Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 595,846 A→G K83E (AAA→GAA)  cusC → copper/silver export system outer membrane channel

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_000913595,8460AG100.0% 61.4 / NA 18K83E (AAA→GAA) cusCcopper/silver export system outer membrane channel
Reads supporting (aligned to +/- strand):  ref base A (0/0);  new base G (6/12);  total (6/12)

TTGATAATCAGGTGAAGACGCTGATTAGCGAGGCGCTGGTGAATAATCGGGATTTGCGCATGGCGACGCTGAAAGTGCAGGAGGCACGGGCGCAATATCGTCTGACCGATGCCGACCGCTACCCACAGCTCAATGGCGAGGGCAGCGGC  >  NC_000913/595775‑595923
                                                                       |                                                                             
ttgATAATCAGGTGAAGACGCTGATTAGCGAGGCGCTGGTGAATAATCGGGATTTGCGCATGGCGACGCTGGAAGTGCagg                                                                      <  2:127925/81‑1 (MQ=255)
   aTAATCAGGTGAAGACGCTGATTAGCGAGGCGCTGGTGAATAATCGGGATTTGCGCATGGCGACGCTGGAAGTGCaggag                                                                    <  1:127926/80‑1 (MQ=255)
    tAATCAGGTGAAGACGCTGATTAGCGAGGCGCTGGTGAATAATCGGGATTTGCGCATGGCGACGCTGGAAGTGCAGGAGGc                                                                  <  1:127927/81‑1 (MQ=255)
              aaGACGCTGATTAGCGAGGCGCTGGTGAATAATCGGGATTTGCGCATGGCGACGCTGGAAGTGCAGGAGGCACGGGCGCaa                                                        <  2:127928/81‑1 (MQ=255)
                    cTGATTAGCGAGGCGCTGGTGAATAATCGGGATTTGCGCATGGCGACGCTGGAAGTGCAGGAGGCACGGGCGCAATATCGt                                                  <  2:127929/81‑1 (MQ=255)
                         tAGCGAGGCGCTGGTGAATAATCGGGATTTGCGCATGGCGACGCTGGAAGTGCAGGAGGCACGGGCGCAATATCGTCTGAc                                             >  2:127967/1‑81 (MQ=255)
                             gAGGCGCTGGTGAATAATCGGGATTTGCGCATGGCGACGCTGGAAGTGCAGGAGGCACGGGCGCAATATCGTCTGACCGAt                                         <  2:127930/81‑1 (MQ=255)
                               ggCGCTGGTGAATAATCGGGATTTGCGCATGGCGACGCTGGAAGTGCAGGAGGCACGGGCGCAATATCGTCTGACCGATGc                                       <  2:127931/81‑1 (MQ=255)
                                gcgcTGGTGAATAATCGGGATTTGCGCATGGCGACGCTGGAAGTGCAGGAGGCACGGGCGCAATATCGTCTGACCGATGcc                                      <  1:127932/81‑1 (MQ=255)
                                    tGGTGAATAATCGGGATTTGCGCATGGCGACGCTGGAAGTGCAGGAGGCACGGGCGCAATATCGTCTGACCGATGCCGAcc                                  >  1:127970/1‑81 (MQ=255)
                                      gTGAATAATCGGGATTTGCGCATGGCGACGCTGGAAGTGCAGGAGGCACGGGCGCAATATCGTCTGACCGATGCCGACCg                                 <  1:127933/80‑1 (MQ=255)
                                            aatCGGGATTTGCGCATGGCGACGCTGGAAGTGCAGGAGGCACGGGCGCAATATCGTCTGACCGATGCCGACCGCTACCca                          >  1:127976/1‑81 (MQ=255)
                                              tCGGGATTTGCGCATGGCGACGCTGGAAGTGCAGGAGGCACGGGCGCAATATCGTCTGACCGATGCCGACCGCTACCca                          >  1:127975/1‑79 (MQ=255)
                                                      tGCGCATGGCGACGCTGGAAGTGCAGGAGGCACGGGCGCAATATCGTCTGACCGATGCCGACCGCTACCCACAGCTCAAt                 <  2:127934/80‑1 (MQ=255)
                                                         gcATGGCGACGCTGGAAGTGCAGGAGGCACGGGCGCAATATCGTCTGACCGATGCCGACCGCTACCCACAGCTCAATGGc              >  1:127977/1‑80 (MQ=255)
                                                         gcATGGCGACGCTGGAAGTGCAGGAGGCACGGGCGCAATATCGTCTGACCGATGCCGACCGCTACCCACAGCTCAATGGCg             <  1:127935/81‑1 (MQ=255)
                                                                gACGCTGGAAGTGCAGGAGGCACGGGCGCAATATCGTCTGACCGATGCCGACCGCTACCCACAGCTCAATGGCGAGggcag      >  2:127968/1‑81 (MQ=255)
                                                                    cTGGAAGTGCAGGAGGCACGGGCGCAATATCGTCTGACCGATGCCGACCGCTACCCACAGCTCAATGGCGAGggcagcggc  <  2:127936/81‑1 (MQ=255)
                                                                       |                                                                             
TTGATAATCAGGTGAAGACGCTGATTAGCGAGGCGCTGGTGAATAATCGGGATTTGCGCATGGCGACGCTGAAAGTGCAGGAGGCACGGGCGCAATATCGTCTGACCGATGCCGACCGCTACCCACAGCTCAATGGCGAGGGCAGCGGC  >  NC_000913/595775‑595923

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: