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 |