Esrrg Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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40 records found for search term Esrrg

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15193126	CV777087	single nucleotide variant	NM_001438.4(ESRRG):c.472+9C>T	not provided [RCV000955281]	benign	1	216677067	216677067	Human		name
14398893	CV610443	microsatellite	NM_001438.4(ESRRG):c.56+15867GT[3]	Premature ovarian insufficiency [RCV000766155]	uncertain significance	1	216707373	216707374	Human		name
8575606	CV109954	single nucleotide variant	NM_001134285.2(ESRRG):c.521-4344T>C	Lung cancer [RCV000090479]	uncertain significance	1	216572442	216572442	Human		name
8575610	CV109958	single nucleotide variant	NM_001134285.2(ESRRG):c.404-9650G>C	Lung cancer [RCV000090483]	uncertain significance	1	216660739	216660739	Human		name
8575616	CV109964	single nucleotide variant	NM_001134285.2(ESRRG):c.-14+8500C>A	Lung cancer [RCV000090489]	uncertain significance	1	216931082	216931082	Human		name
8575617	CV109965	single nucleotide variant	NM_001134285.2(ESRRG):c.-14+5285C>T	Lung cancer [RCV000090490]	uncertain significance	1	216934297	216934297	Human		name
8575618	CV109966	single nucleotide variant	NM_001134285.2(ESRRG):c.-14+4767C>G	Lung cancer [RCV000090491]	uncertain significance	1	216934815	216934815	Human		name
8575605	CV109953	single nucleotide variant	NM_001134285.2(ESRRG):c.793+17948C>A	Lung cancer [RCV000090478]	uncertain significance	1	216546271	216546271	Human		name
8575607	CV109955	single nucleotide variant	NM_001134285.2(ESRRG):c.521-19922T>G	Lung cancer [RCV000090480]	uncertain significance	1	216588020	216588020	Human		name
8575608	CV109956	single nucleotide variant	NM_001134285.2(ESRRG):c.520+22318G>T	Lung cancer [RCV000090481]	uncertain significance	1	216628655	216628655	Human		name
8575609	CV109957	single nucleotide variant	NM_001134285.2(ESRRG):c.520+19360G>T	Lung cancer [RCV000090482]	uncertain significance	1	216631613	216631613	Human		name
8575611	CV109959	single nucleotide variant	NM_001134285.2(ESRRG):c.-13-84299G>C	Lung cancer [RCV000090484]	uncertain significance	1	216761790	216761790	Human		name
8575612	CV109960	single nucleotide variant	NM_001134285.2(ESRRG):c.-13-93602C>T	Lung cancer [RCV000090485]	uncertain significance	1	216771093	216771093	Human		name
8575615	CV109963	single nucleotide variant	NM_001134285.2(ESRRG):c.-14+25154A>C	Lung cancer [RCV000090488]	uncertain significance	1	216914428	216914428	Human		name
8575613	CV109961	single nucleotide variant	NM_001134285.2(ESRRG):c.-14+119129C>T	Lung cancer [RCV000090486]	uncertain significance	1	216820453	216820453	Human		name
8575614	CV109962	single nucleotide variant	NM_001134285.2(ESRRG):c.-14+102306A>T	Lung cancer [RCV000090487]	uncertain significance	1	216837276	216837276	Human		name
8575619	CV109967	single nucleotide variant	NM_001134285.2(ESRRG):c.-229-47241C>A	Lung cancer [RCV000090492]	uncertain significance	1	217006926	217006926	Human		name
8575620	CV109968	single nucleotide variant	NM_001134285.2(ESRRG):c.-229-87895C>A	Lung cancer [RCV000090493]	uncertain significance	1	217047580	217047580	Human		name
156049746	CV2378321	single nucleotide variant	NM_001438.4(ESRRG):c.16C>T (p.Leu6Phe)	not specified [RCV004226349]	uncertain significance	1	216723284	216723284	Human		name
156334943	CV2214841	single nucleotide variant	NM_001438.4(ESRRG):c.73T>C (p.Ser25Pro)	not specified [RCV004090634]	uncertain significance	1	216677475	216677475	Human		name
156086889	CV2388059	single nucleotide variant	NM_001438.4(ESRRG):c.86G>A (p.Arg29Gln)	not specified [RCV004241188]	uncertain significance	1	216677462	216677462	Human		name
405757882	CV3255918	single nucleotide variant	NM_001438.4(ESRRG):c.41T>C (p.Leu14Pro)	not specified [RCV004382983]	uncertain significance	1	216723259	216723259	Human		name
15110524	CV718641	single nucleotide variant	NM_001438.4(ESRRG):c.492C>T (p.Cys164=)	not provided [RCV000894083]	benign	1	216651070	216651070	Human		name
155922449	CV2350835	single nucleotide variant	NM_001438.4(ESRRG):c.157G>A (p.Val53Ile)	not specified [RCV004207163]	uncertain significance	1	216677391	216677391	Human		name
407481134	CV3442274	single nucleotide variant	NM_001438.4(ESRRG):c.250C>G (p.Leu84Val)	not specified [RCV004618150]	uncertain significance	1	216677298	216677298	Human		name
407481139	CV3442275	single nucleotide variant	NM_001438.4(ESRRG):c.127C>T (p.Pro43Ser)	not specified [RCV004618151]	uncertain significance	1	216677421	216677421	Human		name
407481150	CV3442277	single nucleotide variant	NM_001438.4(ESRRG):c.104G>A (p.Cys35Tyr)	not specified [RCV004618153]	uncertain significance	1	216677444	216677444	Human		name
598193144	CV3958281	single nucleotide variant	NM_001438.4(ESRRG):c.178G>A (p.Gly60Ser)	not specified [RCV005335131]	uncertain significance	1	216677370	216677370	Human		name
156250311	CV2232160	single nucleotide variant	NM_001438.4(ESRRG):c.940G>A (p.Val314Ile)	not specified [RCV004104966]	uncertain significance	1	216519344	216519344	Human		name
156250571	CV2311230	single nucleotide variant	NM_001438.4(ESRRG):c.400A>G (p.Ile134Val)	not specified [RCV004166315]	uncertain significance	1	216677148	216677148	Human		name
156263955	CV2329411	single nucleotide variant	NM_001438.4(ESRRG):c.634C>T (p.Arg212Cys)	not specified [RCV004187420]	uncertain significance	1	216568054	216568054	Human		name
405757890	CV3255919	single nucleotide variant	NM_001438.4(ESRRG):c.487A>G (p.Ser163Gly)	not specified [RCV004382984]	uncertain significance	1	216651075	216651075	Human		name
405757897	CV3255920	single nucleotide variant	NM_001438.4(ESRRG):c.700T>A (p.Tyr234Asn)	not specified [RCV004382985]	uncertain significance	1	216567988	216567988	Human		name
407481128	CV3442273	single nucleotide variant	NM_001438.4(ESRRG):c.775G>A (p.Asp259Asn)	not specified [RCV004618149]	uncertain significance	1	216564306	216564306	Human		name
407481145	CV3442276	single nucleotide variant	NM_001438.4(ESRRG):c.362A>G (p.Asn121Ser)	not specified [RCV004618152]	uncertain significance	1	216677186	216677186	Human		name
155974386	CV2221086	single nucleotide variant	NM_001438.4(ESRRG):c.1289A>G (p.Lys430Arg)	not specified [RCV004094541]	uncertain significance	1	216507027	216507027	Human		name
156007653	CV2299752	single nucleotide variant	NM_001438.4(ESRRG):c.1136C>G (p.Ser379Cys)	not specified [RCV004148912]	uncertain significance	1	216507180	216507180	Human		name
14399870	CV610442	single nucleotide variant	NM_001438.4(ESRRG):c.1067A>G (p.Tyr356Cys)	Premature ovarian insufficiency [RCV000766138]	uncertain significance	1	216519217	216519217	Human	2	name
8629311	CV84456	single nucleotide variant	NM_001134285.2(ESRRG):c.931G>A (p.Glu311Lys)	Malignant melanoma [RCV000064538]	not provided	1	216519284	216519284	Human		name
8629310	CV84455	single nucleotide variant	NM_001134285.2(ESRRG):c.1264C>T (p.Pro422Ser)	Malignant melanoma [RCV000064537]	not provided	1	216506983	216506983	Human		name

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