579632	single nucleotide variant	NM_024122.5(APOO):c.294C>G (p.Asp98Glu)	not specified [RCV004844447]	uncertain significance	X	23868687	23868687	Human		name
598164433	CV4005889	single nucleotide variant	NM_024122.5(APOO):c.223A>T (p.Thr75Ser)	not specified [RCV005391156]	uncertain significance	X	23878929	23878929	Human		name
156062627	CV2232030	single nucleotide variant	NM_024122.5(APOO):c.488G>C (p.Gly163Ala)	not specified [RCV004093082]	uncertain significance	X	23856375	23856375	Human		name
597740215	CV3579625	single nucleotide variant	NM_024122.5(APOO):c.520T>C (p.Tyr174His)	not specified [RCV004844446]	uncertain significance	X	23856343	23856343	Human		name
597740236	CV3579635	single nucleotide variant	NM_024122.5(APOO):c.406C>A (p.Leu136Ile)	not specified [RCV004844450]	uncertain significance	X	23858716	23858716	Human		name
598195902	CV4005899	single nucleotide variant	NM_024122.5(APOO):c.443C>A (p.Ser148Tyr)	not specified [RCV005397607]	uncertain significance	X	23858679	23858679	Human		name
598164548	CV4005914	single nucleotide variant	NM_024122.5(APOO):c.305A>G (p.Tyr102Cys)	not specified [RCV005391174]	uncertain significance	X	23868676	23868676	Human		name
15115106	CV717763	single nucleotide variant	NM_024122.5(APOO):c.496T>G (p.Leu166Val)	not provided [RCV000961791]	benign	X	23856367	23856367	Human		name
8637828	CV93054	single nucleotide variant	NM_024122.4(APOO):c.561G>T (p.Lys187Asn)	Malignant melanoma [RCV000073152]	not provided	X	23856302	23856302	Human		name
38598722	CV964792	single nucleotide variant	NM_024122.5(APOO):c.350T>C (p.Ile117Thr)	Lactic acidosis [RCV001254025]\|not provided [RCV001375911]	pathogenic\|uncertain significance	X	23868631	23868631	Human	2	name
405673185	CV3289952	single nucleotide variant	NM_198450.6(APOOL):c.44G>C (p.Gly15Ala)	not specified [RCV004419967]	uncertain significance	X	85046474	85046474	Human		name
598164669	CV4005939	single nucleotide variant	NM_198450.6(APOOL):c.34A>G (p.Met12Val)	not specified [RCV005391199]	uncertain significance	X	85046464	85046464	Human		name
156128310	CV2223904	single nucleotide variant	NM_198450.6(APOOL):c.175G>T (p.Gly59Cys)	not specified [RCV004093900]	uncertain significance	X	85051443	85051443	Human		name
405673177	CV3289950	single nucleotide variant	NM_198450.6(APOOL):c.188T>C (p.Met63Thr)	not specified [RCV004419965]	uncertain significance	X	85051456	85051456	Human		name
407525047	CV3460934	single nucleotide variant	NM_198450.6(APOOL):c.206G>A (p.Arg69His)	not specified [RCV004653898]	uncertain significance	X	85051474	85051474	Human		name
598164638	CV4005932	single nucleotide variant	NM_198450.6(APOOL):c.129A>G (p.Ile43Met)	not specified [RCV005391192]	uncertain significance	X	85051397	85051397	Human		name
155921752	CV2276368	single nucleotide variant	NM_198450.6(APOOL):c.710C>A (p.Ser237Tyr)	not specified [RCV004144108]	uncertain significance	X	85074383	85074383	Human		name
155905688	CV2283134	single nucleotide variant	NM_198450.6(APOOL):c.440T>C (p.Leu147Ser)	not specified [RCV004145822]	uncertain significance	X	85067172	85067172	Human		name
156290202	CV2342548	single nucleotide variant	NM_198450.6(APOOL):c.525T>G (p.Ile175Met)	not specified [RCV004196645]	uncertain significance	X	85074036	85074036	Human		name
156074843	CV2365556	single nucleotide variant	NM_198450.6(APOOL):c.502G>A (p.Val168Ile)	not specified [RCV004211670]	likely benign	X	85074013	85074013	Human		name
401729220	CV2690104	single nucleotide variant	NM_198450.6(APOOL):c.732T>A (p.Phe244Leu)	not specified [RCV004300337]	uncertain significance	X	85087603	85087603	Human		name
401759506	CV2690922	single nucleotide variant	NM_198450.6(APOOL):c.721G>T (p.Ala241Ser)	not specified [RCV004298611]	uncertain significance	X	85087592	85087592	Human		name
401778803	CV2705696	single nucleotide variant	NM_198450.6(APOOL):c.519G>T (p.Gln173His)	not specified [RCV004318549]	uncertain significance	X	85074030	85074030	Human		name
401778383	CV2732466	single nucleotide variant	NM_198450.6(APOOL):c.533C>G (p.Ala178Gly)	not specified [RCV004332569]	uncertain significance	X	85074044	85074044	Human		name
401876559	CV2782962	single nucleotide variant	NM_198450.6(APOOL):c.645C>A (p.His215Gln)	not specified [RCV004361756]	uncertain significance	X	85074318	85074318	Human		name
401919167	CV2826589	single nucleotide variant	NM_198450.6(APOOL):c.584C>G (p.Pro195Arg)	not provided [RCV003430591]	likely benign	X	85074095	85074095	Human		name
405673181	CV3289951	single nucleotide variant	NM_198450.6(APOOL):c.338C>T (p.Pro113Leu)	not specified [RCV004419966]	uncertain significance	X	85055869	85055869	Human		name
405673189	CV3289953	single nucleotide variant	NM_198450.6(APOOL):c.682A>G (p.Ser228Gly)	not specified [RCV004419968]	uncertain significance	X	85074355	85074355	Human		name
405673194	CV3289954	single nucleotide variant	NM_198450.6(APOOL):c.719G>T (p.Gly240Val)	not specified [RCV004419969]	uncertain significance	X	85087590	85087590	Human		name
407525036	CV3460925	single nucleotide variant	NM_198450.6(APOOL):c.472G>A (p.Val158Ile)	not specified [RCV004653892]	likely benign	X	85067204	85067204	Human		name
597740567	CV3579646	single nucleotide variant	NM_198450.6(APOOL):c.724A>G (p.Thr242Ala)	not specified [RCV004844460]	uncertain significance	X	85087595	85087595	Human		name

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