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15 records found for search term Gtf3c6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405719291CV3255602single nucleotide variantNM_138408.4(GTF3C6):c.23G>C (p.Arg8Pro)not specified [RCV004388559]likely benign6110958792110958792Humanname
156265406CV2198654single nucleotide variantNM_138408.4(GTF3C6):c.86G>A (p.Gly29Glu)not specified [RCV004075666]uncertain significance6110959200110959200Humanname
598253193CV3974874single nucleotide variantNM_138408.4(GTF3C6):c.37G>A (p.Gly13Arg)not specified [RCV005346218]uncertain significance6110958806110958806Humanname
405719278CV3255600single nucleotide variantNM_138408.4(GTF3C6):c.116G>A (p.Cys39Tyr)not specified [RCV004388557]uncertain significance6110959230110959230Humanname
407464548CV3443602single nucleotide variantNM_138408.4(GTF3C6):c.155G>C (p.Arg52Thr)not specified [RCV004635106]uncertain significance6110960430110960430Humanname
598253207CV3974876single nucleotide variantNM_138408.4(GTF3C6):c.157C>T (p.Pro53Ser)not specified [RCV005346220]uncertain significance6110960432110960432Humanname
156270433CV2326458single nucleotide variantNM_138408.4(GTF3C6):c.399C>G (p.Phe133Leu)not specified [RCV004183022]uncertain significance6110967547110967547Humanname
329358970CV2450776single nucleotide variantNM_138408.4(GTF3C6):c.482T>C (p.Leu161Ser)not specified [RCV004267703]uncertain significance6110967630110967630Humanname
405719299CV3255603single nucleotide variantNM_138408.4(GTF3C6):c.365G>A (p.Gly122Glu)not specified [RCV004388560]uncertain significance6110967513110967513Humanname
405719306CV3255604single nucleotide variantNM_138408.4(GTF3C6):c.578C>T (p.Pro193Leu)not specified [RCV004388561]uncertain significance6110967726110967726Humanname
597757195CV3688877single nucleotide variantNM_138408.4(GTF3C6):c.301A>C (p.Lys101Gln)not specified [RCV004925027]uncertain significance6110962445110962445Humanname
597771890CV3688878single nucleotide variantNM_138408.4(GTF3C6):c.509T>C (p.Met170Thr)not specified [RCV004928566]uncertain significance6110967657110967657Humanname
597771896CV3688879single nucleotide variantNM_138408.4(GTF3C6):c.577C>T (p.Pro193Ser)not specified [RCV004928567]uncertain significance6110967725110967725Humanname
598253199CV3974875single nucleotide variantNM_138408.4(GTF3C6):c.298A>G (p.Met100Val)not specified [RCV005346219]uncertain significance6110962442110962442Humanname
598253219CV3974878single nucleotide variantNM_138408.4(GTF3C6):c.514G>A (p.Asp172Asn)not specified [RCV005346222]uncertain significance6110967662110967662Humanname