Predicted mutation
evidence seq id position mutation freq annotation gene description
RA BS168_reference_genome 961,032:1 +A 100% intergenic (‑46/‑362) katA ← / → ssuB vegetative catalase 1/aliphatic sulfonate ABC transporter (ATP‑binding protein)

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*BS168_reference_genome961,0321.A100.0% 39.8 / NA 13intergenic (‑46/‑362)katA/ssuBvegetative catalase 1/aliphatic sulfonate ABC transporter (ATP‑binding protein)
Reads supporting (aligned to +/- strand):  ref base . (0/0);  new base A (4/9);  total (4/9)
Rejected as polymorphism: Frequency below/above cutoff threshold.
Rejected as polymorphism: Variant not supported by required number of reads on each strand.

GGTCCGCGAGAACCGGCAGTCATTGAGTTTTGATTATCTCCAACCGGAGCGCCCCAGCTAGTTGTCAGTTTATTTGAACTCATGTTATCACCTCTTGGAATTTATAAGAACATAATATCATCTCTAAGTAAAAAGTCAATATTATTTTATAATTATTATAAAATAGTTATCTCTATTAATCGATATATAGTATCGAAATTGTTGAAAAACCTTGTTGTAACAGCTTTTTATGACACTTAATAATTTTTGGAGAAATAA  >  BS168_reference_genome/960904‑961161
                                                                                                                                 |                                                                                                                                 
ggTCCGCGAGAACCGGCAGTCATTGAGTTTTGATTATCTCCAACCGGAGCGCCCCAGCTAGTTGTCAGTTTATTTGAACTCATGTTATCACCTCTTGGAATTTATAAGAACATAATATCATCTCTAAGTaaaaaagtc                                                                                                                          >  8:150934/1‑134 (MQ=255)
               gCAGTCATTGAGTTTTGATTATCCCCAACCGGAGCGCCCCAGCTAGTTGTCAGTTTATTTGAACTCATGTTATCACCTCTTGGAATTTATAAGAACATAATATCATCTCTAAGTAAAAAAGTCAATATTATTTTATAat                                                                                                           <  7:72235/139‑1 (MQ=255)
                                 ttATCTCCAACCGGAGCGCCCCAGCTAGTTGTCAGTTTATTTGAACTCATGTTATCACCTCTTGGAATTTATAAGAACATAATATCATCTCTAAGTAAAAAAGTCAATATTATTTTATAATTATTATAAAATAGTTAt                                                                                          <  6:83328/138‑1 (MQ=255)
                                          aCCGGAGCGCCCCAGCTAGTTGTCAGTTTATTTGAACTCATGTTATCACCTCTTGGAATTTATAAGAACATAATATCATCTCTAAGTAAAAAAGTCAATATTATTTTATAATTATTATAAAATAGTTATCTCTATTAAt                                                                                <  7:150934/139‑1 (MQ=255)
                                          aCCGGAGCGCCCCAGCTAGTTGTCAGTTTATTTGAACTCATGTTATCACCTCTTGGAATTTATAAGAACATAATATCATCTCTAAGTAAAAAAGTCAATATTATTTTATAATTATTATAAAATAGTTATCTCTATTAAt                                                                                <  7:73961/139‑1 (MQ=255)
                                           ccGGAGCGCCCCAGCTAGTTGTCAGTTTATTTGAACTCATGTTATCACCTCTTGGAATTTATAAGAACATAATATCATCTCTAAGTAAAAAAGTCAATATTATTTTATAATTATTATAAAATAGTTATCTCTATTAATc                                                                               <  1:146076/139‑1 (MQ=255)
                                               aGCGCCCCAGCTAGTTGTCAGTTTATTTGAACTCATGTTATCACCTCTTGGAATTTATAAGAACATAATATCATCTCTAAGTAAAAAAGTCAATATTATTTTATAATTATTATAAAATAGTTATCTCTATTAAt                                                                                <  1:214562/134‑1 (MQ=255)
                                               aGCGCCCCAGCTAGTTGTCAGTTTATTTGAACTCATGTTATCACCTCTTGGAATTTATAAGAACATAATATCATCTCTAAGTAAAAAAGTCAATATTATTTTATAATTATTATAAAATAGTTATCTCTATTAAt                                                                                >  2:214562/1‑134 (MQ=255)
                                                             ttGTCAGTTTATTTGAACTCATGTTATCACCTCTTGGAATTTATAAGAACATAATATCATCTCTAAGTAAAAAAGTCAATATTATTTTATAATTATTATAAAATAGTTATCTCTATTAAt                                                                                >  1:114193/1‑120 (MQ=255)
                                                             ttGTCAGTTTATTTGAACTCATGTTATCACCTCTTGGAATTTATAAGAACATAATATCATCTCTAAGTAAAAAAGTCAATATTATTTTATAATTATTATAAAATAGTTATCTCTATTAAt                                                                                <  2:114193/120‑1 (MQ=255)
                                                                                      aTCACCTCTTGGAATTTATAAGAACATAATATCATCTCTAAGTAAAAAAGTCAATATTATTTTATAATTATTATAAAATAGTTATCTCTATTAATCGATATATAGTATCGAAATTGTTGAAAAACCTTGTTGTAACAg                                     <  5:102375/138‑1 (MQ=255)
                                                                                                      tataAGAACATAATATCATCTCTAAGTAAAAAAGTCAATATTATTTTATAATTATTATAAAATAGTTATCTCTATTAATCGATATATAGTATCGAAATTGTTGAAAAACCTTGTTGTAACAGCTTTTTATGaca                         >  7:96372/1‑134 (MQ=255)
                                                                                                      tataAGAACATAATATCATCTCTAAGTAAAAAAGTCAATATTATTTTATAATTATTATAAAATAGTTATCTCTATTAATCGATATATAGTATCGAAATTGTTGAAAAACCTTGTTGTAACAGCTTTTTATGaca                         <  8:96372/134‑1 (MQ=255)
                                                                                                                        tctcTAAGTAAAAAAGTCAATATTATTTTATAATTATTATAAAATAGTTATCTCTATTAATCGAAATATAGTATCGAAATTGTTCAAAAACCTTGTTGTAACAGCTTTTTATGACACTTAATAATTTTTGGAGAaataa  >  5:115796/1‑139 (MQ=255)
                                                                                                                                 |                                                                                                                                 
GGTCCGCGAGAACCGGCAGTCATTGAGTTTTGATTATCTCCAACCGGAGCGCCCCAGCTAGTTGTCAGTTTATTTGAACTCATGTTATCACCTCTTGGAATTTATAAGAACATAATATCATCTCTAAGTAAAAAGTCAATATTATTTTATAATTATTATAAAATAGTTATCTCTATTAATCGATATATAGTATCGAAATTGTTGAAAAACCTTGTTGTAACAGCTTTTTATGACACTTAATAATTTTTGGAGAAATAA  >  BS168_reference_genome/960904‑961161

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 21 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: