Predicted mutation
evidence seq id position mutation freq annotation gene description
RA NC_000913 1,434,459 C→T 100% intergenic (‑235/+499) ynaE ← / ← ttcC cold shock protein, Rac prophage/pseudogene, prophage Rac integration site ttcA duplication;Phage or Prophage Related

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,434,4590CT83.4% 21.7 / 1.2 18intergenic (‑235/+499)ynaE/ttcCcold shock protein, Rac prophage/pseudogene, prophage Rac integration site ttcA duplication;Phage or Prophage Related
Reads supporting (aligned to +/- strand):  ref base C (0/3);  new base T (8/7);  total (8/10)
Fisher's exact test for biased strand distribution p-value = 2.16e-01
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 1.00e+00

CTGAATATGATAAGGAGCGAAGTGATTATCAGTATGCTGTTCATATAGCCTCGAATTAGTAATGTGTTATATATGATATAGTTGACAATTTTTATCCTGGGTGTTCTTAAAGTTCGTAGATAAACATTGTCGTTTCAGGTATACAGGAATGCTAACAGGTGGCGGCAAAAATCAG  >  NC_000913/1434363‑1434537
                                                                                                |                                                                              
cTGAATATGATAAGGAGCGAAGTGATTATCAGTATGCTGTTCATATAGCCTCGAATTAGTAATGTGTTATATATGATATAGTTGACAATTTTTATCTTgn                                                                             <  1:1283420/100‑2 (MQ=25)
cTGAATATGATAAGGAGCGAAGTGATTATCAGTATGCTGTTCATATAGCCTCGAATTAGTAATGTGTTATATATGATATAGTTGACAATTTTTATCTTgg                                                                             <  2:22925/100‑1 (MQ=18)
cTGAATATGATAAGGAGCGAAGTGATTATCAGTATGCTGTTCATATAGCCTCGAATTAGTAATGTGTTATATATGATATAGTTGACAATTTTTATCTTg                                                                              >  1:624258/1‑99 (MQ=25)
  gAATATGATAAGGAGCGAAGTGATTATCAGTATGCTGTTCATATAGCCTCGAATTAGTAATTTGTTATATATGATATAGTTGACAATTTTTATCTTGGgt                                                                           <  2:303685/100‑1 (MQ=255)
   aaTATGATAAGGAGCGAAGTGATTATCAGTATGCTGTTTATATAGTCTCGAATTAGTAATGTGTTATATATGATATAGTTGACAATTTTTATCTTGGgtg                                                                          <  1:122659/100‑1 (MQ=255)
    atatGATAAGGAGCGAAGTGATTATCAGTATGCTGTTCATATAGCCTCGAATTAGTAATGTGTTATATATGATATAGTTGACAATTTTTATCTTGGgtgt                                                                         >  2:214762/1‑100 (MQ=25)
          tAAGGAGCGAAGTGATTATCAGTATGCTGTTCATATAGCCTCGAATTAGTAATGTGTTATATATGATATAGTTGACAATTTTTATCTTGGGTGTTCTTaa                                                                   <  2:61722/100‑1 (MQ=17)
           aaGGAGCGAAGTGATTATCAGTATGCTGTTCATATAGCCTCGAATTAGTAATGTGTTATATATGATATAGTTGACAATTTTTATCTTGGGTGTTCTTaaa                                                                  >  2:1754399/1‑100 (MQ=18)
           aaGGAGCGAAGTGATTATCAGTATGCTGTTCATATAGCCTCGAATTAGTAATGTGTTATATATGATATAGTTGACAATTTTTATCTTGGGTGTTCTTaaa                                                                  >  1:2078677/1‑100 (MQ=25)
           aaGGAGCGAAGTGATTATCAGTATGCTGTTCATATAGCCTCGAATTAGTAATGTGTTATATATGATATAGTTGACAATTTTTATCCTGGGTGTTCTTaaa                                                                  <  1:1079456/100‑1 (MQ=40)
            aGGAGCGAAGTGATTATCAGTATGCTGTTCATATAGCCTCGAATTAGTAATGTGTTATATATGATATAGTTGACAATTTTTATCTTGGGTGTTCTTAAAg                                                                 >  2:657663/1‑100 (MQ=18)
             ggAGCGAAGTGATTATCAGTATGCTGTTCATATAGCCTCGTATTAGTAATGTGTTATATATGATATAGTTGATAATTTTAATCTTGGGTGTTCTTAAAg                                                                 <  2:846840/99‑1 (MQ=11)
             ggAGCGAAGTGATTATCAGTATGCTGTTCATATAGCCTCGAATTAGTAATGTGTTATATATGATATAGTTGACAATTTTTATCTTGGGTGTTCTTAAAGt                                                                >  2:1489529/1‑100 (MQ=17)
              gAGCGAAGTGATTATCAGTATGCTGTTCATATAGCCTCGAATTAGTAATGTGTTATATATGATATAGTTGACAATTTTTATCTTGGGTGTTCTTAAAGtt                                                               <  2:499017/100‑1 (MQ=14)
               agttaaGTGATTATCAGTATGCTGTTCATATAGCCTCGAATTAGTATGGTGTTATATATAATATAGTTGACCATTTTTATCCTGGGTGTTCTTAACGtt                                                               <  2:1550423/95‑1 (MQ=11)
               aGCGAAGTGATTATCAGTATGCTGTTCATATAGCCTCGAATTAGTAATGTGTTATATATGATATAGTTGACAATTTTTATCTTGGGTGTTCTTAAAGTTc                                                              >  2:2221760/1‑100 (MQ=17)
                 cGAAGTGATTATCAGTATGCTGTTCATATAGCCTCGAATTAGTAATGTGTTATATATGATATAGTTGACAATTTTTATCTTGGGTGTTCTTAAAGTTCGt                                                            >  2:617816/1‑100 (MQ=1)
                                                                           atatAGTTGACAATTTTTATCCTGGGTGTTCTCAAAGTTCGTAGATAAACATTGTCGTTTCAGGTATACAGGAATGCTAACAGGTGGCGGCAAAAATCAg  <  1:2317881/100‑1 (MQ=38)
                                                                                                |                                                                              
CTGAATATGATAAGGAGCGAAGTGATTATCAGTATGCTGTTCATATAGCCTCGAATTAGTAATGTGTTATATATGATATAGTTGACAATTTTTATCCTGGGTGTTCTTAAAGTTCGTAGATAAACATTGTCGTTTCAGGTATACAGGAATGCTAACAGGTGGCGGCAAAAATCAG  >  NC_000913/1434363‑1434537

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 22 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: