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Variants search result for Homo sapiens
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7 records found for search term Ctxn3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405700656CV3242943single nucleotide variantNM_001048252.3(CTXN3):c.37C>A (p.Pro13Thr)not specified [RCV004375191]uncertain significance5127657558127657558Humanname
597653563CV3661503single nucleotide variantNM_001048252.3(CTXN3):c.94G>A (p.Val32Ile)not specified [RCV004910852]uncertain significance5127657615127657615Humanname
401780624CV2685577single nucleotide variantNM_001048252.3(CTXN3):c.177G>C (p.Met59Ile)not specified [RCV004294588]uncertain significance5127657698127657698Humanname
401768317CV2735261single nucleotide variantNM_001048252.3(CTXN3):c.139C>T (p.Arg47Trp)not specified [RCV004333935]uncertain significance5127657660127657660Humanname
405700652CV3242942single nucleotide variantNM_001048252.3(CTXN3):c.188C>T (p.Thr63Ile)not specified [RCV004375190]uncertain significance5127657709127657709Humanname
407472939CV3426455single nucleotide variantNM_001048252.3(CTXN3):c.182C>A (p.Thr61Asn)not specified [RCV004616063]uncertain significance5127657703127657703Humanname
598221943CV3955961single nucleotide variantNM_001048252.3(CTXN3):c.140G>A (p.Arg47Gln)not specified [RCV005317794]uncertain significance5127657661127657661Humanname