Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 2,819,860 C→T A718T (GCG→ACG)  alaS ← alanine‑‑tRNA ligase/DNA‑binding transcriptional repressor

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009132,819,8600CT100.0% 30.0 / NA 13A718T (GCG→ACG) alaSalanine‑‑tRNA ligase/DNA‑binding transcriptional repressor
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base T (5/8);  total (5/8)

CGGCTCAACACCGCTAAGCTCGCTAACCAACAGCTTAACACCATTAACATCAATTGCCTTACTGGAAAGATTTGCGCTCTCCTGTGCGGCAGCTTGTTCTTTAAGCTGTTGTAACTCTTTTTCCAGCTGACGCGTACGTTCCAGTACTGAGCGCACTTTATCAGCCAGATTATTGCTATCGCCTTTCAGCAGATGCGCGACTTCGCTTAAGCGATCGCTGTCTGCATGAACGGTGGCGATAGCACCTTCTCCGGTTACCGCTTCGATACGACGAACGCCTGCAGCAGTACCCGATTCAGAGATGATGCGGAACAGACCAATATCACCAGTGCGGCTGGCGTGAGTACCGCCACACAACTCGGTAGAGAAATCGCCCATGCTCAGCACGCGTACGCGCTCATCATACTTCTCGCCGAACAGCGCC  >  NC_000913/2819663‑2820086
                                                                                                                                                                                                     |                                                                                                                                                                                                                                  
gcgCTCAACACCGCTAAGCTCGCTAACCAACAGCTTAACACCATTAACATCAATTGCCTTACTGGAAAGATTTGCGCTCTCCTGTTCGGCAGCTTGTTCTTTAAGCTGTTGTAACTCTTTTTCCAGCTGACGCGTACGTTCCAGTACTGAGCGCACTTTATCAGCCAGATTAGTGCTATCGCCTTTCAGCAGATGCGTGACTTCGCTTAAGCGATCGCTGTCTGCATGAACGTGGGCGATAGCACCTtctn                                                                                                                                                                               <  1:77585/249‑2 (MQ=255)
  ncTCAACACCGCTAAGCTCGCTAACCAACAGCTTAACACCATTAACATCAATTGCCTTACTGGAAAGATTTGCGCTCTCCTGTGCGGCAGCTTGTTCTTTAAGCTGTTGTAACTCTTTTTCCAGCTGACGCGTACGTTCCAGTACTGAGCGCACTTTATCAGCCAGATTATTGCTATCGCCTTTCAGCAGATGCGTGACTTCGCTTAAGCGATCGCTGTCTGCATGAACGGTGGCGATAGCACCTTCTCCg                                                                                                                                                                             >  1:55466/2‑251 (MQ=255)
      aaCACCGCTAAGCTCGCTAACCAACAGCTTAACACCATTAACATCAATTGCCTTACTGGAAAGATTTGCGCTCTCCTGTGCGGCAGCTTGTTCTTTAAGCTGTTGTAACTCTTTTTCCAGCTGACGCGTACGTTCCAGTACTGAGCGCACTTTATCAGCCAGATTATTGCTATCGCCTTTCAGCAGATGCGTGACTTCGCTTAAGCGATCGCTGTCTGCATGAACGGTGGCGATAGccc                                                                                                                                                                                     <  1:1638/239‑3 (MQ=255)
      aaCACCGCTAAGCTCGCTAACCAACAGCTTAACACCATTAACATCAATTGCCTTACTGGAAAGATTTGCGCTCTCCTGTGCGGCAGCTTGTTCTTTAAGCTGTTGTAACTCTTTTTCCAGCTGACGCGTACGTTCCAGTACTGAGCGCACTTTATCAGCCAGATTATTGCTATCGCCTTTCAGCAGATGCGTGACTTCGCTTAAGCGATCGCTGTCTGCATGAACGGTGGCGATAGCACCTTCTCCGGtt                                                                                                                                                                          >  1:110125/1‑250 (MQ=255)
                                                           tACTGGAAAGATTTGCGCTCTCCTGTGCGGCAGCTTGTTCTTTAAGCTGTTGTAACTCTTTTTCCAGCTGACGCGTACGTTCCAGTACTGAGCGCACTTTATCAGCCAGATTATTGCTATCGCCTTTCAGCAGATGCGTGACTTCGCTTAAGCGATCGCTGTCTGCATGAACGGTGGCGATAGCACCTTCTCCGGTTAC‑‑CTCCGATACGACGAACGCCTGCAGCAGTACCCGATTCAGAGATGATGCgg                                                                                                                    <  1:35821/249‑1 (MQ=255)
                                                                  aaGATTTGCGCACTCCTGTGCGGCAGCTTGTTCTTTAAGCTGTTGTAACTCTTTTTCCAGCTGACGCGTACGTTCCAGTACTGAGCGCACTTTATCAGCCAGATTATTGCTATCGCCTTTCAGCAGATGCGTGACTTCGCTTAAGCGATCGCTGTCTGCATGAACGGGGGCGATAGCACCTTCTCCGGTTACCGCTTCGATACGACGAACGACTGCAGCAGTACCCGATTCAGAGATGATGCGTAACAGAc                                                                                                             <  1:193623/251‑1 (MQ=255)
                                                                              ctcCTGTGCGGCAGCTTGTTCTGTAAGCTGTTGTAACTCTTTTTCCAGCTGACGCGTACGTTCCAGTACTGAGCGCACTTTATCAGCCAGATTATTGCTATCGCCTTTCAGCAGATGCGTGACTTCGCTTAAGCGATCGCTGTCTGCATGAACGGTGGCGATAGCACCTTCTCCGGTTACCGCTTCGATACGACGAACGCCTGCAGCAGTACCCGATTCAGAGATGATGCGGAACAGACCAATATCAcc                                                                                                   <  1:88736/249‑1 (MQ=255)
                                                                                ccTGTGCGGCAGCTTGTTCTTTAAGCTGTTGTAACTCTTTTTCCAGCTGACGCGTACGTTCCAGTACGGAGCGCACTTTATCAGCCAGATTATTGCTATCGCCTTTCAGCAGATGCGTGACTTCGCTTAAGCGATCGCTGTCTGCATGAACGGTGGCGATAGCACCTTCGCCGTTTACCGCGTCGATACGACTAACGCCTGCAGCAGTACCCGATTCAGAGATGATGCGGAACAGACCAATATCACCAGTg                                                                                               <  1:223034/251‑1 (MQ=255)
                                                                                                                 aCTCTTTTTCCAGCTGACGCGTACGTTCCATTACTGAGCGCACTTTATCAGCCATATTATTGCTATCGCCTTTCAGCAGATTCGTGACTTCGCTTAAGCGATCTCGGGCTGCATGTACGTTGGCGATGGCACCTTCTCCGGTTCCCGCTTCGATACGACGAACGCCTGCAGCAGTAc                                                                                                                                        <  1:187537/177‑1 (MQ=255)
                                                                                                                 aCTCTNNTTNNNGCNNACGCGTACGTTCCAGTACTGAGCNCACTTTATCAGCCAGATTATTGCTATCGCNTNTNAGCANNTGCNTGACTTCGCTNAAGCGATCGCTGTCTGCATGAACGGTGGCGATAGCCCCTTCTCCGGTTNCNGCTTCGATACGACGAACGCATGCAGCAGTAc                                                                                                                                        >  2:187537/1‑177 (MQ=255)
                                                                                                                                                           cttgaTCAGCCAGATTATTGCTATCGCCTTTCAGCAGATGCGTGACTTCGCTTAAGCGAGCGCTGTCTGCATGAGCGGTGTCGATAGCACCTGCTCCGGTTACCGCTTCGAGACGACGAACGCCGGCAGCAGTACCCGATTCATAGAAGAGGCGGAACAGACCAATATCACCAGTGCGGCTGGCGTGAGTACCGCcacac                                                                       <  1:168173/196‑1 (MQ=255)
                                                                                                                                                                       gATTATTGCTATCGCCTTTCAGCAGATGCGTGACTTCGCTTAAGCGATCGCTGTCTGCATGAACGGTGGCGATAGCACCTTCTCCGGTTACCGCTTCGATACGACGAACGCCTGCAGCAGTACCCGATTCAGAGATGATGCGGAACAGACCAATATCACCAGTGCGGCTGGCGTGAGTACCGCCACACAACTCGGTAGAGAAATCGCCCATGCTCAGCACGCGTACGCGCTCATCATACTTCTCGCCGAAc        >  1:4598/1‑251 (MQ=255)
                                                                                                                                                                              gCTATCGCCTTTCAGCAGATGCGTGACTTCGCTTAAGCGATCGCTGTCTGCATGAACGGAGGCGATAGCAACTTCTCCGGTTACCGCTTCGATACGACGAACGCCTGCAGCAGTACCCGATTCAGAGATGATGCGGAACAGACCAATATCACCAGTGCGGCTGGCGTGAGTACCGCCACACAACTCGGTAGAGAAATCGCCCATGCTCAGCACGCGTACGCGCTCATCATACTTCTCGCCGAACAgcgca  >  1:100708/1‑249 (MQ=255)
                                                                                                                                                                                                     |                                                                                                                                                                                                                                  
CGGCTCAACACCGCTAAGCTCGCTAACCAACAGCTTAACACCATTAACATCAATTGCCTTACTGGAAAGATTTGCGCTCTCCTGTGCGGCAGCTTGTTCTTTAAGCTGTTGTAACTCTTTTTCCAGCTGACGCGTACGTTCCAGTACTGAGCGCACTTTATCAGCCAGATTATTGCTATCGCCTTTCAGCAGATGCGCGACTTCGCTTAAGCGATCGCTGTCTGCATGAACGGTGGCGATAGCACCTTCTCCGGTTACCGCTTCGATACGACGAACGCCTGCAGCAGTACCCGATTCAGAGATGATGCGGAACAGACCAATATCACCAGTGCGGCTGGCGTGAGTACCGCCACACAACTCGGTAGAGAAATCGCCCATGCTCAGCACGCGTACGCGCTCATCATACTTCTCGCCGAACAGCGCC  >  NC_000913/2819663‑2820086

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 13 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 31 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: