Predicted mutation
evidence seq id position mutation annotation gene description
MC JC NC_000913 603,467 Δ5,885 bp [ybdG]insL‑2 [ybdG], nfsB, ybdF, ybdJ, ybdK, sokE, hokE, insL‑2

Missing coverage evidence...
   seq id start end size ←reads reads→ gene description
* * ÷ NC_000913 603467 609351 5885 38 [0] [0] 37 [ybdG]–insL‑2 [ybdG],nfsB,ybdF,ybdJ,ybdK,sokE,hokE,insL‑2

New junction evidence
  seq id position reads (cov) reads (cov) score skew freq annotation gene product
* ? NC_000913 = 6034660 (0.000)37 (1.040) 32/92 0.0 100% coding (1198/1248 nt) ybdG miniconductance mechanosensitive channel YbdG
?NC_000913 609352 = 0 (0.000)intergenic (+175/+107) insL‑2/entD IS186/IS421 transposase/phosphopantetheinyl transferase EntD

CTGCTTAAATGCACCCGCCAGAGAGCGAATATCATTGCCGGTTGGCGA‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑  >  NC_000913/603419‑603466
‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑gaGTAATCCCCGCATATCCGGTTGTCAGGTCAGGATGGTAAGGCACCT  >  NC_000913/609352‑609397
                                                                                              
CTGCTTAAATGCACCCGCCAGAGAGCGAATATCATTGCCGGTTGGCGAG                                               <  1:2702513/49‑1
CTGCTTAAATGCACCCGCCAGAGAGCGAATATCATTGCCGGTTGGCGAG                                               >  1:557784/1‑49
CTGCTTAAATGCACCCGCCAGAGAGCGAATATCATTGCCGGTTGGCGA                                                <  1:2867101/48‑1
 TGCTTAAATGCACCCGCCAGAGAGCGAATATCATTGCCGGTTGGCGAG                                               >  1:976617/1‑48
   CTTAAATGCCCCCGCCAGAGAGCGAATATCATTGCCGGTTGGCGAGTA                                             <  1:850311/48‑1
   CTTAAATGCACCCGCCAGAGAGCGAATATCATTGCCGGTTGGCGAGTAA                                            >  1:1390785/1‑49
      AAATGCACCCGCCAGAGAGCGAATATCATTGCCGGTTGGCGAGTAATCC                                         >  1:711927/1‑49
      AAATGCACCCGCCAGAGAGCGAATATCATTGCCGGTTGGCGAGTAATC                                          <  1:1675567/48‑1
       AATGCACCCGCCAGAGAGCGAATATCATTGCCGGTTGGCGAGTAATCCC                                        >  1:2664952/1‑49
        ATGCACCCGCCAGAGAGCGAATATCATTGCCGGTTGGCGAGTAATCCCC                                       <  1:1573297/49‑1
        ATGCACCCGCCAGAGAGCGAATATCATTGCCGGTTGGCGAGTAATCCCC                                       <  1:1863518/49‑1
        ATGCACCCGCCAGAGAGCGAATATCATTGCCGGTTGGCGAGTAATCCCC                                       >  1:213045/1‑49
            ACCCGCCAGAGAGCGAATATCATTGCCGGTTGGCGAGTAATCCCCGCA                                    >  1:1845686/1‑48
              CCGCCAGAGAGCGAATATCATTGCCGGTTGGCGAGTAATCCCCGCATAT                                 >  1:426331/1‑49
              CCGCCAGAGAGCGAATATCATTGCCGGTTGGCGAGTAATCCCCGCATAT                                 >  1:2817485/1‑49
                GCCAGAGAGCGAATATCATTGCCGGTTGGCGAGTAATCCCCGCATATCC                               >  1:1440778/1‑49
                  CAGAGAGCGAATATCATTGCCGGTTGGCGAGTAATCCCCGCATATCCGG                             >  1:782626/1‑49
                   AGAGAGCGAATATCATTGCCGGTTGGCGAGTAATCCCCGCATATCCGGT                            <  1:2505069/49‑1
                   AGAGAGCGAATATCATTGCCGGTTGGCGAGTAATCCCCGCATATCCGGT                            >  1:2312374/1‑49
                   AGAGAGCGAATATCATTGCCGGTTGGCGAGTAATCCCCGCATATCCGGT                            >  1:182275/1‑49
                    GAGAGCGAATATCATTGCCGGTTGGCGAGTAATCCCCGCATATCCGGTT                           <  1:1167068/49‑1
                    GAGAGCGAATATCATTGCCGGTTGGCGAGTAATCCCCGCATATCCGGTT                           >  1:86776/1‑49
                         CGAATATCATTGCCGGTTGGCGAGTAATCCCCGCATATCCGGTTGTCAG                      <  1:697312/49‑1
                          GAATATCATTGCCGGTTGGCGAGTAATCCCCGCATATCCGGTTGTCAGG                     <  1:1081936/49‑1
                          GAATATCATTGCCGGTTGGCGAGTAATCCCCGCATATCCGGTTGTCAGG                     >  1:163094/1‑49
                          GAATATCATTGCCGGTTGGCGAGTAATCCCCGCATATCCGGTTGTCAGG                     >  1:2652460/1‑49
                            ATATCATTGCCGGTTGGCGAGTAATCCCCGCATATCCGGTTGTCAGGT                    >  1:2530880/1‑48
                               TCATTGCCGGTTGGCGAGTAATCCCCGCATATCCGGTTGTCAGGTCAG                 >  1:2101405/1‑48
                               TCATTGCCGGTTGGCGAGTAATCCCCGCATATCCGGTTGTCAGGTCAG                 <  1:1325720/48‑1
                                 ATTGCCGGTTGGCGAGTAATCCCCGCATATCCGGTTGTCAGGTCAGGAT              >  1:339082/1‑49
                                 ATTGCCGGTTGGCGAGTAATCCCCGCATATCCGGTTGTCAGGTCAGGAT              >  1:2569910/1‑49
                                  TTGCCGGTTGGCGAGTAATCCCCGCATATCCGGTTGTCAGGTCAGGATG             <  1:813674/49‑1
                                      CGGTTGGCGAGTAATCCCCGCATATCCGGTTGTCAGGTCAGGATGGTAA         <  1:202808/49‑1
                                          TGGCGAGTAATCCCCGCATATCCGGTTGTCAGGTCAGGATGGTAAGGCA     >  1:1200271/1‑49
                                           GGCGAGTAATCCCCGCATATCCGGTTGTCAGGTCAGGATGGTAAGGCAC    >  1:2685347/1‑49
                                            GCGAGTAATCCCCGCATATCCGGTTGTCAGGTCAGGATGGTAAGGCACC   <  1:2244690/49‑1
                                            GCGAGTAATCCCCGCATATCCGGTTGTCAGGTCAGGATGGTAAGGCAC    <  1:1907304/48‑1
                                             CGAGTAATCCCCGCATATCCGGTTGTCAGGTCAGGATGGTAAGGCACCT  >  1:1566120/1‑49
                                                                                              
CTGCTTAAATGCACCCGCCAGAGAGCGAATATCATTGCCGGTTGGCGA‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑  >  NC_000913/603419‑603466
‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑gaGTAATCCCCGCATATCCGGTTGTCAGGTCAGGATGGTAAGGCACCT  >  NC_000913/609352‑609397

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: 
Reads not counted as support for junction
read_name Not counted due to insufficient overlap past the breakpoint.
read_name Not counted due to not crossing MOB target site duplication.