Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 390,136 A→G intergenic (‑409/‑115) hemB ← / → yaiT porphobilinogen synthase/putative autotransporter YaiT

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_000913390,1360AG100.0% 44.4 / NA 14intergenic (‑409/‑115)hemB/yaiTporphobilinogen synthase/putative autotransporter YaiT
Reads supporting (aligned to +/- strand):  ref base A (0/0);  new base G (6/8);  total (6/8)

ATACTGTGCTTTTATGAATTTGATGCGTGTTTTTCTCCATAAATTATATATGTCCACATTCGGACTTAGGGGAAAGAATAATTGAACCATTCGTCTGTAACGCAGCATAATCGTTAGCGCGAAACATAATATGTTTTCTATGCATTGATAATTGA  >  NC_000913/390059‑390213
                                                                             |                                                                             
aTACTGTGCTTTTATGAATTTGATGCGTGTTTTTCTCCATAAATTATATATGTCCACATTCGGACTTAGGGGAAAGagtaa                                                                            >  1:80003/1‑81 (MQ=255)
   cTGTGCTTTTATGAATTTGATGCGTGTTTTTCTCCATAAATTATATATGTCCACATTCGGACTTAGGGGAAAGAGTAAtt                                                                          >  1:80005/1‑80 (MQ=255)
        cTTTTATGAATTTGATGCGTGTTTTTCTCCATAAATTATATATGTCCACATTCGGACTTAGGGGAAAGAGTAATTGAAcc                                                                     <  1:79986/80‑1 (MQ=255)
                 aTTTGATGCGTGTTTTTCTCCATAAATTATATATGTCCACATTCGGACTTAGGGGAAAGAGTAATTGAACCATTCGTCTGt                                                           <  2:79987/81‑1 (MQ=255)
                     gaagCGTGTTTTTCTCCATAAATTATATATGTCCACATTCGCACTTAGGGGAAAGAGTAATTGAACTATTCGTTTGTACCg                                                       >  2:80010/4‑81 (MQ=255)
                              ttttCTCCATAAATTATATATGTCCACATTCGGACTTAGGGGAAAGAGTAATTGAACCATTCGTCTGTAACGCAGCATAAt                                              >  1:80011/1‑81 (MQ=255)
                                 tctcCATAAATTATATATGTCCACATTCGGACTTAGGGGAAAGAGTAATTGAACCATTCGTCTGTAACGCAGCATAATCGt                                           >  2:80009/1‑81 (MQ=255)
                                         aaTTATATATGTCCACATTCGGACTTAGGGGAAAGAGTAATTGAACCATTCGTCTGTAACGCAGCATAATCGTTAGcgcg                                    <  1:79988/80‑1 (MQ=255)
                                           ttATATATGTCCACATTCGGACTTAGGGGAAAGAGTAATTGAACCATTCGTCTGTAACGCAGCATAATCGTTAGCGCGaaa                                 >  1:80021/1‑81 (MQ=255)
                                             atatatGTCCACATTCGGACTTAGGGGAAAGAGTAATTGAACCATTCGTCTGTAACGCAGCATAATCGTTAGCGCGAAAc                                <  1:79989/80‑1 (MQ=255)
                                                        caTTCGGACTTAGGGGAAAGAGTAATTGAACCATTCGTCTGTAACGCAGCATAATCGTTAGCGCGAAACATAATATGtttt                    <  1:79991/81‑1 (MQ=255)
                                                        caTTCGGACTTAGGGGAAAGAGTAATTGAACCATTCGTCTGTAACGCAGCATAATCGTTAGCGCGAAACATAATATGtttt                    <  2:79990/81‑1 (MQ=255)
                                                         aTTCGGACTTAGGGGAAAGAGTAATTGAACCATTCGTCTGTAACGCAGCATAATCGTTAGCGCGAAACATAATATGTTTTc                   <  2:79992/81‑1 (MQ=255)
                                                              gACTTAGGGGAAAGAGTAATTGAACCATTCGTCTGTAACGCAGCATAATCGTTAGCGCGAAACATAATATGTTTTCTATg               >  2:80018/1‑80 (MQ=255)
                                                                        aaaGAGTAATTGAACCATTCGTCTGTAACGCAGCATAATCGTTAGCGCGAAACATAATATGTTTTCTATGCATTGATAAtt    <  2:79993/81‑1 (MQ=255)
                                                                          agagTAATTGAACCATTCGTCTGTAACGCAGCATAATCGTTAGCGCGAAACATAATATGTTTTCTATGCATTGATAATTGa  >  1:80027/1‑81 (MQ=255)
                                                                             |                                                                             
ATACTGTGCTTTTATGAATTTGATGCGTGTTTTTCTCCATAAATTATATATGTCCACATTCGGACTTAGGGGAAAGAATAATTGAACCATTCGTCTGTAACGCAGCATAATCGTTAGCGCGAAACATAATATGTTTTCTATGCATTGATAATTGA  >  NC_000913/390059‑390213

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: