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["Supplementary Table 2: Potential driver mutations in samples identified from COSMIC or ATLAS databases."]
["PATIENT1 POTENTIAL DRIVER GENES"]
["ENSEMBL GENE ID","GENE NAME","*MUTATION EFFECT","*MUTATION TYPE","MUTATED SAMPLES","**BASE CONVERSION"]
["ENSG00000118058","KMT2A","MODERATE","MISSENSE","all tumours shared","TpC*>TpT*"]
["ENSG00000167548","KMT2D","MODERATE","MISSENSE","all tumours shared","TpC*>TpT*"]
["ENSG00000196159","FAT4","MODERATE","MISSENSE","all tumours shared","TpC*>TpT*"]
["ENSG00000104884","ERCC2","MODERATE","MISSENSE","all tumours shared","GpA*>GpC*"]
["ENSG00000145362","ANK2","MODERATE","MISSENSE","all tumours shared","TpA*>TpG*"]
["ENSG00000147050","KDM6A","MODERATE","MISSENSE","all tumours shared","TpA*>TpG*"]
["ENSG00000121879","PIK3CA","MODERATE","MISSENSE","Tumour1.Base private","GpC*>GpG*,TpT*>TpA*"]
["ENSG00000068078","FGFR3","MODERATE","MISSENSE","Tumour1.Base private","TpC*>TpT*"]
["ENSG00000165699","TSC1","HIGH","FRAMESHIFT","Tumour1.Apex private","C deletion"]
["ENSG00000143341","HMCN1","MODERATE","MISSENSE","all samples shared","T insertion"]
["ENSG00000117713","ARID1A","MODERATE","MISSENSE","all samples shared","ApA*>ApG*"]
["ENSG00000164588","HCN1","MODERATE","MISSENSE","all samples shared","ApA*>ApG*"]
["ENSG00000178104","PDE4DIP","HIGH","FRAMESHIFT","all samples shared","A insertion"]
["ENSG00000095015","MAP3K1","MODERATE","CODON DELETION","all samples shared","CAA deletion"]
[]
["PATIENT2 POTENTIAL DRIVER GENES"]
["GENE ENS","GENE NAME","*MUTATION EFFECT","*MUTATION TYPE","MUTATED SAMPLES","**BASE CONVERSION"]
["ENSG00000139687","RB1","HIGH","NON SENSE","all tumours shared","ApC*>ApG*"]
["ENSG00000149311","ATM","MODERATE","MISSENSE","all tumours shared","TpC*>TpG*, CpC*>CpT*"]
["ENSG00000168702","LRP1B","MODERATE","MISSENSE","all tumours shared","TpC*>TpG*"]
["ENSG00000181143","MUC16","MODERATE","MISSENSE","all tumours shared,Tumour1.Apex,Tumour1.Base","TpC*>TpT*"]
["ENSG00000055609","KMT2C","MODERATE","MISSENSE","all samples shared","GpC*>GpG*"]
["ENSG00000143341","HMCN1","MODERATE","MISSENSE","all samples shared","GpC*>GpT*"]
[]
["PATIENT3 POTENTIAL DRIVER GENES"]
["GENE ENS","GENE NAME","MUTATION EFFECT","*MUTATION TYPE","*MUTATED SAMPLES","**BASE CONVERSION"]
["ENSG00000147050","KDM6A","HIGH","nonsense","all samples","TpC*>TpT*"]
["ENSG00000198626","RYR2","MODERATE","missense","all samples","TpC*>TpT*"]
["ENSG00000167548","KMT2D","MODERATE","codon chabge+codon deletion","all samples","TGCTGCTGT deletion"]
["ENSG00000196712","NF1","MODERATE","missense","all samples","TpC*>TpG*"]
["ENSG00000168702","LRP1B","MODERATE","missense","all samples","ApA*>ApG*"]
["ENSG00000131018","SYNE1","MODERATE","missense","private to one sample","TpC*>TpG*"]
["ENSG00000101972","STAG2","HIGH","splice site donor","shared by 3 samples","ApC*>ApA*"]
[]
["*They are annotated according to \"snpEff\" software"]
["**The nucleotide mutated with the preceding SNV"]