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Variants search result for Homo sapiens
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15 records found for search term Med6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156262882CV2391623single nucleotide variantNM_005466.4(MED6):c.10G>T (p.Val4Leu)not specified [RCV004241787]uncertain significance147060062870600628Humanname
597676737CV3560259single nucleotide variantNM_005466.4(MED6):c.137A>G (p.Asn46Ser)not specified [RCV004830386]uncertain significance147059766370597663Humanname
598225265CV3985648single nucleotide variantNM_005466.4(MED6):c.173A>G (p.Glu58Gly)not specified [RCV005380366]uncertain significance147059762770597627Humanname
598241074CV3985650single nucleotide variantNM_005466.4(MED6):c.220C>G (p.Gln74Glu)not specified [RCV005364752]uncertain significance147059666570596665Humanname
155925499CV2277312single nucleotide variantNM_005466.4(MED6):c.511A>G (p.Ile171Val)not specified [RCV004142924]uncertain significance147059133770591337Humanname
156103064CV2291561single nucleotide variantNM_005466.4(MED6):c.697G>A (p.Val233Met)not specified [RCV004155863]uncertain significance147058485770584857Humanname
405692488CV3281769single nucleotide variantNM_005466.4(MED6):c.499G>C (p.Glu167Gln)not specified [RCV004423920]uncertain significance147059134970591349Humanname
407502407CV3449731single nucleotide variantNM_005466.4(MED6):c.713C>G (p.Pro238Arg)not specified [RCV004645141]uncertain significance147058484170584841Humanname
407502411CV3449732single nucleotide variantNM_005466.4(MED6):c.452A>T (p.Asp151Val)not specified [RCV004645142]uncertain significance147059289470592894Humanname
407518029CV3453679single nucleotide variantNM_005466.4(MED6):c.463C>A (p.Gln155Lys)not specified [RCV004628726]uncertain significance147059288370592883Humanname
597634588CV3560258single nucleotide variantNM_005466.4(MED6):c.367G>A (p.Val123Met)not specified [RCV004824185]uncertain significance147059297970592979Humanname
598225253CV3985646single nucleotide variantNM_005466.4(MED6):c.494A>C (p.Lys165Thr)not specified [RCV005380364]uncertain significance147059135470591354Humanname
598225259CV3985647single nucleotide variantNM_005466.4(MED6):c.632C>T (p.Ala211Val)not specified [RCV005380365]uncertain significance147058492270584922Humanname
598241066CV3985649single nucleotide variantNM_005466.4(MED6):c.355G>C (p.Val119Leu)not specified [RCV005364751]uncertain significance147059329870593298Humanname
598241081CV3985651single nucleotide variantNM_005466.4(MED6):c.713C>A (p.Pro238His)not specified [RCV005364753]uncertain significance147058484170584841Humanname