Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 119,028 T→C V99A (GTC→GCC)  ampD → 1,6‑anhydro‑N‑acetylmuramoyl‑L‑alanine amidase

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_000913119,0280TC100.0% 79.2 / NA 22V99A (GTC→GCC) ampD1,6‑anhydro‑N‑acetylmuramoyl‑L‑alanine amidase
Reads supporting (aligned to +/- strand):  ref base T (0/0);  new base C (14/8);  total (14/8)

TAGTCCAGTATGTTCCTTTCGATAAACGTGCATGGCATGCGGGAGTCTCTCAGTATCAGGGGCGCGAACGCTGCAATGATTTTTCTATTG  >  NC_000913/118983‑119072
                                             |                                            
tAGTCCAGTATGTTCCTTTCGATAAACGTGCATGGCATGCGGGAGcctct                                          <  1:354219/50‑1 (MQ=255)
  gTCCAGTATGTTCCTTTCGATAAACGTGCATGGCATGCGGGAGcctct                                          >  1:100393/1‑48 (MQ=255)
  gTCCAGTATGTTCCTTTCGATAAACGTGCATGGCATGCGGGAGcctct                                          >  1:568622/1‑48 (MQ=255)
   tCCAGTATGTTCCTTTCGATAAACGTGCATGGCATGCGGGAGCCTCTCAg                                       >  1:1175908/1‑50 (MQ=255)
     cAGTATGTTCCTTTCGATAAACGTGCATGGCATGCGGGAGCCTCTCAGTa                                     >  1:1468463/1‑50 (MQ=255)
     cAGTATGTTCCTTTCGATAAACGTGCATGGCATGCGGGAGCCTCTCAGTa                                     <  1:507666/50‑1 (MQ=255)
      aGTATGTTCCTTTCGATAAACGTGCATGGCATGCGGGAGCCTCTCAGTAt                                    <  1:1393420/50‑1 (MQ=255)
      aGTATGTTCCTTTCGATAAACGTGCATGGCATGCGGGAGCCTCTCAGTAt                                    >  1:1507894/1‑50 (MQ=255)
              ccTTTCGATAAACGTGCATGGCATGCGGGAGCCTCTCAGTATCAGGGgcg                            >  1:1029517/1‑50 (MQ=255)
              ccTTTCGATAAACGTGCATGGCATGCGGGAGCCTCTCAGTATCAGGGgc                             <  1:1038917/49‑1 (MQ=255)
               cTTTCGATAAACGTGCATGGCATGCGGGAGCCTCTCAGTATCAGGGgcgc                           >  1:1652948/1‑50 (MQ=255)
                     aTAAACGTGCATGGCATGCGGGAGCCTCTCAGTATCAGGGGCGCGAACGc                     >  1:271945/1‑50 (MQ=255)
                     aTAAACGTGCATGGCATGCGGGAGCCTCTCAGTATCAGGGGCGCGAACGc                     >  1:263293/1‑50 (MQ=255)
                       aaaCGTGCATGGCATGCGGGAGCCTCTCAGTATCAGGGGCGCGAACGCTg                   >  1:1555201/1‑50 (MQ=255)
                        aaCGTGCATGGCATGCGGGAGCCTCTCAGTATCAGGGGCGCGAACGCTg                   >  1:418638/1‑49 (MQ=255)
                        aaCGTGCATGGCATGCGGGAGCCTCTCAGTATCAGGGGCGCGAACGCTGc                  <  1:67124/50‑1 (MQ=255)
                          cGTGCATGGCATGCGGGAGCCTCTCAGTATCAGGGGCGCGAACGCTGCaa                <  1:1693210/50‑1 (MQ=255)
                             gcatggcatgCGGGAGCCTCTCAGTATCAGGGGCGCGAACGCTGCAATGa             >  1:1158495/1‑50 (MQ=255)
                              catggcatgCGGGAGCCTCTCAGTATCAGGGGCGCGAACGCTGCAATGAt            >  1:1835184/1‑50 (MQ=255)
                              catggcatgCGGGAGCCTCTCAGTATCAGGGGCGCGAACGCTGCAATGAt            <  1:1306042/50‑1 (MQ=255)
                                    atgCGGGAGCCTCTCAGTATCAGGGGCGCGAACGCTGCAATGATTTTTc       >  1:1976837/1‑49 (MQ=255)
                                    atgCGGGAGCCTCTCAGTATCAGGGGCGCGAACGCTGCAATGATTTTTCt      <  1:1721156/50‑1 (MQ=255)
                                    atgCGGGAGCCTCTCAGTATCAGGGGCGCGAACGCTGCAATGATTTTTCt      <  1:1704268/50‑1 (MQ=255)
                                       cGGGAGCCTCTCAGTATCAGGGGCGCGAACGCTGCAATGATTTTTCTAtt   >  1:480215/1‑50 (MQ=255)
                                        gggAGCCTCTCAGTATCAGGGGCGCGAACGCTGCAATGATTTTTCTATTg  >  1:617833/1‑50 (MQ=255)
                                             |                                            
TAGTCCAGTATGTTCCTTTCGATAAACGTGCATGGCATGCGGGAGTCTCTCAGTATCAGGGGCGCGAACGCTGCAATGATTTTTCTATTG  >  NC_000913/118983‑119072

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: