Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 314,734 Δ1 bp pseudogene (378/888 nt) eaeH → putative porin domain‑containing protein EaeH

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_000913314,7320A.100.0% 54.9 / NA 14pseudogene (376/888 nt)eaeHputative porin domain‑containing protein EaeH
Reads supporting (aligned to +/- strand):  ref base A (0/0);  new base . (11/3);  total (11/3)

CAGCTAAAGCTAACCAGGAAATACAGGAGTGGCTCGGGAAATATGGTACTGCGCGCGTCAAACTGAATGTCGATAAAGATTTCTCGCTGAAGGATTCTTCGCTGGAAATGCTTTATCCGATTTATGATACGCCGACAAATATGTTGTT  >  NC_000913/314658‑314805
                                                                          |                                                                         
caGCTAAAGCTAACCAGGAAATACAGGAGTGGCTCGGGAAATATGGTACTGCGCGCGTCAAACTGAATGTCGATAAGAttt                                                                    >  1:65666/1‑81 (MQ=255)
             ccAGGAAATACAGGAGTGGCTCGGGAAATATGGTACTGCGCGCGTCAAACTGAATGTCGATAAGATTTCTCGCTGAAGGAt                                                       >  1:65659/1‑81 (MQ=255)
                 gAAATACAGGAGTGGCTCGGGAAATATGGTACTGCGCGCGTCAAACTGAATGTCGATAAGATTTCTCGCTGAAGGAttctt                                                   <  2:65640/81‑1 (MQ=255)
                    aTACAGGAGTGGCTCGGGAAATATGGTACTGCGCGCGTCAAACTGAATGTCGATAAGATTTCTCGCTGAAGGATTCTTCGc                                                >  2:65661/1‑81 (MQ=255)
                       cAGGAGTGGCTCGGGAAATATGGTACTGCGCGCGTCAAACTGAATGTCGATAAGATTTCTCGCTGAAGGATTCTTCGCTg                                              >  2:65667/1‑80 (MQ=255)
                        aGGAGTGGCTCGGGAAATATGGTACTGCGCGCGTCAAACTGAATGTCGATAAGATTTCTCGCTGAAGGATTCTTCGCTgg                                             >  1:65657/1‑80 (MQ=255)
                              ggCTCGGGAAATATGGTACTGCGCGCGTCAAACTGAATGTCGATAAGATTTCTCGCTGAAGGATTCTTCGCTGGAAATGCt                                      >  1:65660/1‑81 (MQ=255)
                                       aaTATGGTACTGCGCGCGTCAAACTGAATGTCGATAAGATTTCTCGCTGAAGGATTCTTCGCTGGAAATGCTTTATCCGAt                             >  2:65658/1‑81 (MQ=255)
                                         tatGGTACTGCGCGCGTCAAACTGAATGTCGATAAGATTTCTCGCTGAAGGATTCTTCGCTGGAAATGCTTTATCCGAttt                           <  2:65641/81‑1 (MQ=255)
                                                    gcgcgTCAAACTGAATGTCGATAAGATTTCTCGCTGAAGGATTCTTCGCTGGAAATGCTTTATCCGATTTATGATACGcc                 >  1:65669/1‑80 (MQ=255)
                                                     cgcgTCAAACTGAATGTCGATAAGATTTCTCGCTGAAGGATTCTTCGCTGGAAATGCTTTATCCGATTTATGATACGCCGa               >  1:65674/1‑81 (MQ=255)
                                                         tCAAACTGAATGTCGATAAGATTTCTCGCTGAAGGATTCTTCGCTGGAAATGCTTTATCCGATTTATGATACGCCGACaaa           >  2:65665/1‑81 (MQ=255)
                                                                  aTGTCGATAAGATTTCTCGCTGAAGGATTCTTCGCTGGAAATGCTTTATCCGATTTATGATACGCCGACAAATATgttgtt  <  1:65642/81‑1 (MQ=255)
                                                                  aTGTCGATAAGATTTCTCGCTGAAGGATTCTTCGCTGGAAATGCTTTATCCGATTTATGATACGCCGACAAATATgttgtt  >  2:65662/1‑81 (MQ=255)
                                                                          |                                                                         
CAGCTAAAGCTAACCAGGAAATACAGGAGTGGCTCGGGAAATATGGTACTGCGCGCGTCAAACTGAATGTCGATAAAGATTTCTCGCTGAAGGATTCTTCGCTGGAAATGCTTTATCCGATTTATGATACGCCGACAAATATGTTGTT  >  NC_000913/314658‑314805

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: