Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,197,362 T→C L57L (TTA→TTG ymfD ← e14 prophage; putative SAM‑dependent methyltransferase

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,197,3620TC100.0% 43.2 / NA 13L57L (TTA→TTGymfDe14 prophage; putative SAM‑dependent methyltransferase
Reads supporting (aligned to +/- strand):  ref base T (0/0);  new base C (6/7);  total (6/7)

TTAATTCCTCTAATAATTTGCTCTCTTTCAAGTTGCCTTTTCGAGTCTAGAAAAGTAACTTCATCAAATTTACTGATTAATTCATCAGAATATCTAAGTTTTCCGCAGCCAAAATCAAGGGCGTGGCCATTTTTCTCAATGCTTCTAATATACTC  >  NC_000913/1197285‑1197439
                                                                             |                                                                             
ttAATTCCTCTAATAATTTGCTCTCTTTCAAGTTGCCTTTTCGAGTCTAGAAAAGTAACTTCATCAAATTTACTGATCAAt                                                                            >  1:237402/1‑81 (MQ=255)
  aaTTCCTCTAATAATTTGCTCTCTTTCAAGTTGCCTTTTCGAGTCTAGAAAAGTAACTTCATCAAATTTACTGATCAAtt                                                                           >  2:237392/1‑80 (MQ=255)
              aatTTGCTCTCTTTCAAGTTGCCTTTTCGAGTCTAGAAAAGTAACTTCATCAAATTTACTGATCAATTCATCAGAATATc                                                               >  1:237396/1‑80 (MQ=255)
               atTTGCTCTCTTTCAAGTTGCCTTTTCGAGTCTAGAAAAGTAACTTCATCAAATTTACTGATCAATTCATCAGAATATCTa                                                             <  2:237381/81‑1 (MQ=255)
                    ctctctTTCAAGTTGCCTTTTCGAGTCTAGAAAAGTAACTTCATCAAATTTACTGATCAATTCATCAGAATATCTAAGtt                                                         <  1:237382/80‑1 (MQ=255)
                         tttCAAGTTGCCTTTTCGAGTCTAGAAAAGTAACTTCATCAAATTTACTGATCAATTCATCAGAATATCTAAGTTTTc                                                      <  1:237383/78‑1 (MQ=255)
                                          gAGTCTAGAAAAGTAACTTCATCAAATTTACTGATCAATTCATCAGAATATCTAAGTTTTCCGCAGCCAAAATCAAGGGc                                   <  1:237384/80‑1 (MQ=255)
                                            gTCTAGAAAAGTAACTTCATCAAATTTACTGATCAATTCATCAGAATATCTAAGTTTTCCGCAGCCAAAATCAAGGGCGTg                                >  1:237399/1‑81 (MQ=255)
                                                 gAAAAGTAACTTCATCAAATTTACTGATCAATTCATCAGAATATCTAAGTTTTCCGCAGCCAAAATCAAGGGCGTGGCCa                            <  1:237385/80‑1 (MQ=255)
                                                         aCTTCATCAAATTTACTGATCAATTCATCAGAATATCTAAGTTTTCCGCAGCCAAAATCAAGGGCGTGGCCATTTTtctc                    <  2:237386/80‑1 (MQ=255)
                                                           ttCATCAAATTTACTGATCAATTCATCAGAATATCTAAGTTTTCCGCAGCCAAAATCAAGGGCGTGGCCATTTTTCTCAAt                 >  1:237403/1‑81 (MQ=255)
                                                              atcaAATTTACTGATCAATTCATCAGAATATCTAAGTTTTCCGCAGCCAAAATCAAGGGCGTGGCCATTTTTCTCAATGCt              <  2:237387/81‑1 (MQ=255)
                                                                          gATCAATTCATCAGAATATCTAAGTTTTCCGCAGCCAAAATCAAGGGCGTGGCCATTTTTCTCAATGCTTCTAATATACTc  >  1:237401/1‑81 (MQ=255)
                                                                             |                                                                             
TTAATTCCTCTAATAATTTGCTCTCTTTCAAGTTGCCTTTTCGAGTCTAGAAAAGTAACTTCATCAAATTTACTGATTAATTCATCAGAATATCTAAGTTTTCCGCAGCCAAAATCAAGGGCGTGGCCATTTTTCTCAATGCTTCTAATATACTC  >  NC_000913/1197285‑1197439

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: