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Variants search result for Homo sapiens
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24 records found for search term Mrpl16
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405771333CV3363933single nucleotide variantNM_017840.4(MRPL16):c.19C>T (p.Arg7Cys)not specified [RCV004502287]uncertain significance115981064059810640Humanname
407525162CV3450295single nucleotide variantNM_017840.4(MRPL16):c.73C>T (p.Pro25Ser)not specified [RCV004631636]uncertain significance115980990359809903Humanname
156361775CV2322853single nucleotide variantNM_017840.4(MRPL16):c.141A>T (p.Lys47Asn)not specified [RCV004185312]uncertain significance115980783059807830Humanname
401765521CV2712829single nucleotide variantNM_017840.4(MRPL16):c.195A>T (p.Glu65Asp)not specified [RCV004314248]uncertain significance115980777659807776Humanname
405771535CV3363930single nucleotide variantNM_017840.4(MRPL16):c.196C>T (p.Pro66Ser)not specified [RCV004502284]uncertain significance115980777559807775Humanname
156379824CV2211598single nucleotide variantNM_017840.4(MRPL16):c.620G>A (p.Arg207His)not specified [RCV004084495]uncertain significance115980648359806483Humanname
155923693CV2351833single nucleotide variantNM_017840.4(MRPL16):c.542A>G (p.His181Arg)not specified [RCV004197979]uncertain significance115980656159806561Humanname
156255347CV2358994single nucleotide variantNM_017840.4(MRPL16):c.549G>C (p.Leu183Phe)not specified [RCV004212322]uncertain significance115980655459806554Humanname
155931458CV2362561single nucleotide variantNM_017840.4(MRPL16):c.298G>A (p.Gly100Ser)not specified [RCV004215220]uncertain significance115980680559806805Humanname
329378269CV2463604single nucleotide variantNM_017840.4(MRPL16):c.514G>A (p.Val172Met)not specified [RCV004277403]uncertain significance115980658959806589Humanname
401770458CV2678684single nucleotide variantNM_017840.4(MRPL16):c.386A>G (p.Lys129Arg)not specified [RCV004294721]uncertain significance115980671759806717Humanname
401776709CV2711288single nucleotide variantNM_017840.4(MRPL16):c.407T>C (p.Val136Ala)not specified [RCV004313067]uncertain significance115980669659806696Humanname
401898934CV2792134single nucleotide variantNM_017840.4(MRPL16):c.620G>C (p.Arg207Pro)not specified [RCV004361352]uncertain significance115980648359806483Humanname
405770946CV3363941single nucleotide variantNM_017840.4(MRPL16):c.317G>A (p.Arg106His)not specified [RCV004502295]uncertain significance115980678659806786Humanname
405770959CV3363943single nucleotide variantNM_017840.4(MRPL16):c.364T>C (p.Trp122Arg)not specified [RCV004502297]uncertain significance115980673959806739Humanname
405771035CV3363957single nucleotide variantNM_017840.4(MRPL16):c.593T>C (p.Met198Thr)not specified [RCV004502311]uncertain significance115980651059806510Humanname
407525166CV3450297single nucleotide variantNM_017840.4(MRPL16):c.587A>G (p.Glu196Gly)not specified [RCV004631638]uncertain significance115980651659806516Humanname
407474395CV3450298single nucleotide variantNM_017840.4(MRPL16):c.338T>C (p.Met113Thr)not specified [RCV004638143]uncertain significance115980676559806765Humanname
597633555CV3561091single nucleotide variantNM_017840.4(MRPL16):c.694C>G (p.Pro232Ala)not specified [RCV004830824]uncertain significance115980640959806409Humanname
597633562CV3561092single nucleotide variantNM_017840.4(MRPL16):c.493G>A (p.Gly165Arg)not specified [RCV004830825]uncertain significance115980661059806610Humanname
597633569CV3561094single nucleotide variantNM_017840.4(MRPL16):c.715G>A (p.Gly239Arg)not specified [RCV004830826]uncertain significance115980638859806388Humanname
598178784CV3982828single nucleotide variantNM_017840.4(MRPL16):c.562A>G (p.Lys188Glu)not specified [RCV005371823]uncertain significance115980654159806541Humanname
598178790CV3982830single nucleotide variantNM_017840.4(MRPL16):c.350A>G (p.Asn117Ser)not specified [RCV005371824]uncertain significance115980675359806753Humanname
13462137CV438958single nucleotide variantNM_017840.4(MRPL16):c.619C>T (p.Arg207Cys)not provided [RCV000513779]likely benign115980648459806484Humanname