Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,128,283 G→T A149S (GCG→TCG)  murJ → putative lipid II flippase MurJ

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,128,2830GT100.0% 83.1 / NA 24A149S (GCG→TCG) murJputative lipid II flippase MurJ
Reads supporting (aligned to +/- strand):  ref base G (0/0);  new base T (17/7);  total (17/7)

AATTTGCCCTGACCAGCCAGCTACTAAAGATTACCTTTCCCTATATCTTGCTGATCTCCCTGGCGTCGCTGGTGGGAGCGATTCTGAATACGTGGAACCGCTTCTCGATTCCGGCGTTTGCTCCAACACTGCTTAACATCAGCATGATTGGTTTC  >  NC_000913/1128206‑1128360
                                                                             |                                                                             
aaTTTGCCCTGACCAGCCAGCTACTAAAGATTACCTTTCCCTATATCTTGCTGATCTCCCTGGCGTCGCTGGTGGGATCGa                                                                            >  1:205059/1‑81 (MQ=255)
      cccTGACCAGCCAGCTACTAAAGATTACCTTTCCCTATATCTTGCTGATCTCCCTGGCGTCGCTGGTGGGATCGATTCTg                                                                       >  2:205050/1‑80 (MQ=255)
        cTGACCAGCCAGCTACTAAAGATTACCTTTCCCTATATCTTGCTGATCTTCCTGGCGTCGCTGGTGGGATCGATTCTGaa                                                                     >  2:205063/1‑80 (MQ=255)
           aCCAGCCAGCTACTAAAGATTACCTTTCCCTATATCTTGCTGATCTCCCTGGCGTCGCTGGTGGGATCGATTCTGAATACg                                                                 >  2:205065/1‑81 (MQ=255)
            ccagccagCTACTAAAGATTACCTTTCCCTATATCTTGCTGATCTCCCTGGCGTCGCTGGTGGGATCGATTCTGAATACGt                                                                >  1:205058/1‑81 (MQ=255)
            ccagccagCTACTAAAGATTACCTTTCCCTATATCTTGCTGATCTCCCTGGCGTCGCTGGTGGGATCGATTCTGAATACGt                                                                <  2:205033/81‑1 (MQ=255)
                  agcTACTAAAGATTACCTTTCCCTATATCTTGCTGATCTCCCTGGCGTCGCTGGTGGGATCGATTCTGAATACGTGGAAcc                                                          <  2:205034/81‑1 (MQ=255)
                  agcTACTAAAGATTACCTTTCCCTATATCTTGCTGATCTCCCTGGCGTCGCTGGTGGGATCGATTCTGAATACGTGGAAcc                                                          >  2:205061/1‑81 (MQ=255)
                  agcTACTAAAGATTACCTTTCCCTATATCTTGCTGATCTCCCTGGCGTCGCTGGTGGGATCGATTCTGAATACGTGGAAcc                                                          <  2:205035/81‑1 (MQ=255)
                           aGATTACCTTTCCCTATATCTTGCTGATCTCCCTGGCGTCGCTGGTGGGATCGATTCTGAATACGTGGAACCGCTTCTCGa                                                 >  2:205071/1‑81 (MQ=255)
                           aGATTACCTTTCCCTATATCTTGCTGATCTCCCTGGCGTCGCTGGTGGGATCGATTCTGAATACGTGGAACCGCTTCTCGa                                                 >  1:205062/1‑81 (MQ=255)
                               tACCTTTCCCTATATCTTGCTGATCTCCCTGGCGTCGCTGGTGGGATCGATTCTGAATACGTGGAACCGCTTCTCGATTcc                                             >  2:205057/1‑81 (MQ=255)
                                    ttCCCTATATCTTGCTGATCTCCCTGGCGTCGCTGGTGGGATCGATTCTGAATACGTGGAACCGCTTCTCGATTCCGGCGt                                        >  2:205069/1‑81 (MQ=255)
                                      cccTATATCTTGCTGATCTCCCTGGCGTCGCTGGTGGGATCGATTCTGAATACGTGGAACCGCTTCTCGATTCCGGCGtt                                       <  2:205036/80‑1 (MQ=255)
                                                   tGATCTCCCTGGCGTCGCTGGTGGGATCGATTCTGAATACGTGGAACCGCTCCTCGATTTCGGCGTTTTCTCCAACACTGc                         >  1:910473/1‑81 (MQ=255)
                                                     aTCTCCCTGGCGTCGCTGGTGGGATCGATTCTGAATACGTGGAACCGCTTCTCGATTCCGGCGTTTGCTCCAACACTGc                         <  2:205037/79‑1 (MQ=255)
                                                       ctcCCTGGCGTCGCTGGTGGGATCGATTCTGAATACGTGGAACCGCTTCTCGATTCCGGCGTTTGCTCCAACACTGCTTaa                     >  2:205068/1‑81 (MQ=255)
                                                          ccTGGCGTCGCTGGTGTGATCGATTCTGAATACGTGGAACCGCTTCTCGATTCCGGCGTTTGCTCCAACACTGCTTAACAt                  <  1:205038/81‑1 (MQ=255)
                                                            tGGCGTCGCTGGTGGGATCGATTCTGAATACGTGGAACCGCTTCTCGATTCCGGCGTTTGCTCCAACACTGCTTAACAt                  >  1:205079/1‑79 (MQ=255)
                                                             ggCGTCGCTGGTGGGATCGATTCTGAATACGTGGAACCGCTTCTCGATTCCGGCGTTTGCTCCAACACTGCTTAACATCAg               >  2:205085/1‑81 (MQ=255)
                                                                   gCTGGTGGGATCGATTCTGAATACGTGGAACCGCTTCTCGATTCCGGCGTTTGCTCCAACACTGCTTAACATCAGCATGAt         >  2:205064/1‑81 (MQ=255)
                                                                    cTGGTGGGATCGATTCTGAATACGTGGAACCGCTTCTCGATTCCGGCGTTTGCTCCAACACTGCTTAACATCAGCATGAtt        <  1:205039/81‑1 (MQ=255)
                                                                        tggGATCGATTCTGAATACGTGGAACCGCTTCTCGATTCCGGCGTTTGCTCCAACACTGCTTAACATCAGCATGATTGGtt    >  1:205073/1‑81 (MQ=255)
                                                                          ggATCGATTCTGAATACGTGGAACCGCTTCTCGATCCCGGCGTTTGCTCCAACACTGCTTAACATCAGCATGATTGGTTTc  >  1:205067/1‑81 (MQ=255)
                                                                             |                                                                             
AATTTGCCCTGACCAGCCAGCTACTAAAGATTACCTTTCCCTATATCTTGCTGATCTCCCTGGCGTCGCTGGTGGGAGCGATTCTGAATACGTGGAACCGCTTCTCGATTCCGGCGTTTGCTCCAACACTGCTTAACATCAGCATGATTGGTTTC  >  NC_000913/1128206‑1128360

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 24 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: