Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 698,220 C→T D320N (GAT→AAT)  asnB ← asparagine synthetase B

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_000913698,2200CT100.0% 121.6 / NA 34D320N (GAT→AAT) asnBasparagine synthetase B
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base T (22/12);  total (22/12)

ACCATTTTAATGCCCATCGCCTTGATCTTACGCGACATTAAATACATCGGTGTTGAAGCGCGAATAGTGGTCACATCATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTCCTGTACAGTGAAGTGAATTTCGTGATG  >  NC_000913/698144‑698295
                                                                            |                                                                           
aCCATTTTAATGCCCATCGCCTTGATCTTACGCGACATTAAATACATCGGTGTTGAAGCGCGAATAGTGGTCACATTATaa                                                                         <  2:150055/81‑1 (MQ=255)
   aTTTTAATGCCCATCGCCTTGATCTTACGCGACATTAAATACATCGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGtt                                                                      <  2:150056/81‑1 (MQ=255)
         aTGCCCATCGCCTTGATCTTACGCGACATTAAATACATCGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGAt                                                                 <  1:150057/80‑1 (MQ=255)
            cccATCGCCTTGATCTTACGCGACATTAAATACATCGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTgg                                                             >  1:150083/1‑81 (MQ=255)
              cATCGCCTTGATCTTACGCGACATTAAATACATCGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGt                                                            >  2:150090/1‑80 (MQ=255)
                tCGCCTTGATCTTACGCGACATTAAATACATCGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTaaa                                                         >  2:150069/1‑81 (MQ=255)
                  gCCTTGATCTTACGCGACATTAAATACATCGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAAt                                                        >  2:150121/1‑80 (MQ=255)
                    cTTGATCTTACGCGACATTAAATACATCGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCAc                                                     >  1:150099/1‑81 (MQ=255)
                     ttGATCTTACGCGACATTAAATACATCGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACg                                                    >  2:150093/1‑81 (MQ=255)
                     ttGATCTTACGCGACATTAAATACATCGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACg                                                    >  2:150096/1‑81 (MQ=255)
                       gATCTTACGCGACATTAAATACATCGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGt                                                   <  2:150058/80‑1 (MQ=255)
                                 gACATTAAATACATCGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCa                                        >  1:150086/1‑81 (MQ=255)
                                 aaCATTAAATACATCGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCa                                        >  2:150106/2‑81 (MQ=255)
                                       aaaTACATCGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGa                                  >  2:150108/1‑81 (MQ=255)
                                        aaTACATCGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGAc                                 <  1:150059/81‑1 (MQ=255)
                                          tACATCGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCt                               >  1:150100/1‑81 (MQ=255)
                                           aCATCGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCtt                              >  2:150091/1‑81 (MQ=255)
                                            cATCGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTc                             >  1:150125/1‑81 (MQ=255)
                                               cGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTCCTg                          >  1:150103/1‑81 (MQ=255)
                                               cGGTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTCCTg                          >  2:150112/1‑81 (MQ=255)
                                                ggTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTCCTg                          >  1:150097/1‑80 (MQ=255)
                                                ggTGTTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTCCTGt                         <  2:150060/81‑1 (MQ=255)
                                                 gtgtTGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTCCTGTa                        <  1:150061/81‑1 (MQ=255)
                                                    ttGAAGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTCCTGTACag                     >  1:150102/1‑81 (MQ=255)
                                                       aaGCGCGAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTCCTGTACagtga                  <  2:150062/81‑1 (MQ=255)
                                                           gcgAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTCCTGTACagtgaagtg              <  1:150063/81‑1 (MQ=255)
                                                           gcgAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTCCTGTACagtgaagt               >  2:150107/1‑80 (MQ=255)
                                                             gAATAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTCCTGTACAgtgaagtgaa            >  2:150104/1‑81 (MQ=255)
                                                               aTAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTCCTGTACAGTGAAGTGAAtt          <  2:150064/81‑1 (MQ=255)
                                                                tAGTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTCCTGTACAGTGAAGTGAAttt         <  2:150065/81‑1 (MQ=255)
                                                                  gTGGTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTCCTGTACAGTGAAGTGAATTTc        <  1:150066/80‑1 (MQ=255)
                                                                    ggTCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTCCTGTACAGTGAAGTGAATTTCGt      >  2:150098/1‑80 (MQ=255)
                                                                      tCACATTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTCCTGTACAGTGAAGTGAATTTCGTGAt   >  2:150129/1‑81 (MQ=255)
                                                                       cacaTTATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTCCTGTACAGTGAAGTGAATTTCGTGATg  >  1:150127/1‑81 (MQ=255)
                                                                            |                                                                           
ACCATTTTAATGCCCATCGCCTTGATCTTACGCGACATTAAATACATCGGTGTTGAAGCGCGAATAGTGGTCACATCATAAGTTTCGATGTGGTAAATCACGTCGCGGATGGCATCCAGACCTTCCTGTACAGTGAAGTGAATTTCGTGATG  >  NC_000913/698144‑698295

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: