Predicted mutation
evidence seq id position mutation freq annotation gene description
RA NC_000913 3,427,068 Δ1 bp 100% intergenic (‑35/+8) alaU ← / ← ileU tRNA‑Ala/tRNA‑Ile

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009133,427,0680T.60.0% ‑6.5 / 4.8 5intergenic (‑35/+8)alaU/ileUtRNA‑Ala/tRNA‑Ile
Reads supporting (aligned to +/- strand):  ref base T (0/0);  major base . (0/3);  minor base G (0/2);  total (0/5)
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

CGAACCGCAGACCTCCTGCGTGCAAAGCAGGCGCTCTCCCAGCTGAGCTATAGCCCCATAACATGTAGTTAAAACCTCTTCAAATTTGCCGTGCAAATTTGGTAG  >  NC_000913/3426977‑3427081
                                                                                            |             
cGAACCGCAGACCTCCTGCGTGCAAAGCAGGCGCTCTCCCAGCTGAGCTATAGCCCCATAACATGTAGTTAAAACCTCTTCAAATTTGCACGGCAAAttt       <  1:3341829/100‑1 (MQ=1)
cGAACCGCAGACCTCCTGCGTGCAAAGCAGGCGCTCTCCCAGCTGAGCTATAGCCCCATAACATGTAGTTAAAACCTCTTCAAATTTGCACGGCAAAttt       <  2:1635714/100‑1 (MQ=1)
cGAACCGCAGACCTCCTGCGTGCAAAGCAGGCGCTCTCCCAGCTGAGCTATAGCCCCATAACATGTAGTTAAAACCTCTTCAAATTTGCACGGCAAAttt       <  2:4004250/100‑1 (MQ=1)
  agcctcAGACCTCTTGCGGGCAAAGCAGGCGCTCTCCCAGCTGAGCTATAGACGCATAACATGTAGTTAAAACCTCTTCAAATTTGCACGGCAAATTTg      <  1:220575/94‑1 (MQ=1)
     cggaGACGTGCTGCGTGCAAAGCAGGCGCTCTCCCAGCTGAGCTAGAGCCCCATAACATGTAGTTAAAACCTCGTCAAATTTGCACGGCAAATTTgaaga  <  1:1837425/97‑5 (MQ=1)
                                                                                            |             
CGAACCGCAGACCTCCTGCGTGCAAAGCAGGCGCTCTCCCAGCTGAGCTATAGCCCCATAACATGTAGTTAAAACCTCTTCAAATTTGCCGTGCAAATTTGGTAG  >  NC_000913/3426977‑3427081

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 22 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: