Cd177 Variant Search Result - Rat Genome Database

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66 records found for search term Cd177

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401910597	CV2808857	single nucleotide variant	NM_020406.4(CD177):c.380-1G>C	not provided [RCV003425241]	likely benign	19	43355660	43355660	Human		name
401775405	CV2710555	single nucleotide variant	NM_020406.4(CD177):c.16C>G (p.Leu6Val)	not specified [RCV004319477]	uncertain significance	19	43353730	43353730	Human		name
155941313	CV2294230	single nucleotide variant	NM_020406.4(CD177):c.35T>A (p.Phe12Tyr)	not specified [RCV004149582]	uncertain significance	19	43353749	43353749	Human		name
401928940	CV2808858	single nucleotide variant	NM_020406.4(CD177):c.699G>T (p.Ser233=)	not provided [RCV003407022]	likely benign	19	43360344	43360344	Human		name
401910689	CV2808859	single nucleotide variant	NM_020406.4(CD177):c.954T>C (p.Pro318=)	not provided [RCV003425242]	likely benign	19	43361452	43361452	Human		name
156384034	CV2220268	single nucleotide variant	NM_020406.4(CD177):c.128C>T (p.Thr43Ile)	not specified [RCV004095696]	uncertain significance	19	43353928	43353928	Human		name
156345969	CV2356440	single nucleotide variant	NM_020406.4(CD177):c.168G>C (p.Gln56His)	not specified [RCV004206239]	uncertain significance	19	43353968	43353968	Human		name
401743931	CV2688061	single nucleotide variant	NM_020406.4(CD177):c.253C>A (p.Arg85Ser)	not specified [RCV004305128]	uncertain significance	19	43354266	43354266	Human		name
405758742	CV3303550	single nucleotide variant	NM_020406.4(CD177):c.184A>T (p.Ile62Phe)	not specified [RCV004433236]	uncertain significance	19	43353984	43353984	Human		name
407497857	CV3424878	single nucleotide variant	NM_020406.4(CD177):c.206G>A (p.Ser69Asn)	not specified [RCV004606472]	likely benign	19	43354219	43354219	Human		name
597777760	CV3638614	single nucleotide variant	NM_020406.4(CD177):c.187G>C (p.Glu63Gln)	not specified [RCV004898846]	uncertain significance	19	43353987	43353987	Human		name
597777782	CV3638620	single nucleotide variant	NM_020406.4(CD177):c.254G>T (p.Arg85Leu)	not specified [RCV004898851]	uncertain significance	19	43354267	43354267	Human		name
597777793	CV3638625	single nucleotide variant	NM_020406.4(CD177):c.118C>T (p.Arg40Trp)	not specified [RCV004898854]	uncertain significance	19	43353918	43353918	Human		name
598206689	CV3940086	single nucleotide variant	NM_020406.4(CD177):c.283C>A (p.Leu95Ile)	not specified [RCV005315154]	uncertain significance	19	43354296	43354296	Human		name
156263774	CV2201193	single nucleotide variant	NM_020406.4(CD177):c.727G>C (p.Val243Leu)	not specified [RCV004077338]	uncertain significance	19	43360372	43360372	Human		name
156147151	CV2265184	single nucleotide variant	NM_020406.4(CD177):c.638G>A (p.Arg213Gln)	not specified [RCV004126307]	uncertain significance	19	43360283	43360283	Human		name
156333157	CV2270528	single nucleotide variant	NM_020406.4(CD177):c.728T>C (p.Val243Ala)	not specified [RCV004137485]	uncertain significance	19	43360373	43360373	Human		name
156054301	CV2320451	single nucleotide variant	NM_020406.4(CD177):c.798C>A (p.Ser266Arg)	not specified [RCV004172092]	uncertain significance	19	43361180	43361180	Human		name
156051151	CV2323327	single nucleotide variant	NM_020406.4(CD177):c.415A>G (p.Met139Val)	not specified [RCV004171736]	uncertain significance	19	43355696	43355696	Human		name
156340986	CV2348132	single nucleotide variant	NM_020406.4(CD177):c.500G>A (p.Gly167Glu)	not specified [RCV004197809]	uncertain significance	19	43355781	43355781	Human		name
156035208	CV2376743	single nucleotide variant	NM_020406.4(CD177):c.361G>A (p.Ala121Thr)	not specified [RCV004227024]	likely benign	19	43354374	43354374	Human		name
401723848	CV2725058	single nucleotide variant	NM_020406.4(CD177):c.713G>A (p.Cys238Tyr)	not specified [RCV004319811]	uncertain significance	19	43360358	43360358	Human		name
401886108	CV2771080	single nucleotide variant	NM_020406.4(CD177):c.385G>A (p.Gly129Arg)	not specified [RCV004346086]	uncertain significance	19	43355666	43355666	Human		name
401891695	CV2780676	single nucleotide variant	NM_020406.4(CD177):c.983G>T (p.Cys328Phe)	not specified [RCV004352019]	uncertain significance	19	43361481	43361481	Human		name
405758754	CV3303552	single nucleotide variant	NM_020406.4(CD177):c.688T>A (p.Trp230Arg)	not specified [RCV004433238]	uncertain significance	19	43360333	43360333	Human		name
407497869	CV3424881	single nucleotide variant	NM_020406.4(CD177):c.333C>A (p.Asn111Lys)	not specified [RCV004606475]	uncertain significance	19	43354346	43354346	Human		name
597738588	CV3638615	single nucleotide variant	NM_020406.4(CD177):c.754G>C (p.Asp252His)	not specified [RCV004890149]	uncertain significance	19	43360399	43360399	Human		name
597777764	CV3638616	single nucleotide variant	NM_020406.4(CD177):c.641G>A (p.Gly214Glu)	not specified [RCV004898847]	uncertain significance	19	43360286	43360286	Human		name
597777769	CV3638617	single nucleotide variant	NM_020406.4(CD177):c.902G>T (p.Ser301Ile)	not specified [RCV004898848]	uncertain significance	19	43361284	43361284	Human		name
597777790	CV3638623	single nucleotide variant	NM_020406.4(CD177):c.301A>G (p.Thr101Ala)	not specified [RCV004898853]	uncertain significance	19	43354314	43354314	Human		name
598206666	CV3940082	single nucleotide variant	NM_020406.4(CD177):c.452G>A (p.Cys151Tyr)	not specified [RCV005315150]	uncertain significance	19	43355733	43355733	Human		name
598206677	CV3940084	single nucleotide variant	NM_020406.4(CD177):c.715G>C (p.Glu239Gln)	not specified [RCV005315152]	uncertain significance	19	43360360	43360360	Human		name
598206682	CV3940085	single nucleotide variant	NM_020406.4(CD177):c.307G>A (p.Val103Met)	not specified [RCV005315153]	uncertain significance	19	43354320	43354320	Human		name
15200889	CV705075	single nucleotide variant	NM_020406.4(CD177):c.629C>T (p.Thr210Ile)	not provided [RCV000957462]	benign\|likely benign	19	43360274	43360274	Human		name
15165938	CV728237	single nucleotide variant	NM_020406.4(CD177):c.622T>G (p.Phe208Val)	not provided [RCV000882522]	benign	19	43360267	43360267	Human		name
150488886	CV1237551	single nucleotide variant	NM_020406.4(CD177):c.1291G>A (p.Gly431Arg)	not provided [RCV001654400]	benign	19	43362297	43362297	Human	2	name
150488886	CV1237551	single nucleotide variant	NM_020406.4(CD177):c.1291G>A (p.Gly431Arg)	not provided [RCV001654400]	benign	19	43362297	43362298	Human	2	name
156319935	CV2197183	single nucleotide variant	NM_020406.4(CD177):c.1111G>A (p.Gly371Ser)	not specified [RCV004078973]	uncertain significance	19	43362117	43362117	Human		name
155975680	CV2211299	single nucleotide variant	NM_020406.4(CD177):c.1116C>G (p.Cys372Trp)	not specified [RCV004090231]	uncertain significance	19	43362122	43362122	Human		name
155928744	CV2281224	single nucleotide variant	NM_020406.4(CD177):c.1156C>A (p.Gln386Lys)	not specified [RCV004147473]	uncertain significance	19	43362162	43362162	Human		name
156258935	CV2366178	single nucleotide variant	NM_020406.4(CD177):c.1259T>G (p.Val420Gly)	not specified [RCV004210206]	uncertain significance	19	43362265	43362265	Human		name
156177418	CV2374518	single nucleotide variant	NM_020406.4(CD177):c.1178G>A (p.Arg393His)	not specified [RCV004232021]	uncertain significance	19	43362184	43362184	Human		name
329357951	CV2427892	single nucleotide variant	NM_020406.4(CD177):c.1177C>T (p.Arg393Cys)	not specified [RCV004252663]	uncertain significance	19	43362183	43362183	Human		name
329359421	CV2451008	single nucleotide variant	NM_020406.4(CD177):c.1181A>G (p.Glu394Gly)	not specified [RCV004269676]	uncertain significance	19	43362187	43362187	Human		name
329392913	CV2469068	single nucleotide variant	NM_020406.4(CD177):c.1140G>T (p.Leu380Phe)	not specified [RCV004274312]	uncertain significance	19	43362146	43362146	Human		name
401768502	CV2675391	single nucleotide variant	NM_020406.4(CD177):c.1295T>C (p.Val432Ala)	not specified [RCV004292195]	likely benign	19	43362301	43362301	Human		name
401762164	CV2722668	single nucleotide variant	NM_020406.4(CD177):c.1006T>A (p.Ser336Thr)	not specified [RCV004325116]	uncertain significance	19	43361504	43361504	Human		name
405758681	CV3303541	single nucleotide variant	NM_020406.4(CD177):c.1001C>T (p.Thr334Ile)	not specified [RCV004433227]	uncertain significance	19	43361499	43361499	Human		name
405758693	CV3303543	single nucleotide variant	NM_020406.4(CD177):c.1030T>G (p.Cys344Gly)	not specified [RCV004433229]	uncertain significance	19	43361528	43361528	Human		name
405758700	CV3303544	single nucleotide variant	NM_020406.4(CD177):c.1034C>T (p.Pro345Leu)	not specified [RCV004433230]	uncertain significance	19	43361532	43361532	Human		name
405758709	CV3303545	single nucleotide variant	NM_020406.4(CD177):c.1162G>A (p.Gly388Arg)	not specified [RCV004433231]	uncertain significance	19	43362168	43362168	Human		name
405758722	CV3303547	single nucleotide variant	NM_020406.4(CD177):c.1190A>T (p.Asp397Val)	not specified [RCV004433233]	uncertain significance	19	43362196	43362196	Human		name
405758728	CV3303548	single nucleotide variant	NM_020406.4(CD177):c.1238T>A (p.Leu413Gln)	not specified [RCV004433234]	uncertain significance	19	43362244	43362244	Human		name
405758736	CV3303549	single nucleotide variant	NM_020406.4(CD177):c.1261G>A (p.Gly421Arg)	not specified [RCV004433235]	uncertain significance	19	43362267	43362267	Human		name
407497854	CV3424877	single nucleotide variant	NM_020406.4(CD177):c.1040G>A (p.Gly347Asp)	not specified [RCV004606471]	uncertain significance	19	43361538	43361538	Human		name
407497861	CV3424879	single nucleotide variant	NM_020406.4(CD177):c.1013G>T (p.Gly338Val)	not specified [RCV004606473]	uncertain significance	19	43361511	43361511	Human		name
597777773	CV3638618	single nucleotide variant	NM_020406.4(CD177):c.1117G>A (p.Val373Met)	not specified [RCV004898849]	likely benign	19	43362123	43362123	Human		name
597777786	CV3638621	single nucleotide variant	NM_020406.4(CD177):c.1186C>T (p.Arg396Cys)	not specified [RCV004898852]	uncertain significance	19	43362192	43362192	Human		name
597738593	CV3638622	single nucleotide variant	NM_020406.4(CD177):c.1255G>T (p.Gly419Trp)	not specified [RCV004890150]	uncertain significance	19	43362261	43362261	Human		name
597738596	CV3638624	single nucleotide variant	NM_020406.4(CD177):c.1285T>C (p.Trp429Arg)	not specified [RCV004890151]	uncertain significance	19	43362291	43362291	Human		name
598206652	CV3940079	single nucleotide variant	NM_020406.4(CD177):c.1187G>A (p.Arg396His)	not specified [RCV005315147]	uncertain significance	19	43362193	43362193	Human		name
598206661	CV3940081	single nucleotide variant	NM_020406.4(CD177):c.1175C>T (p.Ala392Val)	not specified [RCV005315149]	likely benign	19	43362181	43362181	Human		name
598206672	CV3940083	single nucleotide variant	NM_020406.4(CD177):c.1246C>G (p.Leu416Val)	not specified [RCV005315151]	uncertain significance	19	43362252	43362252	Human		name
598228771	CV3940087	single nucleotide variant	NM_020406.4(CD177):c.1165A>G (p.Ile389Val)	not specified [RCV005319124]	likely benign	19	43362171	43362171	Human		name
15150144	CV716502	single nucleotide variant	NM_020406.4(CD177):c.1090T>A (p.Ser364Thr)	not provided [RCV000967888]	benign	19	43362096	43362096	Human		name
15150151	CV716503	single nucleotide variant	NM_020406.4(CD177):c.1097A>G (p.Lys366Arg)	not provided [RCV000967889]	benign	19	43362103	43362103	Human		name

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