Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,680,663 C→T P369P (CCC→CCT ydgI → putative arginine:ornithine antiporter

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,680,6630CT100.0% 96.2 / NA 27P369P (CCC→CCTydgIputative arginine:ornithine antiporter
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base T (16/11);  total (16/11)

TCTGGTACTCATCTGGCTGACCGGTTCCGATTACAACACGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCCTATTTCCTGGTCGGCGCGTTCTTGCTGAAAATCGCAACCCGTCCACTGCATAAAGCGGTAGGTGTC  >  NC_000913/1680588‑1680729
                                                                           |                                                                  
tCTGGTACTCATCTGGCTGACCGGTTCCGATTACAACACGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTAttt                                                               >  1:307237/1‑81 (MQ=255)
       cTCATCTGGCTGACCGGTTCCGATTACAACACGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTc                                                        <  1:307185/81‑1 (MQ=255)
       cTCATCTGGCTGACCGGTTCCGATTACAACACGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTc                                                        >  1:307214/1‑81 (MQ=255)
         cATCTGGCTGACCGGTTCCGATTACAACACGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCgg                                                      >  1:307220/1‑81 (MQ=255)
          aTCTGGCTGACCGGTTCCGATTACAACACGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGgc                                                     >  2:307228/1‑81 (MQ=255)
          aTCTGGCTGACCGGTTCCGATTACAACACGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGgc                                                     >  1:307223/1‑81 (MQ=255)
            cTGGCTGACCGGTTCCGATTACAACACGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGgcgc                                                   >  2:307233/1‑81 (MQ=255)
              ggCTGACCGGTTCCGATTACAACACGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGGCGCGt                                                 >  2:307227/1‑81 (MQ=255)
               gCTGACCGGTTCCGATTACAACACGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGgcgc                                                   <  1:307187/78‑1 (MQ=255)
               gCTGACCGGTTCCGATTACAACACGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGgcgc                                                   <  2:307188/78‑1 (MQ=255)
               gCTGACCGGTTCCGATTACAACACGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGgcg                                                    <  2:307186/77‑1 (MQ=255)
               gCTGACCGGTTCCGATTACAACACGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGGCGCGtt                                                >  2:307222/1‑81 (MQ=255)
                      ggTTCCGATTACAACACGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGGCGCGTTCTTGCt                                          >  1:307219/1‑80 (MQ=255)
                      ggTTCCGATTACAACACGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGGCGCGTTCTTGCTg                                         <  1:307189/81‑1 (MQ=255)
                        ttCCGATTACAACACGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGGCGCGTTCTTGCTGaa                                       <  1:307190/81‑1 (MQ=255)
                                 caacaCGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGGCGCGTTCTTGCTGAAAATCGCAAc                              >  2:307234/1‑81 (MQ=255)
                                 caacaCGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGGCGCGTTCTTGCTGAAAATCGCAAc                              >  1:307232/1‑81 (MQ=255)
                                   acacGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGGCGCGTTCTTGCTGAAAATCGCAAccc                            >  1:307226/1‑81 (MQ=255)
                                     acGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGGCGCGTTCTTGCTGAAAATCGCAACCCGt                          <  2:307192/81‑1 (MQ=255)
                                     acGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGGCGCGTTCTTGCTGAAAATCGCAACCCGt                          <  1:307191/81‑1 (MQ=255)
                                             gACCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGGCGCGTTCTTGCTGAAAATCGCAACCCGTCCACTGCa                  >  1:307229/1‑81 (MQ=255)
                                              aCCATCGCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGGCGCGTTCTTGCTGAAAATCGCAACCCGTCCACTGCAt                 <  1:307193/81‑1 (MQ=255)
                                                    gCCTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGGCGCGTTCTTGCTGAAAATCGCAACCCGTCCACTGCATAAAGCg           >  2:307244/1‑81 (MQ=255)
                                                      cTCAGAAATGATTCTGGTGCCTTATTTCCTGGTCGGCGCGTTCTTGCTGAAAATCGCAACCCGTCCACTGCATAAAGCGGt         <  1:307194/81‑1 (MQ=255)
                                                         aGAAATGATTCTGGTGCCTTATTTCCTGGTCGGCGCGTTCTTGCTGAAAATCGCAACCCGTCCACTGCATAAAGCGGTAgg      >  1:307242/1‑81 (MQ=255)
                                                            aaTGATTCTGGTGCCTTATTTCCTGGTCGGCGCGTTCTTGCTGAAAATCGCAACCCGTCCACTGCATAAAGCGGTAGgtgt   >  1:307238/1‑81 (MQ=255)
                                                             aTGATTCTGGTGCCTTATTTCCTGGTCGGCGCGTTCTTGCTGAAAATCGCAACCCGTCCACTGCATAAAGCGGTAGGTGTc  <  2:307195/81‑1 (MQ=255)
                                                                           |                                                                  
TCTGGTACTCATCTGGCTGACCGGTTCCGATTACAACACGTTGCTGACCATCGCCTCAGAAATGATTCTGGTGCCCTATTTCCTGGTCGGCGCGTTCTTGCTGAAAATCGCAACCCGTCCACTGCATAAAGCGGTAGGTGTC  >  NC_000913/1680588‑1680729

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 35 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: