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Variants search result for Homo sapiens
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7 records found for search term Ctxn1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156031646CV2274948single nucleotide variantNM_206833.4(CTXN1):c.67G>A (p.Gly23Ser)not specified [RCV004135001]uncertain significance1979254727925472Humanname
329399571CV2470183single nucleotide variantNM_206833.4(CTXN1):c.77C>T (p.Ala26Val)not specified [RCV004287425]uncertain significance1979254627925462Humanname
598221939CV3955960single nucleotide variantNM_206833.4(CTXN1):c.31C>T (p.Pro11Ser)not specified [RCV005317793]uncertain significance1979255087925508Humanname
155968637CV2312860single nucleotide variantNM_206833.4(CTXN1):c.125T>C (p.Leu42Pro)not specified [RCV004171353]uncertain significance1979254147925414Humanname
401737153CV2717986single nucleotide variantNM_206833.4(CTXN1):c.180G>A (p.Met60Ile)not specified [RCV004321933]uncertain significance1979253597925359Humanname
405700643CV3242941single nucleotide variantNM_206833.4(CTXN1):c.167C>T (p.Pro56Leu)not specified [RCV004375189]uncertain significance1979253727925372Humanname
597783040CV3661502single nucleotide variantNM_206833.4(CTXN1):c.106C>G (p.Leu36Val)not specified [RCV004900145]uncertain significance1979254337925433Humanname