Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,741,062 T→C C384C (TGT→TGC ydhC → putative transporter YdhC

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,741,0620TC100.0% 93.6 / NA 25C384C (TGT→TGCydhCputative transporter YdhC
Reads supporting (aligned to +/- strand):  ref base T (0/0);  new base C (13/12);  total (13/12)

ATCAACAGTAGTGCTGGTCGCGCTGGGTTACATGATGCAACGTTGTGAAGAAGTTGGCTGCCAGAATCATGGCAATGCCGAAGTCGCTCA  >  NC_000913/1741017‑1741106
                                             |                                            
aTCAACAGTAGTGCTGGTCGCGCTGGGTTACATGATGCAACGTTGCga                                            <  1:1423633/48‑1 (MQ=255)
    aCAGTAGTGCTGGTCGCGCTGGGTTACATGATGCAACGTTGCGaagaag                                       >  1:586971/1‑49 (MQ=255)
     cAGTAGTGCTGGTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGt                                      <  1:289615/49‑1 (MQ=255)
      agtagtGCTGGTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGtt                                     <  1:865800/49‑1 (MQ=255)
        tagtGCTGGTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTgg                                   <  1:1531020/49‑1 (MQ=255)
        tagtGCTGGTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTgg                                   >  1:468822/1‑49 (MQ=255)
          gtGCTGGTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGc                                  <  1:1568442/48‑1 (MQ=255)
             cTGGTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGc                               <  1:1374985/48‑1 (MQ=255)
               ggTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGc                               >  1:1513018/1‑46 (MQ=255)
                gTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGcct                             <  1:847501/47‑2 (MQ=255)
                gTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCa                             <  1:2078727/47‑1 (MQ=255)
                gTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAg                            <  1:1875058/48‑1 (MQ=255)
                gTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAg                            >  1:2052594/1‑48 (MQ=255)
                    cgcTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAATCa                       >  1:948367/1‑49 (MQ=255)
                      cTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATg                     >  1:413558/1‑49 (MQ=255)
                      cTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATg                     >  1:1995284/1‑49 (MQ=255)
                       tGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATgg                    >  1:581137/1‑49 (MQ=255)
                       tGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATgg                    >  1:1721951/1‑49 (MQ=255)
                       tGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATgg                    >  1:716622/1‑49 (MQ=255)
                           ttACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATGGCAAt                >  1:1257847/1‑49 (MQ=255)
                             aCATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATGGCAATg               <  1:703883/48‑1 (MQ=255)
                              cATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATGGCAATGc              <  1:2110245/48‑1 (MQ=255)
                                tgatgCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATGGCAATGCCg            >  1:14064/1‑48 (MQ=255)
                                        cGTTGCGAAGAAGTTGGCTGCCAGAATCATGGCAATGCCGAAGTCGCTc   <  1:1231758/49‑1 (MQ=255)
                                          ttGCGAAGAAGTTGGCTGCCAGAATCATGGCAATGCCGAAGTCGCTCa  >  1:2011493/1‑48 (MQ=255)
                                             |                                            
ATCAACAGTAGTGCTGGTCGCGCTGGGTTACATGATGCAACGTTGTGAAGAAGTTGGCTGCCAGAATCATGGCAATGCCGAAGTCGCTCA  >  NC_000913/1741017‑1741106

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: