Msgn1 Variant Search Result - Rat Genome Database

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31 records found for search term Msgn1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156288497	CV2299201	single nucleotide variant	NM_001105569.3(MSGN1):c.18G>C (p.Glu6Asp)	not specified [RCV004152537]	uncertain significance	2	17816536	17816536	Human		name
401769693	CV2689893	single nucleotide variant	NM_001105569.3(MSGN1):c.11T>G (p.Leu4Arg)	not specified [RCV004297787]	uncertain significance	2	17816529	17816529	Human		name
598179647	CV3993683	single nucleotide variant	NM_001105569.3(MSGN1):c.13C>A (p.Arg5Ser)	not specified [RCV005371971]	uncertain significance	2	17816531	17816531	Human		name
401742705	CV2677659	single nucleotide variant	NM_001105569.3(MSGN1):c.82G>T (p.Asp28Tyr)	not specified [RCV004291745]	uncertain significance	2	17816600	17816600	Human		name
405789499	CV3372084	single nucleotide variant	NM_001105569.3(MSGN1):c.28A>G (p.Ser10Gly)	not specified [RCV004505503]	likely benign	2	17816546	17816546	Human		name
597635768	CV3557623	single nucleotide variant	NM_001105569.3(MSGN1):c.97G>A (p.Ala33Thr)	not specified [RCV004831135]	uncertain significance	2	17816615	17816615	Human		name
597638539	CV3557625	single nucleotide variant	NM_001105569.3(MSGN1):c.55G>A (p.Asp19Asn)	not specified [RCV004824911]	uncertain significance	2	17816573	17816573	Human		name
8629982	CV85129	single nucleotide variant	NM_001105569.1(MSGN1):c.369C>G (p.Val123=)	Malignant melanoma [RCV000065211]	not provided	2	17816887	17816887	Human		name
156382187	CV2212625	single nucleotide variant	NM_001105569.3(MSGN1):c.253G>A (p.Gly85Ser)	not specified [RCV004085160]	uncertain significance	2	17816771	17816771	Human		name
156084389	CV2249259	single nucleotide variant	NM_001105569.3(MSGN1):c.167A>C (p.Tyr56Ser)	not specified [RCV004118292]	uncertain significance	2	17816685	17816685	Human		name
155983821	CV2344348	single nucleotide variant	NM_001105569.3(MSGN1):c.120G>C (p.Gln40His)	not specified [RCV004195105]	uncertain significance	2	17816638	17816638	Human		name
329393870	CV2472176	single nucleotide variant	NM_001105569.3(MSGN1):c.137G>A (p.Ser46Asn)	not specified [RCV004283298]	uncertain significance	2	17816655	17816655	Human		name
407475248	CV3450540	single nucleotide variant	NM_001105569.3(MSGN1):c.287A>G (p.Asn96Ser)	not specified [RCV004638329]	uncertain significance	2	17816805	17816805	Human		name
597635773	CV3557622	single nucleotide variant	NM_001105569.3(MSGN1):c.113T>C (p.Leu38Pro)	not specified [RCV004831134]	uncertain significance	2	17816631	17816631	Human		name
597635579	CV3557627	single nucleotide variant	NM_001105569.3(MSGN1):c.149C>G (p.Ala50Gly)	not specified [RCV004831138]	uncertain significance	2	17816667	17816667	Human		name
598179639	CV3993680	single nucleotide variant	NM_001105569.3(MSGN1):c.122C>T (p.Ala41Val)	not specified [RCV005371969]	uncertain significance	2	17816640	17816640	Human		name
156229196	CV2199470	single nucleotide variant	NM_001105569.3(MSGN1):c.352A>G (p.Lys118Glu)	not specified [RCV004071027]	uncertain significance	2	17816870	17816870	Human		name
155934424	CV2225288	single nucleotide variant	NM_001105569.3(MSGN1):c.551G>A (p.Arg184His)	not specified [RCV004098931]	uncertain significance	2	17817069	17817069	Human		name
156346046	CV2356485	single nucleotide variant	NM_001105569.3(MSGN1):c.475G>A (p.Gly159Ser)	not specified [RCV004199402]	uncertain significance	2	17816993	17816993	Human		name
401765348	CV2712665	single nucleotide variant	NM_001105569.3(MSGN1):c.320G>A (p.Gly107Asp)	not specified [RCV004307984]	uncertain significance	2	17816838	17816838	Human		name
405789529	CV3372091	single nucleotide variant	NM_001105569.3(MSGN1):c.460G>A (p.Val154Ile)	not specified [RCV004505510]	uncertain significance	2	17816978	17816978	Human		name
405789549	CV3372096	single nucleotide variant	NM_001105569.3(MSGN1):c.550C>T (p.Arg184Cys)	not specified [RCV004505515]	uncertain significance	2	17817068	17817068	Human		name
405789571	CV3372101	single nucleotide variant	NM_001105569.3(MSGN1):c.577G>A (p.Ala193Thr)	not specified [RCV004505520]	uncertain significance	2	17817095	17817095	Human		name
407475120	CV3450539	single nucleotide variant	NM_001105569.3(MSGN1):c.305C>A (p.Pro102His)	not specified [RCV004638328]	uncertain significance	2	17816823	17816823	Human		name
597635778	CV3557621	single nucleotide variant	NM_001105569.3(MSGN1):c.323G>T (p.Gly108Val)	not specified [RCV004831133]	uncertain significance	2	17816841	17816841	Human		name
597635762	CV3557624	single nucleotide variant	NM_001105569.3(MSGN1):c.374G>A (p.Arg125Gln)	not specified [RCV004831136]	uncertain significance	2	17816892	17816892	Human		name
597635757	CV3557626	single nucleotide variant	NM_001105569.3(MSGN1):c.524T>C (p.Ile175Thr)	not specified [RCV004831137]	uncertain significance	2	17817042	17817042	Human		name
598179644	CV3993681	single nucleotide variant	NM_001105569.3(MSGN1):c.468C>G (p.Ser156Arg)	not specified [RCV005371970]	uncertain significance	2	17816986	17816986	Human		name
598213746	CV3993682	single nucleotide variant	NM_001105569.3(MSGN1):c.449A>G (p.Tyr150Cys)	not specified [RCV005378413]	uncertain significance	2	17816967	17816967	Human		name
8629981	CV85128	single nucleotide variant	NM_001105569.1(MSGN1):c.347G>A (p.Gly116Asp)	Malignant melanoma [RCV000065210]	not provided	2	17816865	17816865	Human		name
8629983	CV85130	single nucleotide variant	NM_001105569.1(MSGN1):c.370C>T (p.Gln124Ter)	Malignant melanoma [RCV000065212]	not provided	2	17816888	17816888	Human		name

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