Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 4,485,906 C→A A16S (GCC→TCC)  pepA ← aminopeptidase A/I

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009134,485,9060CA100.0% 146.8 / NA 36A16S (GCC→TCC) pepAaminopeptidase A/I
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base A (19/17);  total (19/17)

ATCGGAGAAAGGCGACGTGGTTCGAAGACGCCCACGACGATGCAGGCACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACTAAACTCCAT  >  NC_000913/4485860‑4485951
                                              |                                             
aTCGGAGAAAGGCGACGTGGTTCGAAGACGCCCACGACGATGCAGGAAc                                             >  1:621566/1‑49 (MQ=255)
   ggAGAAAGGCGACGTGGTTCGAAGACGCCCACGACGATGCAGGAACTcc                                          >  1:598304/1‑49 (MQ=255)
   ggAGAAAGGCGACGTGGTTCGAAGACGCCCACGACGATGCAGGAACTcc                                          >  1:1142623/1‑49 (MQ=255)
   ggAGAAAGGCGACGTGGTTCGAAGACGCCCACGACGATGCAGGAACTc                                           <  1:2097993/48‑1 (MQ=255)
    gagaAAGGCGACGTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCg                                         >  1:2076192/1‑49 (MQ=255)
       aaaGGCGACGTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTg                                      >  1:1033079/1‑49 (MQ=255)
       aaaGGCGACGTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTg                                      <  1:1880218/49‑1 (MQ=255)
        aaGGCGACGTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTGt                                     >  1:1061769/1‑49 (MQ=255)
          ggCGACGTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTGttt                                   >  1:1792293/1‑49 (MQ=255)
            cGACGTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTGTTtct                                 >  1:998730/1‑49 (MQ=255)
            cGACGTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTGTTtct                                 <  1:685303/49‑1 (MQ=255)
             gACGTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTGTTtctc                                <  1:1295032/49‑1 (MQ=255)
              aCGTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTGTTTCTcc                               >  1:1588741/1‑49 (MQ=255)
              aCGTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTGTTTCTcc                               <  1:1144781/49‑1 (MQ=255)
                gTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTGTTTCTCCgg                             >  1:1017022/1‑49 (MQ=255)
                  ggTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTGTTTCTCCGGGc                           >  1:441189/1‑49 (MQ=255)
                   gTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTGTTTCTCCGGGCt                          <  1:1677726/49‑1 (MQ=255)
                   gTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTGTTTCTCCGGGCt                          <  1:1227025/49‑1 (MQ=255)
                       gAAGACGCCCACGACGATGCAGGAACTCCGCTGTTTCTCCGGGCTAcc                       <  1:1280685/48‑1 (MQ=255)
                        aaGACGCCCACGACGATGCAGGAACTCCGCTGTTTCTCCGGGCTACCGc                     >  1:1742213/1‑49 (MQ=255)
                             gCCCACGACGATGCAGGAACTCCGCTGTTTCTCCGGGCTACCGCtttt                 >  1:1337100/1‑48 (MQ=255)
                                  cgacgaTGCAGGAACTCCGCTGTTTCTCCGGGCTACCGCTTTTTacac            >  1:1004338/1‑48 (MQ=255)
                                   gacgaTGCAGGAACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACt           >  1:756734/1‑48 (MQ=255)
                                     cgaTGCAGGAACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACTaaa        <  1:205326/49‑1 (MQ=255)
                                     cgaTGCAGGAACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACTaaa        <  1:1104600/49‑1 (MQ=255)
                                      gaTGCAGGAACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACTAAAc       >  1:1183239/1‑49 (MQ=255)
                                       aTGCAGGAACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACTAAACt      <  1:638529/49‑1 (MQ=255)
                                       aTGCAGGAACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACTAAACt      >  1:1223230/1‑49 (MQ=255)
                                        tGCAGGAACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACTAAACTc     <  1:48770/49‑1 (MQ=255)
                                         gCAGGAACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACTAAACTc     >  1:1255051/1‑48 (MQ=255)
                                          cAGGAACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACTAAACTcc    <  1:710863/48‑1 (MQ=255)
                                          cAGGAACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACTAAACTCCa   <  1:1894983/49‑1 (MQ=255)
                                          cAGGAACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACTAAACTCCa   <  1:1063821/49‑1 (MQ=255)
                                          cAGGAACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACTAAACTCCa   <  1:776592/49‑1 (MQ=255)
                                           aGGAACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACTAAACTCCAt  <  1:1963735/49‑1 (MQ=255)
                                           aGGAACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACTAAACTCCAt  >  1:215254/1‑49 (MQ=255)
                                              |                                             
ATCGGAGAAAGGCGACGTGGTTCGAAGACGCCCACGACGATGCAGGCACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACTAAACTCCAT  >  NC_000913/4485860‑4485951

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: