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% 68.4 / NA 18A16S (GCC→TCC) pepAaminopeptidase A/I
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base A (6/12);  total (6/12)

ATCGGAGAAAGGCGACGTGGTTCGAAGACGCCCACGACGATGCAGGCACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACTAAACTCCAT  >  NC_000913/4485860‑4485951
                                              |                                             
aTCGGAGAAAGGCGACGTGGTTCGAAGACGCCCACGACGATGCAGGAAc                                             <  1:618603/49‑1 (MQ=255)
      gaAAGGCGACGTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCGCt                                       >  1:129372/1‑49 (MQ=255)
      gaAAGGCGACGTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCGCt                                       <  1:2280960/49‑1 (MQ=255)
        aaGGCGACGTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTGt                                     <  1:2072663/49‑1 (MQ=255)
         aGGCGACGTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTGtt                                    >  1:1271986/1‑49 (MQ=255)
         aGGCGACGTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTGtt                                    >  1:1362547/1‑49 (MQ=255)
              aCGTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTGTTTCTcc                               >  1:920832/1‑49 (MQ=255)
              aCGTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTGTTTCTcc                               <  1:2047456/49‑1 (MQ=255)
               cGTGGTTCGAAGACGCCCACGACGATGCAGGAACTCCGCTGTTTCTCCg                              <  1:621092/49‑1 (MQ=255)
                       gAAGACGCCCACGACGATGCAGGAACTCCGCTGTTTCTCCGGGCTAcc                       <  1:698616/48‑1 (MQ=255)
                       gAAGACGCCCACGACGATGCAGGAACTCCGCTGTTTCTCCGGGCTACCg                      >  1:759301/1‑49 (MQ=255)
                        aaGACGCCCACGACGATGCAGGAACTCCGCTGTTTCTCCGGGCTACCGc                     <  1:1253038/49‑1 (MQ=255)
                        aaGACGCCCACGACGATGCAGGAACTCCGCTGTTTCTCCGGGCTACCGc                     <  1:1037012/49‑1 (MQ=255)
                            cGCCCACGACGATGCAGGAACTCCGCTGTTTCTCCGGGCTACCGCtttt                 <  1:1679698/49‑1 (MQ=255)
                             gCCCACGACGATGCAGGAACTCCGCTGTTTCTCCGGGCTACCGCttttt                <  1:1443414/49‑1 (MQ=255)
                                 acgacgATGCAGGAACTCCGCTGTTTCTCCGGGCTACCGCTTTTTacac            >  1:1931762/1‑49 (MQ=255)
                                  cgacgaTGCAGGAACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACt           <  1:1404177/49‑1 (MQ=255)
                                           aGGAACTCCGCTGTTTCTCCGGGCTACCGCTTTTTACACTAAACTCCAt  <  1:1146266/49‑1 (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: