Slain2 Variant Search Result - Rat Genome Database

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63 records found for search term Slain2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8579941	CV114343	single nucleotide variant	NM_020846.1(SLAIN2):c.390-231A>T	Lung cancer [RCV000094866]	uncertain significance	4	48369618	48369618	Human		name
597739699	CV3599278	single nucleotide variant	NM_020846.2(SLAIN2):c.7G>A (p.Asp3Asn)	not specified [RCV004864519]	uncertain significance	4	48341746	48341746	Human		name
405765802	CV3332380	single nucleotide variant	NM_020846.2(SLAIN2):c.22G>T (p.Val8Leu)	not specified [RCV004456111]	uncertain significance	4	48341761	48341761	Human		name
401758189	CV2729580	single nucleotide variant	NM_020846.2(SLAIN2):c.29C>T (p.Ala10Val)	not specified [RCV004331848]	uncertain significance	4	48341768	48341768	Human		name
15196439	CV698531	single nucleotide variant	NM_020846.2(SLAIN2):c.897G>A (p.Arg299=)	not provided [RCV000956192]	benign	4	48382602	48382602	Human		name
156319826	CV2200601	single nucleotide variant	NM_020846.2(SLAIN2):c.223T>G (p.Ser75Ala)	not specified [RCV004078941]	uncertain significance	4	48341962	48341962	Human		name
156048597	CV2241692	single nucleotide variant	NM_020846.2(SLAIN2):c.281C>T (p.Ala94Val)	not specified [RCV004106637]	uncertain significance	4	48342020	48342020	Human		name
156360599	CV2269069	single nucleotide variant	NM_020846.2(SLAIN2):c.268G>C (p.Glu90Gln)	not specified [RCV004130250]	uncertain significance	4	48342007	48342007	Human		name
156191965	CV2335963	single nucleotide variant	NM_020846.2(SLAIN2):c.173C>T (p.Ser58Phe)	not specified [RCV004189572]	uncertain significance	4	48341912	48341912	Human		name
156281949	CV2363084	single nucleotide variant	NM_020846.2(SLAIN2):c.241T>G (p.Ser81Ala)	not specified [RCV004211210]	uncertain significance	4	48341980	48341980	Human		name
156392717	CV2386629	single nucleotide variant	NM_020846.2(SLAIN2):c.239G>C (p.Gly80Ala)	not specified [RCV004230971]	uncertain significance	4	48341978	48341978	Human		name
329355923	CV2430536	single nucleotide variant	NM_020846.2(SLAIN2):c.139G>C (p.Gly47Arg)	not specified [RCV004252122]	uncertain significance	4	48341878	48341878	Human		name
401727591	CV2678385	single nucleotide variant	NM_020846.2(SLAIN2):c.109G>A (p.Ala37Thr)	not specified [RCV004292413]	uncertain significance	4	48341848	48341848	Human		name
401865671	CV2755590	single nucleotide variant	NM_020846.2(SLAIN2):c.112G>A (p.Val38Met)	not specified [RCV004340163]	uncertain significance	4	48341851	48341851	Human		name
401857459	CV2759236	single nucleotide variant	NM_020846.2(SLAIN2):c.169C>T (p.Pro57Ser)	not specified [RCV004335834]	uncertain significance	4	48341908	48341908	Human		name
405765779	CV3332376	single nucleotide variant	NM_020846.2(SLAIN2):c.146C>G (p.Pro49Arg)	not specified [RCV004456107]	uncertain significance	4	48341885	48341885	Human		name
407502650	CV3477040	single nucleotide variant	NM_020846.2(SLAIN2):c.281C>G (p.Ala94Gly)	not specified [RCV004670025]	uncertain significance	4	48342020	48342020	Human		name
597739717	CV3599282	single nucleotide variant	NM_020846.2(SLAIN2):c.224C>T (p.Ser75Leu)	not specified [RCV004864523]	uncertain significance	4	48341963	48341963	Human		name
156380701	CV2208358	single nucleotide variant	NM_020846.2(SLAIN2):c.695G>C (p.Gly232Ala)	not specified [RCV004088791]	uncertain significance	4	48378052	48378052	Human		name
156331941	CV2220601	single nucleotide variant	NM_020846.2(SLAIN2):c.424A>T (p.Met142Leu)	not specified [RCV004097788]	uncertain significance	4	48369883	48369883	Human		name
156249164	CV2222078	single nucleotide variant	NM_020846.2(SLAIN2):c.829G>A (p.Asp277Asn)	not specified [RCV004104846]	uncertain significance	4	48379815	48379815	Human		name
155915831	CV2274412	single nucleotide variant	NM_020846.2(SLAIN2):c.754A>G (p.Ile252Val)	not specified [RCV004136784]	uncertain significance	4	48379740	48379740	Human		name
156292371	CV2306211	single nucleotide variant	NM_020846.2(SLAIN2):c.605C>T (p.Pro202Leu)	not specified [RCV004162952]	uncertain significance	4	48377962	48377962	Human		name
156225736	CV2400960	single nucleotide variant	NM_020846.2(SLAIN2):c.322G>C (p.Glu108Gln)	not specified [RCV004244245]	uncertain significance	4	48342061	48342061	Human		name
329373813	CV2434621	single nucleotide variant	NM_020846.2(SLAIN2):c.539C>T (p.Ala180Val)	not specified [RCV004248346]	uncertain significance	4	48377896	48377896	Human		name
329366613	CV2441749	single nucleotide variant	NM_020846.2(SLAIN2):c.434C>T (p.Ser145Leu)	not specified [RCV004261963]	uncertain significance	4	48369893	48369893	Human		name
329398880	CV2471767	single nucleotide variant	NM_020846.2(SLAIN2):c.560A>G (p.Tyr187Cys)	not specified [RCV004280811]	uncertain significance	4	48377917	48377917	Human		name
401738386	CV2714438	single nucleotide variant	NM_020846.2(SLAIN2):c.310G>T (p.Gly104Cys)	not specified [RCV004317967]	uncertain significance	4	48342049	48342049	Human		name
405765809	CV3332381	single nucleotide variant	NM_020846.2(SLAIN2):c.321C>A (p.Asp107Glu)	not specified [RCV004456112]	uncertain significance	4	48342060	48342060	Human		name
405765813	CV3332382	single nucleotide variant	NM_020846.2(SLAIN2):c.337C>G (p.Arg113Gly)	not specified [RCV004456113]	uncertain significance	4	48342076	48342076	Human		name
405765819	CV3332383	single nucleotide variant	NM_020846.2(SLAIN2):c.431A>G (p.Lys144Arg)	not specified [RCV004456114]	uncertain significance	4	48369890	48369890	Human		name
405765823	CV3332384	single nucleotide variant	NM_020846.2(SLAIN2):c.532A>G (p.Met178Val)	not specified [RCV004456115]	uncertain significance	4	48369991	48369991	Human		name
405765828	CV3332385	single nucleotide variant	NM_020846.2(SLAIN2):c.580A>G (p.Met194Val)	not specified [RCV004456116]	likely benign	4	48377937	48377937	Human		name
405765836	CV3332387	single nucleotide variant	NM_020846.2(SLAIN2):c.685A>T (p.Ile229Leu)	not specified [RCV004456118]	uncertain significance	4	48378042	48378042	Human		name
597739685	CV3599275	single nucleotide variant	NM_020846.2(SLAIN2):c.932G>A (p.Arg311Gln)	not specified [RCV004864516]	uncertain significance	4	48382637	48382637	Human		name
597739690	CV3599276	single nucleotide variant	NM_020846.2(SLAIN2):c.682C>T (p.Leu228Phe)	not specified [RCV004864517]	uncertain significance	4	48378039	48378039	Human		name
155918554	CV2236858	single nucleotide variant	NM_020846.2(SLAIN2):c.1349A>C (p.Gln450Pro)	not specified [RCV004112615]	uncertain significance	4	48383773	48383773	Human		name
156248623	CV2263996	single nucleotide variant	NM_020846.2(SLAIN2):c.1096T>C (p.Ser366Pro)	not specified [RCV004138021]	uncertain significance	4	48382801	48382801	Human		name
156361066	CV2269163	single nucleotide variant	NM_020846.2(SLAIN2):c.1060C>T (p.Pro354Ser)	not specified [RCV004130330]	uncertain significance	4	48382765	48382765	Human		name
155935967	CV2379740	single nucleotide variant	NM_020846.2(SLAIN2):c.1415G>A (p.Arg472Gln)	not specified [RCV004219860]	uncertain significance	4	48420179	48420179	Human		name
401780152	CV2676843	single nucleotide variant	NM_020846.2(SLAIN2):c.1000G>T (p.Ala334Ser)	not specified [RCV004291010]	uncertain significance	4	48382705	48382705	Human		name
401745176	CV2681208	single nucleotide variant	NM_020846.2(SLAIN2):c.1588A>G (p.Thr530Ala)	not specified [RCV004289348]	uncertain significance	4	48420352	48420352	Human		name
401760871	CV2695191	single nucleotide variant	NM_020846.2(SLAIN2):c.1625C>T (p.Pro542Leu)	not specified [RCV004303333]	uncertain significance	4	48420389	48420389	Human		name
401729998	CV2700355	single nucleotide variant	NM_020846.2(SLAIN2):c.1055C>T (p.Pro352Leu)	not specified [RCV004311011]	uncertain significance	4	48382760	48382760	Human		name
401863408	CV2765769	single nucleotide variant	NM_020846.2(SLAIN2):c.1513A>G (p.Met505Val)	not specified [RCV004335770]	likely benign	4	48420277	48420277	Human		name
405765761	CV3332373	single nucleotide variant	NM_020846.2(SLAIN2):c.1120A>G (p.Ser374Gly)	not specified [RCV004456104]	uncertain significance	4	48382825	48382825	Human		name
405765767	CV3332374	single nucleotide variant	NM_020846.2(SLAIN2):c.1206C>A (p.Ser402Arg)	not specified [RCV004456105]	uncertain significance	4	48382911	48382911	Human		name
405765772	CV3332375	single nucleotide variant	NM_020846.2(SLAIN2):c.1361T>C (p.Ile454Thr)	not specified [RCV004456106]	uncertain significance	4	48420125	48420125	Human		name
405765784	CV3332377	single nucleotide variant	NM_020846.2(SLAIN2):c.1568T>C (p.Leu523Pro)	not specified [RCV004456108]	uncertain significance	4	48420332	48420332	Human		name
405765792	CV3332378	single nucleotide variant	NM_020846.2(SLAIN2):c.1670C>G (p.Pro557Arg)	not specified [RCV004456109]	uncertain significance	4	48420434	48420434	Human		name
405765797	CV3332379	single nucleotide variant	NM_020846.2(SLAIN2):c.1715A>G (p.Lys572Arg)	not specified [RCV004456110]	uncertain significance	4	48422046	48422046	Human		name
407502636	CV3477036	single nucleotide variant	NM_020846.2(SLAIN2):c.1088G>A (p.Arg363His)	not specified [RCV004670021]	uncertain significance	4	48382793	48382793	Human		name
407502643	CV3477038	single nucleotide variant	NM_020846.2(SLAIN2):c.1705G>T (p.Gly569Cys)	not specified [RCV004670023]	uncertain significance	4	48422036	48422036	Human		name
407502647	CV3477039	single nucleotide variant	NM_020846.2(SLAIN2):c.1015G>A (p.Val339Ile)	not specified [RCV004670024]	uncertain significance	4	48382720	48382720	Human		name
597739694	CV3599277	single nucleotide variant	NM_020846.2(SLAIN2):c.1594A>T (p.Met532Leu)	not specified [RCV004864518]	uncertain significance	4	48420358	48420358	Human		name
597739703	CV3599279	single nucleotide variant	NM_020846.2(SLAIN2):c.1105C>T (p.Arg369Trp)	not specified [RCV004864520]	uncertain significance	4	48382810	48382810	Human		name
597739708	CV3599280	single nucleotide variant	NM_020846.2(SLAIN2):c.1306A>C (p.Asn436His)	not specified [RCV004864521]	uncertain significance	4	48383730	48383730	Human		name
597739712	CV3599281	single nucleotide variant	NM_020846.2(SLAIN2):c.1084C>T (p.Pro362Ser)	not specified [RCV004864522]	uncertain significance	4	48382789	48382789	Human		name
598259014	CV3910995	single nucleotide variant	NM_020846.2(SLAIN2):c.1631C>T (p.Ala544Val)	not specified [RCV005279499]	uncertain significance	4	48420395	48420395	Human		name
598259019	CV3910996	single nucleotide variant	NM_020846.2(SLAIN2):c.1703A>G (p.Tyr568Cys)	not specified [RCV005279500]	uncertain significance	4	48422034	48422034	Human		name
598259025	CV3910997	single nucleotide variant	NM_020846.2(SLAIN2):c.1636G>A (p.Gly546Ser)	not specified [RCV005279501]	uncertain significance	4	48420400	48420400	Human		name
8631197	CV86353	single nucleotide variant	NM_020846.1(SLAIN2):c.1496C>T (p.Ser499Phe)	Malignant melanoma [RCV000066444]	not provided	4	48420260	48420260	Human		name
8631198	CV86354	single nucleotide variant	NM_020846.1(SLAIN2):c.1628C>T (p.Ser543Phe)	Malignant melanoma [RCV000066445]	not provided	4	48420392	48420392	Human		name

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