Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 522,992 C→T intergenic (+162/‑269) ybbP → / → rhsD putative ABC transporter membrane subunit YbbP/protein RhsD

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_000913522,9920CT100.0% 40.3 / NA 12intergenic (+162/‑269)ybbP/rhsDputative ABC transporter membrane subunit YbbP/protein RhsD
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base T (4/8);  total (4/8)

ATTGGTGATTTCCTATCTTTCTATTGCTGATATTAATCTGAATCGGTGGAGTTTATTGATTTTAAATATAGCCCTACAAAAATAACTCAGACTAATAAAATCATAAATCATATGCGTTGAATGGATATTATCCATATAGTGAATTTGTTGA  >  NC_000913/522916‑523066
                                                                            |                                                                          
aTTGGTGATTTCCTATCTTTCTATTGCTGATATTAATCTGAATCGGTGGAGTTTATTGATTTTAAATATAGCCCTATaaaa                                                                        <  1:110707/81‑1 (MQ=255)
  tGGTGATTTCCTATCTTTCTATTGCTGATATTAATCTGAATCGGTGGAGTTTATTGATTTTAAATATAGCCCTATaaaaa                                                                       >  1:110728/1‑80 (MQ=255)
       aTTTCCTATCTTTCTATTGCTGATATTAATCTGAATCGGTGGAGTTTATTGATTTTAAATATAGCCCTATAAAAATAACTc                                                                 <  2:110708/81‑1 (MQ=255)
         ttCCTATCTTTCTATTGCTGATATTAATCTGAATCGGTGGAGTTTATTGATTTTAAATATAGCCCTATAAAAATAACt                                                                  >  1:110726/1‑78 (MQ=255)
                                  aaTCTGAATCGGTGGAGTTTATTGATTTTAAATATAGCCCTATAAAAATAACTCAGACTAATAAAATCATAAATCATATg                                       <  1:110709/80‑1 (MQ=255)
                                        aaTCGGTGGAGTTTATTGATTTTAAATATAGCCCTATAAAAATAACTCAGACTAATAAAATCATAAATCATATGCGTTg                                  <  2:110710/79‑1 (MQ=255)
                                        aaTCGGTGGAGTTTATTGATTTTAAATATAGCCCTATAAAAATAACTCAGACTAATAAAATCATAAATCATATGCGTTGa                                 <  1:110711/80‑1 (MQ=255)
                                                gAGTTTATTGATTTTAAATATAGCCCTATAAAAATAACTCAGACTAATAAAATCATAAATCATATGCGTTGAATGGatat                         <  1:110712/80‑1 (MQ=255)
                                                     tATTGATTTTAAATATAGCCCTATAAAAATAACTCAGACTAATAAAATCATAAATCATATGCGTTGAATGGATATTATcc                    <  2:110713/80‑1 (MQ=255)
                                                          aTTTTAAATATAGCCCTATAAAAATAACTCAGACTAATAAAATCATAAATCATATGCGTTGAATGGATATTATCCATATAg              <  1:110714/81‑1 (MQ=255)
                                                          aTTTTAAATATAGCCCTATAAAAATAACTCAGACTAATAAAATCATAAATCATATGCGTTGAATGGATATTATCCATATAg              >  1:110734/1‑81 (MQ=255)
                                                                      gCCCTATAAAAATAACTCAGACTAATAAAATCATAAATCATATGCGTTGAATGGATATTATCCATATAGTGAATTTGTtga  >  1:110729/1‑81 (MQ=255)
                                                                            |                                                                          
ATTGGTGATTTCCTATCTTTCTATTGCTGATATTAATCTGAATCGGTGGAGTTTATTGATTTTAAATATAGCCCTACAAAAATAACTCAGACTAATAAAATCATAAATCATATGCGTTGAATGGATATTATCCATATAGTGAATTTGTTGA  >  NC_000913/522916‑523066

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: