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Variants search result for Homo sapiens
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36 records found for search term Mrps18a
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8632086CV87292single nucleotide variantNM_001193343.1(MRPS18A):c.376+210C>TMalignant melanoma [RCV000067383]not provided64367528443675284Humanname
156330642CV2210672single nucleotide variantNM_018135.4(MRPS18A):c.13A>C (p.Lys5Gln)not specified [RCV004083814]uncertain significance64368776743687767Humanname
598213234CV3993495single nucleotide variantNM_018135.4(MRPS18A):c.25T>G (p.Ser9Ala)not specified [RCV005378310]uncertain significance64368775543687755Humanname
597634243CV3557380single nucleotide variantNM_018135.4(MRPS18A):c.91C>A (p.Pro31Thr)not specified [RCV004830961]uncertain significance64368768943687689Humanname
156142194CV2199996single nucleotide variantNM_018135.4(MRPS18A):c.220C>T (p.Arg74Cys)not specified [RCV004074159]uncertain significance64367855043678550Humanname
156188364CV2226761single nucleotide variantNM_018135.4(MRPS18A):c.122C>T (p.Thr41Ile)not specified [RCV004101980]likely benign64368111143681111Humanname
156089750CV2295614single nucleotide variantNM_018135.4(MRPS18A):c.154C>T (p.Arg52Cys)not specified [RCV004160697]uncertain significance64367861643678616Humanname
156348935CV2380965single nucleotide variantNM_018135.4(MRPS18A):c.221G>A (p.Arg74His)not specified [RCV004220543]uncertain significance64367854943678549Humanname
329349455CV2431415single nucleotide variantNM_018135.4(MRPS18A):c.206A>G (p.Gln69Arg)not specified [RCV004254580]uncertain significance64367856443678564Humanname
329350192CV2441940single nucleotide variantNM_018135.4(MRPS18A):c.279C>G (p.Ile93Met)not specified [RCV004262117]uncertain significance64367559143675591Humanname
401747616CV2733312single nucleotide variantNM_018135.4(MRPS18A):c.136A>G (p.Thr46Ala)not specified [RCV004332219]uncertain significance64368109743681097Humanname
407484308CV3450414single nucleotide variantNM_018135.4(MRPS18A):c.101G>C (p.Gly34Ala)not specified [RCV004638227]uncertain significance64368767943687679Humanname
597638049CV3557381single nucleotide variantNM_018135.4(MRPS18A):c.155G>A (p.Arg52His)not specified [RCV004824850]uncertain significance64367861543678615Humanname
598179178CV3993496single nucleotide variantNM_018135.4(MRPS18A):c.226A>T (p.Asn76Tyr)not specified [RCV005371887]uncertain significance64367854443678544Humanname
598213239CV3993498single nucleotide variantNM_018135.4(MRPS18A):c.248A>G (p.Tyr83Cys)not specified [RCV005378311]uncertain significance64367852243678522Humanname
156318046CV2200233single nucleotide variantNM_018135.4(MRPS18A):c.520A>G (p.Met174Val)not specified [RCV004076578]uncertain significance64367183343671833Humanname
156275869CV2287667single nucleotide variantNM_018135.4(MRPS18A):c.422C>T (p.Pro141Leu)not specified [RCV004141095]uncertain significance64367522643675226Humanname
155969475CV2309075single nucleotide variantNM_018135.4(MRPS18A):c.466C>T (p.Pro156Ser)not specified [RCV004171438]uncertain significance64367188743671887Humanname
156100872CV2351669single nucleotide variantNM_018135.4(MRPS18A):c.401G>A (p.Arg134Gln)not specified [RCV004195379]uncertain significance64367524743675247Humanname
156107929CV2355363single nucleotide variantNM_018135.4(MRPS18A):c.542T>C (p.Leu181Pro)not specified [RCV004205226]uncertain significance64367181143671811Humanname
156225006CV2399554single nucleotide variantNM_018135.4(MRPS18A):c.526G>A (p.Val176Met)not specified [RCV004244080]uncertain significance64367182743671827Humanname
329349712CV2424384single nucleotide variantNM_018135.4(MRPS18A):c.562T>C (p.Ser188Pro)not specified [RCV004252285]uncertain significance64367179143671791Humanname
329349950CV2437627single nucleotide variantNM_018135.4(MRPS18A):c.505T>C (p.Trp169Arg)not specified [RCV004260945]uncertain significance64367184843671848Humanname
405773379CV3374618single nucleotide variantNM_018135.4(MRPS18A):c.311T>A (p.Ile104Asn)not specified [RCV004502677]uncertain significance64367555943675559Humanname
405773400CV3374622single nucleotide variantNM_018135.4(MRPS18A):c.371G>A (p.Arg124Gln)not specified [RCV004502681]uncertain significance64367549943675499Humanname
405773494CV3374637single nucleotide variantNM_018135.4(MRPS18A):c.475G>A (p.Val159Ile)not specified [RCV004502696]uncertain significance64367187843671878Humanname
405773505CV3374639single nucleotide variantNM_018135.4(MRPS18A):c.482C>T (p.Pro161Leu)not specified [RCV004502698]uncertain significance64367187143671871Humanname
405773540CV3374645single nucleotide variantNM_018135.4(MRPS18A):c.502C>G (p.Arg168Gly)not specified [RCV004502704]uncertain significance64367185143671851Humanname
405773589CV3374653single nucleotide variantNM_018135.4(MRPS18A):c.517C>G (p.Arg173Gly)not specified [RCV004502712]uncertain significance64367183643671836Humanname
407484408CV3450412single nucleotide variantNM_018135.4(MRPS18A):c.310A>G (p.Ile104Val)not specified [RCV004631670]likely benign64367556043675560Humanname
407484302CV3450413single nucleotide variantNM_018135.4(MRPS18A):c.338G>A (p.Arg113His)not specified [RCV004638226]uncertain significance64367553243675532Humanname
597634225CV3557377single nucleotide variantNM_018135.4(MRPS18A):c.458G>T (p.Arg153Leu)not specified [RCV004830958]uncertain significance64367189543671895Humanname
597634231CV3557378single nucleotide variantNM_018135.4(MRPS18A):c.518G>T (p.Arg173Leu)not specified [RCV004830959]uncertain significance64367183543671835Humanname
597634237CV3557379single nucleotide variantNM_018135.4(MRPS18A):c.345C>G (p.Ile115Met)not specified [RCV004830960]uncertain significance64367552543675525Humanname
598179184CV3993497single nucleotide variantNM_018135.4(MRPS18A):c.533C>T (p.Ser178Leu)not specified [RCV005371888]uncertain significance64367182043671820Humanname
598213244CV3993499single nucleotide variantNM_018135.4(MRPS18A):c.481C>G (p.Pro161Ala)not specified [RCV005378312]uncertain significance64367187243671872Humanname