Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 809,980 C→T P213S (CCG→TCG)  bioB → biotin synthase

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_000913809,9800CT100.0% 13.3 / NA 7P213S (CCG→TCG) bioBbiotin synthase
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base T (4/3);  total (4/3)

CGCGATGCCGGGATCAAAGTCTGTTCTGGCGGCATTGTGGGCTTAGGCGAAACGGTAAAAGATCGCGCCGGATTATTGCTGCAACTGGCAAACCTGCCGACGCCGCCGGAAAGCGTGCCAATCAACATGCTGGTGAAGGTGAAAGGCACGCCGCTTGCCGATAACGATGATGTCGATGCCTTTGATTTTATTCGCACCATTGCGGTCGCGCGGATCATGATGCCAACCTCTTACGTGCGCCTTTCTGCCGGACGCGAGCAGATGAACGAACAGACTCAGGCGATGTGCTTTATGGCAGGCGCAAACTCGATTTTCTACGGTTGCAAACTGC  >  NC_000913/809884‑810214
                                                                                                |                                                                                                                                                                                                                                          
cgcgATGCCGGGATCAAAGTCTGTTCTGGCGGCATTGTGGGCTTAGGCGAAACGGTAAAAGATCGCGCCGGATTATTGCTGCAACTGGCAAACCTGTCGACGCCGCCGGAAAGc                                                                                                                                                                                                                           >  1:190038/1‑114 (MQ=255)
cgcgATGCCGGGATCAAAGNCTGTTCTGGCNGCANNGTGGNCNTNGGCGAAACGGTAAAAGATCGCGCCGGATTNTTGCTGCAACTGGCAAACCTGTCNNCGNNNCCNNAAAGc                                                                                                                                                                                                                           <  2:190038/114‑1 (MQ=255)
   gATGCCGGGATCAAAGTCTGTTCTGGAGGCATTGTGGGCATCGGCGAAACGGTCACAGATCGCGCCGGACTATTGCTGCCATTGGCACACCTGTCGAcgcc                                                                                                                                                                                                                                     >  1:98754/1‑101 (MQ=255)
                                                       tAAAAGATCGCGCCGGATTATGGCTGCAACTGGCAAACCTGTCGACGCCGCCGGAAAGCGTGCCAATCAACATGCTggtgaaggn                                                                                                                                                                                                 <  1:48539/85‑2 (MQ=255)
                                                                     ggattagcgctgcAACTGGCAAACCTGTCGTCACCGCCGAGAAGCGCGCCAGTCAGCACGCTGGTGAAGGTGAAAGGCACGCCGCTTGCCTAGAACGATGATGTCGATGCCTTTGATTTTATTCGc                                                                                                                                          <  1:109506/118‑1 (MQ=255)
                                                                                gcAACTGGCAAACCTGTCGACGCCGCCGGAAAGCGTGCCACTCAACATGATGGTGCAGGTGAAAGGCACGCAGATTGCCGATAACGATGATGTCGCTGCCTTTGATTTTATTCGCACCATTGCGGTCGCGCGGATCATGATGCCAACCTCTTACGTGCGCCTTTCTGCCGGACGCGAGCAGATGAACGAACAGACTCAGGCGATGTGCTTTATGGCAGGCGCAAACTCGATTTTCTACGGTTGCAAActgc  >  1:248263/1‑251 (MQ=255)
                                                                                          naCCTGTCGACGCAGCCGGAAAGCGAGCCCATCAACATGCTGGTGAAGGTGAAAGGCACGCCGCTTGCCGATAACgat                                                                                                                                                                     >  1:77922/2‑78 (MQ=255)
                                                                                                |                                                                                                                                                                                                                                          
CGCGATGCCGGGATCAAAGTCTGTTCTGGCGGCATTGTGGGCTTAGGCGAAACGGTAAAAGATCGCGCCGGATTATTGCTGCAACTGGCAAACCTGCCGACGCCGCCGGAAAGCGTGCCAATCAACATGCTGGTGAAGGTGAAAGGCACGCCGCTTGCCGATAACGATGATGTCGATGCCTTTGATTTTATTCGCACCATTGCGGTCGCGCGGATCATGATGCCAACCTCTTACGTGCGCCTTTCTGCCGGACGCGAGCAGATGAACGAACAGACTCAGGCGATGTGCTTTATGGCAGGCGCAAACTCGATTTTCTACGGTTGCAAACTGC  >  NC_000913/809884‑810214

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 30 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: