Predicted mutation
evidence seq id position mutation freq annotation gene description
RA W3110S.gb 2,058,034 C→T 100% G279G (GGC→GGT amn → AMP nucleosidase

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*W3110S.gb2,058,0340CT80.0% 38.7 / 6.0 20G279G (GGC→GGTamnAMP nucleosidase
Reads supporting (aligned to +/- strand):  ref base C (1/3);  new base T (10/6);  total (11/9)
Fisher's exact test for biased strand distribution p-value = 2.85e-01
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 6.70e-01
Rejected as polymorphism: Variant not supported by required number of reads on each strand.

TGGCATTTAATTACCGCCGATGGTCAGGGTATTACTCTGGTGAATATTGGCGTGGGACCGTCAAATGCTAAAACCATCTGCGATCATCTGGCAGTGCTACGCCCGGATGTCTGGTT  >  W3110S.gb/2057984‑2058099
                                                  |                                                                 
tGGCATTTAATTACCGCCGATGGTCAGGGTATTACTCTGGTGAATATTGGTGTGGGACCGTCAAATGCTa                                                >  1:1574302/1‑70 (MQ=255)
tGGCATTTAATTACCGCCGATGGTCAGGGTATTACTCTGGTGAATATTGGTGTGGGACCGTCAAATGATa                                                >  1:1159597/1‑70 (MQ=255)
      ttAATTACCGCCGATGGTCAGGGTATTACTCTGGTGAATATTGGTGTGGGACCGTCaaa                                                     <  1:358937/59‑1 (MQ=255)
       tAATTACCGCCGATGGTCAGGGTATTACTCTGGTGAATATTGGTGTGGGACCGTCAAATg                                                   >  1:664337/1‑60 (MQ=255)
       tAATTACCGCCGATGGTCAGGGTATTACTCTGGTGAATATTGGTGTGGGACCGTCAAATGCTAAAAcc                                           <  1:751867/68‑1 (MQ=255)
         aTTACCGCCGATGGTCAGGGTATTACTCTGGTGAATATTGGTGTGGGa                                                             >  1:181527/1‑48 (MQ=255)
                     ggTCAGGGTATTACTCTGGTGAATATTGGTGTGGGATCGTCAAATGCTAAAACCATCTGCGatcatc                              >  1:1821539/1‑67 (MQ=255)
                     ggTCAGGGTATTACTCTGGTGAATATTGGTGTGGGACCGTCAAATGCTAAAAcc                                           <  1:332519/54‑1 (MQ=255)
                      gTCAGGGTATTACTCTGGTGAATATTGGTGTGGGACCGTCAAATGCTAAAACCATCTGCGATCATCTGGc                          <  1:1458746/70‑1 (MQ=255)
                      gTCAGGGTATTACTCTGGTGAATATTGGTGTGGGACCGTCAAATGCTAAAACCATCTGCGATCATCTGGc                          <  1:619754/70‑1 (MQ=255)
                      gTCAGGGTATTACTCTGGTGAATATTGGTGTGGGACCGTCAAATGCTAAAACCATCTGCGATCATCTGGc                          <  1:744584/70‑1 (MQ=255)
                        cAGGGTATTACTCTGGTGAATATTGGCGTGGGACCGTCAAATGCTAAAACCATCTGCGATCATCTGGCAGt                       >  1:502294/1‑71 (MQ=255)
                                 aCTCTGGTGAATATTGGTGTGGGACCGTCAAATGCTAAAACCATCTGCGATCATCTGGCAGTGCTACGccc              >  1:1626494/1‑71 (MQ=255)
                                 aCTCTGGTGAATATTGGTGTGGGACCGTCAAATGCTAAAACCATCTGCGATCATCTGGCAGTGCTACGccc              >  1:1801527/1‑71 (MQ=255)
                                          aaTATTGGTGTGGGACCGTCAAATGCTAAAACCATCTGCGATCATCTGGCAGTGCTACGCCCGGATGTCTg     >  1:1325248/1‑71 (MQ=255)
                                          aaTATTGGTGTGGGACCGTCAAATGCTAAAACCATCTGCGATCATCTGGCAGTGCTACGCCCGGATGTCTg     >  1:1257564/1‑71 (MQ=255)
                                              ttGGTGTGGGACCGTCAAATGCTAAAACCATCTGCGATCATCTGGCAGTGCTACGCCCGGATGTCTGGtt  >  1:1794204/1‑70 (MQ=255)
                                              ttGGCGTGGGACCGTCAAATGCTAAAACCATCTGCGATCATCTgg                           <  1:1805154/45‑1 (MQ=255)
                                              ttGGCGTGGGACCGTCAAATGCTAAAACCATCTGCGATCATCTgg                           <  1:425974/45‑1 (MQ=255)
                                              ttGGCGTGGGACCGTCAAATGCTAAAACCATCTGCGATCATCTgg                           <  1:1006161/45‑1 (MQ=255)
                                                  |                                                                 
TGGCATTTAATTACCGCCGATGGTCAGGGTATTACTCTGGTGAATATTGGCGTGGGACCGTCAAATGCTAAAACCATCTGCGATCATCTGGCAGTGCTACGCCCGGATGTCTGGTT  >  W3110S.gb/2057984‑2058099

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