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Variants search result for Homo sapiens
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26 records found for search term Trub1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
38466829CV920816single nucleotide variantNM_139169.5(TRUB1):c.27G>A (p.Val9=)not provided [RCV001200076]likely benign10114938280114938280Humanname
156305184CV2305047single nucleotide variantNM_139169.5(TRUB1):c.25G>A (p.Val9Met)not specified [RCV004168933]likely benign10114938278114938278Humanname
405777684CV3344556single nucleotide variantNM_139169.5(TRUB1):c.67G>C (p.Glu23Gln)not specified [RCV004471401]uncertain significance10114938320114938320Humanname
597681540CV3621417single nucleotide variantNM_139169.5(TRUB1):c.79A>G (p.Thr27Ala)not specified [RCV004883640]uncertain significance10114938332114938332Humanname
598237154CV3928442single nucleotide variantNM_139169.5(TRUB1):c.47C>G (p.Thr16Arg)not specified [RCV005296191]uncertain significance10114938300114938300Humanname
598215621CV3928446single nucleotide variantNM_139169.5(TRUB1):c.35C>T (p.Pro12Leu)not specified [RCV005292764]uncertain significance10114938288114938288Humanname
407527971CV3488960single nucleotide variantNM_139169.5(TRUB1):c.173A>C (p.Lys58Thr)not specified [RCV004680218]uncertain significance10114938426114938426Humanname
407527980CV3488963single nucleotide variantNM_139169.5(TRUB1):c.225C>G (p.His75Gln)not specified [RCV004680221]uncertain significance10114938478114938478Humanname
407527982CV3488964single nucleotide variantNM_139169.5(TRUB1):c.221T>A (p.Val74Glu)not specified [RCV004680222]uncertain significance10114938474114938474Humanname
598237165CV3928445single nucleotide variantNM_139169.5(TRUB1):c.112A>G (p.Arg38Gly)not specified [RCV005296193]uncertain significance10114938365114938365Humanname
156260248CV2204800single nucleotide variantNM_139169.5(TRUB1):c.323A>G (p.Lys108Arg)not specified [RCV004075055]uncertain significance10114942681114942681Humanname
156115338CV2221425single nucleotide variantNM_139169.5(TRUB1):c.914A>G (p.Glu305Gly)not specified [RCV004096716]uncertain significance10114975243114975243Humanname
156367436CV2266795single nucleotide variantNM_139169.5(TRUB1):c.701C>G (p.Ser234Cys)not specified [RCV004137614]uncertain significance10114972239114972239Humanname
156067939CV2320338single nucleotide variantNM_139169.5(TRUB1):c.695G>A (p.Ser232Asn)not specified [RCV004178500]uncertain significance10114972233114972233Humanname
155917398CV2336326single nucleotide variantNM_139169.5(TRUB1):c.367G>A (p.Ala123Thr)not specified [RCV004192075]uncertain significance10114942725114942725Humanname
329370032CV2424915single nucleotide variantNM_139169.5(TRUB1):c.812A>G (p.Asn271Ser)not specified [RCV004248792]uncertain significance10114975141114975141Humanname
329356368CV2460285single nucleotide variantNM_139169.5(TRUB1):c.880A>G (p.Lys294Glu)not specified [RCV004266832]uncertain significance10114975209114975209Humanname
405777674CV3344554single nucleotide variantNM_139169.5(TRUB1):c.590C>T (p.Pro197Leu)not specified [RCV004471399]uncertain significance10114970434114970434Humanname
405777678CV3344555single nucleotide variantNM_139169.5(TRUB1):c.646A>G (p.Arg216Gly)not specified [RCV004471400]uncertain significance10114972184114972184Humanname
405777689CV3344557single nucleotide variantNM_139169.5(TRUB1):c.971C>G (p.Ser324Cys)not specified [RCV004471402]uncertain significance10114975300114975300Humanname
407527974CV3488961single nucleotide variantNM_139169.5(TRUB1):c.422G>A (p.Ser141Asn)not specified [RCV004680219]uncertain significance10114951130114951130Humanname
407527977CV3488962single nucleotide variantNM_139169.5(TRUB1):c.991T>A (p.Cys331Ser)not specified [RCV004680220]uncertain significance10114975320114975320Humanname
597681548CV3621418single nucleotide variantNM_139169.5(TRUB1):c.697A>G (p.Ile233Val)not specified [RCV004883641]uncertain significance10114972235114972235Humanname
598237149CV3928440single nucleotide variantNM_139169.5(TRUB1):c.545T>C (p.Ile182Thr)not specified [RCV005296190]uncertain significance10114970389114970389Humanname
598215609CV3928441single nucleotide variantNM_139169.5(TRUB1):c.664G>C (p.Ala222Pro)not specified [RCV005292762]uncertain significance10114972202114972202Humanname
598215616CV3928444single nucleotide variantNM_139169.5(TRUB1):c.889A>G (p.Ile297Val)not specified [RCV005292763]uncertain significance10114975218114975218Humanname