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Variants search result for Homo sapiens
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20 records found for search term Gemin6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156039632CV2390352single nucleotide variantNM_024775.10(GEMIN6):c.14T>C (p.Met5Thr)not specified [RCV004240714]uncertain significance23877900438779004Humanname
405786423CV3258237single nucleotide variantNM_024775.10(GEMIN6):c.36G>T (p.Trp12Cys)not specified [RCV004387741]uncertain significance23877902638779026Humanname
597704019CV3687875single nucleotide variantNM_024775.10(GEMIN6):c.47T>C (p.Ile16Thr)not specified [RCV004916768]likely benign23877903738779037Humanname
597704029CV3687876single nucleotide variantNM_024775.10(GEMIN6):c.62G>A (p.Arg21Gln)not specified [RCV004916769]uncertain significance23877905238779052Humanname
156065937CV2270742single nucleotide variantNM_024775.10(GEMIN6):c.233T>C (p.Val78Ala)not specified [RCV004131803]uncertain significance23878162138781621Humanname
156270089CV2293462single nucleotide variantNM_024775.10(GEMIN6):c.115C>T (p.Pro39Ser)not specified [RCV004152705]uncertain significance23877910538779105Humanname
156004641CV2396971single nucleotide variantNM_024775.10(GEMIN6):c.223G>A (p.Asp75Asn)not specified [RCV004234081]uncertain significance23878161138781611Humanname
401766395CV2725511single nucleotide variantNM_024775.10(GEMIN6):c.157G>A (p.Gly53Ser)not specified [RCV004320131]uncertain significance23878154538781545Humanname
405786413CV3258235single nucleotide variantNM_024775.10(GEMIN6):c.198G>T (p.Gln66His)not specified [RCV004387739]uncertain significance23878158638781586Humanname
155925501CV2211845single nucleotide variantNM_024775.10(GEMIN6):c.463G>T (p.Val155Phe)not specified [RCV004086669]uncertain significance23878185138781851Humanname
329360484CV2443568single nucleotide variantNM_024775.10(GEMIN6):c.370C>G (p.Pro124Ala)not specified [RCV004262393]uncertain significance23878175838781758Humanname
401876097CV2789293single nucleotide variantNM_024775.10(GEMIN6):c.409C>T (p.Pro137Ser)not specified [RCV004365319]uncertain significance23878179738781797Humanname
405786418CV3258236single nucleotide variantNM_024775.10(GEMIN6):c.339C>A (p.Asn113Lys)not specified [RCV004387740]uncertain significance23878172738781727Humanname
405786427CV3258238single nucleotide variantNM_024775.10(GEMIN6):c.440C>G (p.Ser147Cys)not specified [RCV004387742]uncertain significance23878182838781828Humanname
405786439CV3258241single nucleotide variantNM_024775.10(GEMIN6):c.450T>G (p.Ile150Met)not specified [RCV004387745]uncertain significance23878183838781838Humanname
405786444CV3258242single nucleotide variantNM_024775.10(GEMIN6):c.458C>T (p.Ser153Leu)not specified [RCV004387746]uncertain significance23878184638781846Humanname
407512780CV3432994single nucleotide variantNM_024775.10(GEMIN6):c.454C>G (p.Leu152Val)not specified [RCV004626912]uncertain significance23878184238781842Humanname
598186210CV3970652single nucleotide variantNM_024775.10(GEMIN6):c.404T>C (p.Ile135Thr)not specified [RCV005353495]uncertain significance23878179238781792Humanname
598186219CV3970653single nucleotide variantNM_024775.10(GEMIN6):c.484C>G (p.His162Asp)not specified [RCV005353496]uncertain significance23878187238781872Humanname
598186225CV3970654single nucleotide variantNM_024775.10(GEMIN6):c.392G>C (p.Gly131Ala)not specified [RCV005353497]uncertain significance23878178038781780Humanname