Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 736,714 A→G intergenic (+15/‑186) ybfQ → / → ybfL inactive transposase YbfQ/putative transposase YbfL

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_000913736,7140AG100.0% 47.7 / NA 15intergenic (+15/‑186)ybfQ/ybfLinactive transposase YbfQ/putative transposase YbfL
Reads supporting (aligned to +/- strand):  ref base A (0/0);  new base G (5/10);  total (5/10)

AAAATGGTATTCCTGTTCACGATACCATTGCCAGAGTTGTATCCCAGGGAAAGATCACGTAACGCTACTTTTTTGTACTAAATAATTCGCATTTTATGTTTAAAAATTGAGATATTCCTTATTACCTAAAGCTGTTTTTCATAGCTTATACAT  >  NC_000913/736638‑736790
                                                                            |                                                                            
aaaaTGGTATTCCTGTTCACGATACCATTGCCAGAGTTGTATCCCAGGGAAAGATCACGTAACGCTACTTTTTTGTGCTaa                                                                          <  2:142348/81‑1 (MQ=255)
    tGGTATTCCTGTTCACGATACCATTGCCAGAGTTGTATCCCAGGGAAAGATCACGTAACGCTACTTTTTTGTGCTAaataa                                                                      >  2:142371/1‑81 (MQ=255)
       tATTCCTGTTCACGATACCATTGCCAGAGTTGTATCCCAGGGAAAGATCACGTAACGCTACTTTTTTGTGCTAAATAATTc                                                                   <  2:142349/81‑1 (MQ=255)
         ttCCTGTTCACGATACCATTGCCAGAGTTGTATCCCAGGGAAAGATCACGTAACGCTACTTTTTTGTGCTAAATAATTCGc                                                                 <  2:142350/81‑1 (MQ=255)
            cTGTTCACGATACCATTGCCAGAGTTGTATCCCAGGGAAAGATCACGTAACGCTACTTTTTTGTGCTAAATAATTCGCAt                                                               <  2:142351/80‑1 (MQ=255)
               ttCACGATACCATTGCCAGAGTTGTATCCCAGGGAAAGATCACGTAACGCTACTTTTTTGTGCTAAATAATTCGCAtttt                                                            <  1:142352/80‑1 (MQ=255)
               ttCACGATACCATTGCCAGAGTTGTATCCCAGGGAAAGATCACGTAACGCTACTTTTTTGTGCTAAATAATTCGCATTTTa                                                           <  2:142353/81‑1 (MQ=255)
                    gATACCATTGCCAGAGTTGTATCCCAGGGAAAGATCACGTAACGCTACTTTTTTGTGCTAAATAATTCGCATTTTATGttt                                                      <  2:142354/81‑1 (MQ=255)
                           ttGCCAGAGTTGTATCCCAGGGAAAGATCACGTAACGCTACTTTTTTGTGCTAAATAATTCGCATTTTATGTTTAAAAAtt                                               >  1:142373/1‑81 (MQ=255)
                                  agTTGTATCCCAGGGAAAGATCACGTAACGCTACTTTTTTGTGCTAAATAATTCGCATTTTATGTTTAAAAATTGAGatat                                        >  1:142376/1‑81 (MQ=255)
                                   gTTGTATCCCAGGGAAAGATCACGTAACGCTACTTTTTTGTGCTAAATAATTCGCATTTTATGTTTAAAAATTGAGATAtt                                       <  1:142355/81‑1 (MQ=255)
                                           ccAGGGAAAGATCACGTAACGCTACTTTTTTGTGCTAAATAATTCGCATTTTATGTTTAAAAATTGAGATATTCCttatt                                <  2:142356/80‑1 (MQ=255)
                                                   aGATCACGTAACGCTACTTTTTTGTGCTAAATAATTCGCATTTTATGTTTAAAAATTGAGATATTCCTTATTACCTAAAGc                       >  2:142377/1‑81 (MQ=255)
                                                       cACGTAACGCTACTTTTTTGTGCTAAATAATTCGCATTTTATGTTTAAAAATTGAGATATTCCTTATTACCTAAAGCTGtt                   >  1:142382/1‑81 (MQ=255)
                                                          gTAACGCTACTTTTTTGTGCTAAATAATTCGCATTTTATGTTTAAAAATTGAGATATTCCTTATTACCTAAAGCTGttttt                <  2:142357/81‑1 (MQ=255)
                                                                         tgtgCTAAATAATTCGCATTTTATGTTTAAAAATTGAGATATTCCTTATTACCTAAAGCTGTTTTTCATAGCTTATACAt  <  1:142358/80‑1 (MQ=255)
                                                                            |                                                                            
AAAATGGTATTCCTGTTCACGATACCATTGCCAGAGTTGTATCCCAGGGAAAGATCACGTAACGCTACTTTTTTGTACTAAATAATTCGCATTTTATGTTTAAAAATTGAGATATTCCTTATTACCTAAAGCTGTTTTTCATAGCTTATACAT  >  NC_000913/736638‑736790

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: