Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,229,560 (T)7→8 coding (835/912 nt) hlyE ← hemolysin E

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,229,5531.T100.0% 42.6 / NA 13M281K (ATG→AAG) hlyEhemolysin E
Reads supporting (aligned to +/- strand):  ref base . (0/0);  new base T (5/8);  total (5/8)

AATCGCTTATCAGACTTCAGGTACCTCAAAGAGTGTCTTTTTACCGTGTCTTTTCTGATACTCATTACAGGTGTTAATCATTTTTTTGGCCGCTTCTTTTAGCAAAGAAAGCATTAAATCATCATAATCAACGTAGAATCTGGTTGTTTCA  >  NC_000913/1229474‑1229624
                                                                                |                                                                       
aatCGCTTATCAGACTTCAGGTACCTCAAAGAGTGTCTTTTTACCGTGTCTTTTCTGATACTCATTACAGGTGTTAATCAt                                                                        >  1:242196/1‑81 (MQ=255)
                  aGGTACCTCAAAGAGTGTCTTTTTACCGTGTCTTTTCTGATACTCATTACAGGTGTTAATCATTTTTTTTGGCCGcttctt                                                       >  2:242193/1‑81 (MQ=255)
                       ccTCAAAGAGTGTCTTTTTACCGTGTCTTTTCTGATACTCATTACAGGTGTTAATCATTTTTTTTGGCCGCTTCTTTTAGc                                                  <  1:242177/81‑1 (MQ=255)
                       ccTCAAAGAGTGTCTTTTTACCGTGTCTTTTCTGATACTCATTACAGGTGTTAATCATTTTTTTTGGCCGCTTCTTTTAGc                                                  <  2:242176/81‑1 (MQ=255)
                            aaGAGTGTCTTTTTACCGTGTCTTTTCTGATACTCATTACAGGTGTTAATCATTTTTTTTGGCCGCTTCTTTTAGCaaaga                                             <  2:242178/81‑1 (MQ=255)
                             agagTGTCTTTTTACCGTGTCTTTTCTGATACTCATTACAGGTGTTAATCATTTTTTTTGGCCGCTTCTTTTAGCaaaga                                             >  2:242198/1‑80 (MQ=255)
                                  gtCTTTTTACCGTGTCTTTTCTGATACTCATTACAGGTGTTAATCATTTTTTTTGGCCGCTTCTTTTAGCAAAGAAAGCAt                                       >  2:242208/1‑81 (MQ=255)
                                                         aTACTCATTACAGGTGTTAATCATTTTTTTTGGCCGCTTCTTTTAGCAAAGAAAGCATTAAATCATCATAATCAACGTAg                 >  2:242195/1‑80 (MQ=255)
                                                            cTCATTACAGGTGTTAATCATTTTTTTTGGCCGCTTCTTTTAGCAAAGAAAGCATTAAATCATCATAATCAACGTAGAAt              <  1:242179/80‑1 (MQ=255)
                                                               aTTACAGGTGTTAATCATTTTTTTTGGCCGCTTCTTTTAGCAAAGAAAGCATTAAATCATCATAATCAACGTAGAATCt            <  1:242180/79‑1 (MQ=255)
                                                               aTTACAGGTGTTAATCATTTTTTTTGGCCGCTTCTTTTAGCAAAGAAAGCATTAAATCATCATAATCAACGTAGAATCTgg          <  1:242181/81‑1 (MQ=255)
                                                               aTTACAGGTGTTAATCATTTTTTTTGGCCGCTTCTTTTAGCAAAGAAAGCATTAAATCATCATAATCAACGTAGAATCTgg          >  2:242199/1‑81 (MQ=255)
                                                                  aCAGGTGTTAATCATTTTTTTTGGCCGCTTCTTTTAGCAAAGAAAGCATTAAATCATCATAATCAACGTAGAATCTGgtt        <  2:242182/80‑1 (MQ=255)
                                                                       tgtTAATCATTTTTTTTGGCCGCTTCTTTTAGCAAAGAAAGCATTAAATCATCATAATCAACGTAGAATCTGGTTGTTTCa  <  2:242183/81‑1 (MQ=255)
                                                                                |                                                                       
AATCGCTTATCAGACTTCAGGTACCTCAAAGAGTGTCTTTTTACCGTGTCTTTTCTGATACTCATTACAGGTGTTAATCATTTTTTTGGCCGCTTCTTTTAGCAAAGAAAGCATTAAATCATCATAATCAACGTAGAATCTGGTTGTTTCA  >  NC_000913/1229474‑1229624

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 35 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: