Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,898,152 G→A A407A (GCG→GCA sdaA → L‑serine deaminase I

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,898,1520GA100.0% 71.7 / NA 19A407A (GCG→GCAsdaAL‑serine deaminase I
Reads supporting (aligned to +/- strand):  ref base G (0/0);  new base A (7/12);  total (7/12)

CATTGAGCGTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCGCGGATGGCTCTGCGCCGCACCAGTGCACCGCGCGTCTCGCTGGA  >  NC_000913/1898107‑1898196
                                             |                                            
cATTGAGCGTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCACgg                                           <  1:411633/49‑1 (MQ=255)
cATTGAGCGTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCACgg                                           <  1:360221/49‑1 (MQ=255)
 aTTGAGCGTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCACGGa                                          >  1:2211068/1‑49 (MQ=255)
     aGCGTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCACGGATgg                                       <  1:1649768/48‑1 (MQ=255)
      gCGTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCACGGATGGct                                     <  1:708283/49‑1 (MQ=255)
      gCGTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCACGGATGGct                                     >  1:498656/1‑49 (MQ=255)
        gTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCACGGATGGctct                                   <  1:351602/49‑1 (MQ=255)
         tAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCACGGATGGCTCTg                                  >  1:616308/1‑49 (MQ=255)
               cATTGCCTCTGTGAAGGCGATTAACGCCGCACGGATGGCTCTGcgccgc                            <  1:479750/49‑1 (MQ=255)
                     ctctGTGAAGGCGATTAACGCCGCACGGATGGCTCTGCGCCGCACCAGt                      >  1:343855/1‑49 (MQ=255)
                     ctctGTGAAGGCGATTAACGCCGCACGGATGGCTCTGCGCCGCACCAGt                      >  1:1640478/1‑49 (MQ=255)
                        tgtgAAGGCGATTAACGCCGCACGGATGGCTCTGCGCCGCACCAGTg                     <  1:224810/47‑1 (MQ=255)
                        tgtgAAGGCGATTAACGCCGCACGGATGGCTCTGCGCCGCACCAGTGCa                   >  1:492706/1‑49 (MQ=255)
                            aaGGCGATTAACGCCGCACGGATGGCTCTGCGCCGCACCAGTGCACcgc               <  1:731693/49‑1 (MQ=255)
                              ggCGATTAACGCCGCACGGATGGCTCTGCGCCGCACCAGTGCACcgcgc             <  1:2294046/49‑1 (MQ=255)
                                     aaCGCCGCACGGATGGCTCTGCGCCGCACCAGTGCACCGCGCGTCTCg       <  1:2357734/48‑1 (MQ=255)
                                     aaCGCCGCACGGATGGCTCTGCGCCGCACCAGTGCACCGCGCGTCTCg       <  1:1849645/48‑1 (MQ=255)
                                       cgccgcACGGATGGCTCTGCGCCGCACCAGTGCACCGCGCGTCTCGCTg    <  1:1966562/49‑1 (MQ=255)
                                         ccgcACGGATGGCTCTGCGCCGCACCAGTGCACCGCGCGTCTCGCTGGa  >  1:1974707/1‑49 (MQ=255)
                                             |                                            
CATTGAGCGTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCGCGGATGGCTCTGCGCCGCACCAGTGCACCGCGCGTCTCGCTGGA  >  NC_000913/1898107‑1898196

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: