Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,652,682 C→T pseudogene (1171/1197 nt) intQ → Qin prophage; putative defective integrase

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,652,6820CT100.0% 46.6 / NA 14pseudogene (1171/1197 nt)intQQin prophage; putative defective integrase
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base T (5/9);  total (5/9)

AAAATGGATGTCTGAAAACAATAATGCACAGGTAGCTTTGTTAAATACACAGTTAAGCGAGTTTGCCCCAACCATGCCCCATAACGAAGCAATGAAAAATTAATTTAATATTTATCAAATAGTTAACACGCATGACTCTTGAAATCCATAAATT  >  NC_000913/1652606‑1652759
                                                                            |                                                                             
aaaaTGGATGTCTGAAAACAATAATGCACAGGTAGCTTTGTTAAATACACAGTTAAGCGAGTTTGCCCCAACCATGTCCCa                                                                           <  2:300373/81‑1 (MQ=255)
          tCTGAAAACAATAATGCACAGGTAGCTTTGTTAAATACACAGTTAAGCGAGTTTGCCCCAACCATGTCCCATAACGAAGc                                                                  >  2:300390/1‑80 (MQ=255)
              aaaaCAATAATGCACAGGTAGCTTTGTTAAATACACAGTTAAGCGAGTTTGCCCCAACCATGTCCCATAACGAAGCAAt                                                               <  1:300374/79‑1 (MQ=255)
              aaaaCAATAATGCACAGGTAGCTTTGTTAAATACACAGTTAAGCGAGTTTGCCCCAACCATGTCCCATAACGAAGCAAt                                                               <  2:300375/79‑1 (MQ=255)
              aaaaCAATAATGCACAGGTAGCTTTGTTAAATACACAGTTAAGCGAGTTTGCCCCAACCATGTCCCATAACGAAGCAATg                                                              <  1:300376/80‑1 (MQ=255)
                aaCAATAATGCACAGGTAGCTTTGTTAAATACACAGTTAAGCGAGTTTGCCCCAACCATGTCCCATAACGAAGCAATGaaa                                                           <  1:300377/81‑1 (MQ=255)
                 aCAATAATGCACAGGTAGCTTTGTTAAATACACAGTTAAGCGAGTTTGCCCCAACCATGTCCCATAACGAAGCAATGaaaa                                                          <  1:300378/81‑1 (MQ=255)
                             aGGTAGCTTTGTTAAATACACAGTTAAGCGAGTTTGCCCCAACCATGTCCCATAACGAAGCAATGAAAAATTAATTTAata                                              >  2:300386/1‑81 (MQ=255)
                                   cTTTGTTAAATACACAGTTAAGCGAGTTTGCCCCAACCATGTCCCATAACGAAGCAATGAAAAATTAATTTAATATTTATc                                        <  1:300379/81‑1 (MQ=255)
                                         tAAATACACAGTTAAGCGAGTTTGCCCCAACCATGTCCCATAACGAAGCAATGAAAAACTAATTTAATATTTATCAAATAg                                  >  1:300394/1‑81 (MQ=255)
                                                          gAGTTTGCCCCAACCATGTCCCATAACGAAGCAATGAAAAATTAATTTAATATTTATCAAATAGTTAACACGCATGActct                 >  1:300396/1‑81 (MQ=255)
                                                          gAGTTTGCCCCAACCATGTCCCATAACGAAGCAATGAAAAATTAATTTAATATTTATCAAATAGTTAACACGCATGActct                 >  1:300403/1‑81 (MQ=255)
                                                                         aTGTCCCATAACGAAGCAATGAAAAATTAATTTAATATTTATCAAATAGTTAACACGCATGACTCTTGAAATCCATAAAtt  <  1:300381/81‑1 (MQ=255)
                                                                         aTGTCCCATAACGAAGCAATGAAAAATTAATTTAATATTTATCAAATAGTTAACACGCATGACTCTTGAAATCCATAAAtt  <  2:300380/81‑1 (MQ=255)
                                                                            |                                                                             
AAAATGGATGTCTGAAAACAATAATGCACAGGTAGCTTTGTTAAATACACAGTTAAGCGAGTTTGCCCCAACCATGCCCCATAACGAAGCAATGAAAAATTAATTTAATATTTATCAAATAGTTAACACGCATGACTCTTGAAATCCATAAATT  >  NC_000913/1652606‑1652759

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: