Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 3,919,455 C→T G135S (GGC→AGC)  atpA ← ATP synthase F1 complex subunit alpha

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009133,919,4550CT85.7% 10.6 / ‑5.3 7G135S (GGC→AGC) atpAATP synthase F1 complex subunit alpha
Reads supporting (aligned to +/- strand):  ref base C (0/1);  new base T (5/1);  total (5/2)
Fisher's exact test for biased strand distribution p-value = 2.86e-01
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 1.00e+00

CCACGTTAGAAATGGTGGACGCTTTCTGGCCGATAGCGACATAGATACATTTGATACCGGAATCGCGCTGGTTGATGATGGCATCGATAGCCAGTGCGGTTTTACCTGTCTGACGGTCACCGATGATCAATTCACGCTGACCACGACCGATTGGGATCATGGAGTCAACGGCTTTATAACCGGTCTGTACCGGCTGATCTACGGACTGACGTTCGATAACGCCCGGAGCGATTGCTTCTACAGCAGAGAAGCCGTCGTGATCCAGCGGACCTTTACCGTCGATTGGTGCACCCAGAGTGTTAACCACACGGCCCAGCAGGCCACGGCCAACCGGAACTTCCAGGATACGGCCAGTACACTTAACTTTCATGCCTTCGGCAAGGTCAGCGTACGGACCCATAACAACCGCACCTACAGAGTCGCGCTCGAGGTTCAGTGC  >  NC_000913/3919233‑3919671
                                                                                                                                                                                                                              |                                                                                                                                                                                                                        
ccACGTTAGAAATGGTGGACGCTTTCTGGCCGATAGCGACATAGATACATTTGATACCGGAATCGCGATGGTTGATGATGGCATCGATAGCCCGTGCGGTTTTACCTGTCTGACGGTCACCGATGATCAATTCACGCTGACCACGACCGATTGGGATCATGGAGTCAACGGCTTTATAACCGGTCTGTACCGGCTGATCTACGGACTGACGTTCGATAACGCTCGGAGCGATTGCTTCt                                                                                                                                                                                                          >  1:115978/1‑239 (MQ=255)
                                                                  gcTGGTTGATGATGGCATCGATAGCCAGTGCGGTTTTACCTGTCTGACGGTCACCGATGATCAATTCACGCTGACCACGACCGATTGGGATCATGGAGTCAACGGCTTTATAACCGGTCTGTACCGGCTGATCTACGGACTGACGTTCGATAACGCTCGGAGCGATTGCTTCTACAGCAGAGAAGCCGTCGTGATCCAGCGGACCTTTACCGTCGATTGGTGCACCCAGAGTGTTAACCACACGGCCcagc                                                                                                                            >  1:54512/1‑251 (MQ=255)
                                                                                    cGATAGCCAGTGCGGTTTTACCTGTCTGACGGTCACCGATGATCAATTCACGCTGACCACGACCGATTGGGATCATGGAGTCAACGGCTTTATAACCGGTCTGTACCGGCTGATCTACGGACTGACGTTCGATAACGCTCGGAGCGATTGCTTCTACAGCAGAGAAGCCGTCGTGATCCAGCGGACCTTTACCGTCGATTGGTGCACCCAGAgtg                                                                                                                                              <  1:80818/215‑1 (MQ=255)
                                                                                                                               cAATTCACGCTGACCACGACCGATTGGGATCATGGAGTCAACGGCTTTATAACCGGTCTGTACCGGCTGATCTACGGACTGACGTTCGATAACGCTCGGAGCGAtt                                                                                                                                                                                                                >  1:62116/1‑106 (MQ=255)
                                                                                                                                                                     naaCGGCTTTATAACCGGTCTGTACCGGCTGATCTACGGACTGACGTTCGATAACGCTCGGAGCGCTTGCTTCTAca                                                                                                                                                                                                       >  1:31019/2‑77 (MQ=255)
                                                                                                                                                                       aNGGNTTTATNACCGNTCTGTACCGGCTGATNTACGGACTGACGTTCGATANNGNCCGGANCGAtt                                                                                                                                                                                                                <  2:62116/66‑1 (MQ=255)
                                                                                                                                                                                            aCCGGCTGATCTACGGACTGACGTTCGATAACGCTCGGAGCGATTGCTTCTACAGCGGAGAAGCAGTCGGGATCCAGCGGACCTTTACCGTCGATTGGTGCACCCAGAGTGTTAACCACAGGGCCCAGAAGGCCACGGCCAAACGGAACTTCCAGGAAACGCCCAGAACACTTAACTTTCATGCCTTCGGCAAGGTCAGCGTACGGACCCATAACAACCGCACCTACAGAGTCGCGCTCGAGGTTCAgagc  >  1:75384/1‑248 (MQ=255)
                                                                                                                                                                                                                              |                                                                                                                                                                                                                        
CCACGTTAGAAATGGTGGACGCTTTCTGGCCGATAGCGACATAGATACATTTGATACCGGAATCGCGCTGGTTGATGATGGCATCGATAGCCAGTGCGGTTTTACCTGTCTGACGGTCACCGATGATCAATTCACGCTGACCACGACCGATTGGGATCATGGAGTCAACGGCTTTATAACCGGTCTGTACCGGCTGATCTACGGACTGACGTTCGATAACGCCCGGAGCGATTGCTTCTACAGCAGAGAAGCCGTCGTGATCCAGCGGACCTTTACCGTCGATTGGTGCACCCAGAGTGTTAACCACACGGCCCAGCAGGCCACGGCCAACCGGAACTTCCAGGATACGGCCAGTACACTTAACTTTCATGCCTTCGGCAAGGTCAGCGTACGGACCCATAACAACCGCACCTACAGAGTCGCGCTCGAGGTTCAGTGC  >  NC_000913/3919233‑3919671

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 13 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: