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22 records found for search term Tmx1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8583829CV118394single nucleotide variantNM_030755.4(TMX1):c.664+1633G>TLung cancer [RCV000098914]uncertain significance145125139851251398Humanname
156166651CV2200934single nucleotide variantNM_030755.5(TMX1):c.23C>G (p.Ala8Gly)not specified [RCV004081547]uncertain significance145124031551240315Humanname
401886911CV2767955single nucleotide variantNM_030755.5(TMX1):c.474A>C (p.Leu158=)not provided [RCV003395761]|not specified [RCV004348204]likely benign145124935651249356Humanname
597801426CV3620638single nucleotide variantNM_030755.5(TMX1):c.58G>A (p.Gly20Ser)not specified [RCV004880709]uncertain significance145124035051240350Humanname
155920315CV2210777single nucleotide variantNM_030755.5(TMX1):c.134G>A (p.Gly45Glu)not specified [RCV004085872]uncertain significance145124042651240426Humanname
598253127CV3935040single nucleotide variantNM_030755.5(TMX1):c.172G>A (p.Ala58Thr)not specified [RCV005278197]uncertain significance145124387551243875Humanname
156342867CV2222510single nucleotide variantNM_030755.5(TMX1):c.430C>G (p.Pro144Ala)not specified [RCV004099352]uncertain significance145124720751247207Humanname
156265729CV2299266single nucleotide variantNM_030755.5(TMX1):c.655T>C (p.Tyr219His)not specified [RCV004152594]uncertain significance145124975651249756Humanname
156076795CV2350982single nucleotide variantNM_030755.5(TMX1):c.372A>G (p.Ile124Met)not specified [RCV004211809]uncertain significance145124714951247149Humanname
156189593CV2390882single nucleotide variantNM_030755.5(TMX1):c.754G>A (p.Glu252Lys)not specified [RCV004234899]uncertain significance145125443051254430Humanname
156158640CV2398052single nucleotide variantNM_030755.5(TMX1):c.581T>C (p.Leu194Ser)not specified [RCV004241642]uncertain significance145124955951249559Humanname
329392874CV2469027single nucleotide variantNM_030755.5(TMX1):c.701A>T (p.Lys234Ile)not specified [RCV004274277]uncertain significance145125437751254377Humanname
401730643CV2689767single nucleotide variantNM_030755.5(TMX1):c.796A>G (p.Ile266Val)not specified [RCV004297677]uncertain significance145125447251254472Humanname
401752681CV2707090single nucleotide variantNM_030755.5(TMX1):c.542A>G (p.Tyr181Cys)not specified [RCV004321673]uncertain significance145124952051249520Humanname
401725551CV2721823single nucleotide variantNM_030755.5(TMX1):c.839C>A (p.Ser280Tyr)not specified [RCV004326339]uncertain significance145125451551254515Humanname
405786737CV3343700single nucleotide variantNM_030755.5(TMX1):c.421T>C (p.Trp141Arg)not specified [RCV004472994]uncertain significance145124719851247198Humanname
407458975CV3479129single nucleotide variantNM_030755.5(TMX1):c.391G>C (p.Glu131Gln)not specified [RCV004686997]uncertain significance145124716851247168Humanname
597801422CV3620636single nucleotide variantNM_030755.5(TMX1):c.656A>G (p.Tyr219Cys)not specified [RCV004880707]uncertain significance145124975751249757Humanname
597801424CV3620637single nucleotide variantNM_030755.5(TMX1):c.635G>A (p.Arg212His)not specified [RCV004880708]uncertain significance145124973651249736Humanname
598228850CV3935041single nucleotide variantNM_030755.5(TMX1):c.802C>G (p.Gln268Glu)not specified [RCV005294798]uncertain significance145125447851254478Humanname
598228858CV3935042single nucleotide variantNM_030755.5(TMX1):c.749A>C (p.Glu250Ala)not specified [RCV005294799]uncertain significance145125442551254425Humanname
598253132CV3935043single nucleotide variantNM_030755.5(TMX1):c.470A>G (p.Gln157Arg)not specified [RCV005278198]uncertain significance145124935251249352Humanname