Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,483,868 A→G T270A (ACC→GCC)  hrpA → ATP‑dependent RNA helicase HrpA

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,483,8680AG100.0% 30.7 / NA 10T270A (ACC→GCC) hrpAATP‑dependent RNA helicase HrpA
Reads supporting (aligned to +/- strand):  ref base A (0/0);  new base G (5/5);  total (5/5)

ATTATCACTTCCGCGACTATCGACCCGGAACGCTTTTCGCGCCACTTTAATAATGCGCCGATTATTGAAGTCTCCGGTCGGACCTATCCGGTGGAAGTGCGCTATCGCCCGATTGTTGAAGAAGCCGATGACACCGAGCGCGATCAGTTGCAGGCGATTTTTGACGCCGTAGACGAACTGAGTCAGGAAAGCCATGGCGACATTCTGATCTTTATGAGCGGCGAGCGGGAAATCCGCGATACCGCCGATGCGCTGAACAAGCT  >  NC_000913/1483736‑1483998
                                                                                                                                    |                                                                                                                                  
aTTATCACTTCCGCGACTATCGACCCGGAACGCTTTTCGCGCCACTTTAATAATGCGCCGATTATTGAAGTCTCCGGTCGGACCTATCCGGTGGAAGTGCGCTATCGCCCGATTGTTGAAGAAGCCGATGACGCCGAgcg                                                                                                                             <  2:48413/140‑1 (MQ=255)
                                           aCTTTAATAATGCGCCGATTATTGAAGTCTCCGGTCGGACCTATCCGGTGGAAGTGCGCTATCGCCCGATTGTTGAAGAAGCCGATGACGCCGAGCGCGATCAGTTGCAGGCGATTTTTGACGCCGTAGACGAACTGAGt                                                                                  <  1:264948/140‑1 (MQ=255)
                                           aCTTTAATAATGCGCCGATTATTGAAGTCTCCGGTCGGACCTATCCGGTGGAAGTGCGCTATCGCCCGATTGTTGAAGAAGCCGATGACGCCGAGCGCGATCAGTTGCAGGCGATTTTTGACGCCGTAGACGAACTGAGt                                                                                  >  2:264948/1‑140 (MQ=255)
                                                       cgcCGATTATTGAAGTCTCCGGTCGGACCTATCCGGTGGAAGTGCGCTATCGCCCGATTGTTGAAGAAGCCGATGACGCCGAGCGCGATCAGTTGCAGGCGATTTTTGACGCCGTAGACGAACTGAGTCAGGAAAGCCAt                                                                      >  2:200559/1‑140 (MQ=255)
                                                           gATTATTGAAGTCTCCGGTCGGACCTATCCGGTGGAAGTGCGCTATCGCCCGATTGTTGAAGAAGCCGATGACGCCGAGCGCGATCAGTTGCAGGCGATTTTTGACGCCGTAGACGAACTGAGTCAGGAAAGCCATGGCg                                                                  <  1:200559/140‑1 (MQ=255)
                                                                                           tGGAAGTGCGCTATCGCCCGATTGTTGAAGAAGCCGATGACGCCGAGCGCGATCAGTTGCAGGCGATTTTTGACGCCGTAGACGAACTGAGTCAGGAAAGCCATGGCGACATTCTGATCTTTATGAGCGGCGAGCGGGaa                                  >  1:243554/1‑140 (MQ=255)
                                                                                                        tCGCCCGATTGTTGAAGAAGCCGATGACGCCGAGCGCGATCAGTTGCAGGCGATTTTTGACGCCGTAGACGAACTGAGTCAGGAAAGCCATGGCGACATTCTGATCTTTATGAGCGGCGAGCggg                                    <  1:191580/125‑1 (MQ=255)
                                                                                                        tCGCCCGATTGTTGAAGAAGCCGATGACGCCGAGCGCGATCAGTTGCAGGCGATTTTTGACGCCGTAGACGAACTGAGTCAGGAAAGCCATGGCGACATTCTGATCTTTATGAGCGGCGAGCggg                                    >  2:191580/1‑125 (MQ=255)
                                                                                                                ttgttgAAGAAGCCGATGACGCCGAGCGCGATCAGTTGCAGGCGATTTTTGACGCCGTAGACGAACTGAGTCAGGAAAGCCATGGCGACATTCTGATCTTTATGAGCGGCGAGCGGGAAATCCGCGATACCGCCGATgcg             >  2:70501/1‑140 (MQ=255)
                                                                                                                           gCCGATGACGCCGAGCGCGATCAGTTGCAGGCGATTTTTGACGCCGTAGACGAACTGAGTCAGGAAAGCCATGGCGACATTCTGATCTTTATGAGCGGCGAGCGGGAAATCCGCGATACCGCCGATGCGCTGAACAAGCt  <  1:70501/140‑1 (MQ=255)
                                                                                                                                    |                                                                                                                                  
ATTATCACTTCCGCGACTATCGACCCGGAACGCTTTTCGCGCCACTTTAATAATGCGCCGATTATTGAAGTCTCCGGTCGGACCTATCCGGTGGAAGTGCGCTATCGCCCGATTGTTGAAGAAGCCGATGACACCGAGCGCGATCAGTTGCAGGCGATTTTTGACGCCGTAGACGAACTGAGTCAGGAAAGCCATGGCGACATTCTGATCTTTATGAGCGGCGAGCGGGAAATCCGCGATACCGCCGATGCGCTGAACAAGCT  >  NC_000913/1483736‑1483998

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: