Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 510,440 G→A L314L (CTG→TTG)  copA ← Cu(+) exporting P‑type ATPase

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_000913510,4400GA100.0% 11.4 / NA 7L314L (CTG→TTG) copACu(+) exporting P‑type ATPase
Reads supporting (aligned to +/- strand):  ref base G (0/0);  new base A (4/3);  total (4/3)

GGCATGGACGCTATCGCCTTCGCCTTTTTGCTGCGGGATTGGTTCGCCCGTCAGCATCGCTTCATCCAGCCATGCTTCGCCCTGGGTAATCTCGCCATCTACCGGCACGCGATCGCCGGTCGTCAGGCGCAGCAACATACCTGGCTGCACTTCTGCCAGAGGCACGCTTTTTTCACCTTCGTCAGTAACCAGGCGTGCCGTCGGCGGGGTTAAATCGAGTAACTTTTCCAGCGCCTTAGAAGAACGCTGGCGTGCGCGCGCTTCCAGCATATGGCCGAGATTGATCAGACCGATAATCATCGCGCTGGCTTCGTAATAAAGATGTCGCGCTTCCATCGGGAACCACTGCGGCCACAGGTTGACGCTCATCGAATAGAGCCACGCCACGCCAGTACCCAGCGCCACCAGCGTATCCATCGTCGCCGCACCGTTCAGCAGGCTTTTCCATGCACTGCGGTAAAAATGG  >  NC_000913/510210‑510675
                                                                                                                                                                                                                                      |                                                                                                                                                                                                                                           
ngCATGGACGCTATCGCCTTCGCCTTTTTGCTGCGGGATTGGTTCGCCCGTCAGCATCGCTTCATCCAGCCATGCTTCGCCCTGGGTAATCTCGCCATCTACCGGCACGCGATCGCCGGTCGTCAGGCGCAGCAACATACCTGGCTGCACTTCTGCCAGAGGCACGCTTTTTTCACCTTCGTCAGTAACCAGGCGTGCCGTCGGCGGGGTTAAATCGAGTAACTTTTTCAACGCCTTAGAAGAACGCTGGc                                                                                                                                                                                                                         >  1:15758/2‑251 (MQ=255)
     ggACGCTATCGCCTTCGCCTTTTTGCTGCTGGATTGGTTCGCCCGTCAGCATCGCTTCATCCAGCCATGCTTCGCCCTGGGTAATCTCGCCATCTCCCGGCCCGCGATCGCCGGTCGTCAGGCGCAGCAACATACCTGCCTGCACTTCTGCCAGAGGCACGCTTTTTTCTCCTTCGTCAGTAACCAGGCGTGCCGTCGGCGGGGTTAAATCGAGTAACTTTTCCAACGCCTTAGAAGAACGCTGGCGTgn                                                                                                                                                                                                                     <  1:42279/250‑2 (MQ=255)
            aTCGCCTTCGCCTTTTTGCTGCGGGATTGGTTCGCCCGTAAGCATCGCTTCAGCCAGCCATGCTTCGCCCTGGGTAATCTCGCCATCTACCGACACGCGAACGCCGGGCTTGATGCGCAGCAACATACCTGGCGGCACTTCTGCCAGAGGCACGCAGTTTTCACCGTCGTCAGTAACCAAGCGTGCCGTCGGCGGGTGTAAAGCGAGCAGCGTTTCCAACGCCTTAGAAGAACTCTGGCGTgcgcgcgc                                                                                                                                                                                                               <  1:167111/249‑1 (MQ=255)
                              ctgcGGGATTGGTTCGCCCGTCCGCATAGCTTCATCCAGCCATGCTTCGCCCTGGGTAATCTCGCCATCTACCGGCACGCGATCGCCGGTCGTCAGGCGCAGCAACATACCTGGCTGCACTTCTGCCAGAGGCACGCTTTTTTCACCTTCGTCAGTAACCAGGCGTGCCGTCGGCGGGGTTAAATCGAGTAACTTTTCCAACGCCTTAGAAGAACGCTGGCGAGCGCGAGCTTCCAGCATATGGCCg                                                                                                                                                                                               >  1:141600/1‑247 (MQ=255)
                                                              cATCCAGCCATGCTTCGCCCTGGGTAATCTCGCCATCTACCGGCACGCGATCGCCGGTCGTCAGGCGCAGCAACATACCTGGCTGCACTTCTGCCAGAGGCACGCTTTTTTCACCTTCGTCAGTAACCAGGCGTGCCGTCGGCGGGGTTAAATCGAGTAACTTTTCCAACGCCTTAGAAGAACGCTGGCGTGCGCGCGCTTCCAGCATATGGCCGAGATTGATCAGACCGATAATCATCGCGCTGGCTTCg                                                                                                                                                           <  1:58412/251‑1 (MQ=255)
                                                                                                                                                                                   cGTCAGTAACCAGGCGTGCCGTCGGCGGGGTTAAATCGAGTAACTTTTACAAACCCCTAACAGAACGATGGCGCGACAGCGATTCCAGCATAAGGCCGAGATTGAACAGAACCATAATCATCGCGCTGGCTTCGTAATAAAGATGACGCGCTTCCATTGGGAACCACTGCGGCCACAGGTTGACCCTCATCGAATAACGACACGCCACGCCAGAACCACCCGCCCCCAGCGTaacaaacgacgccgccccg                                      >  1:90716/1‑233 (MQ=255)
                                                                                                                                                                                                                       cGAGTAACTTTTCCAACGCCTTAGAAGAACGCTGGCGTGCGCGCGCTTCCAGCATATGGCCGAGATTGATCAGACCGATAATCATCGCGCTGGCTTCGTAATAAAGATGTCGCGCTTCCATCGGGAACCACTGCGGCCACAGGTTGACGCTCATCGAATAGAGCCACGCCACGCCAGTACCCAGCGCCACCAGCGTATCCATCGTCGCCGCACCGTTCAGCAGGCTTTTCCATGCACTGCGGTAAAAATgg  >  1:89650/1‑251 (MQ=255)
                                                                                                                                                                                                                                      |                                                                                                                                                                                                                                           
GGCATGGACGCTATCGCCTTCGCCTTTTTGCTGCGGGATTGGTTCGCCCGTCAGCATCGCTTCATCCAGCCATGCTTCGCCCTGGGTAATCTCGCCATCTACCGGCACGCGATCGCCGGTCGTCAGGCGCAGCAACATACCTGGCTGCACTTCTGCCAGAGGCACGCTTTTTTCACCTTCGTCAGTAACCAGGCGTGCCGTCGGCGGGGTTAAATCGAGTAACTTTTCCAGCGCCTTAGAAGAACGCTGGCGTGCGCGCGCTTCCAGCATATGGCCGAGATTGATCAGACCGATAATCATCGCGCTGGCTTCGTAATAAAGATGTCGCGCTTCCATCGGGAACCACTGCGGCCACAGGTTGACGCTCATCGAATAGAGCCACGCCACGCCAGTACCCAGCGCCACCAGCGTATCCATCGTCGCCGCACCGTTCAGCAGGCTTTTCCATGCACTGCGGTAAAAATGG  >  NC_000913/510210‑510675

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 29 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: