ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL ME018 PHPT1 SNP Missense_Mutation 9 139743925 G A 37 64 LUAD TCGA-05-4427 PHPT1 SNP Missense_Mutation 9 139745268 A T 14 64 CRC TCGA-AA-3516 PHPT1 SNP Nonsense_Mutation 9 139745255 A T 5 53 UCEC TCGA-B5-A11E PHPT1 SNP Missense_Mutation 9 139745229 C T 26 80 HNSC TCGA-CV-6936 PHPT1 SNP Missense_Mutation 9 139744530 G A 39 75