Predicted mutation
evidence seq id position mutation freq annotation gene description
RA NC_000913 696,470 C→T 100% noncoding (35/75 nt) glnX ← tRNA‑Gln

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_000913696,4700CT100.0% 26.5 / ‑6.7 14noncoding (35/75 nt)glnXtRNA‑Gln
Reads supporting (aligned to +/- strand):  ref base C (0/0);  major base T (7/6);  minor base G (0/1);  total (7/7)
Rejected as polymorphism: E-value score below prediction cutoff.
Rejected as polymorphism: Frequency below/above cutoff threshold.
Rejected as polymorphism: Variant not supported by required number of reads on each strand.

GCATCCGACATTGAAGGATAAGACGTGTCAACATCGCATTCGACATTGAATGAACGCAGAAAAGCAAAAAGCTCGCCGAAGCGAGCTTTTTTAATGTGGCTGGGGTACGAGGATTCGAACCTCGGAATGCCGGAATCAGAATCCGGTGCCTTACCGCTTGGCGATACCCCAACTGGGTGCACTTACAAGGTAAGCGTCTTGAATAAATTGGCTGGGGTACGAGGATTCGAACCTCGGAATG  >  NC_000913/696334‑696574
                                                                                                                                        |                                                                                                        
gCATCCGACATTGAAGGATAAGACGTGTCAACATCGCATTCGACATTGAATGAACGCAGAAAAGCAAAAAGCTCGCCGACGCGAGCTTTTTTAATGTGGCTGGGGTACGAGGATTCGAACCTCGGAATGCCGGAATTAGAATc                                                                                                    >  1:152850/1‑143 (MQ=255)
 cATCCGACATTGAAGGATAAGACGTGTCAACATCGCATTCGACATTGAATGAACGCAGAAAAGCAAAAAGCTCGCCGAAGCGAGCTTTTTTAATGTGGCTGGGGTACGAGGATTCGAACCTCGGAATGCCGGAATTAGAATcc                                                                                                   >  1:114254/1‑143 (MQ=255)
 cATCCGACATTGAAGGATAAGACGTGTCAACATCGCATTCGACATTGAATGAACGCAGAAAAGCAAAAAGCTCGCCGAAGCGAGCTTTTTTAATGTGGCTGGGGTACGAGGATTCGAACCTCGGAATGCCGGAATTAGAATcc                                                                                                   >  2:108461/1‑143 (MQ=255)
  aTCCGACATTGAAGGATAAGACGTGTCAACATCGCATTCGACATTGAATGAACGCAGAAAAGCAAAAAGCTCGCCGAAGCGAGCTTTTTTAATGTGGCTGGGGTACGAGGATTCGAACCTCGGAATGCCGGAATTAGAATCCg                                                                                                  >  2:111650/1‑143 (MQ=255)
       gcATTGAAGGAGAAGACGTGTGAACATCGCATTCGACATTGAATGAACGCAGAAAAGCAAAAAGCTCGCCGAAGCGAGCTTTTTTAATGTGGCTGGGGTACGAGGATTCGAACCTCGGAATGCCGGAATTAGAATCCGGTGcc                                                                                             <  2:179289/142‑1 (MQ=255)
                        gtgtCAACATCGCATTCGACATTGAATGAACGCAGAAAAGCAAAAAGCTCGCCGAAGCGAGCTTTTTTAATGTGGCTGGGGTACGAGGATTCGAACCTCGGAATGCCGGAATTAGAATCCGGTGCCTTACCGCTTGAAGATaa                                                                            >  1:112076/1‑142 (MQ=255)
                                         gACAGTGAATGAACGCAGAAAAGCAAAAAGCCCGCCGAAGCGAGCTTTTTTAATGTGGCTGGGGTACGAGGATTCGAACCTCGGAATGCCGGAATTAGAATCCGGTGCCTTACCGCTTGGCGATACCCCAACTGGGTGCACtt                                                           <  2:173688/143‑1 (MQ=255)
                                              tgaatgaaCGCAGAAAAGCAAAAAGCTCGCCGAAGCGAGCTTTTTTAATGTGGCTGGGGTACGAGGGTTTGAACCTCAGAATGCCGGAATTAGAATCCGGTGCCTTACCGCTTGGCGATACCCCAACTGGGTGCACttcccag                                                      >  2:177407/1‑138 (MQ=25)
                                                 atgaaCGTAGAAAAGCAAAAAGCTTGTCGCTGCTTGCATTATTAATGTGGCTGGGGTACGAGGATTCGAACCTCGGAATGCCGGAATTAGAATCCGGTGCCTTACCGCTTGGCGATACCCCAACTGGGTGCACTTACAAGGTa                                                   <  1:191968/143‑1 (MQ=18)
                                                                          gCCGAGGCGAGCTTTTTTGATGTGGCTGGGGTACGGGGATTCGTACCTCGGAATGCCGGAATTAGAATCCGGTGCCTTACCGCTTGGCGATACCCCAACTGGGTGCACTTACAAGGTAAGCGTCTTGAATAAATTGGCTgggg                          <  2:8825/143‑1 (MQ=25)
                                                                                        ttttAATGTGGCTGGGGTACGAGGATTCGAACCTCGGAATGCCGGAATTAGAATCCGGTGCCTTACCGCTTGGCGATGCCCCAACTGGGTGCACTTACAAGGTACGCGCCTTGAGGAGACTGGCTGGGGTCCGCGGATTCggc            >  1:50451/1‑141 (MQ=18)
                                                                                             gtgtgGCTCGGGTACGAGGAGTTGAACCGCGGAATGCCGGCATTAGAATCCGGTGCCTTACCGCTTGGAGACACCCCAACTGAGTGCACTTACAAGGTAAGCGTCTTGAATAAATTGGCTGGGGTACGAGGATTCGAACCTCg       <  2:33134/142‑1 (MQ=25)
                                                                                             agttgGCTGGGGTACGAGGATTCGAACCTCGGAATGCCGGAATTAGAATCCGGTGCCTTACCGCTTGGCGATACCCCAACTGGGTGCACTTACAAGGTAAGCGTCTTGAATAAATTGGCTGGGGTACGAGGATTCGAACCTCg       <  2:44857/140‑1 (MQ=255)
                                                                                                  gCTGGGGTACGAGGATTCGAACCTCGGAATGGCGGAACGTGTATCCGGTGCCTTACCGCTTGGCGATACCCCGACTGGGTGCACGTACGAGGTAAGCGTCTTGAATAAATTGGCTGGGGTACGAGGATTCGAACCTCGGAATg  <  2:145277/143‑1 (MQ=25)
                                                                                                                                        |                                                                                                        
GCATCCGACATTGAAGGATAAGACGTGTCAACATCGCATTCGACATTGAATGAACGCAGAAAAGCAAAAAGCTCGCCGAAGCGAGCTTTTTTAATGTGGCTGGGGTACGAGGATTCGAACCTCGGAATGCCGGAATCAGAATCCGGTGCCTTACCGCTTGGCGATACCCCAACTGGGTGCACTTACAAGGTAAGCGTCTTGAATAAATTGGCTGGGGTACGAGGATTCGAACCTCGGAATG  >  NC_000913/696334‑696574

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 8 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: