Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 3,969,234 G→A M68I (ATG→ATA wzzE → enterobacterial common antigen polysaccharide co‑polymerase

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009133,969,2340GA100.0% 90.6 / NA 26M68I (ATG→ATAwzzEenterobacterial common antigen polysaccharide co‑polymerase
Reads supporting (aligned to +/- strand):  ref base G (0/0);  new base A (12/14);  total (12/14)

TCGCGCTGGCGTATACGTTTTTTGCTCGTCAGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATGCTGGGGGGATATTACTCGCAGCAGCAATTTTTGCGTAACCTGGATGTCCGTTCAAACATGGCTTCTGCCGACCAACC  >  NC_000913/3969158‑3969311
                                                                            |                                                                             
tCGCGCTGGCGTATACGTTTTTTGCTCGTCAGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATACTgg                                                                           >  1:778656/1‑81 (MQ=255)
  gcgcTGGCGTATACGTTTTTTGCTCGTCAGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATACTgggg                                                                         >  1:778644/1‑81 (MQ=255)
     cTGGCGTATACGTTTTTTGCTCGTCAGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATACTGGGGGGa                                                                      >  2:778659/1‑81 (MQ=255)
     cTGGCGTATACGTTTTTTGCTCGTCAGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATACTGGGGGGa                                                                      >  1:778649/1‑81 (MQ=255)
        gCGTATACGTTTTTTGCTCGTCAGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATACTGGGGGGata                                                                    <  2:778609/80‑1 (MQ=255)
          gTATACGTTTTTTGCTCGTCAGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATACTGGGGGGATATTa                                                                 >  1:778645/1‑81 (MQ=255)
           tataCGTTTTTTGCTCGTCAGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATACTGGGGGGATATTAc                                                                <  1:778610/81‑1 (MQ=255)
           tataCGTTTTTTGCTCGTCAGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATACTGGGGGGATATTAc                                                                <  2:778611/81‑1 (MQ=255)
             taCGTTTTTTGCTCGTCAGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATACTGGGGGGATATTACTc                                                              <  2:778612/81‑1 (MQ=255)
              aCGTTTTTTGCTCGTCAGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATACTGGGGGGATATTACTCg                                                             >  1:778654/1‑81 (MQ=255)
                    tttGCTCGTCAGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATACTGGGGGGATATTACTCgcagcag                                                       >  1:778658/1‑81 (MQ=255)
                     ttGCTCGTCAGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATACTGGGGGGATATTACTCgcagcag                                                       >  1:778655/1‑80 (MQ=255)
                       gCTCGTCAGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATACTGGGGGGATATTACTCGCAGCAGCaa                                                    >  1:778653/1‑81 (MQ=255)
                        cTCGTCAGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATACTGGGGGGATATTACTCGCAGCAGCAAt                                                   <  2:778613/81‑1 (MQ=255)
                          cGTCAGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATACTGGGGGGATATTACTCGCAGCAGCAAttt                                                 >  2:778647/1‑81 (MQ=255)
                              aGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATACTGGGGGGATATTACTCGCAGCAGCAATTTTTg                                              <  1:778615/80‑1 (MQ=255)
                              aGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATACTGGGGGGATATTACTCGCAGCAGCAATTTTTGc                                             <  1:778616/81‑1 (MQ=255)
                                gAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATACTGGGGGGATATTACTCGCAGCAGCAATTTTTGCGt                                           <  2:778617/81‑1 (MQ=255)
                                           gACGGCGATTACCGATCGTCCAACGGTGAATATACTGGGGGGATATTACTCGCAGCAGCAATTTTTGCGTAACCTGGAt                                  <  1:778618/79‑1 (MQ=255)
                                             cGGCGATTACCGATCGTCCAACGGTGAATATACTGGGGGGATATTACTCGCAGCAGCAATTTTTGCGTAACCTGGATGTcc                              <  1:778619/81‑1 (MQ=255)
                                                 gATTACCGATCGTCCAACGGTGAATATACTGGGGGGATATTACTCGCAGCAGCAATTTTTGCGTAACCTGGATGTCCGTTc                          <  1:778620/81‑1 (MQ=255)
                                                     aCCGATCGTCCAACGGTGAATATACTGGGGGGATATTACTCGCAGCAGCAATTTTTGCGTAACCTGGATGTCCGTTCaaa                       <  2:778621/80‑1 (MQ=255)
                                                               cAACGGTGAATATACTGGGGGGATATTACTCGCAGCAGCAATTTTTGCGTAACCTGGATGTCCGTTCAAACATGGCTTCt             <  1:778622/80‑1 (MQ=255)
                                                                  cGGTGAATATACTGGGGGGATATTACTCGCAGCAGCAATTTTTGCGTAACCTGGATGTCCGTTCAAACATGGCTTCTGcc          >  2:778676/1‑80 (MQ=255)
                                                                   ggTGAATATACTGGGGGGATATTACTCGCAGCAGCAATTTTTGCGTAACCTGGATGTCCGTTCAAACATGGCTTCTGCCGa        >  1:778662/1‑81 (MQ=255)
                                                                    gTGAATATACTGGGGGGATATTACTCGCAGCAGCAATTTTTGCGTAACCTGGATGTCCGTTCAAACATGGCTTCTGCCGac       <  2:778623/81‑1 (MQ=255)
                                                                         tataCTGGGGGGATATTACTCGCAGCAGCAATTTTTGCGTAACCTGGATGTCCGTTCAAACATGGCTTCTGCCGaccaacc  <  2:778624/81‑1 (MQ=255)
                                                                            |                                                                             
TCGCGCTGGCGTATACGTTTTTTGCTCGTCAGGAGTGGAGCTCGACGGCGATTACCGATCGTCCAACGGTGAATATGCTGGGGGGATATTACTCGCAGCAGCAATTTTTGCGTAACCTGGATGTCCGTTCAAACATGGCTTCTGCCGACCAACC  >  NC_000913/3969158‑3969311

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 31 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: