Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 2,998,727 G→A N34N (AAC→AAT ygeQ ← protein YgeQ

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009132,998,7270GA100.0% 86.4 / NA 25N34N (AAC→AATygeQprotein YgeQ
Reads supporting (aligned to +/- strand):  ref base G (0/0);  new base A (12/13);  total (12/13)

AGACGATAATTAGGATACTTATCTGGATTTAACGATAAATAACTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATGTTAAATACAGATTCACTCGTCACTTCTGCCCCTGTCGCCTGGCATGTGCCGCACGAAAATATACCAGCGAGCAGA  >  NC_000913/2998650‑2998802
                                                                             |                                                                           
agaCGATAATTAGGATACTTATCTGGATTTAACGATAAATAACTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATAtt                                                                           >  2:490641/1‑80 (MQ=255)
agaCGATAATTAGGATACTTATCTGGATTTAACGATAAATAACTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATATTa                                                                          <  2:490613/81‑1 (MQ=255)
 gaCGATAATTAGGATACTTATCTGGATTTAACGATAAATAACTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATATTaa                                                                         <  2:490614/81‑1 (MQ=255)
        aTTAGGATACTTATCTGGATTTAACGATAAATAACTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATATTAAATACAGa                                                                  <  2:490615/81‑1 (MQ=255)
                 cTTATCTGGATTTAACGATAAATAACTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGt                                                         <  1:490617/81‑1 (MQ=255)
                  ttATCTGGATTTAACGATAAATAACTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGt                                                         >  2:490645/1‑80 (MQ=255)
                    aTCTGGATTTAACGATAAATAACTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTc                                                        <  2:490617/79‑1 (MQ=255)
                    aTCTGGATTTAACGATAAATAACTTTTATCTGTTGCTGCCCCCGTGGAACTAAGAATATTAAATACAGATTCACTCGTCAc                                                      >  2:490639/1‑81 (MQ=255)
                            ttAACGATAAATAACTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGccc                                              >  1:490641/1‑81 (MQ=255)
                                        aaCTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCa                                 >  2:490644/1‑81 (MQ=255)
                                         aCTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCAt                                <  1:490619/81‑1 (MQ=255)
                                               aTCTGTTGCTGCCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGcc                           <  2:490619/80‑1 (MQ=255)
                                                   gTTGCTGCCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTCCCTCAc                       >  2:490649/1‑80 (MQ=255)
                                                    ttGCTGCCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGCCGCAc                       <  2:490620/79‑1 (MQ=255)
                                                     tgctgcCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGCCGCACGa                     >  2:490642/1‑80 (MQ=255)
                                                         gcCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGCCGCACGAAAata                >  1:490644/1‑81 (MQ=255)
                                                         gcCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGCCGCACGAAAata                >  2:490647/1‑81 (MQ=255)
                                                         gcCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGCCGCACGAAAata                >  2:490656/1‑81 (MQ=255)
                                                          cccccGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGCCGCACGAAAatat               <  2:490621/81‑1 (MQ=255)
                                                                  gAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGCCGCACGAAAATATACCAGCg        <  2:490623/80‑1 (MQ=255)
                                                                  gAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGCCGCACGAAAATATACCAGCg        <  1:490623/80‑1 (MQ=255)
                                                                      tAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGTATGTGCCGCACGAAAATATACCAGCGAg      >  2:490646/1‑78 (MQ=255)
                                                                       aaGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGCCGCACGAAAATATACCAGCGAGCag   <  1:490625/80‑1 (MQ=255)
                                                                       aaGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGCCGCACGAAAATATACCAGCGAGCag   >  2:490651/1‑80 (MQ=255)
                                                                        aGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGCCGCACGAAAATATACCAGCGAGCaga  <  1:490626/80‑1 (MQ=255)
                                                                             |                                                                           
AGACGATAATTAGGATACTTATCTGGATTTAACGATAAATAACTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATGTTAAATACAGATTCACTCGTCACTTCTGCCCCTGTCGCCTGGCATGTGCCGCACGAAAATATACCAGCGAGCAGA  >  NC_000913/2998650‑2998802

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: