Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,573,627 G→A L526F (CTT→TTT)  pqqL ← periplasmic metalloprotease

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,573,6270GA90.9% 23.9 / NA 11L526F (CTT→TTT) pqqLperiplasmic metalloprotease
Reads supporting (aligned to +/- strand):  ref base G (0/0);  major base A (3/7);  minor base C (1/0);  total (4/7)
Fisher's exact test for biased strand distribution p-value = 3.64e-01
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.30e-01

AACGCCGCTTCCGCTAACTGCTTTATTTGCCAGCGCGATAAGTGATTTTTGCTGCGCAGGGAAACTTAAATCGCCTTTATTCGATACGGCAATAATTTGTAGCTTTTGCTCTTCACCCGCGGATTTTGCCAGAATAACCCTGGCACCATTGGAAAGTGTTAATGATGTCAGATTCTCCGCCAGCGTTTCTTTGCTGCTAATTTCCGCCTGTGGGTCTGCGTCTACTGTTAACGATAAATTTCTGCCTGGGAAGACGTAAGCCGCCAGCTTTTTGTTGGCGTACTCCTTTTCCAGCGCCAGGATAGCCGCAGGAGACAATGCTTT  >  NC_000913/1573472‑1573795
                                                                                                                                                           |                                                                                                                                                                        
aaCGCCGCTTCCGCTAACTGCTTTATTTGCCAGCGCGATAAGTGATTTTTGCTGCGCAGGGAAACTTAAATCGCCTTTATTCGATACGGCAATAATTTGTAGCTTTTGCTCTTCACCCGCGGATTTTGCCAGAATAACCCTGGCACCATTGGAAAATGTTAATGATGTCAGATTCTCCGCCAGCGTTTCTTTGCTGCTAATTTCCGCCTGTGGGTCTGCGTCTACTGTTAAcn                                                                                             <  1:159955/233‑2 (MQ=255)
                           tGCCAGCGCGATAAGTGATTTTTGCTGCGCAGGGAAACTTAAATCGCCTTTATTCGATACGGCAATAATTTGTAGCTTTTGCTCTTCACCCGCGGATTTTGCCAGAATAACCCTGGCACCATTGGAAAATGTTNATGNNNNNAgnnnnnnnnnn                                                                                                                                                 >  2:151606/1‑144 (MQ=255)
                           tGCCAGCGCGATAAGTGATTTTTGCTGCGCAGGGAAACTTAAATCGCCTTTATTCGATACGGCAATAATTTGTAGCTTTTGCTCGTCACCCGCGGATTTTGCCAGAATAACCCTGGCACCATTGGAAAATGTTAATGATGTCAGATTCTCCGCCAGCGTTTCTTTGCTGCTAATTTCCGCCTGTGGGTCTGCGTCTACTGTTAACGATAAATTTCTGCCTGGGAAGACGTAAgccgn                                                              <  1:151606/237‑2 (MQ=255)
                                                        cAGGGAAACTAAATCGCCTTTATTCGATACGGCAATAATTTGTAGCTTTTGCTCTTCACCCGCGGATTTTGCCAGAATAACCCTGGCACCATTGGAAAATGTTAATGATGTCAGATTCTCCGCCAGCGTTTCTTTGCTGCTAATTTCCGCCTGTGGGTCTGCGTCTACTGTTAACGATAAATTTCTGCCTGGGAAGACGTAAGCCGCCAGCTTTTTGTTGGCGGACTCCTTATCCAgcg                              <  1:211214/239‑1 (MQ=255)
                                                            gAAACTTAAATCGCCTTTATTCGATACGGCAATAATTTGTAGCTTTTGCTCTTCACCCGCGGATTTTGCCAGAATAACCCTGGCACCATTGGAAACTGTTAATGATGTCAGATTCTCCGCCAGCGTTTCTTTGCTGCTAATTTCCGCCTGTGGGTCTGCGTCTACTGTTAACGATAAATTTCTGCCTGGGAAGACGTAAGCCGCCAGCTTTTTGTTGGCGTACTCCTTTTCCAGCGCCAGGATAGcagc                 >  1:84565/1‑246 (MQ=255)
                                                                cTTAAATCGCCTTTATTCGATACGGCAATAATTTGTAGCTTTTGCTCTTCACCCGCGGATTTTGCCAGAATAACCCTGGCACCATTGGAAAATGTTAATGATGTCAGATTCTCCGCCAGCGTTTCTTtgc                                                                                                                                    <  1:147504/130‑1 (MQ=255)
                                                                         ccTTTATTCGATACGGCAATAATTTGTAGGTTTTGCTCTTCTCTCGCTGATTTTGCCGGAATAGCCCTGGCACCATTGGAAAATGTTAATGATGTCAGATTCCCCGCCAGCGTTTCTTTGCTTGTAATTTCCGCCGGTGTGTCTGCGTCTGCTGGTAACGATAAATTTCTGCCTTGGAATACGTAAGGCGCCAGCTTGTTGTTGGCGTACTCCTTTTCTAGCGTCAGGAGAGCCTCAGGAGACAATGCttt  <  1:80544/251‑1 (MQ=255)
                                                                                                     gCTTTTGCTCTTCACCCGCGGATTTTGCCAGAATAACCCTGGCACCATTGGAAAATGTTAATGATGTCAGATTCTCCGCCAGCGTTTCTTTGCTGCTAATTTCCGCCTGTGGGTCTGCGTCTACTGTTAACGATAAATTTCTGCCTGGGAAg                                                                         <  1:19539/152‑1 (MQ=255)
                                                                                                     gCTTTTGCTCTTCACCCGCGGATTTTGCCAGAATAACCCTGGCACCATTGGAAAATGTTAATGATGTCAGATTCTCCGCCAGCGTTTCNNtgctgc                                                                                                                                 >  2:19539/1‑96 (MQ=255)
                                                                                                                 naCCCGCGGATTTTGCCAGAATAACCCTGGCACCATTGGAAAATGTTAATGATGTCAGATTCTCCGCCAGCGTTTCTTTGCTGCTAATTTCCGCCTGTGGGTCTGCGTCTCCTGTTAACGATAAATTTCTGCCTGGGAAGACGTAAGCCGCCAGCTTTTTGTTGGCGTACTCCt                                       >  1:156150/2‑174 (MQ=255)
                                                                                                                                             nncANNNNNGGANAATGTCAATTAGGTCAGATTTTCCGCCAGCGTTTCTTTTCTGCTAACTTCCGCCTTTGGGTCTGCGTCTACTGTTAACGATAAATGTCTGCCTGGGAAGACGTAAGCCGCCAGCTTGTTGTTGGCGGACTccg                                       <  2:156150/144‑2 (MQ=255)
                                                                                                                                                           |                                                                                                                                                                        
AACGCCGCTTCCGCTAACTGCTTTATTTGCCAGCGCGATAAGTGATTTTTGCTGCGCAGGGAAACTTAAATCGCCTTTATTCGATACGGCAATAATTTGTAGCTTTTGCTCTTCACCCGCGGATTTTGCCAGAATAACCCTGGCACCATTGGAAAGTGTTAATGATGTCAGATTCTCCGCCAGCGTTTCTTTGCTGCTAATTTCCGCCTGTGGGTCTGCGTCTACTGTTAACGATAAATTTCTGCCTGGGAAGACGTAAGCCGCCAGCTTTTTGTTGGCGTACTCCTTTTCCAGCGCCAGGATAGCCGCAGGAGACAATGCTTT  >  NC_000913/1573472‑1573795

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 16 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: