Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,662,872 C→T R773W (CGG→TGG)  ynfF → putative selenate reductase YnfF

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,662,8720CT100.0% 76.7 / NA 20R773W (CGG→TGG) ynfFputative selenate reductase YnfF
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base T (11/9);  total (11/9)

CGGGCAAGGTGCGTGGCTTAAAGCGGATATGTTTGGTGACCGGGTCGATCACGGCGGCAGTATCAATATTCTGACCTCTCA  >  NC_000913/1662832‑1662912
                                        |                                        
cGGGCAAGGTGCGTGGCTTAAAGCGGATATGTTTGGTGACTGGGTCGAt                                  >  1:2041653/1‑49 (MQ=255)
cGGGCAAGGTGCGTGGCTTAAAGCGGATATGTTTGGTGACTGGGTCGAt                                  >  1:955059/1‑49 (MQ=255)
cGGGCAAGGTGCGTGGCTTAAAGCGGATATGTTTGGTGACTGGGTCGAt                                  >  1:348028/1‑49 (MQ=255)
 gggCAAGGTGCGTGGCTTAAAGCGGATATGTTTGGTGACTGGGTCGAt                                  <  1:827404/48‑1 (MQ=255)
 gggCAAGGTGCGTGGCTTAAAGCGGATATGTTTGGTGACTGGGTCGATc                                 <  1:452810/49‑1 (MQ=255)
   gCAAGGTGCGTGGCTTAAAGCGGATATGTTTGGTGACTGGGTCGATCAc                               >  1:1942170/1‑49 (MQ=255)
   gCAAGGTGCGTGGCTTAAAGCGGATATGTTTGGTGACTGGGTCGATCAc                               <  1:1615815/49‑1 (MQ=255)
      aGGTGCGTGGCTTAAAGCGGATATGTTTGGTGACTGGGTCGATCAcggc                            >  1:1414468/1‑49 (MQ=255)
        gTGCGTGGCTTAAAGCGGATATGTTTGGTGACTGGGTCGATCAcggcgg                          >  1:1185614/1‑49 (MQ=255)
           cGTGGCTTAAAGCGGATATGTTTGGTGACTGGGTCGATCACGGCGGCAg                       >  1:195446/1‑49 (MQ=255)
            gTGGCTTAAAGCGGATATGTTTGGTGACTGGGTCGATCACGGCGGCAGt                      <  1:339953/49‑1 (MQ=255)
            gTGGCTTAAAGCGGATATGTTTGGTGACTGGGTCGATCACGGCGGCAGt                      <  1:457090/49‑1 (MQ=255)
                 ttAAAGCGGATATGTTTGGTGACTGGGTCGATCACGGCGGCAGTATCaa                 >  1:1789701/1‑49 (MQ=255)
                 ttAAAGCGGATATGTTTGGTGACTGGGTCGATCACGGCGGCAGTATCaa                 >  1:861898/1‑49 (MQ=255)
                     aGCGGATATGTTTGGTGACTGGGTCGATCACGGCGGCAGTATCAATAtt             <  1:631672/49‑1 (MQ=255)
                       cGGATATGTTTGGTGACTGGGTCGATCACGGCGGCAGTATCAATATTCt           <  1:1935513/49‑1 (MQ=255)
                             tGTTTGGTGACTGGGTCGATCACGGCGGCAGTATCAATATTCTGACctc     >  1:1142316/1‑49 (MQ=255)
                                ttGGTGACTGGGTCGATCACGGCGGCAGTATCAATATTCTGACCTCTCa  >  1:705556/1‑49 (MQ=255)
                                 tGGTGACTGGGTCGATCACGGCGGCAGTATCAATATTCTGACCTCTCa  <  1:1786016/48‑1 (MQ=255)
                                 tGGTGACTGGGTCGATCACGGCGGCAGTATCAATATTCTGACCTCTCa  <  1:1670688/48‑1 (MQ=255)
                                        |                                        
CGGGCAAGGTGCGTGGCTTAAAGCGGATATGTTTGGTGACCGGGTCGATCACGGCGGCAGTATCAATATTCTGACCTCTCA  >  NC_000913/1662832‑1662912

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: