Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 2,247,968 C→T G189S (GGC→AGC)  lysP ← lysine:H(+) symporter

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009132,247,9680CT100.0% 19.2 / NA 8G189S (GGC→AGC) lysPlysine:H(+) symporter
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base T (6/2);  total (6/2)

CCAGAACACCTGACGTACCGCGCGTGGAATGTTTTTCGCCGGATCTTCGGACTCGCCTGCAGCAATACCGATCAGCTCGGTTCCCTGGAAAGAGAAGCCGACAATCATAGCTACGCCGATCATCGCCGCAAAACCACCAGCAAACGGCGCTTCGCCGATTGTCCAGTTGCTCCAGCCCGCAGGCTGCGCGCCTTTGAAGATACCGATAATCATCAGCACGCCAACGATGATAAAGACAATAACTGTCGTGACTTTGATCAGTGAGAACCAGTATTCCGCTTCACCAAAGCCACGAACTGAGATGTAGTTCAGCAGGAAGATAACGCCGAGGAACAACGCACTCCAGATCCAGCCCGGTGTATCCGGGAACCACC  >  NC_000913/2247792‑2248165
                                                                                                                                                                                |                                                                                                                                                                                                      
ccAGAACACCTGACGTACCGCGCGTGGAATGTTTTTCGCCGGATCTTCGGACTCGCCTGCAGCAATACCGATCAGCTCGGTTCCCTGGAAAGAGAAGCCGACAATCATAGCTACGCCGATCATCGCCGCAAAACCACCAGCAAACGGCGCTTCGCCGATTGTCCAGTTGCTCCAGCTCGCAGGCTGCGCGCCTTTGAAGATACCGATAATCATCAGCACGCCAACGATGATAAAGACAATAACTGTCGTg                                                                                                                              >  1:160328/1‑250 (MQ=255)
                                              tCGGACTCGCCTGCAGCAATACCGATCAGCTCGGTTCCCTGGAAAGAGAAGCCGACAATCATAGCTACGCCGATCATCGCCGCAAAACCACCAGCAAACGGCGCTTCGCCGATTGTCCAGTTGCTCCAGCTCGCAGGCTGCGCGCCTTTGAAGATACCGATAATCATCAGCACGCCAACGATGATAAAGACAATAACTGTCGTGACTTTGATCAGTGAGAACCAGTATTCCGCTTCACCAAAGCCAc                                                                                   <  1:57308/247‑1 (MQ=255)
                                                               aaTACCTATCATCGCGGTACCCTGGAAAGAGAAGCCGACAAGCATAGCTACGCTGTTCAGCGCAGCAAAGCCACCAGCAAACGGCGCTTCGCCGATTGTCCTACTGGTCCCGCTCTCATGCAGCGCGCCCTGGGATATACCGATAATGATCATCACGCCAGCGATGATAAAGCCAAGAACGTGCTTGACGTGGAGCAGTTATAACCAGTATTCCGCTTCACCAAAACCACGAACTGAGATGTAGtgcaaca                                                              <  1:98014/251‑7 (MQ=255)
                                                                                        aaaGAGCAGCCGACAATCATAGCTACCCCGATCATCGCCGCAAAACCACCAGCAAACGGCGCTTCGCCGATTGTCCAGTTGCTCCAGCTCGCAGGCTGCGCGCCTTTGAAGATACCGATAATCATCAGCACGCCAACGATGATAAAGACAATAACTGTCGTGACTTTGATCAGTGAGAACCAGTATTCCGCTTCACCAAAGCCACGAACTGAGATGTAGTTCAGCAGGAAGATAACGCAGAGGAACAACGc                                     >  1:132809/1‑251 (MQ=255)
                                                                                                                   ccGATCATCGCCGCAAAACCACCAGCAAACGGCGCTTCGCCGATTGTCCAGTTGCTCCAGCTCGCAGGCTGCGCGCCTTTGCAGATACCGATAATCATCAGCACGCCAACGATGATAAAGACAATAACTGTCGTGACTTTGATCCGTGAGAACCAGTATTCCGCTTCACCAAAGCCACGAACTGAGATGTAGTTCCGCAGGAAGATACCGCCGAGGAACAACGCACTCCAGATCCAGCCCGGTGTATCCgg          >  1:61524/1‑251 (MQ=255)
                                                                                                                       ncatcGCCGCAAAACCACCAGCAAACGGCGCTTCGCCGATTGTCCAGTTGCTCCAGCTCGCAGGCTGCGCGCCTTTGAAGATACCGATAATCATCAGCACGCCAACGATGATAAAGACAATAACTGTCGTGACTTTGATCAGTGAGAACCAGTATTCCGCTTCACCAAAGCCACGAACTGAGATGTAGTTCAGCAGGAAGATAACGCCGAGGAACAACGCACTCCAGATCCAGCCCGGTGTATCCGGGAac      >  1:100177/2‑251 (MQ=255)
                                                                                                                             ccgcAAAACCACCAGCAAACGGCGCTTCGCCGATTGTCCAGTTGCTCCAGCTCGCAGGCTGCGCGCCTTTGAAGATACCGATAATCATCAGCACGCCAACGATGATAAAGACAATAACTGTCGTGACTTTGATCAGTGAGAACCAGTATTCCGCTTCACCAAAGCCACGAACTGAGATGTAGTTCAGCAGGAAGTTAACGCCGAGGAACAACGCACTCCAGATCCAGCCCGGTGTATCCGGGAaccacc  >  1:46029/1‑249 (MQ=255)
                                                                                                                                                         gCCGATTGTCCAGTTGCTCCAGCTCGCAGGCTGCGCGCCTTTGAAGATACCGATAATCATCAGCACGCCAACGATGATAAAGACAATAACTGTCGTGACTTTGATCAGTGAGAACCAGTATTCCGCTTCACCAAAGCCACGAACTGAGATGt                                                                       >  1:818/1‑152 (MQ=255)
                                                                                                                                                                                |                                                                                                                                                                                                      
CCAGAACACCTGACGTACCGCGCGTGGAATGTTTTTCGCCGGATCTTCGGACTCGCCTGCAGCAATACCGATCAGCTCGGTTCCCTGGAAAGAGAAGCCGACAATCATAGCTACGCCGATCATCGCCGCAAAACCACCAGCAAACGGCGCTTCGCCGATTGTCCAGTTGCTCCAGCCCGCAGGCTGCGCGCCTTTGAAGATACCGATAATCATCAGCACGCCAACGATGATAAAGACAATAACTGTCGTGACTTTGATCAGTGAGAACCAGTATTCCGCTTCACCAAAGCCACGAACTGAGATGTAGTTCAGCAGGAAGATAACGCCGAGGAACAACGCACTCCAGATCCAGCCCGGTGTATCCGGGAACCACC  >  NC_000913/2247792‑2248165

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 13 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: