Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,400,309 Δ1 bp coding (1465/1527 nt) abgT ← p‑aminobenzoyl glutamate:H(+) symporter

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,400,3080A.100.0% 71.7 / NA 16coding (1466/1527 nt)abgTp‑aminobenzoyl glutamate:H(+) symporter
Reads supporting (aligned to +/- strand):  ref base A (0/0);  new base . (7/9);  total (7/9)

GGTAAATACCCGGACCTATCGGCAGACCGACAAGATACCACGCCAGCAACATCAGCAGCCATACCACCAAAAAGATAAGTGGATAGGGCAAGA  >  NC_000913/1400261‑1400353
                                               |                                             
ggTAAATACCCGGACCTATCGGCAGACCGACAAGATACCACGCCAGCaca                                             >  1:1880507/1‑48 (MQ=255)
ggTAAATACCCGGACCTATCGGCAGACCGACAAGATACCACGCCAGCac                                              <  1:50624/49‑2 (MQ=255)
             acctATCGGCAGACCGACAAGATACCACGCCAGCACATCGCAGCCATACt                              <  1:1036789‑M1/49‑2 (MQ=255)
             acctATCGGCAGACCGACAAGATACCACGCCAGCACATCGCAGCCATACt                              <  1:557556‑M1/49‑2 (MQ=255)
             acctATCGGCAGACCGACAAGATACCACGCCAGCACATCGCAGCCATACt                              <  1:2303709‑M1/49‑2 (MQ=255)
             aCCTATCGGCAGACCGACAAGATACCACGCCAGCACATCGCAGCCATac                               >  1:2046341/1‑49 (MQ=38)
                 aTCGGCAGACCGACAAGATACCACGCCAGCACATCGCAGCCATACtatg                           >  1:1991921‑M1/1‑45 (MQ=255)
                  tCGGCAGACCGACAAGATACCACGCCAGCACATCGCAGCCATACtatg                           <  1:1169553‑M1/48‑5 (MQ=255)
                  tCGGCAGACCGACAAGATACCACGCCAGCACATCGCAGCCATACtatg                           <  1:2248131‑M1/48‑5 (MQ=255)
                   cGGCAGACCGACAAGATACCACGCCAGCACATCGCAGCCATACtatg                           >  1:894659‑M1/1‑43 (MQ=255)
                    ggCAGACCGACAAGATACCACGCCAGCACATCGCAGCCATACtatgcag                        >  1:766108‑M1/1‑42 (MQ=255)
                                aGATACCACGCCAGCACGTCGCAGCCATACtatgcagaaacaatgctgtc           <  1:2025903‑M1/50‑21 (MQ=255)
                                 gATACCACGCCAGCACATCGCAGCCATACtatgcagaaacaatgctgtcg          <  1:1935905‑M1/50‑22 (MQ=255)
                                  aTACCACGCCAGCACATCGCAGCCATACtatgcagaaacaatgctgtcga         >  1:2312800‑M1/1‑28 (MQ=255)
                                  aTACCACGCCAGCACATCGCAGCCATACtatgcagaaacaatgctgtcga         <  1:338318‑M1/50‑23 (MQ=255)
                                   tACCACGCCAGCACATCGCAGCCATACtatgcagaaacaatgctgtcgat        <  1:210016‑M1/50‑24 (MQ=255)
                                       aCGCCAGCACATCGCAGCCATACtatgcagaaacaatgctgtcgatggct    >  1:1733784‑M1/1‑23 (MQ=255)
                                         gCCAGCACATCGCAGCCATACtatgcagaaacaatgctgtcgatggctgc  >  1:1195258‑M1/1‑21 (MQ=255)
                                               |                                             
GGTAAATACCCGGACCTATCGGCAGACCGACAAGATACCACGCCAGCAACATCAGCAGCCATACCACCAAAAAGATAAGTGGATAGGGCAAGA  >  NC_000913/1400261‑1400353

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 18 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: