Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,143,915 T→A L151F (TTA→TTT rne ← ribonuclease E

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,143,9150TA100.0% 98.5 / NA 27L151F (TTA→TTTrneribonuclease E
Reads supporting (aligned to +/- strand):  ref base T (0/0);  new base A (10/17);  total (10/17)

AGATTTGCCGACGCCAGCGGTGCGCACGATAAGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTTAATTCGGTACGGTCGTCGCCTTCGATACGGCGAGAAATGCCACCCGCGCGCGGGTTGTTCGGCATCAGA  >  NC_000913/1143840‑1143984
                                                                           |                                                                     
agATTTGCCGACGCCAGCGGTGCGCACGATAAGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTc                                                                  >  2:211488/1‑81 (MQ=255)
    ttGCCGACGCCAGCGGTGCGCACGATAAGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTa                                                              >  2:211485/1‑81 (MQ=255)
      gCCGACGCCAGCGGTGCGCACGATAAGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACg                                                            >  1:211495/1‑81 (MQ=255)
       ccGACGCCAGCGGTGCGCACGATAAGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACg                                                            <  1:211450/80‑1 (MQ=255)
        cGACGCCAGCGGTGCGCACGATAAGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACGgt                                                          <  1:211451/81‑1 (MQ=255)
         gACGCCAGCGGTGCGCACGATAAGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACGgtc                                                         >  2:211493/1‑81 (MQ=255)
         gACGCCAGCGGTGCGCACGATAAGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACGgtc                                                         <  2:211452/81‑1 (MQ=255)
          aCGCCAGCGGTGCGCACGATAAGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACGgtcg                                                        <  1:211453/81‑1 (MQ=255)
           cGCCAGCGGTGCGCACGATAAGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACGgtcgt                                                       <  2:211454/81‑1 (MQ=255)
              cAGCGGTGCGCACGATAAGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACGGTCGTCGc                                                    <  2:211455/81‑1 (MQ=255)
                       gcACGATAAGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACGGTCGTCGCCTTCGATAc                                           >  2:211491/1‑81 (MQ=255)
                       gcACGATAAGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACGGTCGTCGCCTTCGATAc                                           <  2:211456/81‑1 (MQ=255)
                          cGATAAGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACGGTCGTCGCCTTCGATACGGc                                        >  2:211503/1‑81 (MQ=255)
                           gATAAGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACGGTCGTCGCCTTCGATACGGc                                        >  1:211483/1‑80 (MQ=255)
                            aTAAGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACGGTCGTCGCCTTCGATACGGc                                        >  2:211497/1‑79 (MQ=255)
                               aGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACGGTCGTCGCCTTCGATACGGCgaga                                    <  2:211457/80‑1 (MQ=255)
                               aGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACGGTCGTCGCCTTCGATACGGCGAGaa                                   <  1:211458/81‑1 (MQ=255)
                                 ccccATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACGGTCGTCGCCTTCGATACGGCGAGAAAt                                 <  1:211459/81‑1 (MQ=255)
                                           tCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACGGTCGTCGCCTTCGATACGGCGAGAAATGCCACCcgcg                       >  1:211492/1‑81 (MQ=255)
                                            ccGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACGGTCGTCGCCTTCGATACGGCGAGAAATGCCACCcgcg                       <  1:211460/80‑1 (MQ=255)
                                             cGGCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACGGTCGTCGCCTTCGATACGGCGAGAAATGCCACCcgcgc                      <  1:211461/80‑1 (MQ=255)
                                              ggCAGTTCAAGGCTTGCCAGTGCTTCTTTAAATTCGGTACGGTCGTCGCCTTCGATACGGCGAGAAATGCCACCcgcgcgc                    <  2:211462/81‑1 (MQ=255)
                                                      aaGGCTTGCCAGTGCTTCTTTAAATTCGGTACGGTCGTCGCCTTCGATACGGCGAGAAATGCCACCCGCGCGCGGgttgtt            <  1:211463/81‑1 (MQ=255)
                                                              ccAGTGCTTCTTTAAATTCGGTACGGTCGTCGCCTTCGATACGGCGAGAAATGCCACCCGCGCGCGGGTTGTTCGGCATc     <  1:211464/80‑1 (MQ=255)
                                                               cAGTGCTTCTTTAAATTCGGTACGGTCGTCGCCTTCGATACGGCGAGAAATGCCACCCGCGCGCGGGTTGTTCGGCAt      >  2:211494/1‑78 (MQ=255)
                                                               cAGTGCTTCTTTAAATTCGGTACGGTCGTCGCCTTCGATACGGCGAGAAATGCCACCCGCGCGCGGGTTGTTCGGCATCAg   <  1:211465/81‑1 (MQ=255)
                                                                aGTGCTTCTTTAAATTCGGTACGGTCGTCGCCTTCGATACGGCGAGAAATGCCACCCGCGCGCGGGTTGTTCGGCATCAGa  <  1:211466/81‑1 (MQ=255)
                                                                           |                                                                     
AGATTTGCCGACGCCAGCGGTGCGCACGATAAGCCCCATGCCTTCCGGCAGTTCAAGGCTTGCCAGTGCTTCTTTTAATTCGGTACGGTCGTCGCCTTCGATACGGCGAGAAATGCCACCCGCGCGCGGGTTGTTCGGCATCAGA  >  NC_000913/1143840‑1143984

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 35 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: