Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,199,190 G→A V166I (GTT→ATT)  lit → e14 prophage; cell death peptidase Lit

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,199,1900GA100.0% 47.4 / NA 14V166I (GTT→ATT) lite14 prophage; cell death peptidase Lit
Reads supporting (aligned to +/- strand):  ref base G (0/0);  new base A (7/7);  total (7/7)

GAAGACTCACAAGTTGCTAGCGAGATATTTCTTTGTGCTATTGCTTGGATTCTTCATCATGAAATAAGTCATGTTGTTTTACAGCATCCATTGGTCACTACAGCATTCTCCACTCAAGAGGAGCGTGAAGCAGATTCACATGCTACAAAATG  >  NC_000913/1199115‑1199266
                                                                           |                                                                            
gAAGACTCACAAGTTGCTAGCGAGATATTTCTTTGTGCTATTGCTTGGATTCTTCATCATGAAATAAGTCATGTTATTTTa                                                                         <  1:237530/81‑1 (MQ=255)
       cacaAGTTGCTAGCGAGATATTTCTTTGTGCTATTGCTTGGATTCTTCATCATGAAATAAGTCATGTTATTTTACAGCATc                                                                  >  1:237546/1‑81 (MQ=255)
                 tAGCGAGATATTTCTTTGTGCTATTGCTTGGATTCTTCATCATGAAATAAGTCATGTTATTTTACAGCATCCATTGGTCAc                                                        >  1:237549/1‑81 (MQ=255)
                  aGCGAGATATTTCTTTGTGCTATTGCTTGGATTCTTCATCATGAAATAAGTCATGTTATTTTACAGCATCCATTGGTCAc                                                        >  2:237548/1‑80 (MQ=255)
                  aGCGAGATATTTCTTTGTGCTATTGCTTGGATTCTTCATCATGAAATAAGTCATGTTATTTTACAGCATCCATTGGTCAc                                                        >  2:237550/1‑80 (MQ=255)
                        atatTTCTTTGTGCTATTGCTTGGATTCTTCATCATGAAATAAGTCATGTTATTTTACAGCATCCATTGGTCACTACAGCa                                                 >  2:237556/1‑81 (MQ=255)
                                 tgtgCTATTGCTTGGATTCTTCATCATGAAATAAGTCATGTTATTTTACAGCATCCATTGGTCACTACAGCATTCTCCa                                          <  2:237531/79‑1 (MQ=255)
                                        ttGCTTGGATTCTTCATCATGAAATAAGTCATGTTATTTTACAGCATCCATTGGTCACTACAGCATTCTCCACTCAAgagg                                 <  2:237532/81‑1 (MQ=255)
                                          gCTTGGATTCTTCATCATGAAATAAGTCATGTTATTTTACAGCATCCATTGGTCACTACAGCATTCTCCACTCAAgagga                                <  2:237533/80‑1 (MQ=255)
                                              ggATTCTTCATCATGAAATAAGTCATGTTATTTTACAGCATCCATTGGTCACTACAGCATTCTCCACTCAAGAGGAGCGt                            <  1:237534/80‑1 (MQ=255)
                                                         catGAAATAAGTCATGTTATTTTACAGCATCCATTGGTCACTACAGCATTCTCCACTCAAGAGGAGCGTGAAGCAGATTca                >  2:237559/1‑81 (MQ=255)
                                                          atGAAATAAGTCATGTTATTTTACAGCATCCATTGGTCACTGCAGCATTCTCCACTCAAGAGGAGCGTGAAGCAGATTcac               <  1:237535/81‑1 (MQ=255)
                                                          atGAAATAAGTCATGTTATTTTACAGCATCCATTGGTCACTACAGCATTCTCCACTCAAGAGGAGCGTGAAGCAGATTca                >  1:237561/1‑80 (MQ=255)
                                                                   gTCATGTTATTTTACAGCATCCATTGGTCACTACAGCATTCTCCACTCAAGAGGAGCGTGAAGCAGATTCACATGCTACaa      <  1:237536/81‑1 (MQ=255)
                                                                       tgttatTTTACAGCATCCATTGGTCACTACAGCATTCTCCACTCAAGAGGAGCGTGAAGCAGATTCACATGCTACAAAATg  >  2:237553/1‑81 (MQ=255)
                                                                           |                                                                            
GAAGACTCACAAGTTGCTAGCGAGATATTTCTTTGTGCTATTGCTTGGATTCTTCATCATGAAATAAGTCATGTTGTTTTACAGCATCCATTGGTCACTACAGCATTCTCCACTCAAGAGGAGCGTGAAGCAGATTCACATGCTACAAAATG  >  NC_000913/1199115‑1199266

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