Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,729,497 A→T A137A (GCA→GCT lhr → putative ATP‑dependent helicase Lhr

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,729,4970AT100.0% 100.6 / NA 31A137A (GCA→GCTlhrputative ATP‑dependent helicase Lhr
Reads supporting (aligned to +/- strand):  ref base A (0/0);  new base T (17/14);  total (17/14)

CCGATGAACGGCGGCGGCGCGGCGAAACGGAAGTCAATCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCACAGGAACGCAGCAAACTCACCCGTAATCCGCCGGATATTCTGATCACCACACCCGAATCACTCTATCTGAT  >  NC_000913/1729424‑1729568
                                                                         |                                                                       
ccGATGAACGGCGGCGGCGCGGCGAAACGGAAGTCAATCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCTCAGGaa                                                                   <  1:298285/80‑1 (MQ=255)
ccGATGAACGGCGGCGGCGCGGCGAAACGGAAGTCAATCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCTCAGGAAc                                                                  <  2:298286/81‑1 (MQ=255)
       aCGGCGGCGGCGCGGCGAAACGGAAGTCAATCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCaa                                                           <  1:298287/81‑1 (MQ=255)
         ggcggcggcGCGGCGAAACGGAAGTCAATCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAAc                                                         >  2:298326/1‑81 (MQ=255)
         ggcggcggcGCGGCGAAACGGAAGTCAATCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAAc                                                         >  1:298340/1‑81 (MQ=255)
            ggcggcgCGGCGAAACGGAAGTCAATCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCa                                                      >  1:298321/1‑81 (MQ=255)
               ggcgcggcgAAACGGAAGTCAATCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCAccc                                                   <  2:298288/81‑1 (MQ=255)
                 cgcggcgAAACGGAAGTCAATCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCg                                                  >  2:298372/1‑80 (MQ=255)
                  gcggcgAAACGGAAGTCAATCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGt                                                 >  2:298336/1‑80 (MQ=255)
                     gcgAAACGGAAGTCAATCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATc                                             <  1:298289/81‑1 (MQ=255)
                       gAAACGGAAGTCAATCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATccg                                           >  1:298328/1‑81 (MQ=255)
                       gAAACGGAAGTCAATCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATccg                                           >  1:298342/1‑81 (MQ=255)
                         aaCGGAAGTCAATCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATccgcc                                         <  2:298290/81‑1 (MQ=255)
                             gAAGTCAATCTTCGCGTAGGGTTCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATCCGCCGGat                                     <  1:298291/81‑1 (MQ=255)
                               aGTCAATCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATCCGCCGGatat                                   >  2:298341/1‑81 (MQ=255)
                                 tCAATCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATCCGCCGGATATTc                                 <  1:298292/81‑1 (MQ=255)
                                  cAATCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATCCGCCGGATATTCt                                >  2:298333/1‑81 (MQ=255)
                                    aTCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATCCGCCGGATATTCTGa                              >  1:298329/1‑81 (MQ=255)
                                         cgcgTAGGGATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATCCGCCGGATATTCTGATcac                          >  1:298345/1‑80 (MQ=255)
                                              aGGGATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATCCGCCGGATATTCTGATCACCACAcc                    >  2:298327/1‑81 (MQ=255)
                                               gggATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATCCGCCGGATATTCTGATCACCACAccc                   >  1:298349/1‑81 (MQ=255)
                                               gggATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATCCGCCGGATATTCTGATCACCACAccc                   <  2:298293/81‑1 (MQ=255)
                                                ggATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATCCGCCGGATATTCTGATCACCACACCCg                  <  2:298294/81‑1 (MQ=255)
                                                 gATCCGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATCCGCCGGATATTCTGATCACCACACCCg                  >  2:298353/1‑80 (MQ=255)
                                                    ccGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATCCGCCGGATATTCTGATCACCACACCCGAAt               >  2:298344/1‑80 (MQ=255)
                                                     cGTACTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATCCGCCGGATATTCTGATCACCACACCCGAATc              <  1:298295/80‑1 (MQ=255)
                                                         cTGGCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATCCGCCGGATATTCTGATCACCACACCCGAATCActc          >  2:298296/1‑80 (MQ=255)
                                                           ggCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATCCGCCGGATATTCTGATCACCACACCCGAATCACTCTAt       >  2:298334/1‑81 (MQ=255)
                                                            gCGATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATCCGCCGGATATTCTGATCACCACACCCGAATCACTCTa        <  2:298297/79‑1 (MQ=255)
                                                              gATACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATCCGCCGGATATTCTGATCACCACACCCGAATCACTCTATCTg    <  1:298298/81‑1 (MQ=255)
                                                                tACGCCTGCTCAGGAACGCAGCAAACTCACCCGTAATCCGCCGGATATTCTGATCACCACACCCGAATCACTCTATCTGAt  <  1:298299/81‑1 (MQ=255)
                                                                         |                                                                       
CCGATGAACGGCGGCGGCGCGGCGAAACGGAAGTCAATCTTCGCGTAGGGATCCGTACTGGCGATACGCCTGCACAGGAACGCAGCAAACTCACCCGTAATCCGCCGGATATTCTGATCACCACACCCGAATCACTCTATCTGAT  >  NC_000913/1729424‑1729568

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 26 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: