Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 2,756,138 Δ1 bp intergenic (+183/‑21) ssrA → / → intA tmRNA/CP4‑57 prophage; integrase

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009132,756,1370C.100.0% 98.6 / NA 21intergenic (+182/‑22)ssrA/intAtmRNA/CP4‑57 prophage; integrase
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base . (8/13);  total (8/13)

AGGCCCATTGATAGGCCCAACGAAAAGCTCTATTGTTTACGTTGGGCCTAAACGCAGGGAGACTCCCCATGGCAAGAAAAACCAAGCC  >  NC_000913/2756091‑2756178
                                              |                                         
aGGCCCATTGATAGGCCCAACGAAAAGCTCTATTGTTTACGTTGGGct                                          <  1:772597/48‑2 (MQ=255)
   cccATTGATAGGCCCAACGAAAAGCTCTATTGTTTACGTTGGGCTAAAc                                     <  1:2045780/49‑1 (MQ=255)
      aTTGATAGGCCCAACGAAAAGCTCTATTGTTTACGTTGGGCTAAACg                                    >  1:1969955/1‑47 (MQ=255)
      aTTGATAGGCCCAACGAAAAGCTCTATTGTTTACGTTGGGCTAAACGCa                                  <  1:1015848/49‑1 (MQ=255)
         gATAGGCCCAACGAAAAGCTCTATTGTTTACGTTGGGCTAAACGCAgg                                <  1:1964799/48‑1 (MQ=255)
          aTAGGCCCAACGAAAAGCTCTATTGTTTACGTTGGGCTAAACGCAgg                                >  1:888431/1‑47 (MQ=255)
          aTAGGCCCAACGAAAAGCTCTATTGTTTACGTTGGGCTAAACGCAgg                                >  1:1976233/1‑47 (MQ=255)
          aTAGGCCCAACGAAAAGCTCTATTGTTTACGTTGGGCTAAACGCAGGga                              <  1:1210183/49‑1 (MQ=255)
           tAGGCCCAACGAAAAGCTCTATTGTTTACGTTGGGCTAAACGCAgg                                >  1:907712/1‑46 (MQ=255)
           tAGGCCCAACGAAAAGCTCTATTGTTTACGTTGGGCTAAACGCAGGgag                             <  1:2049959/49‑1 (MQ=255)
           tAGGCCCAACGAAAAGCTCTATTGTTTACGTTGGGCTAAACGCAGGgag                             <  1:290823/49‑1 (MQ=255)
               cccAACGAAAAGCTCTATTGTTTACGTTGGGCTAAACGCAGGGAGACTc                         <  1:238910/49‑1 (MQ=255)
                      aaaaGCTCTATTGTTTACGTTGGGCTAAACGCAGGGAGACTCCCCAcct                  <  1:1635752‑M1/49‑4 (MQ=255)
                      aaaaGCTCTATTGTTTACGTTGGGCTAAACGCAGGGAGACTCCCCAcct                  >  1:1336955‑M1/1‑46 (MQ=255)
                      aaaaGCTCTATTGTTTACGTTGGGCTAAACGCAGGGAGACTCCCCAcct                  >  1:108320‑M1/1‑46 (MQ=255)
                               aTTGTTTACGTTGGGCTAAACGCAGGGAGACTCCCCAcctttgaaaa           >  1:1509195‑M1/1‑37 (MQ=255)
                                ttGTTTACGTTGGGCTAAACGCAGGGAGACTCCCCAcctttgaaaacag        >  1:880285‑M1/1‑36 (MQ=255)
                                ttGTTTACGTTGGGCTAAACGCAGGGAGACTCCCCAcctttgaaaaca         <  1:2082753‑M1/48‑13 (MQ=255)
                                ttGTTTACGTTGGGCTAAACGCAGGGAGACTCCCCAcctttgaaaa           <  1:1560886‑M1/46‑11 (MQ=255)
                                ttGTTTACGTTGGGCTAAACGCAGGGAGACTCCCCAcctttgaaaa           <  1:261567‑M1/46‑11 (MQ=255)
                                   tttACGTTGGGCTAAACGCAGGGAGACTCCCCAcctttgaaaacagga      <  1:1874605‑M1/48‑16 (MQ=255)
                                       cGTTGGGCTAAACGCAGGGAGACTCCCCAcctttgaaaacaggatgta  <  1:1473986‑M1/48‑20 (MQ=255)
                                              |                                         
AGGCCCATTGATAGGCCCAACGAAAAGCTCTATTGTTTACGTTGGGCCTAAACGCAGGGAGACTCCCCATGGCAAGAAAAACCAAGCC  >  NC_000913/2756091‑2756178

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: