Predicted mutation
evidence seq id position mutation freq annotation gene description
RA CP000730 1,231,411 A→G 100% D19G (GAT→GGT)  USA300HOU_1156 → possible PP2C protein phosphatase

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*CP0007301,231,4110AG100.0% 33.6 / NA 12D19G (GAT→GGT) USA300HOU_1156possible PP2C protein phosphatase
Reads supporting (aligned to +/- strand):  ref base A (0/0);  new base G (5/7);  total (5/7)
Rejected as polymorphism: Frequency below/above cutoff threshold.
Rejected as polymorphism: Variant not supported by required number of reads on each strand.

AAGGTTCGGATATTGACGCAGCTTGTGGTCAATTAAGAGCAAAGGAACGACAAGTAGAAACGAGGTAAAGACAAATGCTAGAGGCACAATTTTTTACTGATACTGGACAACATAGAGATAAGAATGAAGATGCGGGTGGTATTTTTTATAATCAAACTAATCAACAACTTTTAGTTCTGTGTGATGGTATGGGTGGCCATAAAGCAGGAGAAGTTGCAAGTAAATTTGTTACAGATGAGTTGAAATCCCGTTTTGAAGCGGAAAAT  >  CP000730/1231282‑1231547
                                                                                                                                 |                                                                                                                                        
acgtttCGGGTATCGACGCAGCTTGTGGTCAATTAAGAGCAAAGGAACGACAAGTAGAAACGAGGTAAAGACAAATGCTAGAGGCACAATTTTTTACTGATACTGGACAACATAGAGATAAGAATGAAGGTGCGGGTGGTa                                                                                                                               <  2:24907/137‑1 (MQ=255)
                        gtgGTCAATTAAGAGCAAAGGAACGACAAGTAGAAACGCGGTAAAGACAAATGCTAGAGGCACAATTTTTTACTGATACTGAACAACATAGAGGTAAGAATGAAGGTGCGGGTGGTATTTTTTATAGTCAAAATGATcagc                                                                                                       >  1:226630/1‑139 (MQ=255)
                               aTTAAGAGCAAAGGAACGACAAGTAGAAACGAGGTAAAGACAAATGCTAGAGGCACAATTTTTTACTGATACTGGACAACATAGAGATAAGAATGAAGGTGCGGGTGGTATTTTTTATAATCAAACTAATCAACAACtttt                                                                                                >  1:163933/1‑141 (MQ=255)
                                     agCAAAGGAACGACAAGTAGAAACGAGGTAAAGACAAATGCTAGAGGCACAATTTTTTACTGATACTGGACAACATAGAGATAAGAAAGAAGGTGCGGGTGGGATTTTTTATAATCAAACTAATCAACAACTTTTAGTTCt                                                                                          >  1:32806/1‑141 (MQ=255)
                                                         aaaCGAGGTAAAGACAAATGCGAGAGGCAGAAGTTTTTCCTGATCCTGGACAACATAGAGATAAGAATGAAGGTGCGGGTGGTATTTTTTATAATCAAACTAATCAAGGGCCTTGTTTTCTTGGTGATGGTATGGGTGGcc                                                                      <  1:59851/141‑1 (MQ=255)
                                                          aaCGAGGTAAAGACAAATGCTAGAGGCACAATTTTTTACTGATACTGGACAACATAGAGATAAGAATGAAGGTGCGGGTGGTATTTTTTATAATCAAACTAATCAACAACTTTTAGTTCTGTGTGATGGTATGGGTGGCCa                                                                     <  2:220793/141‑1 (MQ=255)
                                                              aGGTAAAGACAAATGCTAGAGGCACAATTTTTTACTGATACTGGACAACATAGAGATAAGAATGAAGGTGCGGGTGGTATTTTTTATAATCAAACTAATCAACAACTTTTAGTTCTGTGTGATGGTATGGGTGGCCATaaa                                                                 >  1:17616/1‑141 (MQ=255)
                                                                 tAAAGACAAATGCTAGAGGCACAATTTTTTACTGATACTGGACAACATAGAGATAAGAATGAAGGTGCGGGTGGTATTTTTTATAATCAAACTAATCAACAACTTTTAGTTCTGTGTGATGGTATGGGTGGCCATAAAGCa                                                              <  1:4334/141‑1 (MQ=255)
                                                                                                             acaTAGAGATAAGAATGAAGGTGCGGGTGGTATTTTTTATAATCAAACTAATCAACAACTTTTAGTTCTGTGTGATGGTATGGGTGGCCATAAAGCAGGAGAAGTTGCAAGTAAATTTGTTACAGATGAGTTGAAATCCCg                  <  2:11104/141‑1 (MQ=255)
                                                                                                                 agagATAAGAATGAAGGTGCGGGTGGTATTTTTTATAATCAAACTAATCAACAACTTTTAGTTCTGTGTGATGGTATGGGTGGCCATAAAGCAGGAGAAGTTGCAAGTAAATTTGTTACAGATGAGTTGAAATCCCGcttt              >  2:44094/1‑141 (MQ=255)
                                                                                                                      aaaGAATGAAGGTGCGGGTGGTACTTTTTAGAATCAAACTAATCAACAACTTTTAGTTCTGTGTGATGGTATGGGTGGCCATAAAGCAGGAGAAGTTGCAAGTAAATTTGTTACAGATGAGTTGAAATCCCGTTTTGAAGc         <  2:197482/140‑1 (MQ=255)
                                                                                                                             gAAGGTGCGGGTGGTATTTTTTATAATCAAACTAATCAACAACTTTTAGTTCTGTGTGATGGTATGGGTGGCCATAAAGCAGGAGAAGTTGCAAGTAAATTTGTTACAGATGAGTTGAAATCCCGTTTTGAAGCGGAAAAt  <  2:17616/141‑1 (MQ=255)
                                                                                                                                 |                                                                                                                                        
AAGGTTCGGATATTGACGCAGCTTGTGGTCAATTAAGAGCAAAGGAACGACAAGTAGAAACGAGGTAAAGACAAATGCTAGAGGCACAATTTTTTACTGATACTGGACAACATAGAGATAAGAATGAAGATGCGGGTGGTATTTTTTATAATCAAACTAATCAACAACTTTTAGTTCTGTGTGATGGTATGGGTGGCCATAAAGCAGGAGAAGTTGCAAGTAAATTTGTTACAGATGAGTTGAAATCCCGTTTTGAAGCGGAAAAT  >  CP000730/1231282‑1231547

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 13 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: