Predicted mutation
evidence seq id position mutation freq annotation gene description
RA minE 1,352,737 T→C 100% E259G (GAG→GGG)  thiM ← hydoxyethylthiazole kinase

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*minE1,352,7370TC97.5% 143.4 / ‑3.7 40E259G (GAG→GGG) thiMhydoxyethylthiazole kinase
Reads supporting (aligned to +/- strand):  ref base T (0/0);  major base C (0/39);  minor base A (0/1);  total (0/40)
Fisher's exact test for biased strand distribution p-value = 1.00e+00
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.55e-01
Rejected as polymorphism: E-value score below prediction cutoff.
Rejected as polymorphism: Frequency below/above cutoff threshold.
Rejected as polymorphism: Variant not supported by required number of reads on each strand.
Rejected as polymorphism: Polymorphic base substitution creates a homopolymer stretch.

AGCGTTAATTCGTTTCATGCCTGCACCTCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACAAA  >  minE/1352710‑1352780
                           |                                           
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCTTCAAGGAAATGTGGAACaaa  <  1:171741/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:561675/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:343983/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:398097/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:431827/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:476111/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:497217/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:506836/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:52485/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:550964/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:390088/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:627428/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:639909/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:641718/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:644015/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:65594/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:68615/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:9278/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:215457/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:120978/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:123097/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:129715/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:155079/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:164738/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:329500/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:240812/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:253520/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:266383/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:282500/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:288399/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:323092/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:324129/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATAAAGGAAATGTGGAACaaa  <  1:152647/71‑1 (MQ=255)
agCGTTAATTCGTTTCATGCCTGCACCACCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:395105/71‑1 (MQ=255)
 gCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:583276/70‑1 (MQ=255)
 gCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:197342/70‑1 (MQ=255)
 gCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:120862/70‑1 (MQ=255)
 gCGTTAATTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:380715/70‑1 (MQ=255)
       aTTCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:564879/64‑1 (MQ=255)
        ttCGTTTCATGCCTGCACCCCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACaaa  <  1:57720/63‑1 (MQ=255)
                           |                                           
AGCGTTAATTCGTTTCATGCCTGCACCTCCTGCGTCAATTGCCAGAGCGCATCAAGGAAATGTGGAACAAA  >  minE/1352710‑1352780

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 21 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: