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% 49.7 / NA 15N34N (AAC→AATygeQprotein YgeQ
Reads supporting (aligned to +/- strand):  ref base G (0/0);  new base A (5/10);  total (5/10)

ATAATTAGGATACTTATCTGGATTTAACGATAAATAACTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATGTTAAATACAGATTCACTCGTCACTTCTGCCCCTGTCGCCTGGCATGTGCCGCACGAAAATATACCAGCGAGC  >  NC_000913/2998655‑2998799
                                                                        |                                                                        
aTAATTAGGATACTTATCTGGATTTAACGATAAATAACTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATATTAAATa                                                                   >  1:547188/1‑80 (MQ=255)
   aTTAGGATACTTATCTGGATTTAACGATAAATAACTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATATTAAATACAGa                                                               <  2:547168/81‑1 (MQ=255)
       ggATACTTATCTGGATTTAACGATAAATAACTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATATTAAATACAGATTc                                                            <  2:547169/80‑1 (MQ=255)
               aTCTGGATTTAACGATAAATAACTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTc                                                     <  2:547170/79‑1 (MQ=255)
                           cGATAAATAACTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGccctgtc                                       >  2:547196/1‑77 (MQ=255)
                                 ataaCTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTgg                                <  2:547171/81‑1 (MQ=255)
                                    aCTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCAt                             <  1:547172/81‑1 (MQ=255)
                                        ttATCTGTTGCTGCCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCAtgt                           <  1:547173/79‑1 (MQ=255)
                                          aTCTGTTGCTGCCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGCCg                       >  2:547195/1‑81 (MQ=255)
                                              gTTGCTGCCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGCCGCAc                    >  2:547194/1‑80 (MQ=255)
                                                    gcCCCCGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGCCGCACGAAAata             >  2:547198/1‑81 (MQ=255)
                                                     cccccGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGCCGCACGAAAat              <  1:562657/79‑1 (MQ=255)
                                                        ccGTGGAATTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGCCGCACGAAAATATAcc         <  2:547174/81‑1 (MQ=255)
                                                              aaTTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGCCGCACGAAAATATACCAGCGAg   <  1:547175/81‑1 (MQ=255)
                                                               aTTAAGAATATTAAATACAGATTCACTCGTCACTTCTGCCCTGTCGCCTGGCATGTGCCGCACGAAAATATACCAGCGAGc  <  2:547176/81‑1 (MQ=255)
                                                                        |                                                                        
ATAATTAGGATACTTATCTGGATTTAACGATAAATAACTTTTATCTGTTGCTGCCCCCGTGGAATTAAGAATGTTAAATACAGATTCACTCGTCACTTCTGCCCCTGTCGCCTGGCATGTGCCGCACGAAAATATACCAGCGAGC  >  NC_000913/2998655‑2998799

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: