Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 3,337,667 C→A A75A (GCG→GCT mlaC ← intermembrane phospholipid transport system ‑ periplasmic binding protein

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009133,337,6670CA91.7% 33.0 / ‑2.0 12A75A (GCG→GCTmlaCintermembrane phospholipid transport system ‑ periplasmic binding protein
Reads supporting (aligned to +/- strand):  ref base C (1/0);  new base A (3/8);  total (4/8)
Fisher's exact test for biased strand distribution p-value = 3.33e-01
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.85e-01

ATCGCCAGCGCCTGACCGTAAGCCTGCTTCAGGTACTCACGGAAAGCGGCAAAGTAGGCTTCACGTTGAGCAGGGGTCGCACTCTTGTAATACTGGCCCAGCACCAGCGCACCGGCGTATTTCACCTGTACGTATGGCAGCAGTTCCTGATCAACAATGGTACGCAGATAATCCGGGTTGGCCCGAATTTGCGGTTGCTCATTCTTCAGGCGATCGAACGTTTTCTGCGCCGCCTCGTCCATC  >  NC_000913/3337560‑3337802
                                                                                                           |                                                                                                                                       
aTCGCCAGCGCCTGACCGTAAGCCTGCTTCAGGTACTCACGGAAAGCGGCAAAGTAGGCTTCACGTTGAGCAGGGGTCGCACTCTTGTAATACTGGCCCAGCACCAGAGCACCGGCGTATTTCACCTGTACGTATGgcag                                                                                                         <  1:167418/140‑1 (MQ=255)
aTCGCCAGCGCCTGACCGTAAGCCTGCTTCAGGTACTCACGGAAAGCGGCAAAGTAGGCTTCACGTTGAGCAGGGGTCGCACTCTTGTAATACTGGCCCAGCACCAGAGCACCGGCGTATTTCACCTGTACGTATGgcag                                                                                                         <  2:304313/140‑1 (MQ=255)
             gACCGTAAGCCTGCTTCAGGTACTCACGGAAAGCGGCAAAGTAGGCTTCACGTTGAGCAGGGGTCGCACTCTTGTAATACTGGCCCAGCACCAGAGCACCGGCGTATTTCACCTGTACGTATGGCAGCAGTTCCTGATca                                                                                            >  2:30907/1‑140 (MQ=255)
              aCCGTAAGCCTGCTTCAGGTACTCACGGAAAGCGGCAAAGTAGGCTTCACGTTGAGCAGGGGTCGCACTCTTGTAATACTGGCCCAGCACCAGAGCACCGGCGTATTTCACCTGTACGTATGGCAGCAGTTCCTGATcaa                                                                                           <  2:217322/140‑1 (MQ=255)
                  tAAGCCTGCTTCAGGTACTCACGGAAAGCGGCAAAGTAGGCTTCACGTTGAGCAGGGGTCGCACTCTTGTAATACTGGCCCAGCACCAGAGCACCGGCGTATTTCACCTGTACGTATGGCAGCAGTTCCTGATCAACAAt                                                                                       <  1:110297/140‑1 (MQ=255)
                                                     gTAGGCTTCACGTTGAGCAGGGGTCGCACTCTTGTAATACTGGCCCAGCACCAGAGCACCGGCGTATTTCACCTGTACGTATGGCAGCAGTTCCTGATCAACAATGGTACGCAGATAATCCGGGTTGGCCCGAATTTGCg                                                    <  1:55183/140‑1 (MQ=255)
                                                                 ttGAGCAGGGGTCGCACTCTTGTAATACTGGCCCAGCACCAGAGCACCGGCGTATTTCACCTGTACGTATGGCAGCAGTTCCTGATCAACAATGGTACGCAGATAATCCGGGTTGGCCCGAATTTGCGGTTGCTCAttct                                        <  2:12573/140‑1 (MQ=255)
                                                                                             tGGCCCAGCACCAGCGCACCGGCGTATTTCACCTGTACGTATGGCAGCAGTTCCTGATCAACAATGGTACGCAGATAATCCGGGTTGGCCCGAATTTGCGGTTGCTCATTCTTCAGGCGATCGAACGTTTTCTGcgccgc            >  1:131374/1‑140 (MQ=255)
                                                                                              ggCCCAGCACCAGAGCACCGGCGTATTTCACCTGTACGTATGGCAGCAGTTCCTGATCAACAATGGTACGCAGATAATCCGGGTTGGCCCGAATTTGCGGTTGCTCATTCTTCAGGCGATCGAACGTTTTCTGCgccgcc           >  2:333337/1‑140 (MQ=255)
                                                                                                cccAGCACCAGAGCACCGGCGTATTTCACCTGTACGTATGGCAGCAGTTCCTGATCAACAATGGTACGCAGATAATCCGGGTTGGCCCGAATTTGCGGTTGCTCATTCTTCAGGCGATCGAACGTTTTCTGCGCCGCCTc         >  2:66218/1‑140 (MQ=255)
                                                                                                     cACCAGAGCACCGGCGTATTTCACCTGTACGTATGGCAGCAGTTCCTGATCAACAATGGTACGCAGATAATCCGGGTTGGCCCGAATTTGCGGTTGCTCATTCTTCAGGCGATCGAACGTTTTCTGCGCCGCCTCGTCCa    <  2:232471/140‑1 (MQ=255)
                                                                                                       ccAGAGCACCGGCGTATTTCACCTGTACGTATGGCAGCAGTTCCTGATCAACAATGGTACGCAGATAATCCGGGTTGGCCCGAATTTGCGGTTGCTCATTCTTCAGGCGATCGAACGTTTTCTGCGCCGCCTCGTCCATc  <  2:198012/140‑1 (MQ=255)
                                                                                                           |                                                                                                                                       
ATCGCCAGCGCCTGACCGTAAGCCTGCTTCAGGTACTCACGGAAAGCGGCAAAGTAGGCTTCACGTTGAGCAGGGGTCGCACTCTTGTAATACTGGCCCAGCACCAGCGCACCGGCGTATTTCACCTGTACGTATGGCAGCAGTTCCTGATCAACAATGGTACGCAGATAATCCGGGTTGGCCCGAATTTGCGGTTGCTCATTCTTCAGGCGATCGAACGTTTTCTGCGCCGCCTCGTCCATC  >  NC_000913/3337560‑3337802

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: