Med15 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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71 records found for search term Med15

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8586831	CV121454	single nucleotide variant	NM_001003891.2(MED15):c.-2076C>T	Lung cancer [RCV000101974]	uncertain significance	22	20505603	20505603	Human		name
8586832	CV121455	single nucleotide variant	NM_001003891.2(MED15):c.69-1274G>A	Lung cancer [RCV000101975]	uncertain significance	22	20535843	20535843	Human		name
150515043	CV1228713	single nucleotide variant	NM_001003891.3(MED15):c.1804-19G>A	not provided [RCV001638701]	benign	22	20584836	20584836	Human		name
150492064	CV1253865	single nucleotide variant	NM_001003891.3(MED15):c.1673-16C>T	not provided [RCV001674961]	benign	22	20583314	20583314	Human		name
15171605	CV778631	duplication	NM_001003891.3(MED15):c.156+8_156+11dup	not provided [RCV000949863]	benign	22	20537211	20537212	Human		name
407502238	CV3453625	single nucleotide variant	NM_001003891.3(MED15):c.13G>C (p.Gly5Arg)	not specified [RCV004645098]	uncertain significance	22	20507691	20507691	Human		name
401920329	CV2821964	single nucleotide variant	NM_001003891.3(MED15):c.387G>A (p.Pro129=)	not provided [RCV003431646]	likely benign	22	20555084	20555084	Human		name
15168645	CV729039	single nucleotide variant	NM_001003891.3(MED15):c.903G>A (p.Pro301=)	not provided [RCV000883107]	likely benign	22	20566679	20566679	Human		name
156040967	CV2342090	single nucleotide variant	NM_001003891.3(MED15):c.262C>G (p.Leu88Val)	not specified [RCV004189521]	uncertain significance	22	20554959	20554959	Human		name
401925927	CV2821967	single nucleotide variant	NM_001003891.3(MED15):c.2232C>T (p.Asp744=)	not provided [RCV003437488]	likely benign	22	20586569	20586569	Human		name
405681867	CV3285490	single nucleotide variant	NM_001003891.3(MED15):c.172C>G (p.Leu58Val)	not specified [RCV004421809]	uncertain significance	22	20551451	20551451	Human		name
407517997	CV3453627	single nucleotide variant	NM_001003891.3(MED15):c.248A>G (p.Asn83Ser)	not specified [RCV004628715]	uncertain significance	22	20554945	20554945	Human		name
597634477	CV3560139	single nucleotide variant	NM_001003891.3(MED15):c.232G>A (p.Val78Ile)	not specified [RCV004824164]	uncertain significance	22	20553168	20553168	Human		name
598225041	CV3985572	single nucleotide variant	NM_001003891.3(MED15):c.289G>A (p.Ala97Thr)	not specified [RCV005380325]	uncertain significance	22	20554986	20554986	Human		name
155926811	CV2230685	single nucleotide variant	NM_001003891.3(MED15):c.820C>T (p.Pro274Ser)	not specified [RCV004097631]	uncertain significance	22	20566596	20566596	Human		name
155993790	CV2286338	single nucleotide variant	NM_001003891.3(MED15):c.332G>A (p.Gly111Asp)	not specified [RCV004146285]	uncertain significance	22	20555029	20555029	Human		name
156188861	CV2395526	single nucleotide variant	NM_001003891.3(MED15):c.345C>G (p.Ser115Arg)	not specified [RCV004241387]	uncertain significance	22	20555042	20555042	Human		name
401770154	CV2719062	single nucleotide variant	NM_001003891.3(MED15):c.331G>A (p.Gly111Ser)	not specified [RCV004322639]	uncertain significance	22	20555028	20555028	Human		name
401728889	CV2729887	single nucleotide variant	NM_001003891.3(MED15):c.524C>T (p.Ala175Val)	not specified [RCV004332890]	likely benign	22	20564522	20564522	Human		name
401859127	CV2775110	single nucleotide variant	NM_001003891.3(MED15):c.787G>A (p.Ala263Thr)	not specified [RCV004346473]	uncertain significance	22	20566563	20566563	Human		name
405681896	CV3285495	single nucleotide variant	NM_001003891.3(MED15):c.301A>T (p.Met101Leu)	not specified [RCV004421814]	uncertain significance	22	20554998	20554998	Human		name
405681901	CV3285496	single nucleotide variant	NM_001003891.3(MED15):c.355A>G (p.Met119Val)	not specified [RCV004421815]	uncertain significance	22	20555052	20555052	Human		name
405681905	CV3285497	single nucleotide variant	NM_001003891.3(MED15):c.357G>A (p.Met119Ile)	not specified [RCV004421816]	uncertain significance	22	20555054	20555054	Human		name
405681910	CV3285498	single nucleotide variant	NM_001003891.3(MED15):c.761A>G (p.Gln254Arg)	not specified [RCV004421817]	uncertain significance	22	20566537	20566537	Human		name
405854720	CV3394835	single nucleotide variant	NM_001003891.3(MED15):c.916C>T (p.Gln306Ter)	not provided [RCV004554976]	uncertain significance	22	20566692	20566692	Human		name
407518000	CV3453629	single nucleotide variant	NM_001003891.3(MED15):c.860C>G (p.Pro287Arg)	not specified [RCV004628716]	uncertain significance	22	20566636	20566636	Human		name
407502251	CV3453630	single nucleotide variant	NM_001003891.3(MED15):c.316C>G (p.Pro106Ala)	not specified [RCV004645101]	uncertain significance	22	20555013	20555013	Human		name
597676035	CV3560140	single nucleotide variant	NM_001003891.3(MED15):c.902C>T (p.Pro301Leu)	not specified [RCV004830316]	uncertain significance	22	20566678	20566678	Human		name
597676054	CV3560142	single nucleotide variant	NM_001003891.3(MED15):c.921G>C (p.Gln307His)	not specified [RCV004830318]	uncertain significance	22	20566697	20566697	Human		name
597676081	CV3560145	single nucleotide variant	NM_001003891.3(MED15):c.583G>A (p.Ala195Thr)	not specified [RCV004830321]	uncertain significance	22	20564581	20564581	Human		name
15174142	CV679160	single nucleotide variant	NM_001003891.3(MED15):c.943C>A (p.Pro315Thr)	Aganglionic megacolon [RCV000984696]	uncertain significance	22	20566719	20566719	Human	2	name
156075056	CV2291367	single nucleotide variant	NM_001003891.3(MED15):c.2320A>G (p.Asn774Asp)	not specified [RCV004162054]	uncertain significance	22	20586657	20586657	Human		name
156199548	CV2293816	single nucleotide variant	NM_001003891.3(MED15):c.1757A>G (p.Gln586Arg)	not specified [RCV004155085]	uncertain significance	22	20584379	20584379	Human		name
155905083	CV2349675	single nucleotide variant	NM_001003891.3(MED15):c.1564G>A (p.Ala522Thr)	not specified [RCV004204091]	uncertain significance	22	20583139	20583139	Human		name
156034461	CV2376679	single nucleotide variant	NM_001003891.3(MED15):c.1950C>A (p.His650Gln)	not specified [RCV004222876]	uncertain significance	22	20585001	20585001	Human		name
329358988	CV2450785	single nucleotide variant	NM_001003891.3(MED15):c.1189A>G (p.Ile397Val)	not specified [RCV004267710]	likely benign	22	20575149	20575149	Human		name
329353542	CV2466860	single nucleotide variant	NM_001003891.3(MED15):c.1579G>A (p.Ala527Thr)	not specified [RCV004282634]	uncertain significance	22	20583154	20583154	Human		name
329392063	CV2470341	single nucleotide variant	NM_001003891.3(MED15):c.1889G>A (p.Arg630His)	not specified [RCV004279730]	uncertain significance	22	20584940	20584940	Human		name
401739896	CV2684205	single nucleotide variant	NM_001003891.3(MED15):c.1477G>T (p.Val493Leu)	not specified [RCV004288872]	uncertain significance	22	20582907	20582907	Human		name
401731875	CV2690181	single nucleotide variant	NM_001003891.3(MED15):c.2020A>G (p.Ile674Val)	not specified [RCV004302193]	uncertain significance	22	20585156	20585156	Human		name
401734710	CV2690659	single nucleotide variant	NM_001003891.3(MED15):c.1211C>T (p.Thr404Ile)	not specified [RCV004298393]	uncertain significance	22	20575171	20575171	Human		name
401772211	CV2708199	single nucleotide variant	NM_001003891.3(MED15):c.2215C>T (p.Arg739Trp)	not specified [RCV004311558]	uncertain significance	22	20585811	20585811	Human		name
401741775	CV2710256	single nucleotide variant	NM_001003891.3(MED15):c.1375G>T (p.Gly459Cys)	not specified [RCV004317151]	uncertain significance	22	20582713	20582713	Human		name
401781153	CV2726437	single nucleotide variant	NM_001003891.3(MED15):c.2324C>A (p.Thr775Asn)	not specified [RCV004328638]	uncertain significance	22	20586661	20586661	Human		name
405681853	CV3285487	single nucleotide variant	NM_001003891.3(MED15):c.1214C>T (p.Thr405Ile)	not specified [RCV004421806]	uncertain significance	22	20575174	20575174	Human		name
405681858	CV3285488	single nucleotide variant	NM_001003891.3(MED15):c.1313C>T (p.Pro438Leu)	not specified [RCV004421807]	uncertain significance	22	20582651	20582651	Human		name
405681872	CV3285491	single nucleotide variant	NM_001003891.3(MED15):c.1951G>A (p.Gly651Ser)	not specified [RCV004421810]	uncertain significance	22	20585002	20585002	Human		name
405681880	CV3285492	single nucleotide variant	NM_001003891.3(MED15):c.2257C>T (p.His753Tyr)	not specified [RCV004421811]	uncertain significance	22	20586594	20586594	Human		name
405681885	CV3285493	single nucleotide variant	NM_001003891.3(MED15):c.2311G>A (p.Ala771Thr)	not specified [RCV004421812]	uncertain significance	22	20586648	20586648	Human		name
405681891	CV3285494	single nucleotide variant	NM_001003891.3(MED15):c.2338G>A (p.Val780Ile)	not specified [RCV004421813]	likely benign	22	20586675	20586675	Human		name
407475133	CV3453622	single nucleotide variant	NM_001003891.3(MED15):c.1405G>A (p.Val469Ile)	not specified [RCV004638127]	uncertain significance	22	20582743	20582743	Human		name
407475126	CV3453623	single nucleotide variant	NM_001003891.3(MED15):c.2108C>T (p.Thr703Ile)	not specified [RCV004638128]	uncertain significance	22	20585244	20585244	Human		name
407502243	CV3453626	single nucleotide variant	NM_001003891.3(MED15):c.1442T>C (p.Leu481Pro)	not specified [RCV004645099]	uncertain significance	22	20582872	20582872	Human		name
407502248	CV3453628	single nucleotide variant	NM_001003891.3(MED15):c.1291C>G (p.Pro431Ala)	not specified [RCV004645100]	uncertain significance	22	20582629	20582629	Human		name
597676044	CV3560141	single nucleotide variant	NM_001003891.3(MED15):c.1481C>T (p.Thr494Met)	not specified [RCV004830317]	uncertain significance	22	20582911	20582911	Human		name
597676062	CV3560143	single nucleotide variant	NM_001003891.3(MED15):c.1274T>C (p.Val425Ala)	not specified [RCV004830319]	uncertain significance	22	20582612	20582612	Human		name
597676070	CV3560144	single nucleotide variant	NM_001003891.3(MED15):c.1448G>T (p.Ser483Ile)	not specified [RCV004830320]	uncertain significance	22	20582878	20582878	Human		name
597676091	CV3560146	single nucleotide variant	NM_001003891.3(MED15):c.2270C>T (p.Thr757Ile)	not specified [RCV004830322]	uncertain significance	22	20586607	20586607	Human		name
598240865	CV3985571	single nucleotide variant	NM_001003891.3(MED15):c.1334C>T (p.Pro445Leu)	not specified [RCV005364715]	uncertain significance	22	20582672	20582672	Human		name
598225047	CV3985573	single nucleotide variant	NM_001003891.3(MED15):c.1283G>A (p.Ser428Asn)	not specified [RCV005380326]	likely benign	22	20582621	20582621	Human		name
598225053	CV3985574	single nucleotide variant	NM_001003891.3(MED15):c.1487G>A (p.Arg496Gln)	not specified [RCV005380327]	uncertain significance	22	20582917	20582917	Human		name
598225059	CV3985575	single nucleotide variant	NM_001003891.3(MED15):c.1938G>C (p.Met646Ile)	not specified [RCV005380328]	uncertain significance	22	20584989	20584989	Human		name
8628642	CV83786	single nucleotide variant	NM_001003891.2(MED15):c.2239C>T (p.Pro747Ser)	Malignant melanoma [RCV000063867]	not provided	22	20586576	20586576	Human		name
155741672	CV1770477	microsatellite	NM_001003891.3(MED15):c.633GCA[7] (p.Gln218del)	Hepatocellular carcinoma [RCV002302702]	pathogenic	22	20564629	20564631	Human		name
155741718	CV1770516	microsatellite	NM_001003891.3(MED15):c.534GCA[6] (p.Gln188del)	Hepatocellular carcinoma [RCV002302741]	pathogenic	22	20564530	20564532	Human		name
155741654	CV1770463	microsatellite	NM_001003891.3(MED15):c.751CAG[11] (p.Gln262del)	Hepatocellular carcinoma [RCV002302687]	pathogenic	22	20566527	20566529	Human		name
401925926	CV2821966	microsatellite	NM_001003891.3(MED15):c.751CAG[9] (p.Gln260_Gln262del)	not provided [RCV003437487]	likely benign	22	20566527	20566535	Human		name
401925924	CV2821965	deletion	NM_001003891.3(MED15):c.629_655del (p.Leu210_Gln218del)	not provided [RCV003437485]	benign	22	20564610	20564636	Human		name
155741674	CV1770478	microsatellite	NM_001003891.3(MED15):c.633GCA[9] (p.Gln218_His219insGln)	not provided [RCV003437486]	pathogenic\|likely benign	22	20564628	20564629	Human		name
155741655	CV1770464	microsatellite	NM_001003891.3(MED15):c.751CAG[13] (p.Gln262_Ala263insGln)	Hepatocellular carcinoma [RCV002302688]	pathogenic	22	20566526	20566527	Human		name
155741692	CV1770494	microsatellite	NM_001003891.3(MED15):c.751CAG[15] (p.Gln262_Ala263insGlnGlnGln)	Hepatocellular carcinoma [RCV002302719]	pathogenic	22	20566526	20566527	Human		name

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