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["Sample_ID","chromosome","start","stop","reference","variant","type","gene_name","transcript_name","strand","effect","c_position","amino_acid_change"]
["dbGaP-298170-361467",20,31022288,31022288,"C","G","SNP","ASXL1","ENST00000375687",1,"nonsense","c.1773","p.Y591*"]
["dbGaP-295088-361485",2,25457242,25457242,"C","T","SNP","DNMT3A","ENST00000264709",-1,"missense","c.2645","p.R882H"]
["dbGaP-295464-361677",2,25457242,25457242,"C","T","SNP","DNMT3A","ENST00000264709",-1,"missense","c.2645","p.R882H"]
["dbGaP-298112-361837",2,25457242,25457242,"C","T","SNP","DNMT3A","ENST00000264709",-1,"missense","c.2645","p.R882H"]
["dbGaP-353698-437130",2,25457242,25457242,"C","T","SNP","DNMT3A","ENST00000264709",-1,"missense","c.2645","p.R882H"]
["dbGaP-353485-437074",2,25459834,25459834,"C","A","SNP","DNMT3A","ENST00000264709",-1,"nonsense","c.2449","p.E817*"]
["dbGaP-353587-436912",2,25457243,25457243,"G","A","SNP","DNMT3A","ENST00000264709",-1,"missense","c.2644","p.R882C"]
["dbGaP-294968-360378",2,25457243,25457243,"G","A","SNP","DNMT3A","ENST00000264709",-1,"missense","c.2644","p.R882C"]
["dbGaP-295037-360660",2,25457243,25457243,"G","A","SNP","DNMT3A","ENST00000264709",-1,"missense","c.2644","p.R882C"]
["dbGaP-295149-361236",20,57428858,57428858,"C","T","SNP","GNAS","ENST00000371100",1,"nonsense","c.538","p.Q180*"]
["dbGaP-295493-361708",20,57484421,57484421,"G","A","SNP","GNAS","ENST00000354359",1,"missense","c.605","R202H"]
["dbGaP-294874-361374",9,5073770,5073770,"G","T","SNP","JAK2","ENST00000381652",1,"missense","c.1849","p.V617F"]
["dbGaP-298062-361478",9,5073770,5073770,"G","T","SNP","JAK2","ENST00000381652",1,"missense","c.1849","p.V617F"]
["dbGaP-295219-361137",9,5073770,5073770,"G","T","SNP","JAK2","ENST00000381652",1,"missense","c.1849","p.V617F"]
["dbGap-390083-851772",2,198266834,198266834,"T","C","SNP","SF3B1","ENST00000335508",-1,"missense","c.2098","p.K700E"]
["dbGaP-297986-360566",2,198266834,198266834,"T","C","SNP","SF3B1","ENST00000335508",-1,"missense","c.2098","p.K700E"]
["dbGaP-399048-661495",4,106180783,106180784,"-","G","INS","TET2","ENST00000380013",1,"frame_shift_ins","c.3811_3812","p.C1271fs"]
[]
[{"$nulls":5},"Supplementary Table 7. Rare truncation variants and known hotspot variants detected in DNMT3A, TET2, ASXL1, GNAS, JAK2, SF3B1, IDH1, and IDH2 in 557 WHISP samples."]