Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,182,497 A→T D111E (GAT→GAA potD ← spermidine preferential ABC transporter periplasmic binding protein

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,182,4970AT100.0% 80.9 / NA 23D111E (GAT→GAApotDspermidine preferential ABC transporter periplasmic binding protein
Reads supporting (aligned to +/- strand):  ref base A (0/0);  new base T (8/15);  total (8/15)

ACCAATCGCCGTCGCACCCCAGATATACGGAATGGAGTAGTCGTTATTCGGGTCAAAAGGCTTGTTGAGCATGTCTGGATCGAGATTGCTGAAGTTTGTTAACTTCGACTTGTCGATCTTCTGGATCATCCCTTCTTTACGCATTTTATCAAC  >  NC_000913/1182419‑1182571
                                                                              |                                                                          
acCAATCGCCGTCGCACCCCAGATATACGGAATGGAGTAGTCGTTATTCGGGTCAAAAGGCTTGTTGAGCATGTCTGGTTc                                                                          >  2:235671/1‑81 (MQ=255)
acCAATCGCCGTCGCACCCCAGATATACGGAATGGAGTAGTCGTTATTCGGGTCAAAAGGCTTGTTGAGCATGTCTGGTTc                                                                          <  2:235642/81‑1 (MQ=255)
   aaTCGCCGTCGCACCCCAGATATACGGAATGGAGTAGTCGTTATTCGGGTCAAAAGGCTTGTTGAGCATGTCTGGTTCgag                                                                       <  2:235643/81‑1 (MQ=255)
     tCGCCGTCGCACCCCAGATATACGGAATGGAGTAGTCGTTATTCGGGTCAAAAGGCTTGTTGAGCATGTCTGGTTCGAGAt                                                                     <  1:235644/81‑1 (MQ=255)
                 cccAGATATACGGAATGGAGTAGTCGTTATTCGGGTCAAAAGGCTTGTTGAGCATGTCTGGTTCGAGATTGCTGAAGTTTg                                                         >  2:235667/1‑81 (MQ=255)
                  ccAGATATACGGAATGGAGTAGTCGTTATTCGGGTCAAAAGGCTTGTTGAGCATGTCTGGTTCGAGATTGCTGAAGTTTGt                                                        <  2:235645/81‑1 (MQ=255)
                      atatACGGAATGGAGTAGTCGTTATTCGGGTCAAAAGGCTTGTTGAGCATGTCTGGTTCGAGATTGCTGAAGTTTGTTAAc                                                    <  1:235646/81‑1 (MQ=255)
                        ataCGGAATGGAGTAGTCGTTATTCGGGTCAAAAGGCTTGTTGAGCATGTCTGGTTCGAGATTGCTGAAGTTTGTTAACtt                                                  >  1:235666/1‑81 (MQ=255)
                         taCGGAATGGAGTAGTCGTTATTCGGGTCAAAAGGCTTGTTGAGCATGTCTGGTTCGAGATTGCTGAAGTTTGTTAACtt                                                  <  1:235647/80‑1 (MQ=255)
                         taCGGAATGGAGTAGTCGTTATTCGGGTCAAAAGGCTTGTTGAGCATGTCTGGTTCGAGATTGCTGAAGTTTGTTAACTTc                                                 <  2:235648/81‑1 (MQ=255)
                          aCGGAATGGAGTAGTCGTTATTCGGGTCAAAAGGCTTGTTGAGCATGTCTGGTTCGAGATTGCTGAAGTTTGTTAACTTc                                                 >  1:235649/1‑80 (MQ=255)
                              aaTGGAGTAGTCGTTATTCGGGTCAAAAGGCTTGTTGAGCATGTCTGGTTCGAGATTGCTGAAGTTTGTTAACTTCGACtt                                            <  1:235650/81‑1 (MQ=255)
                               aTGGAGTAGTCGTTATTCGGGTCAAAAGGCTTGTTGAGCATGTCTGGTTCGAGATTGCTGAAGTTTGTTAACTTCGACTTg                                           >  1:235675/1‑81 (MQ=255)
                                  gAGTAGTCGTTATTCGGGTCAAAAGGCTTGTTGAGCATGTCTGGTTCGAGATTGCTGAAGTTTGTTAACTTCGACTTGTc                                         <  1:235651/80‑1 (MQ=255)
                                   agtagtCGTTATTCGGGTCAAAAGGCTTGTTGAGCATGTCTGGTTCGAGATTGCTGAAGTTTGTTAACTTCGACTTGTCGa                                       <  2:235652/81‑1 (MQ=255)
                                     tagtCGTTATTCGGGTCAAAAGGCTTGTTGAGCATGTCTGGTTCGAGATTGCTGAAGTTTGTTAACTTCGACTTGTCGAtc                                     <  1:235653/81‑1 (MQ=255)
                                                        aaGGCTTGTTGAGCATGTCTGGTTCGAGATTGCTGAAGTTTGTTAACTTCGACTTGTCGATCTTCTGGATCATCCcttctt                  <  2:235654/81‑1 (MQ=255)
                                                               gttgAGCATGTCTGGTTCGAGATTGCTGAAGTTTGTTAACTTCGACTTGTCGATCTTCTGGATCATCCCTTCTTTACGc             <  1:235655/79‑1 (MQ=255)
                                                               gttgAGCATGTCTGGTTCGAGATTGCTGAAGTTTGTTAACTTCGACTTGTCGATCTTCTGGATCATCCCTTCTTTACGCAt           >  2:235668/1‑81 (MQ=255)
                                                                   aGCATGTCTGGTTCGAGATTGCTGAAGTTTGTTAACTTCGACTTGTCGATCTTCTGGATCATCCCTTCTTTACGCATTTTa       >  1:235725/1‑81 (MQ=255)
                                                                     cATGTCTGGTTCGAGATTGCTGAAGTTTGTTAACTTCGACTTGTCGATCTTCTGGATCATCCCTTCTTTACGCATTTTATc     <  1:235656/81‑1 (MQ=255)
                                                                      aTGTCTGGTTCGAGATTGCTGAAGTTTGTTAACTTCGACTTGTCGATCTTCTGGATCATCCCTTCTTTACGCATTTTATc     >  1:235669/1‑80 (MQ=255)
                                                                         tCTGGTTCGAGATTGCTGAAGTTTGTTAACTTCGACTTGTCGATCTTCTGGATCATCCCTTCTTTACGCATTTTATCAAc  <  1:235657/80‑1 (MQ=255)
                                                                              |                                                                          
ACCAATCGCCGTCGCACCCCAGATATACGGAATGGAGTAGTCGTTATTCGGGTCAAAAGGCTTGTTGAGCATGTCTGGATCGAGATTGCTGAAGTTTGTTAACTTCGACTTGTCGATCTTCTGGATCATCCCTTCTTTACGCATTTTATCAAC  >  NC_000913/1182419‑1182571

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: