Schip1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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50 records found for search term Schip1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8578253	CV112632	single nucleotide variant	NM_001197107.1(SCHIP1):c.64-67118A>G	Lung cancer [RCV000093155]	uncertain significance	3	159697325	159697325	Human		name
8578255	CV112634	single nucleotide variant	NM_001197107.1(SCHIP1):c.721-4768C>G	Lung cancer [RCV000093157]	uncertain significance	3	159861395	159861395	Human		name
8578250	CV112629	single nucleotide variant	NM_001197107.1(SCHIP1):c.63+142120A>G	Lung cancer [RCV000093152]	uncertain significance	3	159416003	159416003	Human		name
8578251	CV112630	single nucleotide variant	NM_001197107.1(SCHIP1):c.64-165155G>A	Lung cancer [RCV000093153]	uncertain significance	3	159599288	159599288	Human		name
8578254	CV112633	single nucleotide variant	NM_001197107.1(SCHIP1):c.721-40920T>C	Lung cancer [RCV000093156]	uncertain significance	3	159825243	159825243	Human		name
405281794	CV3224382	single nucleotide variant	NM_014575.4(SCHIP1):c.1354C>T (p.Arg452Ter)	Familial meningioma [RCV003988764]	likely pathogenic	3	159892132	159892132	Human	1	name
156300817	CV2248882	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.401G>C (p.Cys134Ser)	not specified [RCV004115890]	uncertain significance	3	159764552	159764552	Human		name
156015722	CV2270002	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.881C>T (p.Pro294Leu)	not specified [RCV004128991]	uncertain significance	3	159765032	159765032	Human		name
156257504	CV2277666	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.328G>T (p.Ala110Ser)	not specified [RCV004147124]	uncertain significance	3	159764479	159764479	Human		name
156272670	CV2323406	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.724G>A (p.Val242Met)	not specified [RCV004171801]	uncertain significance	3	159764875	159764875	Human		name
156235229	CV2346344	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.398A>G (p.Glu133Gly)	not specified [RCV004203827]	uncertain significance	3	159764549	159764549	Human		name
156003085	CV2347752	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.535G>A (p.Glu179Lys)	not specified [RCV004202718]	uncertain significance	3	159764686	159764686	Human		name
401750807	CV2700076	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.496G>A (p.Asp166Asn)	not specified [RCV004310492]	uncertain significance	3	159764647	159764647	Human		name
401778773	CV2705650	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.763C>T (p.Arg255Cys)	not specified [RCV004318508]	uncertain significance	3	159764914	159764914	Human		name
401877726	CV2761285	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.659C>T (p.Pro220Leu)	not specified [RCV004341156]	uncertain significance	3	159764810	159764810	Human		name
401863852	CV2770867	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.658C>T (p.Pro220Ser)	not specified [RCV004343543]	uncertain significance	3	159764809	159764809	Human		name
401897806	CV2772936	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.767G>A (p.Arg256Gln)	not specified [RCV004357705]	uncertain significance	3	159764918	159764918	Human		name
401897544	CV2787014	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.877C>T (p.Pro293Ser)	not specified [RCV004366138]	uncertain significance	3	159765028	159765028	Human		name
405794528	CV3274935	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.472C>T (p.Pro158Ser)	not specified [RCV004400899]	uncertain significance	3	159764623	159764623	Human		name
405794531	CV3274936	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.476T>G (p.Val159Gly)	not specified [RCV004400900]	uncertain significance	3	159764627	159764627	Human		name
405794537	CV3274938	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.494T>C (p.Ile165Thr)	not specified [RCV004400902]	uncertain significance	3	159764645	159764645	Human		name
405794541	CV3274939	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.515A>T (p.Glu172Val)	not specified [RCV004400903]	uncertain significance	3	159764666	159764666	Human		name
405794544	CV3274940	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.637A>G (p.Arg213Gly)	not specified [RCV004400904]	uncertain significance	3	159764788	159764788	Human		name
405794547	CV3274941	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.745A>G (p.Ser249Gly)	not specified [RCV004400905]	uncertain significance	3	159764896	159764896	Human		name
405794553	CV3274943	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.769G>A (p.Ala257Thr)	not specified [RCV004400907]	uncertain significance	3	159764920	159764920	Human		name
405794555	CV3274944	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.971G>A (p.Arg324Lys)	not specified [RCV004400908]	uncertain significance	3	159765122	159765122	Human		name
407479780	CV3455200	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.643G>T (p.Ala215Ser)	not specified [RCV004630988]	uncertain significance	3	159764794	159764794	Human		name
407479784	CV3455201	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.797G>A (p.Gly266Asp)	not specified [RCV004630989]	uncertain significance	3	159764948	159764948	Human		name
407479788	CV3455202	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.749G>C (p.Cys250Ser)	not specified [RCV004630990]	likely benign	3	159764900	159764900	Human		name
407479419	CV3455203	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.578C>T (p.Ser193Phe)	not specified [RCV004626443]	uncertain significance	3	159764729	159764729	Human		name
597785919	CV3680489	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.689A>G (p.Gln230Arg)	not specified [RCV004932101]	uncertain significance	3	159764840	159764840	Human		name
597785923	CV3680490	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.646A>G (p.Thr216Ala)	not specified [RCV004932102]	uncertain significance	3	159764797	159764797	Human		name
597785927	CV3680491	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.349A>C (p.Ser117Arg)	not specified [RCV004932103]	uncertain significance	3	159764500	159764500	Human		name
597785929	CV3680492	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.598G>A (p.Asp200Asn)	not specified [RCV004932104]	uncertain significance	3	159764749	159764749	Human		name
597785933	CV3680493	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.814G>C (p.Gly272Arg)	not specified [RCV004932105]	uncertain significance	3	159764965	159764965	Human		name
597785937	CV3680494	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.763C>G (p.Arg255Gly)	not specified [RCV004932106]	uncertain significance	3	159764914	159764914	Human		name
598194444	CV3979433	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.355G>T (p.Ala119Ser)	not specified [RCV005354828]	uncertain significance	3	159764506	159764506	Human		name
598194451	CV3979434	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.823G>T (p.Ala275Ser)	not specified [RCV005354829]	uncertain significance	3	159764974	159764974	Human		name
598210694	CV3979435	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.664C>G (p.Pro222Ala)	not specified [RCV005358571]	uncertain significance	3	159764815	159764815	Human		name
598160682	CV3979436	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.501G>C (p.Glu167Asp)	not specified [RCV005368290]	uncertain significance	3	159764652	159764652	Human		name
598194459	CV3979437	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.859A>G (p.Thr287Ala)	not specified [RCV005354830]	uncertain significance	3	159765010	159765010	Human		name
598160688	CV3979438	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.845C>T (p.Pro282Leu)	not specified [RCV005368291]	uncertain significance	3	159764996	159764996	Human		name
598194464	CV3979439	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.718G>A (p.Gly240Ser)	not specified [RCV005354831]	uncertain significance	3	159764869	159764869	Human		name
598160693	CV3979440	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.881C>A (p.Pro294Gln)	not specified [RCV005368292]	uncertain significance	3	159765032	159765032	Human		name
598194471	CV3979441	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.581C>T (p.Pro194Leu)	not specified [RCV005354832]	uncertain significance	3	159764732	159764732	Human		name
405794514	CV3274930	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.1030C>T (p.Leu344Phe)	not specified [RCV004400894]	uncertain significance	3	159866205	159866205	Human		name
405794517	CV3274931	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.1233G>C (p.Gln411His)	not specified [RCV004400895]	uncertain significance	3	159887716	159887716	Human		name
405794520	CV3274932	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.1280C>G (p.Ser427Cys)	not specified [RCV004400896]	uncertain significance	3	159887763	159887763	Human		name
405794522	CV3274933	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.1375G>A (p.Val459Ile)	not specified [RCV004400897]	uncertain significance	3	159887858	159887858	Human		name
405794525	CV3274934	single nucleotide variant	NM_001197113.2(IQCJ-SCHIP1):c.1441A>G (p.Ile481Val)	not specified [RCV004400898]	uncertain significance	3	159888838	159888838	Human		name

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