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6 records found for search term Tpt1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15189699CV739056single nucleotide variantNM_003295.4(TPT1):c.492G>A (p.Lys164=)not provided [RCV000909730]benign134533868445338684Humanname
155910633CV2303638single nucleotide variantNM_003295.4(TPT1):c.122G>T (p.Gly41Val)not specified [RCV004161720]uncertain significance134534016545340165Humanname
597795785CV3620940single nucleotide variantNM_003295.4(TPT1):c.245G>C (p.Ser82Thr)not specified [RCV004878294]uncertain significance134534004245340042Humanname
156225943CV2203090single nucleotide variantNM_003295.4(TPT1):c.349G>A (p.Gly117Arg)not specified [RCV004069335]uncertain significance134533954745339547Humanname
401944584CV2839817single nucleotide variantNM_003295.4(TPT1):c.364A>G (p.Ile122Val)not specified [RCV003457237]benign134533953245339532Humanname
405775543CV3344006single nucleotide variantNM_003295.4(TPT1):c.355G>T (p.Ala119Ser)not specified [RCV004471042]uncertain significance134533954145339541Humanname