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Table 2 Allelic counts for tumor sample SU048 from Jan et al.[17]

From: Inferring clonal evolution of tumors from single nucleotide somatic mutations

SNV Variant allele read counts Read depth Allele frequency Cluster ID
TET2-E1357stop 7,436 19,553 0.380 (95% CI: 0.375-0.386) A
SMC1A 182,974 660,069 0.277 (95% CI: 0.276-0.278) B
ACSM1 17,149 127,236 0.135 (95% CI: 0.133-0.136) B
OLFM2 13,828 122,523 0.113 (95% CI: 0.111-0.114) B
TET2-D1384V 1,833 17,687 0.104 (95% CI: 0.100-0.107) B
ZMYM3 18,536 307,346 0.060 (95% CI: 0.060-0.061) B