Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,450,392 C→T A320T (GCA→ACA)  tynA ← tyramine oxidase, copper‑requiring

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,450,3920CT94.4% 49.1 / ‑6.1 18A320T (GCA→ACA) tynAtyramine oxidase, copper‑requiring
Reads supporting (aligned to +/- strand):  ref base C (0/0);  major base T (9/8);  minor base A (1/0);  total (10/8)
Fisher's exact test for biased strand distribution p-value = 1.00e+00
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 1.00e+00

CAGTTCCGCCAGTGAATCATATCGCCAGTAATGGTGTAATTTTTACCTTCAGGCTCAATGATTTGCATAGGCTTAACTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGCGGTCATTGGCACCGGAACTACCGGACCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGATGGGATGTGCCC  >  NC_000913/1450277‑1450490
                                                                                                                   |                                                                                                  
cAGTTCCGCCAGTGAATCATATCGCCAGTAATGGTGTAATTTTTACCTTCAGGCTCAATGATTTGCATAGGCTTAACTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGTGGTCATTGGCACCGGAACTACCg                                                                             >  2:792581/1‑139 (MQ=255)
       gCCAGTGAATCATATCGCCAGTAATAGTGTCATCTTTACCTCCAGGCGCAATGCCTTGGCTAGGCTCCACTGCCGGAGCAACACGGTCAGGGCCCTCAAAAGGGCGAGTGGTCGTTGGCACCGGAACTACCGGGCctta                                                                      >  1:269120/1‑138 (MQ=255)
                   tatCGCCAGTAATGGTGTAATTTTTACCTTCAGGCTCAATGATTTGCATAGGCTTAACTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGTGGTCATTGGCACCGGAACTACCGGACCTTCTTCAATCTTAAc                                                          >  2:721311/1‑139 (MQ=255)
                            tAATGGTGTAATTTTTACCTTCAGGCTCAATGATTTGCATAGGCTTAACTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGTGGTCATTGGCACCGGAACTACCGGACCTTCTTCAATCTTAACGAttttttt                                                 >  1:417531/1‑139 (MQ=255)
                                  tgtAATTTTTACCTTCAGGCTCAATGATTTGCATAGGCTTAACTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGTGGTCATTGGCACCGGAACTACCGGACCTTCTTCAATCTTAACGATTTTTTTCTGTTc                                           >  2:728505/1‑139 (MQ=255)
                                                     cTCAATGATTTGCATAGGCTTAACTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGTGGTCATTGGCACCGGAACTACCGGACCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGccacc                        <  2:526394/139‑1 (MQ=255)
                                                                gCATAGGCTTAACTGCCGGAGTAACGCGTTCACGGCCATCAGATGGGCGTGTGGTCATTGGCAACGGAACTACCGGACCTTCTTCTAGCTTAACGATTTTTTTCTGTTGTAAATCAACGACCGCCACCAGGTTTTCGAt             <  1:724734/139‑1 (MQ=255)
                                                                gCATAGGCTTAACTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGTGGTCATTGGCACCGGAACTACCGGACCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGAt             <  2:799919/139‑1 (MQ=255)
                                                                      gCTTAACTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGTGGTCATTGGCACCGGAACTACCGGACCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGATGGGAtg       <  2:417531/139‑1 (MQ=255)
                                                                      gCTTAACTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGTGGTCATTGGCACCGGAACTACCGGACCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGATGGGAtg       >  1:390067/1‑139 (MQ=255)
                                                                           aCTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGTGGTCATTGGCACCgg                                                                                     >  2:117721/1‑56 (MQ=255)
                                                                           aCTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGTGGTCATTGGCACCgg                                                                                     <  1:117721/56‑1 (MQ=255)
                                                                           aCTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGTGGTCATTGGCACCGGAACTACCGGACCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGATGGGATGTGacc  >  2:422046/1‑139 (MQ=255)
                                                                                cGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGTGGTCATTGGCAc                                                                                        <  2:336154/48‑1 (MQ=255)
                                                                                cGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGTGGTCATTGGCAc                                                                                        >  1:336154/1‑48 (MQ=255)
                                                                                cGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGTGGTCATTGGCACCGGAACTACCGGACCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGATGGGAt        >  1:734442/1‑128 (MQ=255)
                                                                                cGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGTGGTCATTGGCACCGGAACTACCGGACCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGATGGGAt        <  2:734442/128‑1 (MQ=255)
                                                                                                            gggCGTGTGGTCATTGGCACCGGAACTACCGGACCTTCTTCAATCtt                                                             <  2:524654/47‑1 (MQ=255)
                                                                                                            gggCGTGAGGTCATTGGCACCGGAACTACCGGACCTTCTTCAATCtt                                                             >  1:524654/1‑47 (MQ=255)
                                                                                                                   |                                                                                                  
CAGTTCCGCCAGTGAATCATATCGCCAGTAATGGTGTAATTTTTACCTTCAGGCTCAATGATTTGCATAGGCTTAACTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGCGGTCATTGGCACCGGAACTACCGGACCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGATGGGATGTGCCC  >  NC_000913/1450277‑1450490

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: