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Variants search result for Homo sapiens
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59 records found for search term Kifc1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
12896638CV390551insertionNM_002263.4(KIFC1):c.*15_*16dupnot specified [RCV000455622]benign63340970333409704Humanname
401772788CV2719759single nucleotide variantNM_002263.4(KIFC1):c.19C>T (p.Pro7Ser)not specified [RCV004329193]uncertain significance63339803533398035Humanname
156127191CV2234617single nucleotide variantNM_002263.4(KIFC1):c.70G>T (p.Ala24Ser)not specified [RCV004102583]uncertain significance63339808633398086Humanname
155908486CV2387343single nucleotide variantNM_002263.4(KIFC1):c.44T>C (p.Ile15Thr)not specified [RCV004238426]likely benign63339806033398060Humanname
597768341CV3695337single nucleotide variantNM_002263.4(KIFC1):c.76T>A (p.Ser26Thr)not specified [RCV004927464]uncertain significance63339809233398092Humanname
156076798CV2230239single nucleotide variantNM_002263.4(KIFC1):c.274G>C (p.Gly92Arg)not specified [RCV004099860]uncertain significance63340333733403337Humanname
156287922CV2288442single nucleotide variantNM_002263.4(KIFC1):c.154C>T (p.Arg52Trp)not specified [RCV004151988]uncertain significance63339829133398291Humanname
405652890CV3269108single nucleotide variantNM_002263.4(KIFC1):c.114G>T (p.Arg38Ser)not specified [RCV004414362]uncertain significance63339813033398130Humanname
407524782CV3452230single nucleotide variantNM_002263.4(KIFC1):c.281G>A (p.Arg94Gln)not specified [RCV004631493]uncertain significance63340334433403344Humanname
598248825CV3991125single nucleotide variantNM_002263.4(KIFC1):c.277C>G (p.Pro93Ala)not specified [RCV005366285]uncertain significance63340334033403340Humanname
598220677CV3991129single nucleotide variantNM_002263.4(KIFC1):c.158C>T (p.Thr53Ile)not specified [RCV005360701]likely benign63339829533398295Humanname
156147586CV2196973single nucleotide variantNM_002263.4(KIFC1):c.448C>G (p.Leu150Val)not specified [RCV004071430]uncertain significance63340382133403821Humanname
155945451CV2237987single nucleotide variantNM_002263.4(KIFC1):c.866G>A (p.Arg289His)not specified [RCV004111024]uncertain significance63340496133404961Humanname
156040490CV2261301single nucleotide variantNM_002263.4(KIFC1):c.728G>T (p.Gly243Val)not specified [RCV004128163]uncertain significance63340410133404101Humanname
156299293CV2310717single nucleotide variantNM_002263.4(KIFC1):c.965C>T (p.Pro322Leu)not specified [RCV004157366]uncertain significance63340506033405060Humanname
156276985CV2328126single nucleotide variantNM_002263.4(KIFC1):c.994C>T (p.Leu332Phe)not specified [RCV004173234]uncertain significance63340508933405089Humanname
329397042CV2459856single nucleotide variantNM_002263.4(KIFC1):c.722G>A (p.Arg241Gln)not specified [RCV004279353]uncertain significance63340409533404095Humanname
401771708CV2693467single nucleotide variantNM_002263.4(KIFC1):c.841G>A (p.Ala281Thr)not specified [RCV004295414]likely benign63340493633404936Humanname
401885807CV2774544single nucleotide variantNM_002263.4(KIFC1):c.856C>T (p.Arg286Trp)not specified [RCV004350028]uncertain significance63340495133404951Humanname
405652921CV3269120single nucleotide variantNM_002263.4(KIFC1):c.716A>T (p.Glu239Val)not specified [RCV004414374]uncertain significance63340408933404089Humanname
405652924CV3269121single nucleotide variantNM_002263.4(KIFC1):c.779C>T (p.Ala260Val)not specified [RCV004414375]uncertain significance63340487433404874Humanname
597638101CV3695336single nucleotide variantNM_002263.4(KIFC1):c.401G>A (p.Arg134His)not specified [RCV004941095]uncertain significance63340377433403774Humanname
597638112CV3695339single nucleotide variantNM_002263.4(KIFC1):c.629G>C (p.Arg210Pro)not specified [RCV004941097]uncertain significance63340400233404002Humanname
597638116CV3695340single nucleotide variantNM_002263.4(KIFC1):c.317A>G (p.Gln106Arg)not specified [RCV004941098]uncertain significance63340349733403497Humanname
598248834CV3991126single nucleotide variantNM_002263.4(KIFC1):c.554G>A (p.Arg185His)not specified [RCV005366286]uncertain significance63340392733403927Humanname
598248840CV3991127single nucleotide variantNM_002263.4(KIFC1):c.409T>G (p.Trp137Gly)not specified [RCV005366287]uncertain significance63340378233403782Humanname
598248848CV3991130single nucleotide variantNM_002263.4(KIFC1):c.461G>A (p.Arg154His)not specified [RCV005366288]uncertain significance63340383433403834Humanname
598248856CV3991132single nucleotide variantNM_002263.4(KIFC1):c.461G>T (p.Arg154Leu)not specified [RCV005366289]uncertain significance63340383433403834Humanname
156043026CV2261506single nucleotide variantNM_002263.4(KIFC1):c.1493C>T (p.Thr498Ile)not specified [RCV004130124]likely benign63340558833405588Humanname
155966165CV2329771single nucleotide variantNM_002263.4(KIFC1):c.1735G>A (p.Gly579Ser)not specified [RCV004183242]uncertain significance63340639433406394Humanname
156198560CV2331073single nucleotide variantNM_002263.4(KIFC1):c.1385T>C (p.Val462Ala)not specified [RCV004181687]uncertain significance63340548033405480Humanname
156075084CV2377020single nucleotide variantNM_002263.4(KIFC1):c.1328C>G (p.Ser443Cys)not specified [RCV004229699]uncertain significance63340542333405423Humanname
329359069CV2450825single nucleotide variantNM_002263.4(KIFC1):c.1040G>A (p.Arg347His)not specified [RCV004267741]likely benign63340513533405135Humanname
329360381CV2458707single nucleotide variantNM_002263.4(KIFC1):c.1096C>A (p.Pro366Thr)not specified [RCV004268366]uncertain significance63340519133405191Humanname
401735441CV2672653single nucleotide variantNM_002263.4(KIFC1):c.1846C>T (p.Arg616Trp)not specified [RCV004287674]uncertain significance63340661033406610Humanname
401743757CV2696860single nucleotide variantNM_002263.4(KIFC1):c.1669T>C (p.Cys557Arg)not specified [RCV004290825]uncertain significance63340632833406328Humanname
401776035CV2706858single nucleotide variantNM_002263.4(KIFC1):c.1082G>T (p.Ser361Ile)not specified [RCV004321487]uncertain significance63340517733405177Humanname
401752484CV2707024single nucleotide variantNM_002263.4(KIFC1):c.1134C>G (p.Phe378Leu)not specified [RCV004321619]uncertain significance63340522933405229Humanname
401770830CV2707438single nucleotide variantNM_002263.4(KIFC1):c.1102A>G (p.Thr368Ala)not specified [RCV004312821]uncertain significance63340519733405197Humanname
401862365CV2775269single nucleotide variantNM_002263.4(KIFC1):c.1541A>G (p.Asp514Gly)not specified [RCV004348391]uncertain significance63340620033406200Humanname
401876135CV2777673single nucleotide variantNM_002263.4(KIFC1):c.1066C>T (p.Arg356Trp)not specified [RCV004343509]uncertain significance63340516133405161Humanname
405652885CV3269106single nucleotide variantNM_002263.4(KIFC1):c.1121T>G (p.Phe374Cys)not specified [RCV004414360]uncertain significance63340521633405216Humanname
405652888CV3269107single nucleotide variantNM_002263.4(KIFC1):c.1138C>T (p.Pro380Ser)not specified [RCV004414361]uncertain significance63340523333405233Humanname
405652894CV3269110single nucleotide variantNM_002263.4(KIFC1):c.1366A>C (p.Ser456Arg)not specified [RCV004414364]uncertain significance63340546133405461Humanname
405652897CV3269111single nucleotide variantNM_002263.4(KIFC1):c.1466G>A (p.Arg489His)not specified [RCV004414365]likely benign63340556133405561Humanname
405652899CV3269112single nucleotide variantNM_002263.4(KIFC1):c.1562G>A (p.Arg521His)not specified [RCV004414366]likely benign63340622133406221Humanname
405652900CV3269113single nucleotide variantNM_002263.4(KIFC1):c.1601G>A (p.Arg534Gln)not specified [RCV004414367]uncertain significance63340626033406260Humanname
405652903CV3269114single nucleotide variantNM_002263.4(KIFC1):c.1658G>A (p.Arg553Gln)not specified [RCV004414368]uncertain significance63340631733406317Humanname
405652906CV3269115single nucleotide variantNM_002263.4(KIFC1):c.1669T>G (p.Cys557Gly)not specified [RCV004414369]uncertain significance63340632833406328Humanname
405652908CV3269116single nucleotide variantNM_002263.4(KIFC1):c.1748G>T (p.Arg583Leu)not specified [RCV004414370]uncertain significance63340640733406407Humanname
405652911CV3269117single nucleotide variantNM_002263.4(KIFC1):c.1778A>T (p.Asn593Ile)not specified [RCV004414371]uncertain significance63340643733406437Humanname
405652914CV3269118single nucleotide variantNM_002263.4(KIFC1):c.1931A>G (p.Glu644Gly)not specified [RCV004414372]uncertain significance63340682933406829Humanname
405652917CV3269119single nucleotide variantNM_002263.4(KIFC1):c.2011A>C (p.Asn671His)not specified [RCV004414373]uncertain significance63340967933409679Humanname
407524786CV3452231single nucleotide variantNM_002263.4(KIFC1):c.1741G>A (p.Gly581Arg)not specified [RCV004631494]uncertain significance63340640033406400Humanname
407469671CV3452232single nucleotide variantNM_002263.4(KIFC1):c.1438G>C (p.Gly480Arg)not specified [RCV004636946]uncertain significance63340553333405533Humanname
597638107CV3695338single nucleotide variantNM_002263.4(KIFC1):c.1649A>G (p.His550Arg)not specified [RCV004941096]uncertain significance63340630833406308Humanname
598181954CV3991124single nucleotide variantNM_002263.4(KIFC1):c.1429A>G (p.Thr477Ala)not specified [RCV005352630]likely benign63340552433405524Humanname
598220670CV3991128single nucleotide variantNM_002263.4(KIFC1):c.1912G>C (p.Val638Leu)not specified [RCV005360700]uncertain significance63340681033406810Humanname
598220684CV3991131single nucleotide variantNM_002263.4(KIFC1):c.1105C>T (p.Arg369Cys)not specified [RCV005360702]uncertain significance63340520033405200Humanname