Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_002947 5,948,277 C→T R66H (CGT→CAT)  rho ← transcription termination factor Rho

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0029475,948,2770CT100.0% 34.8 / NA 12R66H (CGT→CAT) rhotranscription termination factor Rho
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base T (5/7);  total (5/7)

CAGGGCGAAGTAACGCTCCCCTTCCTTCGGTGGGCGGATCTTGCCGACGATGGTGTCGCCGGTACGCAGGTTGAAACGGCGGATCTGGCTGGGCGAGACATAGATATCGTCTGGGCCGGCCAGGTAGGACGCATCAGCCGAACGCAGGAAACCGAAACCATCCTGGAGAATCTCCAGCACGCCGTCACCCGAGATCTCTTCGCCGCTTTTCGCATGCTTCTTCAGCAGGGCGAAAATCACGTCCTGTTTGCGCGAACGGGCCATGTTTTCGATGCCCATCTGTTC  >  NC_002947/5948135‑5948419
                                                                                                                                              |                                                                                                                                              
cagGGCGAAGTAACGCTCCCCTTCCTTCGGTGGGCGGATCTTGCCGACGATGGTGTCGCCGGTACGCAGGTTGAAACGGCGGATCTGGCTGGGCGAGACATAGATATCGTCTGGGCCGGCCAGGTAGGACGCATCAGCCGAATGCa                                                                                                                                             >  5:176613/1‑146 (MQ=255)
    gCGAAGTAACGCTCCCCTTCCTTCGGTGGGCGGATCTTGCCGACGATGGTGTCGCCGGTACGCAGGTTGAAACGGCGGATCTGGCTGGGCGAGACATAGATATCGTCTGGGCCGGCCAGGTAGGACGCATCAGCCGAATGCAGgaaa                                                                                                                                        >  1:145895/1‑147 (MQ=255)
     cGAAGTAACGCTCCCCTTCCTTCGGTGGGCGGATCTTGCCGACGATGGTGTCGCCGGTACGCAGGTTGAAACGGCGGATCTGGCTGGGCGAGACATAGATATCGTCTGGGCCGGCCAGGTAGGACGCATCAGCCGAATGCAGgaaac                                                                                                                                       <  7:205100/147‑1 (MQ=255)
        aGTAACGCTCCCCTTCCTTCGGTGGGCGGATCTTGCCGACGATGGTGTCGCCGGTACGCAGGTTGAAACGGCGGATCTGGCTGGGCGAGACATAGATATCGTCTGGGCCGGCCAGGTAGGACGCATCAGCCGAATGCAGgaaaccga                                                                                                                                    <  5:77235/147‑1 (MQ=255)
                            ggTGGGCGGATCTTGCCGACGATGGTGTCGCCGGTACGCAGGTTGAAACGGCGGATCTGGCTGGGCGAGACATAGATATCGTCTGGGCCGGCCAGGTAGGACGCATCAGCCGAATGCAGGAAACCGAAACCATCCTGGAGAAtct                                                                                                                  <  5:26548/145‑1 (MQ=255)
                                 gCGGATCTTGCCGACGATGGTGTCGCCGGTACGCAGGTTGAAACGGCGGATCTGGCTGGGCGAGACATAGATATCGTCTGGGCCGGCCAGGTAGGACGCATCAGCCGAATGCAGGAAACCGAAACCATCCTGGAGAATCTCCAGCAc                                                                                                           >  6:265323/1‑147 (MQ=255)
                                                                          accggcggATCTGGCCTGGCGACACATACATATCGTCTGGGCCGGCCAGGTAGGACGCAGCAGCCGAATGCAGGAACCCGAACCCATCCTGTATAATCTCCAGGACGCCGTCACCCGACATCTCTTCGCCGCTTTTCGCATGcttct                                                                  <  5:228428/145‑1 (MQ=255)
                                                                          aaCGGCGGATCTGGCTGGGCGAGACATAGATATCGTCTGGGCCGGCCAGGTAGGACGCATCAGCCGAATGCAGGAAACCGAAACCATCCTGGAGAATCTCCAGCACGCCGTCACCCGAGATCTCTTCGCCGCTTTTCGCATGcttct                                                                  >  6:14192/1‑147 (MQ=255)
                                                                                                 aCATAGATATCGTCTGGGCCGGCCAGGTAGGACGCATCAGCCGAATGCAGGAAACCGAAACCATCCTGGAGAATCTCCAGCACGCCGTCACCCGAGATCTCTTCGCCGCTTTTCGCATGCTTCTTCAGCAGGGCGAAAATCACGTcc                                           <  6:176613/147‑1 (MQ=255)
                                                                                                                                      cAGCCGAATGCAGGAAACCGAAACCATCCTGGAGAATCTCCAGCACGCCGTCACCCGAGATCTCTTCGCCGCTTTTCGCATGCTTCTTCAGCAGGGCGAAAATCACGTCCTGTTTgc                                    >  3:218743/1‑117 (MQ=255)
                                                                                                                                      cAGCCGAATGCAGGAAACCGAAACCATCCTGGAGAATCTCCAGCACGCCGTCACCCGAGATCTCTTCGCCGCTTTTCGCATGCTTCTTCAGCAGGGCGAAAATCACGTCCTGTTTgc                                    <  4:218743/117‑1 (MQ=255)
                                                                                                                                          agAATGCAGGAAACCGAAACCATCCTGGAGAATCTCCAGCACGCCGTCACCCGAGATCTCTTCGCCGCTTTTCGCATGCTTCTTCAGCAGGGCGAAAATCACGTCCTGTTTGCGCGAACGGGCCATGTTTTCGATGCCCATCTGTTc  <  5:14192/146‑1 (MQ=255)
                                                                                                                                              |                                                                                                                                              
CAGGGCGAAGTAACGCTCCCCTTCCTTCGGTGGGCGGATCTTGCCGACGATGGTGTCGCCGGTACGCAGGTTGAAACGGCGGATCTGGCTGGGCGAGACATAGATATCGTCTGGGCCGGCCAGGTAGGACGCATCAGCCGAACGCAGGAAACCGAAACCATCCTGGAGAATCTCCAGCACGCCGTCACCCGAGATCTCTTCGCCGCTTTTCGCATGCTTCTTCAGCAGGGCGAAAATCACGTCCTGTTTGCGCGAACGGGCCATGTTTTCGATGCCCATCTGTTC  >  NC_002947/5948135‑5948419

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: