Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,068,977 C→G G288A (GGC→GCC)  rutG ← pyrimidine:H(+) symporter

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,068,9770CG100.0% 98.1 / NA 29G288A (GGC→GCC) rutGpyrimidine:H(+) symporter
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base G (13/16);  total (13/16)

ACCGATATTTTCAGCATAGGTGGTCACGCCGCTACCGCCGACAGAGCCGGAAAGCATCGTTGCCAGACCATCGCCTACGAATGCCCGCCCCATATACGGGTCCATATTGCGTCCGGTCATCCCGGCGACTGCCTTGAGATGACC  >  NC_000913/1068904‑1069047
                                                                         |                                                                      
acCGATATTTTCAGCATAGGTGGTCACGCCGCTACCGCCGACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGaa                                                                 <  1:217061/81‑1 (MQ=255)
acCGATATTTTCAGCATAGGTGGTCACGCCGCTACCGCCGACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGaa                                                                 >  2:217112/1‑81 (MQ=255)
acCGATATTTTCAGCATAGGTGGTCACGCCGCTACCGCCGACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGaa                                                                 >  2:217109/1‑81 (MQ=255)
 ccGATATTTTCAGCATAGGTGGTCACGCCGCTACCGCCGACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAAt                                                                <  1:217062/81‑1 (MQ=255)
               aTAGGTGGTCACGCCGCTACCGCCGACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCAtata                                                  >  2:217117/1‑81 (MQ=255)
               aTAGGTGGTCACGCCGCTACCGCCGACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCAtata                                                  >  2:217102/1‑81 (MQ=255)
                tAGGTGGTCACGCCGCTACCGCCGACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATAc                                                 >  1:217100/1‑81 (MQ=255)
                 aGGTGGTCACGCCGCTACCGCCGACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACg                                                >  2:217105/1‑81 (MQ=255)
                  ggtggtCACGCCGCTACCGCCGACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACgg                                               <  2:217064/81‑1 (MQ=255)
                  ggtggtCACGCCGCTACCGCCGACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACgg                                               <  2:217063/81‑1 (MQ=255)
                    tggtCACGCCGCTACCGCCGACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACGGGt                                             >  1:217101/1‑81 (MQ=255)
                          cgccgcTACCGCCGACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACGGGTCCatat                                       <  1:217065/81‑1 (MQ=255)
                           gccgcTACCGCCGACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACGGGTCCATAtt                                      <  2:217066/81‑1 (MQ=255)
                             cgcTACCGCCGACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACGGGTCCATATTGc                                    >  2:217110/1‑81 (MQ=255)
                                  ccgccgACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACGGGTCCATATTGCGTCCg                               <  2:217068/81‑1 (MQ=255)
                                  ccgccgACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACGGGTCCATATTGAGTCCg                               <  1:217067/81‑1 (MQ=255)
                                    gccgACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACGGGTCCATATTGCGTCCGGt                             >  2:217099/1‑81 (MQ=255)
                                     ccgACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACGGGTCCATATTGCGTCCGGTc                            <  1:217070/81‑1 (MQ=255)
                                     ccgACAGAGCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACGGGTCCATATTGCGTCCGGTc                            <  1:217069/81‑1 (MQ=255)
                                          agagCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACGGGTCCATATTGCGTCCGGTCATccc                       >  1:217107/1‑81 (MQ=255)
                                          agagCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACGGGTCCATATTGCGTCCGGTCATccc                       <  2:217071/81‑1 (MQ=255)
                                             gCCGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACGGGTCCATATTGCGTCCGGTCATCCCGGc                    <  1:217072/81‑1 (MQ=255)
                                              ccGGAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACGGGTCCATATTGCGTCCGGTCATCCCGGCg                   <  1:217073/81‑1 (MQ=255)
                                                ggAAAGCATCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACGGGTCCATATTGCGTCCGGTCATCCCGGCGAc                 >  1:217113/1‑81 (MQ=255)
                                                       aTCGTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACGGGTCCATATTGCGTCCGGTCATCCCGGCGACTGCCTTg          <  2:217074/81‑1 (MQ=255)
                                                          gTTGCCAGACCATCGGCTACGAATGCCCGCCCCATATACGGGTCCATATTGCGTCCGGTCATCCCGGCGACTGCCtt           >  1:217115/1‑77 (MQ=255)
                                                             gCCAGACCATCGGCTACGAATGCCCGCCCCATATACGGGTCCATATTGCGTCCGGTCATCCCGGCGACTGCCTTGAGATg     <  1:217075/80‑1 (MQ=255)
                                                               cAGACCATCGGCTACGAATGCCCGCCCCATATACGGGTCCATATTGCGTCCGGTCATCCCGGCGACTGCCTTGAGATGAcc  <  2:217076/81‑1 (MQ=255)
                                                                aGACCATCGGCTACGAATGCCCGCCCCATATACGGGTCCATATTGCGTCCGGTCATCCCGGCGACTGCCTTGAGATGAcc  >  1:217124/1‑80 (MQ=255)
                                                                         |                                                                      
ACCGATATTTTCAGCATAGGTGGTCACGCCGCTACCGCCGACAGAGCCGGAAAGCATCGTTGCCAGACCATCGCCTACGAATGCCCGCCCCATATACGGGTCCATATTGCGTCCGGTCATCCCGGCGACTGCCTTGAGATGACC  >  NC_000913/1068904‑1069047

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: