Predicted mutation
evidence seq id position mutation freq annotation gene description
RA NC_002947 1,484,303 T→G 100% V125G (GTC→GGC)  yhdX → amino acid ABC transporter permease

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0029471,484,3030TG100.0% 40.3 / NA 12V125G (GTC→GGC) yhdXamino acid ABC transporter permease
Reads supporting (aligned to +/- strand):  ref base T (0/0);  new base G (8/4);  total (8/4)
Rejected as polymorphism: Frequency below/above cutoff threshold.
Rejected as polymorphism: Variant not supported by required number of reads on each strand.

TGTTCGTCATCGGCCTGCTCAATACGCTGTTGGTGACCTTCATCGGCGTCATTCTGGCGACGATACTGGGCTTCATCATCGGTGTGGCTCGCCTGTCACCGAACTGGATGATCAACAAGCTGGCGACCGTCTATGTGGAAACCTTCCGCAACATTCCGCCGTTGTTGCAGATCCTGTTCTGGTATTTCGCCGTGTTCCTGACCCTGCCGGGACCGCGGGGCAGCATCAACATCGAGGACATGTTC  >  NC_002947/1484174‑1484418
                                                                                                                                 |                                                                                                                   
tgtTCGTCATCGGCCTGCTCAATACGCTGTTGGTGACCTTCATCGGCGTCATTCTGGCGACGATACTGGGCTTCATCATCGGTGTGGCTCGCCTGTCACCGAACTGGATGATCAACAAGCTGGCGACCGGCTAtgt                                                                                                               <  1:424894/136‑1 (MQ=255)
  ttCGTCATCGGCCTGCTCAATACGCTGTTGGTGACCTTCATCGGCGTCATTCTGGCGACGATACTGGGCTTCATCATCGGTGTGGCTCGCCTGTCACCGAACTGGATGATCAACAAGCTGGCGACCGGCTATGTgg                                                                                                             >  2:466584/1‑136 (MQ=255)
                                  gACCTTGATCGGCGTCATTCTGGCGACGATACTGGGCTTCATCATCGGTGTGGCTCGCCTGTCACCGAACTGGATGATCAACAAGCTGGCGACCGGCTATGTGGAAACCTTCCGCAACATTCCGCCGTTGTTGCAg                                                                             <  1:219403/136‑1 (MQ=255)
                                   aCCTTCATCGGCGTCATTCTGGCGACGATACTGGGCTTCATCATCGGTGTGGCTCGCCTGTCACCGAACTGGATGATCAACAAGCTGGCGACCGGCTATGTGGAAACCTTCCGCAACATTCCGCCGTTGTTGCAgc                                                                            >  1:125261/1‑135 (MQ=255)
                                          tCGGCGTCATTCTGGCGACGATACTGGGCTTCATCATCGGTGTGGCTCGCCTGTCACCGAACTGGATGATCAACAAGCTGGCGACCGGCTATGTGGAAACCTTCCGCAACATTCCGCCGTTGTTGCAGATCCTGtt                                                                     >  1:97478/1‑136 (MQ=255)
                                                    tCTGGCGACGATACTGGGCTTCATCATCGGTGTGGCTCGCCTGTCACCGAACTGGATGATCAATAAGCTGGCGACCGGCTATGTGGAAACCTTCCGCAACATTCCGCCGTTGTTGCAGATCCTGTTCTGGTATTTc                                                           <  1:489603/136‑1 (MQ=255)
                                                                            catcGGTGTGGCTCGCCTGTCACCGAACTGGATGATCAACAAGCTGGCGACCGGCTATGTGGAAACCTTCCGCAACATTCCGCCGTTGTTGCAGATCCTGTTCTGGTATTTCGCCGTGTTCCTGACCCTGCCgggc                                   >  1:263401/1‑135 (MQ=255)
                                                                            catcGGTGTGGCTCGCCTCTCACCGAACAGGATGATCAACAAGCTCGCGACAGGCTATGTGGAAACCTTCCGCAACATTCCGCCGTTGTAGCAGATCCTCTTCTGGTATATCGAAGTGTTCCTGACCCTGCCGGGa                                   >  1:382128/1‑136 (MQ=255)
                                                                                        tCGCCTGTCACCGAACTGGATGATCAACAAGCTGGCGACCGGCTATGTGGAAACCTTCCGCAACATTCCGCCGTTGTTGCAGATCCTGTTCTGGTATTTCGCCGTGTTCCTGACCCTGCCGGGACCGCGGGgcagc                       <  1:466584/136‑1 (MQ=255)
                                                                                              gTCACCGAACTGGATGATCAACAAGCTGGCGACCGGCTATGTGGAAACCTTCCGCAACATTCCGCCGTTGTTGCAGATCCTGTTCTGGTATTTCGCCGTGTTCCTGACCCTGCCGGGACCGCGGGGCAGCATCAAc                 >  2:14728/1‑136 (MQ=255)
                                                                                                             gatCAACAAGCTGGCGACCGGCTATGTGGAAACCTTCCGCAACATTCCGCCGTTGTTGCAGATCCTGTTCTGGTATTTCGCCGTGTTCCTGACCCTGCCGGGACCGCGGGGCAGCATCAACATCGAGGACATGtta  >  1:83800/1‑135 (MQ=255)
                                                                                                             gatCAACAAGCTGGCGACCGGCTATGTGGAAACCTTCAGCAACATTCCGCCGTTGTTGCAGATCCTGTTCTGGTATTTCGCCGTGTTCCTGACCCTGCCGGGACCGCGGGGCAGCATCAACATCGAGGACATGttc  >  1:318225/1‑136 (MQ=255)
                                                                                                                                 |                                                                                                                   
TGTTCGTCATCGGCCTGCTCAATACGCTGTTGGTGACCTTCATCGGCGTCATTCTGGCGACGATACTGGGCTTCATCATCGGTGTGGCTCGCCTGTCACCGAACTGGATGATCAACAAGCTGGCGACCGTCTATGTGGAAACCTTCCGCAACATTCCGCCGTTGTTGCAGATCCTGTTCTGGTATTTCGCCGTGTTCCTGACCCTGCCGGGACCGCGGGGCAGCATCAACATCGAGGACATGTTC  >  NC_002947/1484174‑1484418

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: