Med24 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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81 records found for search term Med24

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15162231	CV778475	single nucleotide variant	NM_014815.4(MED24):c.2853+7A>G	not provided [RCV000947817]	benign	17	40019778	40019778	Human		name
150491693	CV1225345	single nucleotide variant	NM_014815.4(MED24):c.1986-19T>C	not provided [RCV001618860]	benign	17	40023414	40023414	Human		name
8585350	CV119935	single nucleotide variant	NM_001079518.1(MED24):c.1947-1374A>T	Lung cancer [RCV000100455]	uncertain significance	17	40024769	40024769	Human		name
155912645	CV2341624	single nucleotide variant	NM_014815.4(MED24):c.94C>A (p.Pro32Thr)	not specified [RCV004182552]	uncertain significance	17	40053505	40053505	Human		name
401767617	CV2729789	single nucleotide variant	NM_014815.4(MED24):c.86A>G (p.Lys29Arg)	not specified [RCV004332804]	uncertain significance	17	40053513	40053513	Human		name
405682324	CV3285575	single nucleotide variant	NM_014815.4(MED24):c.627G>A (p.Pro209=)	not specified [RCV004421894]	likely benign	17	40033389	40033389	Human		name
150514278	CV1210951	single nucleotide variant	NM_014815.4(MED24):c.2142T>C (p.Ile714=)	not provided [RCV001598994]	benign	17	40023239	40023239	Human		name
150467078	CV1255846	single nucleotide variant	NM_014815.4(MED24):c.2886C>T (p.Ser962=)	not provided [RCV001670480]	benign	17	40019613	40019613	Human		name
329367542	CV2456900	single nucleotide variant	NM_014815.4(MED24):c.164C>T (p.Ser55Phe)	not specified [RCV004270857]	uncertain significance	17	40053347	40053347	Human		name
404980164	CV2850455	single nucleotide variant	NM_014815.4(MED24):c.291G>C (p.Leu97Phe)	not provided [RCV003488024]	uncertain significance	17	40035757	40035757	Human		name
597676431	CV3560210	single nucleotide variant	NM_014815.4(MED24):c.124C>G (p.Leu42Val)	not specified [RCV004830356]	uncertain significance	17	40053475	40053475	Human		name
156323852	CV2201889	single nucleotide variant	NM_014815.4(MED24):c.538A>G (p.Ile180Val)	not specified [RCV004082313]	uncertain significance	17	40035138	40035138	Human		name
156260497	CV2204820	single nucleotide variant	NM_014815.4(MED24):c.319C>T (p.Arg107Cys)	not specified [RCV004075074]	uncertain significance	17	40035729	40035729	Human		name
156380983	CV2219079	single nucleotide variant	NM_014815.4(MED24):c.724C>T (p.Pro242Ser)	not specified [RCV004087242]	uncertain significance	17	40033154	40033154	Human		name
156057643	CV2322869	single nucleotide variant	NM_014815.4(MED24):c.779C>T (p.Thr260Met)	not specified [RCV004185327]	uncertain significance	17	40033099	40033099	Human		name
329392617	CV2439071	single nucleotide variant	NM_014815.4(MED24):c.626C>T (p.Pro209Leu)	not specified [RCV004266363]	uncertain significance	17	40033390	40033390	Human		name
329354865	CV2449003	single nucleotide variant	NM_014815.4(MED24):c.352A>G (p.Ile118Val)	not specified [RCV004264082]	uncertain significance	17	40035324	40035324	Human		name
401861552	CV2756342	single nucleotide variant	NM_014815.4(MED24):c.634C>T (p.Arg212Trp)	not specified [RCV004342888]	uncertain significance	17	40033382	40033382	Human		name
405682309	CV3285572	single nucleotide variant	NM_014815.4(MED24):c.422G>C (p.Arg141Pro)	not specified [RCV004421891]	uncertain significance	17	40035254	40035254	Human		name
405682314	CV3285573	single nucleotide variant	NM_014815.4(MED24):c.524G>A (p.Arg175Gln)	not specified [RCV004421892]	uncertain significance	17	40035152	40035152	Human		name
405682317	CV3285574	single nucleotide variant	NM_014815.4(MED24):c.614A>G (p.Asn205Ser)	not specified [RCV004421893]	uncertain significance	17	40033402	40033402	Human		name
405682330	CV3285576	single nucleotide variant	NM_014815.4(MED24):c.773G>A (p.Gly258Asp)	not specified [RCV004421895]	uncertain significance	17	40033105	40033105	Human		name
405682337	CV3285577	single nucleotide variant	NM_014815.4(MED24):c.778A>C (p.Thr260Pro)	not specified [RCV004421896]	uncertain significance	17	40033100	40033100	Human		name
407502352	CV3453660	single nucleotide variant	NM_014815.4(MED24):c.803C>T (p.Thr268Met)	not specified [RCV004645127]	likely benign	17	40033075	40033075	Human		name
407502356	CV3453661	single nucleotide variant	NM_014815.4(MED24):c.515C>G (p.Thr172Ser)	not specified [RCV004645128]	uncertain significance	17	40035161	40035161	Human		name
597676410	CV3560208	single nucleotide variant	NM_014815.4(MED24):c.635G>A (p.Arg212Gln)	not specified [RCV004830354]	uncertain significance	17	40033381	40033381	Human		name
597634541	CV3560211	single nucleotide variant	NM_014815.4(MED24):c.422G>A (p.Arg141Gln)	not specified [RCV004824176]	uncertain significance	17	40035254	40035254	Human		name
15190820	CV727145	single nucleotide variant	NM_014815.4(MED24):c.610G>A (p.Ala204Thr)	not provided [RCV000888206]	benign	17	40033406	40033406	Human		name
155965270	CV2206406	single nucleotide variant	NM_014815.4(MED24):c.2510G>A (p.Arg837His)	not specified [RCV004078731]	uncertain significance	17	40022407	40022407	Human		name
156094606	CV2213417	single nucleotide variant	NM_014815.4(MED24):c.1160C>T (p.Ala387Val)	not specified [RCV004087397]	uncertain significance	17	40029854	40029854	Human		name
156160437	CV2236344	single nucleotide variant	NM_014815.4(MED24):c.2912C>T (p.Thr971Met)	not specified [RCV004108033]	uncertain significance	17	40019587	40019587	Human		name
156025777	CV2274015	single nucleotide variant	NM_014815.4(MED24):c.2574G>A (p.Met858Ile)	not specified [RCV004134402]	uncertain significance	17	40022004	40022004	Human		name
155999724	CV2287305	single nucleotide variant	NM_014815.4(MED24):c.2287C>T (p.Arg763Trp)	not specified [RCV004146935]	uncertain significance	17	40022790	40022790	Human		name
155901850	CV2301335	single nucleotide variant	NM_014815.4(MED24):c.2320C>A (p.Leu774Met)	not specified [RCV004160494]	uncertain significance	17	40022757	40022757	Human		name
156360891	CV2329699	single nucleotide variant	NM_014815.4(MED24):c.2819G>A (p.Arg940His)	not specified [RCV004180805]	uncertain significance	17	40019819	40019819	Human		name
156192812	CV2344109	single nucleotide variant	NM_014815.4(MED24):c.2269C>G (p.Arg757Gly)	not specified [RCV004195708]	uncertain significance	17	40022808	40022808	Human		name
155981926	CV2351467	single nucleotide variant	NM_014815.4(MED24):c.2483C>T (p.Ala828Val)	not specified [RCV004193151]	uncertain significance	17	40022434	40022434	Human		name
155991298	CV2355389	single nucleotide variant	NM_014815.4(MED24):c.1642C>T (p.Arg548Cys)	not specified [RCV004205248]	uncertain significance	17	40026923	40026923	Human		name
156129635	CV2358710	single nucleotide variant	NM_014815.4(MED24):c.1238C>T (p.Ala413Val)	not specified [RCV004209627]	uncertain significance	17	40029776	40029776	Human		name
156227007	CV2388126	single nucleotide variant	NM_014815.4(MED24):c.2615C>T (p.Ser872Leu)	not specified [RCV004241244]	uncertain significance	17	40021963	40021963	Human		name
156000366	CV2396572	single nucleotide variant	NM_014815.4(MED24):c.2680C>T (p.Arg894Trp)	not specified [RCV004242272]	uncertain significance	17	40020297	40020297	Human		name
329385362	CV2432097	single nucleotide variant	NM_014815.4(MED24):c.2564C>T (p.Ser855Leu)	not specified [RCV004249246]	uncertain significance	17	40022014	40022014	Human		name
401731051	CV2674244	single nucleotide variant	NM_014815.4(MED24):c.2414C>T (p.Pro805Leu)	not specified [RCV004289131]	uncertain significance	17	40022663	40022663	Human		name
401723716	CV2675053	single nucleotide variant	NM_014815.4(MED24):c.2599G>A (p.Asp867Asn)	not specified [RCV004296350]	uncertain significance	17	40021979	40021979	Human		name
401733524	CV2682138	single nucleotide variant	NM_014815.4(MED24):c.1397G>A (p.Arg466Gln)	not specified [RCV004290189]	uncertain significance	17	40028838	40028838	Human		name
401728539	CV2693624	single nucleotide variant	NM_014815.4(MED24):c.2389A>G (p.Lys797Glu)	not specified [RCV004297964]	uncertain significance	17	40022688	40022688	Human		name
401726500	CV2695703	single nucleotide variant	NM_014815.4(MED24):c.2029G>A (p.Val677Met)	not specified [RCV004299505]	uncertain significance	17	40023352	40023352	Human		name
401761396	CV2702320	single nucleotide variant	NM_014815.4(MED24):c.2185A>T (p.Ile729Phe)	not specified [RCV004316853]	uncertain significance	17	40023196	40023196	Human		name
401742846	CV2715332	single nucleotide variant	NM_014815.4(MED24):c.2743C>T (p.Arg915Cys)	not specified [RCV004324667]	uncertain significance	17	40019895	40019895	Human		name
401874441	CV2759211	single nucleotide variant	NM_014815.4(MED24):c.1138A>G (p.Asn380Asp)	not specified [RCV004342497]	uncertain significance	17	40031175	40031175	Human		name
401891994	CV2775870	single nucleotide variant	NM_014815.4(MED24):c.2108C>T (p.Pro703Leu)	not specified [RCV004344902]	uncertain significance	17	40023273	40023273	Human		name
401895567	CV2777905	single nucleotide variant	NM_014815.4(MED24):c.2841G>A (p.Met947Ile)	not specified [RCV004347874]	uncertain significance	17	40019797	40019797	Human		name
401875026	CV2791020	single nucleotide variant	NM_014815.4(MED24):c.2179C>T (p.Arg727Cys)	not specified [RCV004354634]	uncertain significance	17	40023202	40023202	Human		name
405866923	CV2842439	single nucleotide variant	NM_014815.4(MED24):c.2044G>A (p.Ala682Thr)	EBV-positive nodal T- and NK-cell lymphoma [RCV004557796]	likely benign	17	40023337	40023337	Human		name
405682264	CV3285564	single nucleotide variant	NM_014815.4(MED24):c.1013T>C (p.Phe338Ser)	not specified [RCV004421883]	uncertain significance	17	40031592	40031592	Human		name
405682278	CV3285566	single nucleotide variant	NM_014815.4(MED24):c.1882G>A (p.Val628Ile)	not specified [RCV004421885]	uncertain significance	17	40026259	40026259	Human		name
405682283	CV3285567	single nucleotide variant	NM_014815.4(MED24):c.1906C>T (p.Arg636Cys)	not specified [RCV004421886]	uncertain significance	17	40026235	40026235	Human		name
405682289	CV3285568	single nucleotide variant	NM_014815.4(MED24):c.2384C>T (p.Ser795Phe)	not specified [RCV004421887]	uncertain significance	17	40022693	40022693	Human		name
405682294	CV3285569	single nucleotide variant	NM_014815.4(MED24):c.2747C>T (p.Thr916Ile)	not specified [RCV004421888]	uncertain significance	17	40019891	40019891	Human		name
405682299	CV3285570	single nucleotide variant	NM_014815.4(MED24):c.2858C>T (p.Ser953Leu)	not specified [RCV004421889]	uncertain significance	17	40019641	40019641	Human		name
405682304	CV3285571	single nucleotide variant	NM_014815.4(MED24):c.2963C>T (p.Ala988Val)	not specified [RCV004421890]	uncertain significance	17	40019536	40019536	Human		name
407502328	CV3453654	single nucleotide variant	NM_014815.4(MED24):c.1405A>G (p.Ile469Val)	not specified [RCV004645121]	uncertain significance	17	40028830	40028830	Human		name
407502332	CV3453655	single nucleotide variant	NM_014815.4(MED24):c.2014C>T (p.Arg672Cys)	not specified [RCV004645122]	uncertain significance	17	40023367	40023367	Human		name
407502341	CV3453657	single nucleotide variant	NM_014815.4(MED24):c.1005C>G (p.Asn335Lys)	not specified [RCV004645124]	uncertain significance	17	40031600	40031600	Human		name
407502343	CV3453658	single nucleotide variant	NM_014815.4(MED24):c.2765A>G (p.Gln922Arg)	not specified [RCV004645125]	uncertain significance	17	40019873	40019873	Human		name
407502347	CV3453659	single nucleotide variant	NM_014815.4(MED24):c.1147G>A (p.Ala383Thr)	not specified [RCV004645126]	uncertain significance	17	40031166	40031166	Human		name
407502361	CV3453662	single nucleotide variant	NM_014815.4(MED24):c.2782A>C (p.Met928Leu)	not specified [RCV004645129]	uncertain significance	17	40019856	40019856	Human		name
597676403	CV3560206	single nucleotide variant	NM_014815.4(MED24):c.2282C>T (p.Thr761Met)	not specified [RCV004830353]	uncertain significance	17	40022795	40022795	Human		name
597634535	CV3560207	single nucleotide variant	NM_014815.4(MED24):c.2199C>G (p.Asp733Glu)	not specified [RCV004824175]	uncertain significance	17	40023182	40023182	Human		name
597676422	CV3560209	single nucleotide variant	NM_014815.4(MED24):c.2131C>G (p.Leu711Val)	not specified [RCV004830355]	uncertain significance	17	40023250	40023250	Human		name
597676441	CV3560212	single nucleotide variant	NM_014815.4(MED24):c.2810A>G (p.Gln937Arg)	not specified [RCV004830357]	uncertain significance	17	40019828	40019828	Human		name
597676456	CV3560213	single nucleotide variant	NM_014815.4(MED24):c.1492C>T (p.Leu498Phe)	not specified [RCV004830358]	uncertain significance	17	40027421	40027421	Human		name
597676462	CV3560214	single nucleotide variant	NM_014815.4(MED24):c.2108C>G (p.Pro703Arg)	not specified [RCV004830359]	uncertain significance	17	40023273	40023273	Human		name
597676471	CV3560215	single nucleotide variant	NM_014815.4(MED24):c.2291C>T (p.Ala764Val)	not specified [RCV004830360]	uncertain significance	17	40022786	40022786	Human		name
597676480	CV3560216	single nucleotide variant	NM_014815.4(MED24):c.2123A>G (p.Lys708Arg)	not specified [RCV004830361]	uncertain significance	17	40023258	40023258	Human		name
597676499	CV3560218	single nucleotide variant	NM_014815.4(MED24):c.2606A>G (p.Asn869Ser)	not specified [RCV004830363]	uncertain significance	17	40021972	40021972	Human		name
598240987	CV3985619	single nucleotide variant	NM_014815.4(MED24):c.1885C>T (p.Arg629Trp)	not specified [RCV005364738]	uncertain significance	17	40026256	40026256	Human		name
598225168	CV3985620	single nucleotide variant	NM_014815.4(MED24):c.2113C>T (p.Arg705Trp)	not specified [RCV005380350]	uncertain significance	17	40023268	40023268	Human		name
14349987	CV590891	single nucleotide variant	NM_014815.4(MED24):c.2288G>A (p.Arg763Gln)	Short stature [RCV000736133]	likely pathogenic	17	40022789	40022789	Human	2	name
14349985	CV590892	single nucleotide variant	NM_014815.4(MED24):c.1247C>G (p.Thr416Ser)	Short stature [RCV000736132]	likely pathogenic	17	40029767	40029767	Human	2	name
8636123	CV91346	single nucleotide variant	NM_001079518.1(MED24):c.1349C>T (p.Ser450Phe)	Malignant melanoma [RCV000071444]	not provided	17	40028847	40028847	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

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