Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,220,871 G→A pseudogene (1271/2648 nt) ycgH → putative transporter component, N‑terminal fragment

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,220,8710GA100.0% 45.3 / NA 14pseudogene (1271/2648 nt)ycgHputative transporter component, N‑terminal fragment
Reads supporting (aligned to +/- strand):  ref base G (0/0);  new base A (10/4);  total (10/4)

GAATATGAAAGATGACTCCGTTGTTACCCATCTGACTAATTCAGACAGTATTATCAATCTTTCGTATGATGATGGTCAAACATTTACCCAAGGAAAAACATTAACCGTAAAAGGTAATTATGTCGGTAATAATGGTCAGCTTAATATCCGCA  >  NC_000913/1220797‑1220948
                                                                          |                                                                             
gAATATGAAAGATGACTCCGTTGTTACCCATCTGACTAATTCAGACAGTATTATCAATCTTTCGTATGATGATGATCAAAc                                                                         <  2:240962/81‑1 (MQ=255)
    atGAAAGATGACTCCGTTGTTACCCATCTGACTAATTCAGACAGTATTATCAATCTTTCGTATGATGATGATCAAACAtt                                                                      >  2:240973/1‑80 (MQ=255)
      gAAAGATGACTCCGTTGTTACCCATCTGACTAATTCAGACAGTATTATCAATCTTTCGTATGATGATGATCAAACATTTAc                                                                   >  2:240984/1‑81 (MQ=255)
       aaaGATGACTCCGTTGTTACCCATCTGACTAATTCAGACAGTATTATCAATCTTTCGTATGATGATGATCAAACATTTAcc                                                                  <  2:240963/81‑1 (MQ=255)
          gATGACTCCGTTGTTACCCATCTGACTAATTCAGACAGTATTATCAATCCTTCGTATGATGATGATCAAACATTTAccc                                                                 >  2:240983/1‑79 (MQ=255)
              aCTCCGTTGTTACCCATCTGACTAATTCAGACAGTATTATCAATCTTTCGTATGATGATGATCAAACATTTACCCAAGGa                                                            >  1:240981/1‑80 (MQ=255)
                tCCGTTGTTACCCATCTGACTAATTCAGACAGTATTATCAATCTTTCGTATGATGATGATCAAACATTTACCCAAGGaaa                                                          >  2:240991/1‑80 (MQ=255)
                tCCGTTGTTACCCATCTGACTAATTCAGACAGTATTATCAATCTTTCGTATGATGATGATCAAACATTTACCCAAGGaaa                                                          >  2:240993/1‑80 (MQ=255)
                         aCCCATCTGACTAATTCAGACAGTATTATCAATCTTTCGTATGATGATGATCAAACATTTACCCAAGGAAAAACATTAAcc                                                >  1:241006/1‑81 (MQ=255)
                                tGACTAATTCAGACAGTATTATCAATCTTTCGTATGATGACGATCTAACATTTACCCAAGGAAAAACATTAACCGTAAAAg                                         >  2:240994/1‑81 (MQ=255)
                                              aGTATTATCAATCTTTCGTATGATGATGATCAAACATTTACCCAAGGAAAAACATTAACCGTAAAAGGTAATTATGTCgg                            >  2:240985/1‑80 (MQ=255)
                                                  ttatCAATCTTTCGTATGATGATGATCAAACATTTACCCAAGGAAAAACATTAACCGTAAAAGGTAATTATGTCGGtaat                        <  1:240964/80‑1 (MQ=255)
                                                     tCAATCTTTCGTATGATGATGATCAAACATTTACCCAAGGAAAAACATTAACCGTAAAAGGTAATTATGTCGGTAATAATg                    <  1:240965/81‑1 (MQ=255)
                                                                       atgATCAAACATTTACCCAAGGAAAAACATTAACCGTAAAAGGTAATTATGTCGGTAACAATGGTCAGCTTAATATCCGCa  >  1:241005/1‑81 (MQ=255)
                                                                          |                                                                             
GAATATGAAAGATGACTCCGTTGTTACCCATCTGACTAATTCAGACAGTATTATCAATCTTTCGTATGATGATGGTCAAACATTTACCCAAGGAAAAACATTAACCGTAAAAGGTAATTATGTCGGTAATAATGGTCAGCTTAATATCCGCA  >  NC_000913/1220797‑1220948

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 23 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: