breseq  version 0.35.4  
mutation predictions | marginal predictions | summary statistics | genome diff | command line log

Predicted mutations
evidence position mutation annotation gene description
RA 3,547 +A coding (307/798 nt) r1tp05 → ORF5
RA 3,556 +GT coding (316/798 nt) r1tp05 → ORF5
RA 5,234 2 bp→GC coding (325‑326/834 nt) r1tp09 → ORF9
RA 5,237 C→G L110V (CTT→GTT)  r1tp09 → ORF9
RA 8,712 (TGAATT)3→2 coding (21‑26/396 nt) r1tp14 → ORF14
RA 9,972 C→A A59E (GCA→GAA)  r1tp18 → ORF18
RA 13,763 T→C V122A (GTT→GCT)  r1tp24 → ORF24
RA 23,480 A→C E213A (GAA→GCA)  r1tp40 → ORF40

Unassigned missing coverage evidence
   seq id start end size ←reads reads→ gene description
* * ÷ NC_004302 1 11 11 NA [0] [0] 2 –/r1tp01 –/Integrase
* * ÷ NC_004302 33195 33350 156 2 [1] [0] NA [r1tp50] [r1tp50]

Unassigned new junction evidence
  seq id position reads (cov) reads (cov) score skew freq annotation gene product
* ? NC_004302 = 2337927 (0.050)475 (0.810) 19/148 0.2 91.4% coding (537/642 nt) r1tp40 ORF40
?NC_004302 24308 = 62 (0.110)intergenic (+198/‑21) r1tp41/r1tp42 ORF41/ORF42