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Variants search result for Homo sapiens
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22 records found for search term Mat2b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597637344CV3694335single nucleotide variantNM_013283.5(MAT2B):c.26C>T (p.Ser9Phe)not specified [RCV004940953]uncertain significance5163505712163505712Humanname
598199375CV3981700single nucleotide variantNM_013283.5(MAT2B):c.88A>G (p.Arg30Gly)not specified [RCV005375690]uncertain significance5163512026163512026Humanname
156272114CV2299558single nucleotide variantNM_013283.5(MAT2B):c.174T>G (p.Cys58Trp)not specified [RCV004154892]uncertain significance5163512112163512112Humanname
155906415CV2379017single nucleotide variantNM_013283.5(MAT2B):c.166G>T (p.Val56Phe)not specified [RCV004233779]uncertain significance5163512104163512104Humanname
329362664CV2439017single nucleotide variantNM_013283.5(MAT2B):c.161A>T (p.His54Leu)not specified [RCV004264524]uncertain significance5163512099163512099Humanname
401743743CV2684771single nucleotide variantNM_013283.5(MAT2B):c.268A>G (p.Ile90Val)not specified [RCV004293850]uncertain significance5163513564163513564Humanname
405659144CV3278026single nucleotide variantNM_013283.5(MAT2B):c.163G>A (p.Ala55Thr)not specified [RCV004416701]uncertain significance5163512101163512101Humanname
597637339CV3694334single nucleotide variantNM_013283.5(MAT2B):c.155A>G (p.Asn52Ser)not specified [RCV004940952]uncertain significance5163512093163512093Humanname
156236071CV2224094single nucleotide variantNM_013283.5(MAT2B):c.482A>G (p.Lys161Arg)not specified [RCV004095959]uncertain significance5163513950163513950Humanname
156182193CV2327879single nucleotide variantNM_013283.5(MAT2B):c.751T>G (p.Ser251Ala)not specified [RCV004179207]uncertain significance5163517591163517591Humanname
155971114CV2334178single nucleotide variantNM_013283.5(MAT2B):c.758A>G (p.Asn253Ser)not specified [RCV004186166]uncertain significance5163517598163517598Humanname
155902988CV2353489single nucleotide variantNM_013283.5(MAT2B):c.935G>A (p.Arg312Gln)not specified [RCV004199475]uncertain significance5163518293163518293Humanname
156070801CV2356079single nucleotide variantNM_013283.5(MAT2B):c.971T>C (p.Ile324Thr)not specified [RCV004203493]uncertain significance5163518329163518329Humanname
329360643CV2439553single nucleotide variantNM_013283.5(MAT2B):c.551T>C (p.Ile184Thr)not specified [RCV004255577]uncertain significance5163516542163516542Humanname
405659146CV3278027single nucleotide variantNM_013283.5(MAT2B):c.586G>C (p.Ala196Pro)not specified [RCV004416702]uncertain significance5163516577163516577Humanname
405659152CV3278029single nucleotide variantNM_013283.5(MAT2B):c.795T>G (p.Ile265Met)not specified [RCV004416704]uncertain significance5163517635163517635Humanname
597637350CV3694336single nucleotide variantNM_013283.5(MAT2B):c.572A>C (p.Lys191Thr)not specified [RCV004940954]uncertain significance5163516563163516563Humanname
597637354CV3694337single nucleotide variantNM_013283.5(MAT2B):c.913A>G (p.Ile305Val)not specified [RCV004940955]uncertain significance5163518271163518271Humanname
598199361CV3981698single nucleotide variantNM_013283.5(MAT2B):c.599T>C (p.Met200Thr)not specified [RCV005375688]uncertain significance5163516590163516590Humanname
598199366CV3981699single nucleotide variantNM_013283.5(MAT2B):c.685A>G (p.Thr229Ala)not specified [RCV005375689]uncertain significance5163516676163516676Humanname
598177373CV3981702single nucleotide variantNM_013283.5(MAT2B):c.679G>C (p.Val227Leu)not specified [RCV005371586]uncertain significance5163516670163516670Humanname
15197574CV721362single nucleotide variantNM_013283.5(MAT2B):c.905C>T (p.Thr302Ile)not provided [RCV000890098]benign5163518263163518263Humanname