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Variants search result for Homo sapiens
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19 records found for search term Mrpl30
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8630496CV85651single nucleotide variantNM_145212.3(MRPL30):c.57G>A (p.Val19=)Malignant melanoma [RCV000065734]not provided29918818299188182Humanname
156140450CV2260300single nucleotide variantNM_145212.4(MRPL30):c.25G>A (p.Val9Ile)not specified [RCV004129396]uncertain significance29918622899186228Humanname
407474507CV3450336single nucleotide variantNM_145212.4(MRPL30):c.23T>G (p.Val8Gly)not specified [RCV004638171]uncertain significance29918622699186226Humanname
156237854CV2193593single nucleotide variantNM_145212.4(MRPL30):c.65G>T (p.Gly22Val)not specified [RCV004073065]uncertain significance29918819099188190Humanname
156076995CV2350998single nucleotide variantNM_145212.4(MRPL30):c.55G>A (p.Val19Met)not specified [RCV004211823]uncertain significance29918818099188180Humanname
597633750CV3561138single nucleotide variantNM_145212.4(MRPL30):c.59C>A (p.Thr20Lys)not specified [RCV004830854]uncertain significance29918818499188184Humanname
598178868CV3982874single nucleotide variantNM_145212.4(MRPL30):c.79A>G (p.Ile27Val)not specified [RCV005371837]uncertain significance29918820499188204Humanname
156096736CV2210529single nucleotide variantNM_145212.4(MRPL30):c.229A>G (p.Arg77Gly)not specified [RCV004089657]uncertain significance29919484799194847Humanname
156091681CV2256605single nucleotide variantNM_145212.4(MRPL30):c.188C>T (p.Pro63Leu)not specified [RCV004118794]uncertain significance29919480699194806Humanname
407474502CV3450335single nucleotide variantNM_145212.4(MRPL30):c.128A>T (p.Glu43Val)not specified [RCV004638170]uncertain significance29918825399188253Humanname
597633762CV3561140single nucleotide variantNM_145212.4(MRPL30):c.140A>G (p.Gln47Arg)not specified [RCV004830856]uncertain significance29919475899194758Humanname
598178864CV3982872single nucleotide variantNM_145212.4(MRPL30):c.155A>G (p.Asp52Gly)not specified [RCV005371836]uncertain significance29919477399194773Humanname
329391369CV2448002single nucleotide variantNM_145212.4(MRPL30):c.401T>C (p.Met134Thr)not specified [RCV004260798]uncertain significance29919562099195620Humanname
329367434CV2456851single nucleotide variantNM_145212.4(MRPL30):c.477T>A (p.His159Gln)not specified [RCV004270814]uncertain significance29919569699195696Humanname
329361096CV2463275single nucleotide variantNM_145212.4(MRPL30):c.400A>G (p.Met134Val)not specified [RCV004275038]uncertain significance29919561999195619Humanname
405785675CV3374544single nucleotide variantNM_145212.4(MRPL30):c.368A>G (p.Lys123Arg)not specified [RCV004504757]uncertain significance29919558799195587Humanname
407474499CV3450334single nucleotide variantNM_145212.4(MRPL30):c.410C>T (p.Thr137Met)not specified [RCV004638169]uncertain significance29919562999195629Humanname
597633756CV3561139single nucleotide variantNM_145212.4(MRPL30):c.391G>C (p.Glu131Gln)not specified [RCV004830855]uncertain significance29919561099195610Humanname
598212873CV3982873single nucleotide variantNM_145212.4(MRPL30):c.472G>A (p.Ala158Thr)not specified [RCV005378247]likely benign29919569199195691Humanname