Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 2,066,740 A→G G194G (GGT→GGC insH‑6 ← CP4‑44 prophage; IS5 transposase and trans‑activator

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009132,066,7400AG94.7% 50.8 / ‑3.7 19G194G (GGT→GGCinsH‑6CP4‑44 prophage; IS5 transposase and trans‑activator
Reads supporting (aligned to +/- strand):  ref base A (0/1);  new base G (9/9);  total (9/10)
Fisher's exact test for biased strand distribution p-value = 1.00e+00
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.94e-01

TACCCAGCTGATTGAGGTCATGCTCGTTGGCCGCGGTGGTGACTAGGCTGTGGGTCAGGCCGCTCTTGGCATCGACACCAATGTGGGCCTTCATGCCAAAGTGCCACTGATTGCCTTTCTTGGTCTGATGCATCTCCGGATC  >  NC_000913/2066664‑2066805
                                                                            |                                                                 
tACCCAGCTGATTGAGGTCATGCTCGTTGGCCGCGGTGGTGACTAGGCTGTGGGTCAGGCCGCTCTTGGCATCGACGCCaa                                                               >  1:351387/1‑81 (MQ=255)
 aCCCAGCTGATTGAGGTCATGCTCGTTGGCCGCGGTGGTGACTAGGCTGTGGGTCAGGCCGCTCTTGGCATCGACGCCAAt                                                              >  2:351393/1‑81 (MQ=255)
 aCCCAGCTGATTGAGGTCATGCTCGTTGGCCGCGGTGGTGACTAGGCTGTGGGTCAGGCCGCTCTTGGCATCGACGCCAAt                                                              >  1:351382/1‑81 (MQ=255)
          aTTGAGGTCATGCTCGTTGGCCGCGGTGGTGACTAGGCTGTGGGTCAGGCCGCTCTTGGCATCGACGCCAATGTGGGcc                                                       <  1:351353/79‑1 (MQ=255)
          aTTGAGGTCATGCTCGTTGGCCGCGGTGGTGACTAGGCTGTGGGTCAGGCCGCTCTTGGCATCGACGCCAATGTGGGCCtt                                                     <  2:351354/81‑1 (MQ=255)
             gAGGTCATGCTCGTTGGCCGCGGTGGTGACTAGGCTGTGGGTCAGGCCGCTCTTGGCATCGACGCCAATGTGGGCCTTCa                                                   <  1:351355/80‑1 (MQ=255)
                   aTGCTCGTTGGCCGCGGTGGTGACTAGGCTGTGGGTCAGGCCGCTCTTGGCATCGACGCCAATGTGGGCCTTCATGCCaa                                             <  2:351356/80‑1 (MQ=255)
                   aTGCTCGTTGGCCGCGGTGGTGACTAGGCTGTGGGTCAGGCCGCTCTTGGCATCGACGCCAATGTGGGCCTTCATGCCa                                              >  1:351402/1‑79 (MQ=255)
                      cTCGTTGGCCGCGGTGGTGACTAGGCTGTGGGTCAGGCCGCTCTTGGCATCGACGCCAATGTGGGCCTTCATGCCAAAGTg                                         >  2:351381/1‑81 (MQ=255)
                             gCCGCGGTGGTGACTAGGCTGTGGGTCAGGCCGCTCTTGGCATCGACGCCAATGTGGGCCTTCATGCCAAAGTGCCACTg                                   <  2:351357/80‑1 (MQ=255)
                              ccGCGGTGGTGACTAGGCTGTGGGTCAGGCCGCTCTTGGCATCGACGCCAATGTGGGCCTTCATGCCAAAGTGCCACTGAt                                 <  1:351358/81‑1 (MQ=255)
                                  ggtggtGACTAGGCTGTGGGTCAGGCCGCTCTTGGCATCGACGCCAATGTGGGCCTTCATGCCAAAGTGCCACTGATTGcc                             >  1:351406/1‑81 (MQ=255)
                                       tgACTAGGCTGTGGGTCAGGCCGCTCTTGGCATCGACACCAATGTGGGCCTTCATGCCAAAGTGCCACTGATTGCCTTTCt                        <  1:351359/81‑1 (MQ=38)
                                         aCTAGGCTGTGGGTCAGGCCGCTCTTGGCATCGACGCCAATGTGGGCCTTCATGCCAAAGTGCCACTGATTGCCTTTCTTg                      >  1:351398/1‑81 (MQ=255)
                                             ggCTGTGGGTCAGGCCGCTCTTGGCATCGACGCCAATGTGGGCCTTCATGCCAAAGTGCCACTGATTGCCTTTCTTGGTCt                  <  2:351360/81‑1 (MQ=18)
                                              gCTGTGGGTCAGGCCGCTCTTGGCATCGACGCCAATGTGGGCCTTCATGCCAAAGTGCCACTGATTGCCTTTCTTGGTCt                  >  1:351404/1‑80 (MQ=21)
                                                      tCAGGCCGCTCTTGGCATCGACGCCAATGTGGGCCTTCATGCCAAAGTGCCACTGATTGCCTTTCTTGGTCTGATGCAtct         <  2:351361/81‑1 (MQ=18)
                                                             gCTCTTGGCATCGACGCCAATGTGGGCCTTCATGCCAAAGTGCCACTGATTGCCTTTCTTGGTCTGATGCATCTCCGGATc  <  1:351362/81‑1 (MQ=14)
                                                             gCTCTTGGCATCGACGCCAATGTGGGCCTTCATGCCAAAGTGCCACTGATTGCCTTTCTTGGTCTGATGCATCTCCGGATc  >  2:351397/1‑81 (MQ=14)
                                                                            |                                                                 
TACCCAGCTGATTGAGGTCATGCTCGTTGGCCGCGGTGGTGACTAGGCTGTGGGTCAGGCCGCTCTTGGCATCGACACCAATGTGGGCCTTCATGCCAAAGTGCCACTGATTGCCTTTCTTGGTCTGATGCATCTCCGGATC  >  NC_000913/2066664‑2066805

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: