Predicted mutation
evidence seq id position mutation freq annotation gene description
RA NC_002947 2,226,841 T→C 50.0% Y586C (TAC→TGC)  PP_1963 ← hypothetical protein

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0029472,226,8410TC50.0% ‑6.5 / 7.1 8Y586C (TAC→TGC) PP_1963hypothetical protein
Reads supporting (aligned to +/- strand):  ref base T (2/2);  new base C (2/2);  total (4/4)
Fisher's exact test for biased strand distribution p-value = 1.00e+00
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 3.68e-01

AAATTTTACCTTCCCAGCGCAGGTCAGAGGACCGTGCACCTTCGCTTTCATTTTCCAGCTCATACTCAATATGAGCTAGACGCTCCATCAAATAGGGTAGTGAGTCTTCGTAAATTCGAACCTGGGAGCAGCCGATGCACTTGTCTATGCTGTAGCATTTCTTTCCATTAGGAACCGATTGCTCGAATCCCTTCCAGTCTGGTTGATACTGATTTTCGCATCCCCAGAGCGGGCCGGGATGACCA  >  NC_002947/2226731‑2226975
                                                                                                              |                                                                                                                                      
aaaTTTTACCTTCCCAGCGCAGGTCAGAGGACCGTGCACCTTCGCTTTCATTTTCCAGCTCATACTCAATATGAGCTAGACGCTCCATCAAATAGGGTAGTGAGTCTTCGTAAATTCGAACCTGGGAGCAGCCGAt                                                                                                               <  2:48267/136‑1 (MQ=255)
aaaTTTTACCTTCCCAGCGCAGGTCAGAGGACCGTGCACCTTCGCTTTCATTTTCCAGCTCATACTCAATATGAGCTAGACGCTCCATCAAATAGGGTAGTGAGTCTTCGTAAATTCGAACCTGGGAGCAGCCGAt                                                                                                               <  2:552583/136‑1 (MQ=255)
                                   gCACCTTCGCTTTCATTTTCCAGCTCATACTCAATATGAGCTAGACGCTCCATCAAATAGGGTAGTGAGTCTTCGTAAATTCGAACCTGGGAGCAGCCGATGCACTTGTCTATGCTGTAGCATTTCTTTCCATTat                                                                            >  1:95008/1‑135 (MQ=255)
                                            cTTTCATTTTCCAGCTCATACTCAATATGAGCTAGACGCTCCATCAAATAGGGTAGTGAGTCTTCGTAAATTCGAACCTGGGAGCAGCCGATGCACTTGTCTATGCTGTAGCATTTCTTTCCATTAGGAACCGAtt                                                                   >  1:64004/1‑136 (MQ=255)
                                                                                      aTCAAATAGGGTAGTGAGTCTTCGCAAATTCGAACCTGGGAGCAGCCGATGCACTTGTCTATGCTGTAGCAtttc                                                                                      <  1:90282/75‑1 (MQ=255)
                                                                                      aTCAAATAGGGTAGTGAGTCTTCGCAAATTCGAACCTGGGAGCAGCCGATGCACTTGTCTATGCTGTAGCAtttc                                                                                      <  1:92852/75‑1 (MQ=255)
                                                                                      aTCAAATAGGGTAGTGAGTCTTCGCAAATTCGAACCTGGGAGCAGCCGATGCACTTGTCTATGCTGTAGCAtttc                                                                                      >  2:90282/1‑75 (MQ=255)
                                                                                      aTCAAATAGGGTAGTGAGTCTTCGCAAATTCGAACCTGGGAGCAGCCGATGCACTTGTCTATGCTGTAGCAtttc                                                                                      >  2:92852/1‑75 (MQ=255)
                                                                                                             ttAAATTCGAACCTGGGAGCAGCCGATGCACTTGTCTATGCTGTAGCATTTCTTTCCATTAGGAACCGATTGCTCGAATCCCTTCCAGTCTGGTTGATACTGATTTTCGCATCCCCAGAGCGGGCCGGGATGACCa  <  1:76588/135‑1 (MQ=255)
                                                                                                              |                                                                                                                                      
AAATTTTACCTTCCCAGCGCAGGTCAGAGGACCGTGCACCTTCGCTTTCATTTTCCAGCTCATACTCAATATGAGCTAGACGCTCCATCAAATAGGGTAGTGAGTCTTCGTAAATTCGAACCTGGGAGCAGCCGATGCACTTGTCTATGCTGTAGCATTTCTTTCCATTAGGAACCGATTGCTCGAATCCCTTCCAGTCTGGTTGATACTGATTTTCGCATCCCCAGAGCGGGCCGGGATGACCA  >  NC_002947/2226731‑2226975

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: