Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 612,097 G→A T133I (ACT→ATT)  fepA ← ferric enterobactin outer membrane transporter

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_000913612,0970GA100.0% 99.1 / NA 28T133I (ACT→ATT) fepAferric enterobactin outer membrane transporter
Reads supporting (aligned to +/- strand):  ref base G (0/0);  new base A (8/20);  total (8/20)

GTTGCCATAACGCGCAGCTGCCGGACCACGCAGAACTTCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAGTATCACCACGGGTATCGCGCTCGCCACGCCAGCCCTGACGCACCGAGTTACGGCTGCTTACCGGCTTGCCGTCAAT  >  NC_000913/612024‑612173
                                                                         |                                                                            
gTTGCCATAACGCGCAGCTGCCGGACCACGCAGAACTTCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAATATcacc                                                                       <  2:131129/81‑1 (MQ=255)
 ttGCCATAACGCGCAGCTGCCGGACCACGCAGAACTTCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAATATcacca                                                                      <  1:131131/81‑1 (MQ=255)
 ttGCCATAACGCGCAGCTGCCGGACCACGCAGAACTTCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAATATcacca                                                                      <  2:131130/81‑1 (MQ=255)
   gCCATAACGCGCAGCTGCCGGACCACGCAGAACTTCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAATATcaccac                                                                     <  1:131132/80‑1 (MQ=255)
     cATAACGCGCAGCTGCCGGACCACGCAGAACATCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAATATCACCACggg                                                                  <  2:131133/81‑1 (MQ=255)
           gcgcAGCTGCCGGACCACGCAGAACTTCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAATATCACCACGGGTATcgc                                                            <  1:131134/81‑1 (MQ=255)
             gcAGCTGCCGGACCACGCAGAACTTCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAATATCACCACGGGTATCgcgc                                                          >  2:131179/1‑81 (MQ=255)
             gcAGCTGCCGGACCACGCAGAACTTCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAATATCACCACGGGTATCgcgc                                                          <  2:131135/81‑1 (MQ=255)
              cAGCTGCCGGACCACGCAGAACTTCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAATATCACCACGGGTATCGCGCt                                                         <  1:131136/81‑1 (MQ=255)
                    ccGGACCACGCAGAACTTCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAATATCACCACGGGTATCGCGCTcgccac                                                   <  2:131137/81‑1 (MQ=255)
                     cGGACCACGCAGAACTTCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAATATCACCACGGGTATCGCGCTcgccacg                                                  >  2:131180/1‑81 (MQ=255)
                          cACGCAGAACTTCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAATATCACCACGGGTATCGCGCTCGCCACGCCAGc                                             >  2:131181/1‑81 (MQ=255)
                             gCAGAACTTCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAATATCACCACGGGTATCGCGCTCGCCACGCCAGCCCt                                          >  2:131183/1‑81 (MQ=255)
                              cAGAACTTCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAATATCACCACGGGTATCGTGCTCGCCACGCCAGCCCt                                          >  2:131175/1‑80 (MQ=255)
                                gAACTTCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAATATCACCACGGGTATCGCGCTCGCCACGCCAGCCCTGAc                                       <  1:131138/81‑1 (MQ=255)
                                 aaCTTCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAATATCACCACGGGTATCGCGCTCGCCACGCCAGCCCTGACg                                      >  1:131192/1‑81 (MQ=255)
                                  aCTTCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAATATCACCACGGGTATCGCGCTCGCCACGCCAGCCCTGACGc                                     <  2:131139/81‑1 (MQ=255)
                                        aTACGTTCAATCATTTCAGGTGGCACCCAGGAAATATCACCACGGGTATCGCGCTCGCCACGCCAGCCCTGACGCACCGAg                               <  1:131140/81‑1 (MQ=255)
                                           cGTTCAATCATTTCAGGTGGCACCCAGGAAATATCACCACGGGTATCGCGCTCGCCACGCCAGCCCTGACGCACCGAGtt                             <  1:131141/80‑1 (MQ=255)
                                            gTTCAATCATTTCAGGTGGCACCCAGGAAATATCACCACGGGTATCGCGCTCGCCACGCCAGCCCTGACGCACCGAGTTAc                           <  1:131142/81‑1 (MQ=255)
                                                aaTCATTTCAGGTGGCACCCAGGAAATATCACCACGGGTATCGCGCTCGCCACGCCAGCCCTGACGCACCGAGTTACGgct                       <  1:131143/81‑1 (MQ=255)
                                                    aTTTCAGGTGGCACCCAAGAAATATCACCACGGGTATCGCGCTTGCCACGCCAGCCCTGACGCACCGAGTTACGGCTGCtt                   <  2:131144/81‑1 (MQ=255)
                                                      ttCAGGTGGCACCCAGGAAATATCACCACGGGTATCGCGCTCGCCACGCCAGCCCTGACGCACCGAGTTACGGCTGCTTAc                 >  2:131182/1‑81 (MQ=255)
                                                       tCAGGTGGCACCCAGGAAATATCACCACGGGTATCGCGCTCGCCACGCCAGCCCTGACGCACCGAGTTACGGCTGCTTAcc                >  2:131188/1‑81 (MQ=255)
                                                        cAGGTGGCACCCAGGAAATATCACCACGGGTATCGCGCTCGCCACGCCAGCCCTGACGCACCGAGTTACGGCTGCTTAcc                <  2:131145/80‑1 (MQ=255)
                                                            tGGCACCCAGGAAATATCACCACGGGTATCGCGCTCGCCACGCCAGCCCTGACGAACCGAGTTACGGCTGCTTACCGGCtt           <  1:131146/81‑1 (MQ=255)
                                                              gCACCCAGGAAATATCACCACGGGTATCGCGCTCGCCACGCCAGCCCTGACGCACCGAGTTACGGCTGCTTACCGGCTTg          <  2:131147/80‑1 (MQ=255)
                                                                     ggAAATATCACCACGGGTATCGCGCTCGCCACGCCAGCCCTGACGCACCGAGTTACGGCTGCTTACCGGCTTGCCGtcaat  <  1:131148/81‑1 (MQ=255)
                                                                         |                                                                            
GTTGCCATAACGCGCAGCTGCCGGACCACGCAGAACTTCAATACGTTCAATCATTTCAGGTGGCACCCAGGAAGTATCACCACGGGTATCGCGCTCGCCACGCCAGCCCTGACGCACCGAGTTACGGCTGCTTACCGGCTTGCCGTCAAT  >  NC_000913/612024‑612173

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: