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% 85.8 / NA 24A407A (GCG→GCAsdaAL‑serine deaminase I
Reads supporting (aligned to +/- strand):  ref base G (0/0);  new base A (14/10);  total (14/10)

CATTGAGCGTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCGCGGATGGCTCTGCGCCGCACCAGTGCACCGCGCGTCTCGCTGGATA  >  NC_000913/1898107‑1898198
                                             |                                              
cATTGAGCGTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCACgg                                             <  1:178177/49‑1 (MQ=255)
 aTTGAGCGTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCACGGAt                                           <  1:1517217/50‑1 (MQ=255)
    gAGCGTAATACCATTGCCTCTGTGAAGGCGATTAACGCCGCACGGATGGc                                        >  1:2328719/1‑50 (MQ=38)
     aGCGTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCACGGATGGct                                       >  1:456173/1‑50 (MQ=255)
     aGCGTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCACGGATGGc                                        <  1:1173798/49‑1 (MQ=255)
     aGCGTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCACGGATGGc                                        <  1:563032/49‑1 (MQ=255)
      gCGTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCACGGATGGctc                                      >  1:906415/1‑50 (MQ=255)
      gCGTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCACGGATGGctc                                      <  1:455577/50‑1 (MQ=255)
        gTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCACGGATGGCTCTg                                    >  1:1906070/1‑50 (MQ=255)
            tGCCATTGCCTCTGTGAAGGCGATTAACGCCGCACGGATGGCTCTGcgcc                                >  1:416635/1‑50 (MQ=255)
              ccATTGCCTCTGTGAAGGCGATTAACGCCGCACGGATGGCTCTGcgccg                               >  1:17691/1‑49 (MQ=255)
                 ttGCCTCTGTGAAGGCGATTAACGCCGCACGGATGGCTCTGCGCCGCAc                            >  1:222604/1‑49 (MQ=255)
                   gCCTCTGTGAAGGCGATTAACGCCGCACGGATGGCTCTGCGCCGCACCa                          <  1:2317078/49‑1 (MQ=255)
                   gCCTCTGTGAAGGCGATTAACGCCGCACGGATGGCTCTGCGCCGCACCAg                         >  1:888676/1‑50 (MQ=255)
                    ccTCTGTGAAGGCGATTAACGCCGCACGGATGGCTCTGCGCCGCACCAg                         <  1:1630519/49‑1 (MQ=255)
                    ccTCTGTGAAGGCGATTAACGCCGCACGGATGGCTCTGCGCCGCACCAGt                        <  1:728051/50‑1 (MQ=255)
                     ctctGTGAAGGCGATTAACGCCGCACGGATGGCTCTGCGCCGCACCAGTg                       >  1:2318412/1‑50 (MQ=255)
                     ctctGTGAAGGCGATTAACGCCGCACGGATGGCTCTGCGCCGCACCAGTg                       >  1:1861350/1‑50 (MQ=255)
                       ctGTGAAGGCGATTAACGCCGCACGGATGGCTCTGCGCCGCACCAGTGCa                     >  1:1019028/1‑50 (MQ=255)
                          tgAAGGCGATTAACGCCGCACGGATGGCTCTGCGCCGCACCAGTGCACcg                  <  1:2120810/50‑1 (MQ=255)
                               gCGATTAACGCCGCACGGATGGCTCTGCGCCGCACCAGTGCACCGCGCGt             >  1:419939/1‑50 (MQ=255)
                                 gATTAACGCCGCACGGATGGCTCTGCGCCGCACCAGTGCACCGCGCGtct           <  1:679015/50‑1 (MQ=255)
                                     aaCGCCGCACGGATGGCTCTGCGCCGCACCAGTGCACCGCGCGTCTCGCt       >  1:2575163/1‑50 (MQ=255)
                                       cgccgcACGGATGGCTCTGCGCCGCACCAGTGCACCGCGCGTCTCGCTg      >  1:1254633/1‑49 (MQ=255)
                                          cgcacgGATGGCTCTGCGCCGCACCAGTGCACCGCGCGTCTCGCTGGAt   >  1:2470636/1‑49 (MQ=255)
                                          cgcacgGATGGCTCTGCGCCGCACCAGTGCACCGCGCGTCTCGCTGGATa  <  1:460286/50‑1 (MQ=255)
                                             |                                              
CATTGAGCGTAATGCCATTGCCTCTGTGAAGGCGATTAACGCCGCGCGGATGGCTCTGCGCCGCACCAGTGCACCGCGCGTCTCGCTGGATA  >  NC_000913/1898107‑1898198

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: