Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 163,804 T→C V567A (GTA→GCA)  hrpB → putative ATP‑dependent RNA helicase HrpB

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_000913163,8040TC100.0% 23.6 / NA 8V567A (GTA→GCA) hrpBputative ATP‑dependent RNA helicase HrpB
Reads supporting (aligned to +/- strand):  ref base T (0/0);  new base C (6/2);  total (6/2)

ATGGTTGATCGCACCGTTATTATTGCAGGGCAGCGCCTCGCCGGATGCGCGGATTTTACTGGCGCTGCTGGTCGATATTGATGAGTTAGTACAACGCTGCCCGCAGCTGGTACAGCAGTCTGACACTGTGGAGTGGGATGACGCGCAAGGTACGCTGAAAGCCTGGCGTCGGCTACAAATCGGTCAGTTGACGGTGAAAGTGCAGCCGCTGGCGAAACCGTCAGAAGACGAGTTGCA  >  NC_000913/163694‑163930
                                                                                                              |                                                                                                                              
aTGGTTGATCGCACCGTTATTATTGCAGGGCAGCGCCTCGCCGGATGCGCGGATTTTACTGGCGCTGCTGGTCGATATTGATGAGTTAGTACAACGCTGCCCGCAGCTGGCACAGCAGTCTGACACTGTGGAGTGGGATg                                                                                                   <  2:54636/140‑1 (MQ=255)
 tGGTTGATCGCACCGTTATTATTGCAGGGCAGCGCCTCGCCGGATGCGCGGATTTTACTGGCGCTGCTGGTCGATATTGATGAGTTAGTACAACGCTGCCCGCAGCTGGCACAGCAGTCTGACACTGTGGAGTGGGATGa                                                                                                  >  1:305230/1‑140 (MQ=255)
             ccGTTATTATTGCAGGGCAGCGCCTCGCCGGATGCGCGGATTTTACTGGCGCTGCTGGTCGATATTGATGAGTTAGTACAACGCTGCCCGCAGCTGGCACAGCAGTCTGACACTGTGGAGTGGGATGACGCGCAAGGTAc                                                                                      >  2:308535/1‑140 (MQ=255)
                      ttGCAGGGCAGCGCCTCGCCGGATGCGCGGATTTTACTGGCGCTGCTGGTCGATATTGATGAGTTAGTACAACGCTGCCCGCAGCTGGCACAGCAGTCTGACACTGTGGAGTGGGATGACGCGCAAGGTACGCTGAAAGc                                                                             >  2:287668/1‑140 (MQ=255)
                          aGGGCAGCGCCTCGCCGGATGCGCGGATTTTACTGGCGCTGCTGGTCGATATTGATGAGTTAGTACAACGCTGCCCGCAGCTGGCACAGCAGTCTGACACTGTGGAGTGGGATGACGCGCAAGGTACGCTGAAAGCCTgg                                                                         >  2:138785/1‑140 (MQ=255)
                                                                    tgGTCGATATTGATGAGTTAGTACAACGCTGCCCGCAGCTGGCACAGCAGTCTGACACTGTGGAGTGGGATGACGCGCAAGGTACGCTGAAAGCCTGGCGTCGGCTACAAATCGGTCAGTTGACGGTGAAAGTGCAGCCg                               <  2:111523/140‑1 (MQ=255)
                                                                                              cGCTGCCCGCAGCTGGCACAGCAGTCTGACACTGTGGAGTGGGATGACGCGCAAGGTACGCTGAAAGCCTGGCGTCGGCTACAAATCGGTCAGTTGACGGTGAAAGTGCAGCCGCTGGCGAAACCGTCAGAAGACGAGtt     >  2:372124/1‑140 (MQ=255)
                                                                                                 tGCCCGCAGCTGGCACAGCAGTCTGACACTGTGGAGTGGGATGACGCGCAAGGTACGCTGAAAGCCTGGCGTCGGCTACAAATCGGTCAGTTGACGGTGAAAGTGCAGCCGCTGGCGAAACCGTCAGAAGACGAGTTGCa  >  1:9957/1‑140 (MQ=255)
                                                                                                              |                                                                                                                              
ATGGTTGATCGCACCGTTATTATTGCAGGGCAGCGCCTCGCCGGATGCGCGGATTTTACTGGCGCTGCTGGTCGATATTGATGAGTTAGTACAACGCTGCCCGCAGCTGGTACAGCAGTCTGACACTGTGGAGTGGGATGACGCGCAAGGTACGCTGAAAGCCTGGCGTCGGCTACAAATCGGTCAGTTGACGGTGAAAGTGCAGCCGCTGGCGAAACCGTCAGAAGACGAGTTGCA  >  NC_000913/163694‑163930

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: