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% 76.8 / NA 17coding (1466/1527 nt)abgTp‑aminobenzoyl glutamate:H(+) symporter
Reads supporting (aligned to +/- strand):  ref base A (0/0);  new base . (11/6);  total (11/6)

GGTAAATACCCGGACCTATCGGCAGACCGACAAGATACCACGCCAGCAACATCAGCAGCCATACCACCAAAAAGATAAGTGGATAGGGCAAG  >  NC_000913/1400261‑1400352
                                               |                                            
ggTAAATACCCGGACCTATCGGCAGACCGACAAGATACCACGCCAGCac                                             <  1:1725730/49‑2 (MQ=255)
 gTAAATACCCGGACCTATCGGCAGACCGACAAGATACCACGCCAGCaca                                            <  1:1563867/49‑3 (MQ=255)
         ccGGACCTATCGGCAGACCGACAAGATACCACGCCAGCACATCGCAGcc                                  <  1:840601/49‑1 (MQ=38)
           ggACCTATCGGCAGACCGACAAGATACCACGCCAGCACATCGCAGCCAt                                <  1:2102725/49‑1 (MQ=38)
              cctATCGGCAGACCGACAAGATACCACGCCAGCACATCGCAGCCATACt                             <  1:478480‑M1/48‑2 (MQ=255)
                 aTCGGCAGACCGACAAGATACCACGCCAGCACATCGCAGCCATACtatg                          >  1:1898400‑M1/1‑45 (MQ=255)
                    ggCAGACCGACAAGATACCACGCCAGCACATCGCAGCCATACtatg                          >  1:1882518‑M1/1‑42 (MQ=255)
                      cAGACCGACAAGATACCACGCCAGCACATCGCAGCCATACtatgcaga                      >  1:1371263‑M1/1‑40 (MQ=255)
                         aCCGACAAGATACCACGCCAGCACATCGCAGCCATACtatgcagaaac                   >  1:1280449‑M1/1‑37 (MQ=255)
                              cAAGATACCACGCCAGCACATCGCAGCCATACtatgcagaaacaatgct             >  1:1152491‑M1/1‑32 (MQ=255)
                               aaGATACCACGCCAGCACATCGCAGCCATACtatgcagaaacaatgctg            >  1:192147‑M1/1‑31 (MQ=255)
                                aGATACCACGCCAGCACATCGCAGCCATACtatgcagaaacaatgctgt           <  1:1359649‑M1/49‑20 (MQ=255)
                                  aTACCACGCCAGCACATCGCAGCCATACtatgcagaaacaatgctgtcg         <  1:1207274‑M1/49‑22 (MQ=255)
                                  aTACCACGCCAGCACATCGCAGCCATACtatgcagaaacaatgctgtcg         <  1:1305018‑M1/49‑22 (MQ=255)
                                  aTACCACGCCAGCACATCGCAGCCATACtatgcagaaacaatgctgtc          >  1:163659‑M1/1‑28 (MQ=255)
                                    aCCACGCCAGCACATCGCAGCCATACtatgcagaaacaatgctgtcgat       >  1:424227‑M1/1‑26 (MQ=255)
                                    aCCACGCCAGCACATCGCAGCCATACtatgcagaaacaatgctgtcgat       >  1:1192822‑M1/1‑26 (MQ=255)
                                         gCCAGCACATCGCAGCCATACtatgcagaaacaatgctgtcgatggctg  >  1:29936‑M1/1‑21 (MQ=255)
                                         gCCAGCACATCGCAGCCATACtatgcagaaacaatgctgtcgatggctg  >  1:1598266‑M1/1‑21 (MQ=255)
                                               |                                            
GGTAAATACCCGGACCTATCGGCAGACCGACAAGATACCACGCCAGCAACATCAGCAGCCATACCACCAAAAAGATAAGTGGATAGGGCAAG  >  NC_000913/1400261‑1400352

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: