Predicted mutation
evidence seq id position mutation freq annotation gene description
RA NC_002947 5,605,111 T→A 30.8% E115V (GAA→GTA)  PP_4924 ← subtilase family serine protease

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0029475,605,1110TA30.8% 11.5 / 5.9 13E115V (GAA→GTA) PP_4924subtilase family serine protease
Reads supporting (aligned to +/- strand):  ref base T (5/4);  new base A (2/2);  total (7/6)
Fisher's exact test for biased strand distribution p-value = 1.00e+00
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 8.11e-01

TGTAAATTCATCCGTTAGATTCCCCGCTGAGGAAAGCACATGCCGCCAGTAGTCCTCTCGATTTTCGACAGCAATCACATCAAACACCGGACTCAACGTCCATGCCCTCTCAGGATATTCAAGGCTTTCGAAAGTTTCCTTATGAAATGCCGCGACCTCTTTTTGGCTTACCTGACCGACAATAGGACCTTTACTAATCTTCTTTAGCAACACCTCCATATATTTATTTGCCATTTCAACCCTCACC  >  NC_002947/5604984‑5605230
                                                                                                                               |                                                                                                                       
tgtAAATTCATCCGTTAGATTCCCCGCTGAGGAAAGCACATGCCGCCAGTAGTCCTCTCGATTTTCGACAGCAATCACATCAAACACCGGACTCAACGTCCATGCCCTCTCAGGATATTCAAGGCTTTCGAAAGtt                                                                                                                 >  2:299023/1‑136 (MQ=255)
                                            gccAGTAGTCCTCTCGATTTTCGACAGCAATCACATCAAACACCGGACTCAACGTCCATGCCCTCTCAGGATATTCAAGGCTTTCGAAAGTTTCCTTATGAAATGCCGCGACCTCTTTTTTGCTTACCTGACCGAc                                                                     <  1:299023/136‑1 (MQ=255)
                                                 tagtCCTCTCGATTTTCGACAGCAATCACATCAAACACCGGACTCAACGTCCATGCCCTCTCAGGATATTCAAGGCTTTCGAAAGTTTCCTTATGAAATGCCGCGACCTCTTTTTGGCTTACCTGACAGACAATAg                                                                >  2:481160/1‑136 (MQ=255)
                                                                   aCAGCAATCACATCAAACACCGGACTCAACGTCCATGCCCTCTCAGGATATTCAAGGCTTACGAAAGTTTCCTTATGAAATGCCGCGACCTCTTTTTGGCTTACCTGACCGACAATAGGACCTTTACTAAtcttct                                              >  1:298461/1‑136 (MQ=255)
                                                                   aCAGCAATCACATCAAACACCGGACTCAACGTCCATGCCCTCTCAGGATATTCAAGGCTTACGAAAGTTTCCTTATGAAATGCCGCGACCTCTTTTTGGCTTACCTGACCGACAATAGGACCTTTACTAAtcttct                                              >  1:300329/1‑136 (MQ=255)
                                                                          tCACATCAAACACCGGACTCAACGTCCATGCCCTCTCAGGATATTCAAGGCTTACGAAAGTTTCCTTATGAAATGCCGCGACCTCTTTTTGGCTTACCTGACCGACAATAGGACCTTTACTAATCTTCTTTAGCaa                                       <  2:298461/136‑1 (MQ=255)
                                                                          tCACATCAAACACCGGACTCAACGTCCATGCCCTCTCAGGATATTCAAGGCTTACGAAAGTTTCCTTATGAAATGCCGCGACCTCTTTTTGGCTTACCTGACCGACAATAGGACCTTTACTAATCTTCTTTAGCaa                                       <  2:300329/136‑1 (MQ=255)
                                                                                           cTCAACGTCCATGCCCTCTCAGGATATTCAAGGCTTTCGAAAGTTTCCTTATGAAATGCCGCGACCTCTTTTTGGCTTACCTGACCGACAATAg                                                                <  1:305642/94‑1 (MQ=255)
                                                                                           cTCAACGTCCATGCCCTCTCAGGATATTCAAGGCTTTCGAAAGTTTCCTTATGAAATGCCGCGACCTCTTTTTGGCTTACCTGACCGACAATAg                                                                >  2:305642/1‑94 (MQ=255)
                                                                                                         ccTCTCAGGATATTCAAGGCTTTCGAAAGTTTCCTTATGAAATGCCGCGACCTCTTTTTGGCTTACCTGACCGACAATAGGACCTTTACTAATCTTCTTTAGCAACACCTCCATATATTTATTTGCCATTTCAAcc        <  2:426057/136‑1 (MQ=255)
                                                                                                               aGGATATTCAAGGCTTTCGAAAGTTTCCTTATGAAATGCCGCGACCTCTTTTTGGCTTACCTGACCGACAATAGGACCTTTACTAATCTTCTTTAGCAACACCTCCATATATTTATTTGCCATTTCaa          >  1:425899/1‑128 (MQ=255)
                                                                                                               aGGATATTCAAGGCTTTCGAAAGTTTCCTTATGAAATGCCGCGACCTCTTTTTGGCTTACCTGACCGACAATAGGACCTTTACTAATCTTCTTTAGCAACACCTCCATATATTTATTTGCCATTTCaa          <  2:425899/128‑1 (MQ=255)
                                                                                                               aGGATATTCAAGGCTTTCGAAAGTTTCCTTATGAAATGCCGCGACCTCTTTTTGGCTTACCTGACCGACAATAGGACCTTTACTAATCTTCTTTAGCAACACCTCCATATATTTATTTGCCATTTCAACCCTCAcc  >  1:57401/1‑136 (MQ=255)
                                                                                                                               |                                                                                                                       
TGTAAATTCATCCGTTAGATTCCCCGCTGAGGAAAGCACATGCCGCCAGTAGTCCTCTCGATTTTCGACAGCAATCACATCAAACACCGGACTCAACGTCCATGCCCTCTCAGGATATTCAAGGCTTTCGAAAGTTTCCTTATGAAATGCCGCGACCTCTTTTTGGCTTACCTGACCGACAATAGGACCTTTACTAATCTTCTTTAGCAACACCTCCATATATTTATTTGCCATTTCAACCCTCACC  >  NC_002947/5604984‑5605230

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: