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% 63.2 / NA 18C384C (TGT→TGCydhCputative transporter YdhC
Reads supporting (aligned to +/- strand):  ref base T (0/0);  new base C (9/9);  total (9/9)

AACAGTAGTGCTGGTCGCGCTGGGTTACATGATGCAACGTTGTGAAGAAGTTGGCTGCCAGAATCATGGCAATGCCGAAGTCGCTCA  >  NC_000913/1741020‑1741106
                                          |                                            
aaCAGTAGTGCTGGTCGCGCTGGGTTACATGATGCAACGTTGCgaagaa                                        <  1:1259608/49‑1 (MQ=255)
   agtagtGCTGGTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTg                                    >  1:900002/1‑50 (MQ=255)
      agtGCTGGTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCt                                 >  1:1249864/1‑50 (MQ=255)
      agtGCTGGTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCt                                 >  1:364656/1‑50 (MQ=255)
       gtGCTGGTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCt                                 <  1:1503840/49‑1 (MQ=255)
          cTGGTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCa                             <  1:1686386/50‑1 (MQ=255)
             gTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAg                            <  1:1490988/48‑1 (MQ=255)
             gTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGaa                          >  1:130865/1‑50 (MQ=255)
             gTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGaa                          >  1:1090187/1‑50 (MQ=255)
                gcgcTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAATc                        <  1:694883/49‑1 (MQ=255)
                    tGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATgg                    >  1:2104716/1‑49 (MQ=255)
                       gTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATGGCAAt                <  1:2463100/50‑1 (MQ=255)
                        ttACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATGGCAATg               >  1:32727/1‑50 (MQ=255)
                          aCATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATGGCAATGc              <  1:2578710/49‑1 (MQ=255)
                           cATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATGGCAATGCCg            <  1:201362/50‑1 (MQ=255)
                              gatgCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATGGCAATGCCGAAg         >  1:321532/1‑50 (MQ=255)
                                tgCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATGGCAATGCCGAAGTc       <  1:216506/50‑1 (MQ=255)
                                      gTTGCGAAGAAGTTGGCTGCCAGAATCATGGCAATGCCGAAGTCGCTCa  >  1:822812/1‑49 (MQ=255)
                                          |                                            
AACAGTAGTGCTGGTCGCGCTGGGTTACATGATGCAACGTTGTGAAGAAGTTGGCTGCCAGAATCATGGCAATGCCGAAGTCGCTCA  >  NC_000913/1741020‑1741106

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: