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Variants search result for Homo sapiens
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66 records found for search term Mus81
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
11641470CV269843single nucleotide variantNM_025128.5(MUS81):c.1401+1G>Tnot provided [RCV000356408]uncertain significance116586514665865146Humanname
156274504CV2320031single nucleotide variantNM_025128.5(MUS81):c.34C>A (p.Pro12Thr)not specified [RCV004167893]uncertain significance116586078765860787Humanname
401748114CV2687686single nucleotide variantNM_025128.5(MUS81):c.43G>T (p.Ala15Ser)not specified [RCV004302681]uncertain significance116586079665860796Humanname
598229379CV3986844single nucleotide variantNM_025128.5(MUS81):c.98C>A (p.Thr33Asn)not specified [RCV005381011]uncertain significance116586085165860851Humanname
598263820CV3986845single nucleotide variantNM_025128.5(MUS81):c.46T>G (p.Cys16Gly)not specified [RCV005387579]uncertain significance116586079965860799Humanname
155992909CV2252071single nucleotide variantNM_025128.5(MUS81):c.100C>G (p.Arg34Gly)not specified [RCV004122100]uncertain significance116586085365860853Humanname
156311569CV2260199single nucleotide variantNM_025128.5(MUS81):c.164T>C (p.Leu55Pro)not specified [RCV004120976]uncertain significance116586100165861001Humanname
401747937CV2698888single nucleotide variantNM_025128.5(MUS81):c.142C>T (p.Arg48Cys)not specified [RCV004301646]uncertain significance116586097965860979Humanname
401772887CV2720400single nucleotide variantNM_025128.5(MUS81):c.271C>G (p.His91Asp)not specified [RCV004325705]uncertain significance116586135565861355Humanname
401894152CV2770357single nucleotide variantNM_025128.5(MUS81):c.278C>T (p.Pro93Leu)not specified [RCV004358009]uncertain significance116586136265861362Humanname
401909494CV2813360single nucleotide variantNM_025128.5(MUS81):c.1077T>C (p.Cys359=)not provided [RCV003398007]likely benign116586451465864514Humanname
401933231CV2813361single nucleotide variantNM_025128.5(MUS81):c.1477C>T (p.Leu493=)not provided [RCV003409301]likely benign116586529565865295Humanname
407508007CV3457949single nucleotide variantNM_025128.5(MUS81):c.167C>T (p.Pro56Leu)not specified [RCV004646983]uncertain significance116586100465861004Humanname
597644354CV3557868single nucleotide variantNM_025128.5(MUS81):c.269A>G (p.Asp90Gly)not specified [RCV004825949]uncertain significance116586135365861353Humanname
597644370CV3557870single nucleotide variantNM_025128.5(MUS81):c.119G>T (p.Arg40Leu)not specified [RCV004825951]uncertain significance116586087265860872Humanname
156331433CV2220525single nucleotide variantNM_025128.5(MUS81):c.877C>T (p.Arg293Trp)not specified [RCV004097746]uncertain significance116586363765863637Humanname
156218380CV2253946single nucleotide variantNM_025128.5(MUS81):c.440G>A (p.Arg147Gln)not specified [RCV004127620]likely benign116586203565862035Humanname
156288792CV2370699single nucleotide variantNM_025128.5(MUS81):c.844G>A (p.Gly282Arg)not specified [RCV004209103]uncertain significance116586360465863604Humanname
156057958CV2383311single nucleotide variantNM_025128.5(MUS81):c.341C>G (p.Ser114Cys)not specified [RCV004222355]uncertain significance116586142565861425Humanname
329376203CV2438025single nucleotide variantNM_025128.5(MUS81):c.356C>T (p.Pro119Leu)not specified [RCV004263731]uncertain significance116586195165861951Humanname
329351716CV2459319single nucleotide variantNM_025128.5(MUS81):c.401G>A (p.Arg134Gln)not specified [RCV004274735]uncertain significance116586199665861996Humanname
401741366CV2713476single nucleotide variantNM_025128.5(MUS81):c.931G>A (p.Val311Met)not specified [RCV004319081]uncertain significance116586369165863691Humanname
401892155CV2777280single nucleotide variantNM_025128.5(MUS81):c.524C>A (p.Ala175Asp)not specified [RCV004354298]uncertain significance116586244865862448Humanname
401891505CV2779175single nucleotide variantNM_025128.5(MUS81):c.992T>C (p.Ile331Thr)not specified [RCV004349083]uncertain significance116586383465863834Humanname
405692289CV3315237single nucleotide variantNM_025128.5(MUS81):c.620C>T (p.Pro207Leu)not specified [RCV004445567]uncertain significance116586307965863079Humanname
405692306CV3315240single nucleotide variantNM_025128.5(MUS81):c.707G>A (p.Gly236Glu)not specified [RCV004445570]uncertain significance116586316665863166Humanname
405692349CV3315249single nucleotide variantNM_025128.5(MUS81):c.885C>G (p.His295Gln)not specified [RCV004445579]uncertain significance116586364565863645Humanname
405692373CV3315254single nucleotide variantNM_025128.5(MUS81):c.991A>G (p.Ile331Val)not specified [RCV004445584]uncertain significance116586383365863833Humanname
407503841CV3457945single nucleotide variantNM_025128.5(MUS81):c.557G>A (p.Arg186His)not specified [RCV004645603]uncertain significance116586248165862481Humanname
407503844CV3457947single nucleotide variantNM_025128.5(MUS81):c.788G>A (p.Arg263Lys)not specified [RCV004645604]uncertain significance116586345165863451Humanname
407503847CV3457948single nucleotide variantNM_025128.5(MUS81):c.623A>G (p.Glu208Gly)not specified [RCV004645605]uncertain significance116586308265863082Humanname
597644361CV3557869single nucleotide variantNM_025128.5(MUS81):c.401G>C (p.Arg134Pro)not specified [RCV004825950]uncertain significance116586199665861996Humanname
597639999CV3557871single nucleotide variantNM_025128.5(MUS81):c.518G>C (p.Arg173Thr)not specified [RCV004825218]uncertain significance116586227865862278Humanname
597644396CV3557877single nucleotide variantNM_025128.5(MUS81):c.887T>G (p.Val296Gly)not specified [RCV004825955]uncertain significance116586364765863647Humanname
597644409CV3557879single nucleotide variantNM_025128.5(MUS81):c.302G>A (p.Ser101Asn)not specified [RCV004825957]uncertain significance116586138665861386Humanname
598229352CV3986838single nucleotide variantNM_025128.5(MUS81):c.616A>G (p.Thr206Ala)not specified [RCV005381006]uncertain significance116586307565863075Humanname
598229363CV3986840single nucleotide variantNM_025128.5(MUS81):c.641A>G (p.Gln214Arg)not specified [RCV005381008]uncertain significance116586310065863100Humanname
598229368CV3986841single nucleotide variantNM_025128.5(MUS81):c.688G>A (p.Gly230Arg)not specified [RCV005381009]uncertain significance116586314765863147Humanname
598229374CV3986842single nucleotide variantNM_025128.5(MUS81):c.979G>A (p.Val327Ile)not specified [RCV005381010]uncertain significance116586382165863821Humanname
156367303CV2203496single nucleotide variantNM_025128.5(MUS81):c.1256T>A (p.Leu419Gln)not specified [RCV004072706]uncertain significance116586479965864799Humanname
155965328CV2206427single nucleotide variantNM_025128.5(MUS81):c.1330A>G (p.Met444Val)not specified [RCV004078748]uncertain significance116586507465865074Humanname
155971472CV2227857single nucleotide variantNM_025128.5(MUS81):c.1064G>A (p.Arg355Gln)not specified [RCV004094496]uncertain significance116586450165864501Humanname
156269927CV2293394single nucleotide variantNM_025128.5(MUS81):c.1642G>A (p.Gly548Ser)not specified [RCV004150862]likely benign116586603865866038Humanname
156276022CV2318440single nucleotide variantNM_025128.5(MUS81):c.1568T>A (p.Ile523Asn)not specified [RCV004179593]uncertain significance116586587365865873Humanname
156169871CV2337399single nucleotide variantNM_025128.5(MUS81):c.1031T>G (p.Ile344Ser)not specified [RCV004187844]uncertain significance116586387365863873Humanname
156086000CV2340901single nucleotide variantNM_025128.5(MUS81):c.1237G>A (p.Ala413Thr)not specified [RCV004181398]uncertain significance116586478065864780Humanname
156099675CV2378968single nucleotide variantNM_025128.5(MUS81):c.1450G>A (p.Gly484Arg)not specified [RCV004233388]uncertain significance116586526865865268Humanname
329377390CV2462593single nucleotide variantNM_025128.5(MUS81):c.1625A>G (p.Gln542Arg)not specified [RCV004278540]uncertain significance116586602165866021Humanname
401727825CV2678489single nucleotide variantNM_025128.5(MUS81):c.1205C>T (p.Thr402Ile)not specified [RCV004292505]uncertain significance116586474865864748Humanname
401874004CV2757797single nucleotide variantNM_025128.5(MUS81):c.1129C>A (p.Leu377Ile)not specified [RCV004336944]uncertain significance116586456665864566Humanname
401881183CV2789506single nucleotide variantNM_025128.5(MUS81):c.1391T>C (p.Ile464Thr)not specified [RCV004360118]uncertain significance116586513565865135Humanname
405691877CV3319059single nucleotide variantNM_025128.5(MUS81):c.1310G>A (p.Gly437Glu)not specified [RCV004445500]uncertain significance116586505465865054Humanname
405691914CV3319065single nucleotide variantNM_025128.5(MUS81):c.1360C>T (p.Leu454Phe)not specified [RCV004445506]uncertain significance116586510465865104Humanname
405691968CV3319074single nucleotide variantNM_025128.5(MUS81):c.1498C>G (p.Pro500Ala)not specified [RCV004445515]uncertain significance116586531665865316Humanname
405691997CV3319079single nucleotide variantNM_025128.5(MUS81):c.1520A>G (p.Tyr507Cys)not specified [RCV004445520]uncertain significance116586582565865825Humanname
407508004CV3457946single nucleotide variantNM_025128.5(MUS81):c.1371T>A (p.Ser457Arg)not specified [RCV004646982]uncertain significance116586511565865115Humanname
597644376CV3557873single nucleotide variantNM_025128.5(MUS81):c.1247C>T (p.Thr416Met)not specified [RCV004825952]uncertain significance116586479065864790Humanname
597640010CV3557874single nucleotide variantNM_025128.5(MUS81):c.1091G>A (p.Arg364Gln)not specified [RCV004825220]uncertain significance116586452865864528Humanname
597644382CV3557875single nucleotide variantNM_025128.5(MUS81):c.1039G>A (p.Gly347Ser)not specified [RCV004825953]uncertain significance116586388165863881Humanname
597644389CV3557876single nucleotide variantNM_025128.5(MUS81):c.1146C>G (p.Ser382Arg)not specified [RCV004825954]uncertain significance116586458365864583Humanname
597644404CV3557878single nucleotide variantNM_025128.5(MUS81):c.1646C>T (p.Pro549Leu)not specified [RCV004825956]uncertain significance116586604265866042Humanname
598229357CV3986839single nucleotide variantNM_025128.5(MUS81):c.1036G>T (p.Asp346Tyr)not specified [RCV005381007]uncertain significance116586387865863878Humanname
598263823CV3986846single nucleotide variantNM_025128.5(MUS81):c.1358T>G (p.Leu453Arg)not specified [RCV005387580]uncertain significance116586510265865102Humanname
598229384CV3986847single nucleotide variantNM_025128.5(MUS81):c.1187G>T (p.Gly396Val)not specified [RCV005381012]uncertain significance116586473065864730Humanname
15199160CV701893single nucleotide variantNM_025128.5(MUS81):c.1168A>C (p.Asn390His)not provided [RCV000956962]benign116586460565864605Humanname
15183754CV724610single nucleotide variantNM_025128.5(MUS81):c.1409C>T (p.Ser470Leu)not provided [RCV000886294]benign116586522765865227Humanname