Mcam Variant Search Result - Rat Genome Database

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79 records found for search term Mcam

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
407473198	CV3457153	single nucleotide variant	NM_006500.3(MCAM):c.16C>G (p.Leu6Val)	not specified [RCV004637795]	uncertain significance	11	119317086	119317086	Human		name
597648086	CV3703011	single nucleotide variant	NM_006500.3(MCAM):c.25G>C (p.Ala9Pro)	not specified [RCV004942726]	uncertain significance	11	119317077	119317077	Human		name
401725847	CV2687305	single nucleotide variant	NM_006500.3(MCAM):c.61G>A (p.Val21Ile)	not specified [RCV004298239]	uncertain significance	11	119317041	119317041	Human		name
401876526	CV2761093	single nucleotide variant	NM_006500.3(MCAM):c.168C>A (p.Asn56Lys)	not specified [RCV004338752]	uncertain significance	11	119315163	119315163	Human		name
401890835	CV2778379	single nucleotide variant	NM_006500.3(MCAM):c.271C>G (p.Arg91Gly)	not specified [RCV004344063]	uncertain significance	11	119314962	119314962	Human		name
407469421	CV3457148	single nucleotide variant	NM_006500.3(MCAM):c.131C>T (p.Ala44Val)	not specified [RCV004636624]	uncertain significance	11	119315200	119315200	Human		name
407473186	CV3457149	single nucleotide variant	NM_006500.3(MCAM):c.265G>A (p.Glu89Lys)	not specified [RCV004637792]	uncertain significance	11	119314968	119314968	Human		name
597648012	CV3703001	single nucleotide variant	NM_006500.3(MCAM):c.257G>T (p.Gly86Val)	not specified [RCV004942716]	uncertain significance	11	119314976	119314976	Human		name
597648060	CV3703008	single nucleotide variant	NM_006500.3(MCAM):c.133C>T (p.Leu45Phe)	not specified [RCV004942723]	uncertain significance	11	119315198	119315198	Human		name
597648068	CV3703009	single nucleotide variant	NM_006500.3(MCAM):c.161A>G (p.Gln54Arg)	not specified [RCV004942724]	uncertain significance	11	119315170	119315170	Human		name
15138898	CV712643	single nucleotide variant	NM_006500.3(MCAM):c.1719G>A (p.Ala573=)	not provided [RCV000965871]	benign	11	119310830	119310830	Human		name
155976253	CV2236013	single nucleotide variant	NM_006500.3(MCAM):c.440G>A (p.Gly147Asp)	not specified [RCV004113881]	uncertain significance	11	119314710	119314710	Human		name
156083954	CV2244511	single nucleotide variant	NM_006500.3(MCAM):c.827G>C (p.Gly276Ala)	not specified [RCV004100465]	uncertain significance	11	119312561	119312561	Human		name
156292609	CV2246694	single nucleotide variant	NM_006500.3(MCAM):c.705G>A (p.Met235Ile)	not specified [RCV004110421]	uncertain significance	11	119312804	119312804	Human		name
155919862	CV2254945	single nucleotide variant	NM_006500.3(MCAM):c.391C>T (p.Arg131Cys)	not specified [RCV004117179]	uncertain significance	11	119314842	119314842	Human		name
156047903	CV2271684	single nucleotide variant	NM_006500.3(MCAM):c.901G>A (p.Asp301Asn)	not specified [RCV004130536]	uncertain significance	11	119312389	119312389	Human		name
156170594	CV2317150	single nucleotide variant	NM_006500.3(MCAM):c.877G>A (p.Glu293Lys)	not specified [RCV004174618]	uncertain significance	11	119312413	119312413	Human		name
155905006	CV2349651	single nucleotide variant	NM_006500.3(MCAM):c.458A>T (p.Lys153Met)	not specified [RCV004204070]	uncertain significance	11	119314692	119314692	Human		name
155902723	CV2356515	single nucleotide variant	NM_006500.3(MCAM):c.319A>T (p.Thr107Ser)	not specified [RCV004199429]	uncertain significance	11	119314914	119314914	Human		name
156155136	CV2359696	single nucleotide variant	NM_006500.3(MCAM):c.794G>A (p.Gly265Glu)	not specified [RCV004210519]	uncertain significance	11	119312594	119312594	Human		name
156093559	CV2389713	single nucleotide variant	NM_006500.3(MCAM):c.907G>A (p.Gly303Arg)	not specified [RCV004243762]	uncertain significance	11	119312383	119312383	Human		name
329356717	CV2430871	single nucleotide variant	NM_006500.3(MCAM):c.775G>C (p.Val259Leu)	not specified [RCV004248073]	uncertain significance	11	119312613	119312613	Human		name
401730720	CV2677271	single nucleotide variant	NM_006500.3(MCAM):c.683G>A (p.Arg228Gln)	not specified [RCV004295891]	uncertain significance	11	119312826	119312826	Human		name
401883683	CV2754932	single nucleotide variant	NM_006500.3(MCAM):c.743C>T (p.Pro248Leu)	not specified [RCV004341401]	uncertain significance	11	119312645	119312645	Human		name
401865017	CV2757381	single nucleotide variant	NM_006500.3(MCAM):c.989C>G (p.Ser330Trp)	not specified [RCV004340782]	uncertain significance	11	119312301	119312301	Human		name
401856953	CV2759885	single nucleotide variant	NM_006500.3(MCAM):c.457A>G (p.Lys153Glu)	not specified [RCV004345312]	likely benign	11	119314693	119314693	Human		name
401887280	CV2771856	single nucleotide variant	NM_006500.3(MCAM):c.536G>A (p.Arg179Gln)	not specified [RCV004344575]	uncertain significance	11	119314512	119314512	Human		name
401882455	CV2781513	single nucleotide variant	NM_006500.3(MCAM):c.926C>G (p.Pro309Arg)	not specified [RCV004354745]	uncertain significance	11	119312364	119312364	Human		name
401882452	CV2781514	single nucleotide variant	NM_006500.3(MCAM):c.949C>A (p.Arg317Ser)	not specified [RCV004354746]	uncertain significance	11	119312341	119312341	Human		name
405668658	CV3278301	single nucleotide variant	NM_006500.3(MCAM):c.335G>A (p.Arg112His)	not specified [RCV004419046]	uncertain significance	11	119314898	119314898	Human		name
405668662	CV3278302	single nucleotide variant	NM_006500.3(MCAM):c.950G>A (p.Arg317His)	not specified [RCV004419047]	uncertain significance	11	119312340	119312340	Human		name
407473177	CV3457145	single nucleotide variant	NM_006500.3(MCAM):c.380G>A (p.Arg127His)	not specified [RCV004637790]	uncertain significance	11	119314853	119314853	Human		name
597648026	CV3703003	single nucleotide variant	NM_006500.3(MCAM):c.533G>T (p.Gly178Val)	not specified [RCV004942718]	uncertain significance	11	119314515	119314515	Human		name
597648046	CV3703006	single nucleotide variant	NM_006500.3(MCAM):c.407C>T (p.Pro136Leu)	not specified [RCV004942721]	uncertain significance	11	119314743	119314743	Human		name
597648100	CV3703013	single nucleotide variant	NM_006500.3(MCAM):c.976G>A (p.Asp326Asn)	not specified [RCV004942728]	uncertain significance	11	119312314	119312314	Human		name
597648134	CV3703018	single nucleotide variant	NM_006500.3(MCAM):c.519C>G (p.Ile173Met)	not specified [RCV004942733]	uncertain significance	11	119314529	119314529	Human		name
598210559	CV3992615	single nucleotide variant	NM_006500.3(MCAM):c.765A>C (p.Glu255Asp)	not specified [RCV005377882]	uncertain significance	11	119312623	119312623	Human		name
598178454	CV3992616	single nucleotide variant	NM_006500.3(MCAM):c.345G>C (p.Leu115Phe)	not specified [RCV005371775]	uncertain significance	11	119314888	119314888	Human		name
15154484	CV724247	single nucleotide variant	NM_006500.3(MCAM):c.929C>T (p.Ala310Val)	not provided [RCV000880225]	likely benign	11	119312361	119312361	Human		name
156026536	CV2271074	single nucleotide variant	NM_006500.3(MCAM):c.1796C>T (p.Thr599Met)	not specified [RCV004134464]	uncertain significance	11	119310464	119310464	Human		name
156162388	CV2323529	single nucleotide variant	NM_006500.3(MCAM):c.1715T>C (p.Leu572Pro)	not specified [RCV004165731]	uncertain significance	11	119310834	119310834	Human		name
156332469	CV2339786	single nucleotide variant	NM_006500.3(MCAM):c.1637C>A (p.Thr546Asn)	not specified [RCV004196482]	uncertain significance	11	119311098	119311098	Human		name
155902155	CV2356401	single nucleotide variant	NM_006500.3(MCAM):c.1217G>A (p.Arg406His)	not specified [RCV004206202]	uncertain significance	11	119311876	119311876	Human		name
155992502	CV2379319	single nucleotide variant	NM_006500.3(MCAM):c.1757G>A (p.Gly586Asp)	not specified [RCV004223782]	uncertain significance	11	119310792	119310792	Human		name
156003188	CV2396708	single nucleotide variant	NM_006500.3(MCAM):c.1811G>A (p.Arg604His)	not specified [RCV004233863]	uncertain significance	11	119310449	119310449	Human		name
329399239	CV2436457	single nucleotide variant	NM_006500.3(MCAM):c.1060G>A (p.Glu354Lys)	not specified [RCV004251838]	uncertain significance	11	119312135	119312135	Human		name
329388207	CV2437204	single nucleotide variant	NM_006500.3(MCAM):c.1718C>T (p.Ala573Val)	not specified [RCV004256096]	uncertain significance	11	119310831	119310831	Human		name
329398762	CV2442773	single nucleotide variant	NM_006500.3(MCAM):c.1415A>T (p.Glu472Val)	not specified [RCV004251604]	uncertain significance	11	119311414	119311414	Human		name
329401898	CV2457493	single nucleotide variant	NM_006500.3(MCAM):c.1543G>A (p.Glu515Lys)	not specified [RCV004267307]	uncertain significance	11	119311286	119311286	Human		name
401872291	CV2779453	single nucleotide variant	NM_006500.3(MCAM):c.1271A>T (p.Asn424Ile)	not specified [RCV004351088]	uncertain significance	11	119311822	119311822	Human		name
401861619	CV2779956	single nucleotide variant	NM_006500.3(MCAM):c.1846A>G (p.Lys616Glu)	not specified [RCV004353550]	uncertain significance	11	119310414	119310414	Human		name
405668612	CV3278292	single nucleotide variant	NM_006500.3(MCAM):c.1187A>G (p.Asp396Gly)	not specified [RCV004419037]	uncertain significance	11	119311906	119311906	Human		name
405668618	CV3278293	single nucleotide variant	NM_006500.3(MCAM):c.1243C>G (p.Pro415Ala)	not specified [RCV004419038]	uncertain significance	11	119311850	119311850	Human		name
405668622	CV3278294	single nucleotide variant	NM_006500.3(MCAM):c.1304T>A (p.Phe435Tyr)	not specified [RCV004419039]	uncertain significance	11	119311633	119311633	Human		name
405668629	CV3278295	single nucleotide variant	NM_006500.3(MCAM):c.1339G>C (p.Val447Leu)	not specified [RCV004419040]	uncertain significance	11	119311598	119311598	Human		name
405668633	CV3278296	single nucleotide variant	NM_006500.3(MCAM):c.1412G>A (p.Ser471Asn)	not specified [RCV004419041]	uncertain significance	11	119311417	119311417	Human		name
405668639	CV3278297	single nucleotide variant	NM_006500.3(MCAM):c.1658C>T (p.Pro553Leu)	not specified [RCV004419042]	uncertain significance	11	119310891	119310891	Human		name
405668645	CV3278298	single nucleotide variant	NM_006500.3(MCAM):c.1664C>T (p.Pro555Leu)	not specified [RCV004419043]	uncertain significance	11	119310885	119310885	Human		name
405668650	CV3278299	single nucleotide variant	NM_006500.3(MCAM):c.1697T>C (p.Ile566Thr)	not specified [RCV004419044]	likely benign	11	119310852	119310852	Human		name
407473171	CV3457144	single nucleotide variant	NM_006500.3(MCAM):c.1267G>A (p.Val423Ile)	not specified [RCV004637789]	uncertain significance	11	119311826	119311826	Human		name
407473190	CV3457150	single nucleotide variant	NM_006500.3(MCAM):c.1801C>A (p.Pro601Thr)	not specified [RCV004637793]	uncertain significance	11	119310459	119310459	Human		name
407469423	CV3457151	single nucleotide variant	NM_006500.3(MCAM):c.1417C>G (p.Gln473Glu)	not specified [RCV004636625]	uncertain significance	11	119311412	119311412	Human		name
407473194	CV3457152	single nucleotide variant	NM_006500.3(MCAM):c.1361C>T (p.Ala454Val)	not specified [RCV004637794]	uncertain significance	11	119311576	119311576	Human		name
597648005	CV3703000	single nucleotide variant	NM_006500.3(MCAM):c.1874A>C (p.Gln625Pro)	not specified [RCV004942715]	uncertain significance	11	119310386	119310386	Human		name
597648019	CV3703002	single nucleotide variant	NM_006500.3(MCAM):c.1733T>C (p.Val578Ala)	not specified [RCV004942717]	uncertain significance	11	119310816	119310816	Human		name
597648038	CV3703005	single nucleotide variant	NM_006500.3(MCAM):c.1673G>A (p.Arg558Gln)	not specified [RCV004942720]	likely benign	11	119310876	119310876	Human		name
597648053	CV3703007	single nucleotide variant	NM_006500.3(MCAM):c.1172T>A (p.Val391Glu)	not specified [RCV004942722]	uncertain significance	11	119311921	119311921	Human		name
597648079	CV3703010	single nucleotide variant	NM_006500.3(MCAM):c.1198G>A (p.Glu400Lys)	not specified [RCV004942725]	uncertain significance	11	119311895	119311895	Human		name
597648093	CV3703012	single nucleotide variant	NM_006500.3(MCAM):c.1214A>G (p.Tyr405Cys)	not specified [RCV004942727]	uncertain significance	11	119311879	119311879	Human		name
597648106	CV3703014	single nucleotide variant	NM_006500.3(MCAM):c.1618C>T (p.His540Tyr)	not specified [RCV004942729]	uncertain significance	11	119311117	119311117	Human		name
597648120	CV3703016	single nucleotide variant	NM_006500.3(MCAM):c.1148G>C (p.Gly383Ala)	not specified [RCV004942731]	uncertain significance	11	119311945	119311945	Human		name
597648126	CV3703017	single nucleotide variant	NM_006500.3(MCAM):c.1848G>T (p.Lys616Asn)	not specified [RCV004942732]	uncertain significance	11	119310412	119310412	Human		name
598210537	CV3992612	single nucleotide variant	NM_006500.3(MCAM):c.1577C>T (p.Ser526Phe)	not specified [RCV005377879]	uncertain significance	11	119311158	119311158	Human		name
598210545	CV3992613	single nucleotide variant	NM_006500.3(MCAM):c.1315A>C (p.Lys439Gln)	not specified [RCV005377880]	uncertain significance	11	119311622	119311622	Human		name
598210552	CV3992614	single nucleotide variant	NM_006500.3(MCAM):c.1382C>T (p.Thr461Ile)	not specified [RCV005377881]	uncertain significance	11	119311555	119311555	Human		name
598210566	CV3992617	single nucleotide variant	NM_006500.3(MCAM):c.1273G>A (p.Val425Met)	not specified [RCV005377883]	uncertain significance	11	119311820	119311820	Human		name
598178461	CV3992618	single nucleotide variant	NM_006500.3(MCAM):c.1487G>A (p.Gly496Asp)	not specified [RCV005371776]	uncertain significance	11	119311342	119311342	Human		name
598210573	CV3992619	single nucleotide variant	NM_006500.3(MCAM):c.1511A>G (p.Asp504Gly)	not specified [RCV005377884]	uncertain significance	11	119311318	119311318	Human		name
15138904	CV712644	single nucleotide variant	NM_006500.3(MCAM):c.1180T>A (p.Leu394Met)	not provided [RCV000965872]	benign	11	119311913	119311913	Human		name

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