Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 2,103,170 T→C pseudogene (220/446 nt) wbbL ← interrupted rhamnosyltransferase WbbL

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009132,103,1700TC100.0% 45.6 / NA 14pseudogene (220/446 nt)wbbLinterrupted rhamnosyltransferase WbbL
Reads supporting (aligned to +/- strand):  ref base T (0/0);  new base C (8/6);  total (8/6)

AAATCATCATGCTTCATGATGATATCGGGATTCAAAAACAAAATGTAATCATCATCTGCGGGTCTATATTTTTCCTTTACATACGCCACCGCAATATTATTATTATGACCAAAGCCGTATACACCTCCACTAATATAGTCCAGGCCTGCATAA  >  NC_000913/2103094‑2103246
                                                                            |                                                                            
aaaTCATCATGCTTCATGATGATATCGGGATTCAAAAACAAAATGTAATCATCATCTGCGGGTCTATATTTTTCCTCTACa                                                                          >  1:382770/1‑81 (MQ=255)
  atcatcATGCTTCATGATGATATCGGGATTCAAAAACAAAATGTAATCATCATCTGCGGGTCTATATTTTTCCTCTACATa                                                                        <  2:382746/81‑1 (MQ=255)
     atcatGCTTCATGATGATATCGGGATTCAAAAACAAAATGTAATCATCATCTGCGGGTCTATATTTTTCCTCTACATACGc                                                                     >  1:382764/1‑81 (MQ=255)
      tcatGCTTCATGATGATATCGGGATTCAAAAACAAAATGTAATCATCATCTGCGGGTCTATATTTTTCCTCTACATACGcc                                                                    <  1:382747/81‑1 (MQ=255)
        atGCTTCATGATGATATCGGGATTCAAAAACAAAATGTAATCATCATCTGCGGGTCTATATTTTTCCTCTACATACGCCAc                                                                  >  1:382752/1‑81 (MQ=255)
         tGCTTCATGATGATATCGGGATTCAAAAACAAAATGTAATCATCATCTGCGGGTCTATATTTTTCCTCTACATACGCCAcc                                                                 <  1:382748/81‑1 (MQ=255)
                         cGGGATTCAAAAACAAAATGTAATCATCATCTGCGGGTCTATATTTTTCCTCTACATACGCCACCGCAAtattattattat                                                 >  2:382762/1‑81 (MQ=255)
                         cGGGATTCAAAAACAAAATGTAATCATCATCTGCGGGTCTATATTTTTCCTCTACATACGCCACCGCAAtattattattat                                                 >  2:382765/1‑81 (MQ=255)
                                   aaaCAAAATGTAATCATCATCTGCGGGTCTATATTTTTCCTCTACATACGCCACCGCAATATTATTATTATGACCAAAGcc                                       <  2:382749/81‑1 (MQ=255)
                                      cAAAATGTAATCATCATCTGCGGGTCTATATTTTTCCTCTACATACGCCACCGCAATATTATTATTATGACCAAAGCCGta                                    <  1:382750/81‑1 (MQ=255)
                                                    catcTGCGGGTCTATATTTTTCCTCTACATACGCCACCGCAATATTATTATTATGACCAAAGCCGTATACACCTCCACTat                      >  2:592971/1‑80 (MQ=255)
                                                          cGGGTCTATATTTTTCCTCTACATACGCCACCGCAATATTATTATTATGACCAAAGCCGTATACACCTCCACTAata                    <  1:382751/77‑1 (MQ=255)
                                                                     ttttCCTCTACATACGCCACCGCAATATTATTATTATGACCAAAGCCGTATACACCTCCACTAATATAGTCCAGGCCTGCa     >  1:382769/1‑81 (MQ=255)
                                                                        tCCTCTACATACGCCACCGCAATATTATTATTATGACCAAAGCCGTATACACCTCCACTAATATAGTCCAGGCCTGCATaa  >  2:382773/1‑81 (MQ=255)
                                                                            |                                                                            
AAATCATCATGCTTCATGATGATATCGGGATTCAAAAACAAAATGTAATCATCATCTGCGGGTCTATATTTTTCCTTTACATACGCCACCGCAATATTATTATTATGACCAAAGCCGTATACACCTCCACTAATATAGTCCAGGCCTGCATAA  >  NC_000913/2103094‑2103246

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: