Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 3,829,233 C→A L97M (CTG→ATG)  xanP → xanthine:H(+) symporter XanP

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009133,829,2330CA100.0% 64.5 / NA 18L97M (CTG→ATG) xanPxanthine:H(+) symporter XanP
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base A (9/9);  total (9/9)

CATCGATTATTCAAATTAAGGCCTGGGGTCCGGTTGGCTCCGGGCTGTTGTCTATTCAGGGCACCAGCTTCAACTTTGTTGCCCCGCTG  >  NC_000913/3829189‑3829277
                                            |                                            
cATCGATTATTCAAATTAAGGCCTGGGGTCCGGTTGGCTCCGGGAtgtt                                          >  1:1969344/1‑49 (MQ=255)
    gATTATTCAAATTAAGGCCTGGGGTCCGGTTGGCTCCGGGATGTTGTc                                       <  1:943221/48‑1 (MQ=255)
      ttattCAAATTAAGGCCTGGGGTCCGGTTGGCTCCGGGATGTTGTCTAt                                    <  1:2469890/49‑1 (MQ=255)
        attCAAATTAAGGCCTGGGGTCCGGTTGGCTCCGGGATGTTGTCTAtt                                   <  1:2023566/48‑1 (MQ=255)
              aTTAAGGCCTGGGGTCCGGTTGGCTCCGGGATGTTGTCTATTCAGGGCa                            >  1:133888/1‑49 (MQ=255)
                 aaGGCCTGGGGTCCGGTTGGCTCCGGGATGTTGTCTATTCAGGGCAcc                          <  1:2322994/48‑1 (MQ=255)
                     ccTGGGGTCCGGTTGGCTCCGGGATGTTGTCTATTCAGGGCACCAGCtt                     <  1:588868/49‑1 (MQ=255)
                      cTGGGGTCCGGTTGGCTCCGGGATGTTGTCTATTCAGGGCACCAGCtt                     >  1:561377/1‑48 (MQ=255)
                      cTGGGGTCCGGTTGGCTCCGGGATGTTGTCTATTCAGGGCACCAGCTTc                    <  1:2580150/49‑1 (MQ=255)
                       tGGGGTCCGGTTGGCTCCGGGATGTTGTCTATTCAGGGCACCAGCTTc                    >  1:930585/1‑48 (MQ=255)
                         gggTCCGGTTGGCTCCGGGATGTTGTCTATTCAGGGCACCAGCTTCAAc                 >  1:2077007/1‑49 (MQ=255)
                          ggTCCGGTTGGCTCCGGGATGTTGTCTATTCAGGGCACCAGCTTCAACt                <  1:1544734/49‑1 (MQ=255)
                               ggTTGGCTCCGGGATGTTGTCTATTCAGGGCACCAGCTTCAACTttgtt           >  1:2817307/1‑49 (MQ=255)
                                gTTGGCTCCGGGATGTTGTCTATTCAGGGCACCAGCTTCAACTttgttg          >  1:2029527/1‑49 (MQ=255)
                                    gCTCCGGGATGTTGTCTATTCAGGGCACCAGCTTCAACTTTGTTGcccc      >  1:1637869/1‑49 (MQ=255)
                                        cGGGATGTTGTCTATTCAGGGCACCAGCTTCAACTTTGTTGCCCCGCt   >  1:1107249/1‑48 (MQ=255)
                                        cGGGATGTTGTCTATTCAGGGCACCAGCTTCAACTTTGTTGCCCCGCt   <  1:356901/48‑1 (MQ=255)
                                        cGGGATGTTGTCTATTCAGGGCACCAGCTTCAACTTTGTTGCCCCGCTg  <  1:715675/49‑1 (MQ=255)
                                            |                                            
CATCGATTATTCAAATTAAGGCCTGGGGTCCGGTTGGCTCCGGGCTGTTGTCTATTCAGGGCACCAGCTTCAACTTTGTTGCCCCGCTG  >  NC_000913/3829189‑3829277

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 18 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: