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11 records found for search term Tomm22
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156353159CV2324113single nucleotide variantNM_020243.5(TOMM22):c.29C>T (p.Ala10Val)not specified [RCV004178400]uncertain significance223868200738682007Humanname
407461082CV3486732single nucleotide variantNM_020243.5(TOMM22):c.40C>G (p.Gln14Glu)not specified [RCV004687564]uncertain significance223868201838682018Humanname
597786610CV3614318single nucleotide variantNM_020243.5(TOMM22):c.94C>G (p.Leu32Val)not specified [RCV004875388]uncertain significance223868207238682072Humanname
597786615CV3614319single nucleotide variantNM_020243.5(TOMM22):c.44C>T (p.Ser15Phe)not specified [RCV004875389]uncertain significance223868202238682022Humanname
401772270CV2712628single nucleotide variantNM_020243.5(TOMM22):c.182C>T (p.Ser61Phe)not specified [RCV004307954]uncertain significance223868238738682387Humanname
405757128CV3346896single nucleotide variantNM_020243.5(TOMM22):c.122A>G (p.Asp41Gly)not specified [RCV004467996]uncertain significance223868232738682327Humanname
598187898CV3928034single nucleotide variantNM_020243.5(TOMM22):c.199T>G (p.Phe67Val)not specified [RCV005287853]uncertain significance223868240438682404Humanname
156224318CV2395135single nucleotide variantNM_020243.5(TOMM22):c.400G>C (p.Ala134Pro)not specified [RCV004236812]uncertain significance223868381238683812Humanname
329394167CV2450121single nucleotide variantNM_020243.5(TOMM22):c.404T>C (p.Leu135Pro)not specified [RCV004270947]uncertain significance223868381638683816Humanname
401739324CV2673266single nucleotide variantNM_020243.5(TOMM22):c.398G>A (p.Gly133Glu)not specified [RCV004286069]uncertain significance223868381038683810Humanname
405757133CV3346897single nucleotide variantNM_020243.5(TOMM22):c.321A>C (p.Gln107His)not specified [RCV004467997]uncertain significance223868296338682963Humanname