Predicted mutation
evidence seq id position mutation freq annotation gene description
RA minE 1,697,000 T→C 100% intergenic (+69/‑49) suhB → / → yfhR inositol monophosphatase/predicted peptidase

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*minE1,697,0000TC85.7% 46.2 / 1.7 21intergenic (+69/‑49)suhB/yfhRinositol monophosphatase/predicted peptidase
Reads supporting (aligned to +/- strand):  ref base T (3/0);  new base C (18/0);  total (21/0)
Fisher's exact test for biased strand distribution p-value = 1.00e+00
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 6.72e-01
Rejected as polymorphism: E-value score below prediction cutoff.
Rejected as polymorphism: Variant not supported by required number of reads on each strand.

TATCACTCACCCGCCCTCGCCTTTCAGGCGCTATTCCGAAATACTTCCTCACTGCTTTACTTTCTTT  >  minE/1696948‑1697014
                                                    |              
tatCACTCACCCGCCCTCGCCTTTCAGGCGCTATTCCGAAATACTTCCTCACTGCTTTActttcttt  >  1:2315388/1‑67 (MQ=255)
tatCACTCACCCGCCCTCGCCTTTCAGGCGCTATTCCGAAATACTTCCTCACTGCTTTActttcttt  >  1:1137045/1‑67 (MQ=255)
tatCACTCACCCGCCCTCGCCTTTCAGGCGCTATTCCGAAATACTTCCTCACTGCTTTActttcttt  >  1:2082047/1‑67 (MQ=255)
                    cTTTCAGGCGCTATTCCGAAATACTTCCTCACCGCttt           >  1:2159895/1‑38 (MQ=255)
                    cTTTCAGGCGCTATTCCGAAATACTTCCTCACCGCTTTa          >  1:2053752/1‑39 (MQ=255)
                    cTTTCAGGCGCTATTCCGAAATACTTCCTCACCGCTTTa          >  1:707820/1‑39 (MQ=255)
                    cTTTCAGGCGCTATTCCGAAATACTTCCTCACCGCTTTa          >  1:671273/1‑39 (MQ=255)
                    cTTTCAGGCGCTATTCCGAAATACTTCCTCACCGCTTTa          >  1:452919/1‑39 (MQ=255)
                    cTTTCAGGCGCTATTCCGAAATACTTCCTCACCGCTTTa          >  1:418604/1‑39 (MQ=255)
                    cTTTCAGGCGCTATTCCGAAATACTTCCTCACCGCTTTa          >  1:396285/1‑39 (MQ=255)
                    cTTTCAGGCGCTATTCCGAAATACTTCCTCACCGCTTTa          >  1:27633/1‑39 (MQ=255)
                    cTTTCAGGCGCTATTCCGAAATACTTCCTCACCGCTTTa          >  1:2314439/1‑39 (MQ=255)
                    cTTTCAGGCGCTATTCCGAAATACTTCCTCACCGCTTTa          >  1:1954234/1‑39 (MQ=255)
                    cTTTCAGGCGCTATTCCGAAATACTTCCTCACCGCTTTa          >  1:1855693/1‑39 (MQ=255)
                    cTTTCAGGCGCTATTCCGAAATACTTCCTCACCGCTTTa          >  1:1814932/1‑39 (MQ=255)
                    cTTTCAGGCGCTATTCCGAAATACTTCCTCACCGCTTTa          >  1:1807330/1‑39 (MQ=255)
                    cTTTCAGGCGCTATTCCGAAATACTTCCTCACCGCTTTa          >  1:1692772/1‑39 (MQ=255)
                    cTTTCAGGCGCTATTCCGAAATACTTCCTCACCGCTTTa          >  1:1663620/1‑39 (MQ=255)
                    cTTTCAGGCGCTATTCCGAAATACTTCCTCACCGCTTTa          >  1:1512074/1‑39 (MQ=255)
                    cTTTCAGGCGCTATTCCGAAATACTTCCTCACCGCTTTa          >  1:1191097/1‑39 (MQ=255)
                    cTTTCAGGCGCTATTCCGAAATACTTCCTCACCGCTTTa          >  1:1190934/1‑39 (MQ=255)
                                                    |              
TATCACTCACCCGCCCTCGCCTTTCAGGCGCTATTCCGAAATACTTCCTCACTGCTTTACTTTCTTT  >  minE/1696948‑1697014

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: