Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,104,203 A→G T85A (ACA→GCA)  csgB → curlin, minor subunit

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,104,2030AG100.0% 46.5 / NA 14T85A (ACA→GCA) csgBcurlin, minor subunit
Reads supporting (aligned to +/- strand):  ref base A (0/0);  new base G (12/2);  total (12/2)

GTTACGGCAGGGAGGCTCAAAACTTTTGGCGGTTGTTGCGCAAGAAGGTAGTAGCAACCGGGCAAAGATTGACCAGACAGGAGATTATAACCTTGCATATATTGATCAGGCGGGCAGTGCCAACGATGCCAGTATTTCGCAAGGTGC  >  NC_000913/1104127‑1104273
                                                                            |                                                                      
gTTACGGCAGGGAGGCTCAAAACTTTTGGCGGTTGTTGCGCAAGAAGGTAGTAGCAACCGGGCAAAGATTGACcaggcagg                                                                    <  2:222036/81‑1 (MQ=255)
  tACGGCAGGGAGGCTCAAAACTTTTGGCGGTTGTTGCGCAAGAAGGTAGTAGCAACCGGGCAAAGATTGACCAGGCAg                                                                     >  1:222050/1‑78 (MQ=255)
  tACGGCAGGGAGGCTCAAAACTTTTGGCGGTTGTTGCGCAAGAAGGTAGTAGCAACCGGGCAAAGATTGACCAGGCAg                                                                     >  2:222057/1‑78 (MQ=255)
          ggAGGCTCAAAACTTTTGGCGGTTGTTGCGCAAGAAGGTAGTAGCAACCGGGCAAAGATTGACCAGGCAGGAGATTATAAc                                                          >  1:222048/1‑81 (MQ=255)
              gCTCAAAACTTTTGGCGGTTGTTGCGCAAGAAGGTAGTAGCAACCGGGCAAAGATTGACCAGGCAGGAGATTATAACCTTg                                                      <  1:222037/81‑1 (MQ=255)
                   aaaCTTTTGGCGGTTGTTGCGCAAGAAGGTAGTAGCAACCGGGCAAAGATTGACCAGGCAGGAGATTATAACCTTGCatat                                                 <  2:222038/81‑1 (MQ=255)
                    aaCTTTTGGCGGTTGTTGCGCAAGAAGGTAGTAGCAACCGGGCAAAGATTGACCAGGCAGGAGATTATAACCTTGCatata                                                >  1:222054/1‑81 (MQ=255)
                      cTTTTGGCGGTTGTTGCGCAAGAAGGTAGTAGCAACCGGGCAAAGATTGACCAGGCAGGAGATTATAACCTTGCATATAtt                                              >  1:222056/1‑81 (MQ=255)
                              ggTTGTTGCGCAAGAAGGTAGTAGCAACCGGGCAAAGATTGACCAGGCAGGAGATTATAACCTTGCATATATTGATCAGGc                                      >  1:222060/1‑81 (MQ=255)
                                  gttgCGCAAGAAGGTAGTAGCAACCGGGCAAAGATTGACCAGGCAGGAGATTATAACCTTGCATATATTGATCAGGCggg                                   >  1:222064/1‑80 (MQ=255)
                                       gcAAGAAGGTAGTAGCAACCGGGCAAAGATTGACCAGGCAGGAGATTATAACCTTGCATATATTGATCAGGCGGGCAGTGc                             >  1:222063/1‑81 (MQ=255)
                                           gaagGTAGTAGCAACCGGGCAAAGATTGACCAGGCAGGAGATTATAACCTTGCATATATTGATCAGGCGGGCAGTGCCAAc                         >  2:222053/1‑81 (MQ=255)
                                             agGTAGTAGCAACCGGGCAAAGATTGACCAGGCAGGAGATTATAACCTTGCATATATTGATCAGGCGGGCAGTGCCAACGa                       >  1:222055/1‑81 (MQ=255)
                                                    agCAACCGGGCAAAGATTGACCAGGCAGGAGATTATAACCTTGCATATATTGATCAGGCGGGCAGTGCCAACGATGCCAg                 >  2:222058/1‑80 (MQ=255)
                                                                  gATTGACCAGGCAGGAGATTATAACCTTGCATATATTGATCAGGCGGGCAGTGCCAACGATGCCAGTATTTCGCAAGGTGc  >  2:222065/1‑81 (MQ=255)
                                                                            |                                                                      
GTTACGGCAGGGAGGCTCAAAACTTTTGGCGGTTGTTGCGCAAGAAGGTAGTAGCAACCGGGCAAAGATTGACCAGACAGGAGATTATAACCTTGCATATATTGATCAGGCGGGCAGTGCCAACGATGCCAGTATTTCGCAAGGTGC  >  NC_000913/1104127‑1104273

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 31 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: