Predicted mutation
evidence seq id position mutation annotation gene description
RA REL606 825,980 G→A D96N (GAT→AAT)  dinG → ATP‑dependent DNA helicase

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*REL606825,9800GA100.0% 71.5 / NA 20D96N (GAT→AAT) dinGATP‑dependent DNA helicase
Reads supporting (aligned to +/- strand):  ref base G (0/0);  new base A (9/11);  total (9/11)

CGCGAAGAGCAAAAAACGCTGGTGGTGAGTACCGCCAACGTGGCATTGCAGGATCAGATTTACAGCAAAGATTTACCGCTGCTGAAAAAGATCATTCCCGATCTTAAATTCACTGCCGCTTTTGGGCGTGGGCGCTA  >  REL606/825911‑826047
                                                                     |                                                                   
cgcgAAGAGCAAAAAACGCTGGTGGTGAGTACCGCCAACGTGGCATTGCAGGATCAGATTTACAGCAAAAATTTAc                                                               <  1:632166/76‑1 (MQ=255)
   gAAGAGCAAAAAACGCTGGTGGTGAGTACCGCCAACGTGGCATTGCAGGATCAGATTTACAGCAAAAATTTACCgc                                                            <  2:260/76‑1 (MQ=255)
        gCAAAAAACGCTGGTGGTGAGTACCGCCAACGTGGCATTGCAGGATCAGATTTACAGCAAAAATTTACCGatgctg                                                       >  2:712828/1‑76 (MQ=255)
         cAAAAAACGCTGGTGGTGAGTACCGCCAACGTGGCATTGCAGGATCAGATTTACAGCAAAAATTTACCGCTGCTGa                                                      >  1:445043/1‑76 (MQ=255)
          aaaaaaCGCTGGTGGTGAGTACCGCCAACGTGGCATTGCAGGATCAGATTTACAGCAAAAATTTACCGCTGCTGaa                                                     >  2:729/1‑76 (MQ=255)
             aaaCGCTGGTGGTGAGTACCGCCAACGTGGCATTGCAGGATCAGATTTACAGCAAAAATTTACCGCTGCTGaaaaa                                                  >  2:661411/1‑76 (MQ=255)
                cGCTGGTGGTGAGTACCGCCAACGTGGCATTGCAGGATCAGATTTACAGCAAAAATTTACCGCTGCTGAAAAAGAt                                               <  1:142867/76‑1 (MQ=255)
                 gCTGGTGGTGAGTACCGCCAACGTGGCATTGCAGGATCAGATTTACAGCAAAAATTTACCGCTGCTGAAAAAGATc                                              <  1:663859/76‑1 (MQ=255)
                 gCTGGTGGTGAGTACCGCCAACGTGGCATTGCAGGATCAGATTTACAGCAAAAATTTACCGCTGCTGAAAAAGATc                                              <  1:554603/76‑1 (MQ=255)
                 gCTGGTGGTGAGTACCGCCAACGTGGCATTGCAGGATCAGATTTACAGCAAAAATTTACCGCTGCTGAAAAAGATc                                              <  1:471609/76‑1 (MQ=255)
                  atggtggTGAGTACNGCCAACGTGGCATTGCAGGATCAGATTTACAGCAAAAATTTACCGCTGCTGAAAAAGATCa                                             >  1:390750/2‑76 (MQ=255)
                             tACCGCCAACGTGGCATTGCAGGATCAGATTTACAGCAAAAATTTACCGCTGCTGAAAAAGATCATTCCCGATCtt                                  <  1:712828/76‑1 (MQ=255)
                               ccGCCAACGTGGCATTGCAGGATCAGATTTACAGCAAAAATTTACCGCTGCTGAAAAAGATCATTCCCGATCTTaa                                <  1:358767/76‑1 (MQ=255)
                                  ccAACGTGGCATTGCAGGATCAGATTTACAGCAAAAATTTACCGCTGCTGAAAAAGATCATTCCCGATCTTAAAtt                             >  2:13415/1‑76 (MQ=255)
                                  ccAACGTGGCATTGCAGGATCAGATTTACAGCAAAAATTTACCGCTGCTGAAAAAGATCATTCCCGATCTTAAAtt                             <  2:582151/76‑1 (MQ=255)
                                           cATTGCAGGATCAGATTTACAGCAAAAATTTACCGCTGCTGAAAAAGATCATTCCCGATCTTAAATTCACTGCCGc                    >  1:334123/1‑76 (MQ=255)
                                                   gATCAGATTTACAGCAAAAATTTACCGCTGCTGAAAAAGATCATTCCCGATCTTAAATTCACTGCCGCTTTtgggc            <  2:517819/76‑1 (MQ=255)
                                                            tACAGCAAAAATTTACCGCTGCTGAAAAAGATCATTCCCGATCTTAAATTCACTGCCGCTTTTGGGCGTGGGCGCt   >  1:316150/1‑76 (MQ=255)
                                                            tACAGCAAAAATTTACCGCTGCTGAAAAAGATCATTCCCGATCTTAAATTCACTGCCGCTTTTGGGCGTGGGCGCt   >  1:202429/1‑76 (MQ=255)
                                                             aCAGCAAAAATTTACCGCTGCTGAAAAAGATCATTCCCGATCTTAAATTCACTGCCGCTTTTGGGCGTGGGCGCTa  <  1:694541/76‑1 (MQ=255)
                                                                     |                                                                   
CGCGAAGAGCAAAAAACGCTGGTGGTGAGTACCGCCAACGTGGCATTGCAGGATCAGATTTACAGCAAAGATTTACCGCTGCTGAAAAAGATCATTCCCGATCTTAAATTCACTGCCGCTTTTGGGCGTGGGCGCTA  >  REL606/825911‑826047

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 19 ≤ ATCG/ATCG < 25 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: