Lman1l Variant Search Result - Rat Genome Database

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56 records found for search term Lman1l

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155922735	CV2340673	single nucleotide variant	NM_021819.3(LMAN1L):c.8C>T (p.Ala3Val)	not specified [RCV004190346]	likely benign	15	74812862	74812862	Human		name
597623142	CV3693255	single nucleotide variant	NM_021819.3(LMAN1L):c.5C>T (p.Pro2Leu)	not specified [RCV004936175]	likely benign	15	74812859	74812859	Human		name
156224085	CV2395077	single nucleotide variant	NM_021819.3(LMAN1L):c.32T>C (p.Phe11Ser)	not specified [RCV004236761]	uncertain significance	15	74812886	74812886	Human		name
329370038	CV2424963	single nucleotide variant	NM_021819.3(LMAN1L):c.55G>A (p.Asp19Asn)	not specified [RCV004250629]	uncertain significance	15	74812909	74812909	Human		name
401751634	CV2708751	single nucleotide variant	NM_021819.3(LMAN1L):c.47T>G (p.Leu16Arg)	not specified [RCV004307717]	uncertain significance	15	74812901	74812901	Human		name
407470746	CV3449168	single nucleotide variant	NM_021819.3(LMAN1L):c.30A>T (p.Leu10Phe)	not specified [RCV004637184]	uncertain significance	15	74812884	74812884	Human		name
597623139	CV3693250	single nucleotide variant	NM_021819.3(LMAN1L):c.92G>A (p.Arg31His)	not specified [RCV004936172]	uncertain significance	15	74812946	74812946	Human		name
329396176	CV2459375	single nucleotide variant	NM_021819.3(LMAN1L):c.284T>C (p.Val95Ala)	not specified [RCV004275074]	uncertain significance	15	74816265	74816265	Human		name
401782143	CV2686555	single nucleotide variant	NM_021819.3(LMAN1L):c.179C>T (p.Ala60Val)	not specified [RCV004299988]	uncertain significance	15	74816160	74816160	Human		name
401782145	CV2686556	single nucleotide variant	NM_021819.3(LMAN1L):c.185T>A (p.Leu62Gln)	not specified [RCV004299989]	uncertain significance	15	74816166	74816166	Human		name
405809501	CV3287588	single nucleotide variant	NM_021819.3(LMAN1L):c.148G>A (p.Gly50Arg)	not specified [RCV004407550]	uncertain significance	15	74813002	74813002	Human		name
407470742	CV3449167	single nucleotide variant	NM_021819.3(LMAN1L):c.163A>G (p.Ser55Gly)	not specified [RCV004637183]	uncertain significance	15	74813017	74813017	Human		name
597623143	CV3693256	single nucleotide variant	NM_021819.3(LMAN1L):c.203G>A (p.Arg68Gln)	not specified [RCV004936176]	uncertain significance	15	74816184	74816184	Human		name
598237869	CV3980991	single nucleotide variant	NM_021819.3(LMAN1L):c.238G>A (p.Val80Met)	not specified [RCV005364154]	uncertain significance	15	74816219	74816219	Human		name
598261033	CV3980995	single nucleotide variant	NM_021819.3(LMAN1L):c.203G>C (p.Arg68Pro)	not specified [RCV005347749]	uncertain significance	15	74816184	74816184	Human		name
8635573	CV90795	single nucleotide variant	NM_021819.2(LMAN1L):c.259C>T (p.Pro87Ser)	Malignant melanoma [RCV000070893]	not provided	15	74816240	74816240	Human		name
156065675	CV2240311	single nucleotide variant	NM_021819.3(LMAN1L):c.812G>A (p.Arg271His)	not specified [RCV004112866]	uncertain significance	15	74820672	74820672	Human		name
156283437	CV2288898	single nucleotide variant	NM_021819.3(LMAN1L):c.404G>T (p.Gly135Val)	not specified [RCV004149872]	uncertain significance	15	74816500	74816500	Human		name
156150344	CV2307474	single nucleotide variant	NM_021819.3(LMAN1L):c.697G>A (p.Ala233Thr)	not specified [RCV004166132]	uncertain significance	15	74819251	74819251	Human		name
156162534	CV2319557	single nucleotide variant	NM_021819.3(LMAN1L):c.692T>A (p.Val231Asp)	not specified [RCV004185120]	uncertain significance	15	74819246	74819246	Human		name
155973892	CV2333248	single nucleotide variant	NM_021819.3(LMAN1L):c.952C>G (p.Arg318Gly)	not specified [RCV004196578]	uncertain significance	15	74821119	74821119	Human		name
156037151	CV2374044	single nucleotide variant	NM_021819.3(LMAN1L):c.935C>T (p.Thr312Met)	not specified [RCV004227168]	uncertain significance	15	74821102	74821102	Human		name
329381668	CV2471272	single nucleotide variant	NM_021819.3(LMAN1L):c.949C>T (p.Arg317Cys)	not specified [RCV004280295]	uncertain significance	15	74821116	74821116	Human		name
401774550	CV2691776	single nucleotide variant	NM_021819.3(LMAN1L):c.305T>G (p.Leu102Arg)	not specified [RCV004299228]	uncertain significance	15	74816286	74816286	Human		name
401877566	CV2761188	single nucleotide variant	NM_021819.3(LMAN1L):c.299C>T (p.Thr100Met)	not specified [RCV004341073]	uncertain significance	15	74816280	74816280	Human		name
401896393	CV2781236	single nucleotide variant	NM_021819.3(LMAN1L):c.970C>T (p.Arg324Trp)	not specified [RCV004352272]	uncertain significance	15	74821137	74821137	Human		name
405809506	CV3287590	single nucleotide variant	NM_021819.3(LMAN1L):c.371T>C (p.Val124Ala)	not specified [RCV004407552]	uncertain significance	15	74816467	74816467	Human		name
405809508	CV3287591	single nucleotide variant	NM_021819.3(LMAN1L):c.514G>A (p.Gly172Arg)	not specified [RCV004407553]	uncertain significance	15	74818734	74818734	Human		name
405809510	CV3287592	single nucleotide variant	NM_021819.3(LMAN1L):c.595C>T (p.Arg199Cys)	not specified [RCV004407554]	uncertain significance	15	74818815	74818815	Human		name
405809512	CV3287593	single nucleotide variant	NM_021819.3(LMAN1L):c.679G>A (p.Gly227Ser)	not specified [RCV004407555]	uncertain significance	15	74819233	74819233	Human		name
405809517	CV3287595	single nucleotide variant	NM_021819.3(LMAN1L):c.831A>C (p.Glu277Asp)	not specified [RCV004407557]	uncertain significance	15	74820691	74820691	Human		name
405809519	CV3287596	single nucleotide variant	NM_021819.3(LMAN1L):c.971G>A (p.Arg324Gln)	not specified [RCV004407558]	likely benign	15	74821138	74821138	Human		name
405809521	CV3287597	single nucleotide variant	NM_021819.3(LMAN1L):c.997G>A (p.Ala333Thr)	not specified [RCV004407559]	uncertain significance	15	74821164	74821164	Human		name
597795898	CV3693251	single nucleotide variant	NM_021819.3(LMAN1L):c.595C>A (p.Arg199Ser)	not specified [RCV004935032]	uncertain significance	15	74818815	74818815	Human		name
597623140	CV3693252	single nucleotide variant	NM_021819.3(LMAN1L):c.526T>C (p.Cys176Arg)	not specified [RCV004936173]	uncertain significance	15	74818746	74818746	Human		name
597795901	CV3693253	single nucleotide variant	NM_021819.3(LMAN1L):c.950G>C (p.Arg317Pro)	not specified [RCV004935033]	uncertain significance	15	74821117	74821117	Human		name
598261014	CV3980989	single nucleotide variant	NM_021819.3(LMAN1L):c.950G>A (p.Arg317His)	not specified [RCV005347745]	uncertain significance	15	74821117	74821117	Human		name
598261024	CV3980992	single nucleotide variant	NM_021819.3(LMAN1L):c.355G>A (p.Gly119Ser)	not specified [RCV005347747]	uncertain significance	15	74816451	74816451	Human		name
598261029	CV3980993	single nucleotide variant	NM_021819.3(LMAN1L):c.992C>T (p.Ala331Val)	not specified [RCV005347748]	uncertain significance	15	74821159	74821159	Human		name
9687068	CV171562	single nucleotide variant	NM_021819.3(LMAN1L):c.1338G>T (p.Lys446Asn)	Prostate cancer [RCV000149287]	uncertain significance	15	74824365	74824365	Human	2	name
156249522	CV2222129	single nucleotide variant	NM_021819.3(LMAN1L):c.1385A>G (p.Gln462Arg)	not specified [RCV004104887]	likely benign	15	74824412	74824412	Human		name
156299450	CV2248646	single nucleotide variant	NM_021819.3(LMAN1L):c.1213C>T (p.Arg405Cys)	not specified [RCV004121828]	uncertain significance	15	74823572	74823572	Human		name
156282573	CV2252414	single nucleotide variant	NM_021819.3(LMAN1L):c.1234G>A (p.Val412Ile)	not specified [RCV004116254]	uncertain significance	15	74823593	74823593	Human		name
156190792	CV2301757	single nucleotide variant	NM_021819.3(LMAN1L):c.1360C>A (p.Pro454Thr)	not specified [RCV004156570]	uncertain significance	15	74824387	74824387	Human		name
155908866	CV2307165	single nucleotide variant	NM_021819.3(LMAN1L):c.1532C>G (p.Ala511Gly)	not specified [RCV004159640]	uncertain significance	15	74825556	74825556	Human		name
156164546	CV2323682	single nucleotide variant	NM_021819.3(LMAN1L):c.1487C>T (p.Ser496Phe)	not specified [RCV004165860]	uncertain significance	15	74825511	74825511	Human		name
156172955	CV2326814	single nucleotide variant	NM_021819.3(LMAN1L):c.1214G>A (p.Arg405His)	not specified [RCV004176649]	likely benign	15	74823573	74823573	Human		name
156180372	CV2331453	single nucleotide variant	NM_021819.3(LMAN1L):c.1051G>A (p.Gly351Arg)	not specified [RCV004184085]	uncertain significance	15	74821218	74821218	Human		name
401774868	CV2688316	single nucleotide variant	NM_021819.3(LMAN1L):c.1470C>A (p.Ser490Arg)	not specified [RCV004299323]	likely benign	15	74825494	74825494	Human		name
401757091	CV2692804	single nucleotide variant	NM_021819.3(LMAN1L):c.1127A>G (p.Asn376Ser)	not specified [RCV004306348]	likely benign	15	74821896	74821896	Human		name
401879750	CV2769721	single nucleotide variant	NM_021819.3(LMAN1L):c.1192G>A (p.Glu398Lys)	not specified [RCV004351639]	uncertain significance	15	74822702	74822702	Human		name
405809497	CV3287586	single nucleotide variant	NM_021819.3(LMAN1L):c.1313G>A (p.Arg438Gln)	not specified [RCV004407548]	likely benign	15	74823672	74823672	Human		name
405809504	CV3287589	single nucleotide variant	NM_021819.3(LMAN1L):c.1555C>T (p.Pro519Ser)	not specified [RCV004407551]	uncertain significance	15	74825579	74825579	Human		name
598230438	CV3980994	single nucleotide variant	NM_021819.3(LMAN1L):c.1291G>T (p.Gly431Cys)	not specified [RCV005362705]	uncertain significance	15	74823650	74823650	Human		name
598237875	CV3980996	single nucleotide variant	NM_021819.3(LMAN1L):c.1265A>G (p.His422Arg)	not specified [RCV005364155]	uncertain significance	15	74823624	74823624	Human		name
8635574	CV90796	single nucleotide variant	NM_021819.2(LMAN1L):c.1352C>T (p.Pro451Leu)	Malignant melanoma [RCV000070894]	not provided	15	74824379	74824379	Human		name

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