Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 2,681,049 T→C N566S (AAC→AGC)  yphG ← DUF5107 domain‑containing protein YphG

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009132,681,0490TC100.0% 50.5 / NA 15N566S (AAC→AGC) yphGDUF5107 domain‑containing protein YphG
Reads supporting (aligned to +/- strand):  ref base T (0/0);  new base C (8/7);  total (8/7)

GCACTTCCTGATTGGTTGGGCAGGCGCGAAGACTTTGTTGGCAAAAATCCAGACCAGCGTCGAAGTTACCATTACGCGCCGCCAGTCGTGCCAGGCCATAATAGCCACCGGCTTTGCTGTTGCCGCTCCAGACCGCACGCCAGAAATCCTCTTCGGCTTGTTGATATTGTCCCTGACGTTCGTAAGCACTGGCGCGAATCAAACTCGCCTGTCCGCACTGCGGATTTTTGTTCAGCGCATGTGCGCGTTTCAGAGC  >  NC_000913/2680930‑2681185
                                                                                                                       |                                                                                                                                        
gCACTTCCTGATTGGTTGGGCAGGCGCGAAGACTTTGTTGGCAAAAATCCAGACCAGCGTCGAAGTTACCATTACGCGCCGCCAGTCGTGCCAGGCCATAATAGCCACCGGCTTTGCTGCTGCCGCTCCAGACCGCACGc                                                                                                                      >  2:63155/1‑140 (MQ=255)
     tCCTGATTGGTTGGGCAGGCGCGAAGACTTTGTTGGCAAAAATCCAGACCAGCGTCGAAGTTACCATTACGCGCCGCCAGTCGTGCCAGGCCATAATAGCCACCGGCTTTGCTGCTGCCGCTCCAGACCg                                                                                                                           <  1:1993/130‑1 (MQ=255)
     tCCTGATTGGTTGGGCAGGCGCGAAGACTTTGTTGGCAAAAATCCAGACCAGCGTCGAAGTTACCATTACGCGCCGCCAGTCGTGCCAGGCCATAATAGCCACCGGCTTTGCTGCTGCCGCTCCAGACCg                                                                                                                           >  1:250644/1‑130 (MQ=255)
     tCCTGATTGGTTGGGCAGGCGCGAAGACTTTGTTGGCAAAAATCCAGACCAGCGTCGAAGTTACCATTACGCGCCGCCAGTCGTGCCAGGCCATAATAGCCACCGGCTTTGCTGCTGCCGCTCCAGACCg                                                                                                                           >  2:1993/1‑130 (MQ=255)
     tCCTGATTGGTTGGGCAGGCGCGAAGACTTTGTTGGCAAAAATCCAGACCAGCGTCGAAGTTACCATTACGCGCCGCCAGTCGTGCCAGGCCATAATAGCCACCGGCTTTGCTGCTGCCGCTCCAGACCg                                                                                                                           <  2:250644/130‑1 (MQ=255)
              gttggGCAGGCGCGAAGACTTTGTTGGCAAAAATCCAGACCAGCGTCGAAGTTACCATTACGCGCCGCCAGTCGTGCCAGGCCATAATAGCCACCGGCTTTGCTGCTGCCGCTCCAGACCGCACGCCAGAAATCCTCTTc                                                                                                        >  1:110554/1‑140 (MQ=255)
                tggGCAGGCGCGAAGACTTTGTTGGCAAAAATCCAGACCAGCGTCGAAGTTACCATTACGCGCCGCCAGTCGTGCCAGGCCATAATAGCCACCGGCTTTGCTGCTGCCGCTCCAGACCGCACGCCAGAAATCCTCTTCgg                                                                                                      <  1:63155/140‑1 (MQ=255)
                     aGGCGCGAAGACTTTGTTGGCAAAAATCCAGACCAGCGTCGAAGTTACCATTACGCGCCGCCAGTCGTGCCAGGCCATAATAGCCACCGGCTTTGCTGCTGCCGCTCCAGACCGCACGCCAGAAATCCTCTTCGGCttgt                                                                                                 <  2:390091/140‑1 (MQ=255)
                                    tttgGCAAAAATCCAGACCAGCGTCGAAGTTCCCATTACGCGCCGCCAGTCGTGCCAGGCCATAATAGCCACCGGCTTTGCTGCTGCCGCTCCAGACCGCACGCCAGAAATCCTCTTCGGCTTGTTGATATTGTCCCTGa                                                                                  <  1:251751/139‑1 (MQ=255)
                                      tgGCAAAAATCCAGACCAGCGTCGAAGTTACCATTACGCGCCGCCAGTCGTGCCAGGCCATAATAGCCACCGGCTTTGCTGCTGCCGCTCCAGACCGCACGCCAGAAATCCTCTTCGGCTTGTTGATATTGTCCCTGACg                                                                                <  2:110554/140‑1 (MQ=255)
                                                         cGTCGAAGTTACCATTACGCGCCGCCAGTCGTGCCAGGCCATAATAGCCACCGGCTTTGCTGCTGCCGCTCCAGACCGCACGCCAGAAATCCTCTTCGGCTTGTTGATATTGTCCCTGACGTTCGTAAGCACTGGCGCGa                                                             >  1:15561/1‑140 (MQ=255)
                                                                             gccgccAGTCGTGCCAGGCCATAATAGCCACCGGCTTTGCTGCTGCCGCTCCAGACCGCACGCCAGAAATCCTCTTCGGCTTGTTGATATTGTCCCTGACGTTCGTAAGCACTGGCGCGAATCAAACTCGCCTGTCCGCa                                         >  2:254563/1‑140 (MQ=255)
                                                                                                        ccACCGGCTTTGCTGCTGCCGCTCCAGACCGCACGCCAGAAATCCTCTTCGGCTTGTTGATATTGTCCCTGACGTTCGTAAGCACTGGCGCGAATCAAACTCGCCTGTCCGCACTGCGGATTTTTGTTCAGCGCATGTgc              >  1:163996/1‑140 (MQ=255)
                                                                                                          aCCGGCTTTGCTGCTGCCGCTCCAGACCGCACGCCAGAAATCCTCTTCGGCTTGTTGATATTGTCCCTGACGTTCGTAAGCACTGGCGCGAATCAAACTCGCCTGTCCGCACTGCGGATTTTTGTTCAGCGCATGTgcgc            >  2:118621/1‑140 (MQ=255)
                                                                                                                tttGCTGCTGCCGCTCCAGACCGCACGCCAGAAATCCTCTTCGGCTTGTTGATATTGTCCCTGACGTTCGTAAGCACTGGCGCGAATCAAACTCGCCTGTCCGCACTGCGGATTTTTGTTCAGCGCATGTGCGCGTTTCa      <  2:163996/140‑1 (MQ=255)
                                                                                                                    ctgctgCCGCTCCAGACCGCACGCCAGAAATCCTCTTCGGCTTGTTGATATTGTCCCTGACGTTCGTAAGCACTGGCGCGAATCAAACTCGCCTGTCCGCACTGCGGATTTTTGTTCAGCGCATGTGCGCGTTTCAGAGc  <  1:27388/140‑1 (MQ=255)
                                                                                                                       |                                                                                                                                        
GCACTTCCTGATTGGTTGGGCAGGCGCGAAGACTTTGTTGGCAAAAATCCAGACCAGCGTCGAAGTTACCATTACGCGCCGCCAGTCGTGCCAGGCCATAATAGCCACCGGCTTTGCTGTTGCCGCTCCAGACCGCACGCCAGAAATCCTCTTCGGCTTGTTGATATTGTCCCTGACGTTCGTAAGCACTGGCGCGAATCAAACTCGCCTGTCCGCACTGCGGATTTTTGTTCAGCGCATGTGCGCGTTTCAGAGC  >  NC_000913/2680930‑2681185

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: