Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 619,996 G→A G68G (GGC→GGT fepC ← ferric enterobactin ABC transporter ATP binding subunit

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_000913619,9960GA100.0% 93.7 / NA 27G68G (GGC→GGTfepCferric enterobactin ABC transporter ATP binding subunit
Reads supporting (aligned to +/- strand):  ref base G (0/0);  new base A (11/16);  total (11/16)

CGGCGTGGTAGCATTTTGCGCCAACAGACCAATCCGGCGTGCAACCTCTTTACTGGCGTAATGTTGAATGTGCTCGCCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAGGCGGCTTAAGGTACGCAGTAACGTGGATTTAC  >  NC_000913/619921‑620066
                                                                           |                                                                      
cGGCGTGGTAGCATTTTGCGCCAACAGACCAATCCGGCGTGCAACCTCTTTACTGGCGTAATGTTGAATGTGCTCACCATc                                                                   <  2:132850/81‑1 (MQ=255)
   cGTGGTAGCATTTTGCGCCAACAGACCAATCCGGCGTGCAACCTCTTTACTGGCGTAATGTTGAATGTGCTCACCATccag                                                                >  2:132896/1‑81 (MQ=255)
    gTGGTAGCATTTTGCGCCAACAGACCAATCCGGCGTGCAACCTCTTACTGGCGTAATGTTGAATGTGCTCACCATccagc                                                               >  2:132905/1‑80 (MQ=255)
          gCATTTTGCGCCAACAGACCAATCCGGCGTGCAACCTCTTTACTGGCGTAATGTTGAATGTGCTCACCATCCAGCCAGAc                                                          <  1:132851/80‑1 (MQ=255)
                   gcCAACAGACCAATCCGGCGTGCAACCTCTTTACTGGCGTAATGTTGAATGTGCTCACCATCCAGCCAGACATGCCCAt                                                  >  1:132898/1‑79 (MQ=255)
                          gACCAATCCGGCGTGCAACCTCTTTACTGGCGTAATGTTGAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCg                                         <  2:132852/81‑1 (MQ=255)
                            ccAATCCGGCGTGCAACCTCTTTACTGGCGTAATGTTGAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGt                                        >  1:132965/1‑80 (MQ=255)
                                  cGGCGTGCAACCTCTTTACTGGCGTAATGTTGAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCGTCAgg                                 >  2:132904/1‑81 (MQ=255)
                                    gCGTGCAACCTCTTTACTGGCGTAATGTTGAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAggcg                               <  1:132853/81‑1 (MQ=255)
                                    gCGTGCAACCTCTTTACTGGCGTAATGTTGAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAggcg                               <  2:132854/81‑1 (MQ=255)
                                      gTGCAACCTCTTTACTGGCGTAATGTTGAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAggcggc                             >  2:132952/1‑81 (MQ=255)
                                      gTGCAACCTCTTTACTGGCGTAATGTTGAATATGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAggcggc                             <  2:132855/81‑1 (MQ=255)
                                         cAACCTCTTTACTGGCGTAATGTTGAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAGGCGGCTTa                          <  1:132856/81‑1 (MQ=255)
                                           aCCTCTTTACTGGCGTAATGTTGAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAGGCGGCTTAAg                        >  1:132908/1‑81 (MQ=255)
                                           aCCTCTTTACTGGCGTAATGTTGAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAGGCGGCTTAAg                        <  1:132857/81‑1 (MQ=255)
                                                tttACTGGCGTAATGTTGAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAGGCGGCTTAAGGTa                     <  2:132858/79‑1 (MQ=255)
                                                  tACTGGCGTAATGTTGAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAGGCGGCTTAAGGTACg                   <  1:132859/79‑1 (MQ=255)
                                                  tACTGGCGTAATGTTGAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAGGCGGCTTAAGGTACGc                  <  2:132860/80‑1 (MQ=255)
                                                    cTGGCGTAATGTTGAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAGGCGGCTTAAGGTACGCAg                <  1:132861/80‑1 (MQ=255)
                                                     tGGCGTAATGTTGAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAGGCGGCTTAAGGTACGCAGt               >  2:132914/1‑80 (MQ=255)
                                                       gCGTAATGTTGAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAGGCGGCTTAAGGTACGCAGTAAc            <  2:132862/81‑1 (MQ=255)
                                                            aTGTTGAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAGGCGGCTTAAGGTACGCAGTAACGTGGa       <  1:132863/81‑1 (MQ=255)
                                                             tGTTGAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAGGCGGCTTAAGGTACGCAGTAACGTGGAt      <  1:132864/81‑1 (MQ=255)
                                                               ttGAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAGGCGGCTTAAGGTACGCAGTAACGTGGAttt    <  2:132865/81‑1 (MQ=255)
                                                                 gAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAGGCGGCTTAAGGTACGCAGTAACGTGGATTTAc  >  2:132913/1‑81 (MQ=255)
                                                                 gAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAGGCGGCTTAAGGTACGCAGTAACGTGGATTTAc  >  2:132901/1‑81 (MQ=255)
                                                                 gAATGTGCTCACCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAGGCGGCTTAAGGTACGCAGTAACGTGGATTTAc  >  2:132917/1‑81 (MQ=255)
                                                                           |                                                                      
CGGCGTGGTAGCATTTTGCGCCAACAGACCAATCCGGCGTGCAACCTCTTTACTGGCGTAATGTTGAATGTGCTCGCCATCCAGCCAGACATGCCCATGAGCAGGCGTCATCAGGCGGCTTAAGGTACGCAGTAACGTGGATTTAC  >  NC_000913/619921‑620066

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 31 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: