Predicted mutation
evidence seq id position mutation annotation gene description
MC JC NC_000913 687,860 Δ1,185 bp IS5‑mediated insH‑3 insH‑3

Missing coverage evidence...
   seq id start end size ←reads reads→ gene description
* * ÷ NC_000913 687860 689044 1185 25 [0] [0] 27 insH‑3 insH‑3

New junction evidence
  seq id position reads (cov) reads (cov) score skew freq annotation gene product
* ? NC_000913 = 6878590 (0.000)24 (0.890) 22/94 0.1 100% noncoding (1187/1195 nt) IS5 repeat region
?NC_000913 689045 = 0 (0.000)noncoding (1/1195 nt) IS5 repeat region

TATCGTCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCGAATAAGCGGGGAAATTCTTCTCGGCTGACTCAGTCATTTCAT  >  NC_000913/687811‑687902
                                                |                                           
tATCGTCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGC                                             >  1:724012‑M1/1‑49 (MQ=255)
 aTCGTCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCc                                            >  1:1612562‑M1/1‑48 (MQ=255)
   cGTCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCct                                           >  1:1600878‑M1/1‑46 (MQ=255)
    gTCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCctta                                         <  1:1095482‑M1/49‑5 (MQ=255)
    gTCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCctt                                          <  1:1276929‑M1/48‑4 (MQ=255)
    gTCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCctt                                          <  1:573909‑M1/48‑4 (MQ=255)
    gTCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCct                                           >  1:489746‑M1/1‑45 (MQ=255)
     tCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCcttag                                        <  1:1177861‑M1/49‑6 (MQ=255)
      cTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCcttagg                                       >  1:585098‑M1/1‑43 (MQ=255)
      cTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCcttagg                                       >  1:1992725‑M1/1‑43 (MQ=255)
       tGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCcttagg                                       >  1:213373‑M1/1‑42 (MQ=255)
               tATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCcttaggtaacattt                               <  1:687488‑M1/48‑15 (MQ=255)
                    tgCAGTGTTGTGCCTGTTAGGGAAGGTGCcttaggtaacatttagtttg                         <  1:1026648‑M1/49‑21 (MQ=255)
                      cAGTGTTGTGCCTGTTAGGGAAGGTGCcttaggtaacatttagtttggc                       >  1:624456‑M1/1‑27 (MQ=255)
                       aGTGTTGTGCCTGTTAGGGAAGGTGCcttaggtaacatttagtttggc                       >  1:418699‑M1/1‑26 (MQ=255)
                         tgttgtGCCTGTTAGGGAAGGTGCcttaggtaacatttagtttggcta                     >  1:1132030‑M1/1‑24 (MQ=255)
                              tgCCTGTTAGGGAAGGTGCcttaggtaacatttagtttggctaaatgta               <  1:866641‑M1/49‑31 (MQ=255)
                               gCCTGTTAGGGAAGGTGCcttaggtaacatttagtttggctaaatgta               >  1:1871609‑M1/1‑18 (MQ=255)
                                 cTGTTAGGGAAGGTGCcttaggtaacatttagtttggctaaatgtaaag            <  1:1679333‑M1/49‑34 (MQ=255)
                                  tGTTAGGGAAGGTGCcttaggtaacatttagtttggctaaatgta               >  1:1071217‑M1/1‑15 (MQ=255)
                                   gTTAGGGAAGGTGCcttaggtaacatttagtttggctaaatgtaaaga           >  1:836117‑M1/1‑14 (MQ=255)
                                    ttAGGGAAGGTGCcttaggtaacatttagtttggctaaatgtaaaga           <  1:1907091‑M1/47‑35 (MQ=255)
                                         gAAGGTGCcttaggtaacatttagtttggctaaatgtaaagatattgct    <  1:87629‑M1/49‑42 (MQ=255)
                                          aaGGTGCcttaggtaacatttagtttggctaaatgtaaagatattgctg   <  1:1097195‑M1/49‑43 (MQ=255)
                                           aGGTGCcttaggtaacatttagtttggctaaatgtaaagatattgctgt  >  1:1535515‑M1/1‑6 (MQ=255)
                                                |                                           
TATCGTCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCGAATAAGCGGGGAAATTCTTCTCGGCTGACTCAGTCATTTCAT  >  NC_000913/687811‑687902

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: