| Predicted mutation | |||||||
|---|---|---|---|---|---|---|---|
| evidence | seq id | position | mutation | freq | annotation | gene | description |
| RA | NC_002947 | 4,241,017 | A→G | 31.3% | I242I (ATT→ATC) ‡ | PP_3718 ← | aminotransferase |
| Read alignment evidence... | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
| * | NC_002947 | 4,241,017 | 0 | A | G | 31.3% | 15.8 / 8.3 | 16 | I242I (ATT→ATC) ‡ | PP_3718 | aminotransferase |
| Reads supporting (aligned to +/- strand): ref base A (6/5); new base G (3/2); total (9/7) | |||||||||||
| Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
| Kolmogorov-Smirnov test that lower quality scores support variant p-value = 6.00e-01 | |||||||||||
GTGATGATGTCTGGGGTGACGCCAAACAGTTCCTCGCTGGCGAAGAAGGTGCCCAGGCGCCCGAACGAGGTCACCACTTCGTCGGCGACGAACAGGATGTCGTAGGTCTGGCACAGCTGCCACATGCGCTGGAAGTAGCCCTCGGGCGGAATGATCACCCCGCCCGAGCCCATGATCGGCTCGGCGAAGAATGCCGCCACGTTGTCGGCACCCAGCGAGAGGATCTTGTCCTCGAACTCGGCCACCAGGAAGTCGAGGAACTCCGCCTCGTCCATGTCGTCTGGCGCGCGG > NC_002947/4240868‑4241158 | gtgATGATGTCTGGGGTGACGCCAAACAGTTCCTCGCTGGCGAAGAAGGTGCCCAGGCGCCCGAACGAGGTCACCACTTCGTCGGCGACGAACAGGATGTCGTAGGTATGATGCAGCTGCCACATGCGCTGGAAGTAGCCCTCGGGCGGa > 1:468934/1‑150 (MQ=255) ccAAACAGTTCCTCGCTGGCGAAGAAGGTGCCCAGGCGCCCGAACGAGGTCACCACTTCGTCGGCGACGAACAGGATGTCGTAGGTCTGGCACAGCTGCCACATGCGCTGGAAGTAGCCCTCGGGCGGGGTGATCATTCCGCCCGAgg > 1:558911/1‑147 (MQ=255) ccAAACAGTTCCTCGCTGGCGAAGAAGGTGCCCAGGCGCCCGAACGAGGTCACCACTTCGTCGGCGACGAACAGGATGTCGTAGGTCTGGCACAGCTGCCACATGCGCTGGAAGTAGCCCTCGGGCGGGGTGATCATTCCGCCCGAgg < 2:558911/148‑2 (MQ=255) aGTTCCTCGCTGGCGAAGAAGGTGCCCAGGCGCCCGAACGAGGTCACCACTTCGTCGGCGACGAACAGGATGTCGTAGGTCTGGCACAGCTGCCACATGCGCTGGAAGTAGCCCTCGGGCGGAATGATCACCCCGCCCGAGCCCATGAtc < 2:417794/150‑1 (MQ=255) gaagaaGGTGCCCAGGCGCCAGAACGAGGACACCACTTCGTCGGCGACGAAGAGGATGTCGAAGATATAGGACAGCTGCAACATGCGCTGAAAGTAGCCCTCGGGTGGAATGATCATCCCGCCCGACCGCATGATTGGCTCGGTgatgaa > 2:66494/1‑150 (MQ=255) tCACCACTTCGTCGGCGACGAACAGGATGTCGTAGGTCTGGCACAGCTGCCACATGCGCTGGAAGTAGCCCTCGGGCGGAATGATCACCCCGCCCGAGCCCATGATCGGCTCGGCGAAGAATGCCGCCACGTTGTCGGCACCCAGCgaga > 1:158622/1‑150 (MQ=255) gtcgGCGACGAACAGGATGTCGTAGGTCTGGCACAGCTGCCACATGCGCTGGAAGTAGCCCTCGGGCGGAATGATCACCCCGCCCGAGCCCATGATCGGCTCGGCGAAGAATGCCGCCACGTTGTCGGCACCCAGCGAGAGGATCTTGTc < 2:190955/150‑1 (MQ=255) tGTCGTAGGTCTGGCACAGCTGCCACATGCGCTGGAAGTAGCCCTCGGGCGGAATGATCACCCCGCCCGAGCCCATGATCGGCTCGGCGAAGAATGCCGCCACGTTGTCGGCACCCAGCGAGAGGATCTTGTCCTCGAACTCGGccacca < 1:63713/150‑1 (MQ=255) tCTGGCACAGCTGCCACATGCGCTGGAAGTAGCCCTCGGGCGGAATGATCACCCCGCCCGAGCCCATGATCGGCTCGGCGAAGAATGCCGCCACGTTGTCGGCACCCAGCGAGAGGATCTTGTCCTCGAACTCGGCCACCAGGAAGTCGa > 1:480240/1‑150 (MQ=255) cacaGCTGCCACATGCGCTGGAAGTAGCCCTCGGGCGGGGTGATCATTCCGCCCGAg > 1:299372/1‑57 (MQ=18) cacaGCTGCCACATGCGCTGGAAGTAGCCCTCGGGCGGGGTGATCATTCCGCCCGAg < 2:299372/57‑1 (MQ=18) acaTGCGCTGGAAGTAGCCCTCGGGCGGAATGATCACCCCGCCCGAGCCCATGATCGGCTCGGCGAAGAATGCCGCCACGTTGTCGGCACCCAGCGAGAGGATCTTGTCCTCGAACTCGGCCACCAGGAAGTCGAGGAACTCCGCCTCGt > 1:302895/1‑150 (MQ=255) gAAGTAGCCCTCGGGCGGAATGATCACCCCGCCCGAGCCCATGATCGGCTCGGCGAAGAATGCCGCCACGTTGTCGGCACCCAGCGAGAGGATCTTGTCCTCGAACTCGGCCACCAGGAAGTCGAGGAACTCCGCCTCGTCCATgtcgtc < 2:158622/150‑1 (MQ=255) cccTCGGGCGGAATGATCACCCCGCCCGAGCCCATGATCGGCTCGGCGAAGAATGCCGCCACGTTGTCGGCACCCAGCGAGAGGATCTTGTCCTCGAACTCGGCCACCAGGAAGTCGAGGAACTCCGCCTCGTCCATGTCGTCTGgcgcg > 2:74197/1‑150 (MQ=255) gcTCGGGCGGGGTGATCATTCCGCCCGAGCCCATGATCGGCTCGGCGAAGAATGCCGCCACGTTGTCGGCACCCAGCGAGAGGATCTTGTCCTCGAACTCGGCCACCAGGAAGTCGAGGAACTCCGCCTCGTCCATGTCGTCTGgcgcgc > 2:309883/2‑150 (MQ=255) cTCGGGCGGAATGATCACCCCGCCCGAGCCCATGATCGGCTCGGCGAAGAATGCCGCCACGTTGTCGGCACCCAGCGAGAGGATCTTGTCCTCGAACTCGGCCACCAGGAAGTCGAGGAACTCCGCCTCGTCCATGTCGTCTGGcgcgcg > 1:263984/1‑150 (MQ=255) tCGGGCGGAATGATCACCCCGCCCGAGCCCATGATCGGCTCGGCGAAGAATGCCGCCACGTTGTCGGCACCCAGCGAGAGGATCTTGTCCTCGAACTCGGCCACCAGGAAGTCGAGGAACTCCGCCTCGTCCATGTCGTCTGGCGCGCgg < 1:74197/150‑1 (MQ=255) aaTGATCACCCCGCCCGAGCCCATGATCGGCTCGGCGAAGAATGCCGCCACGTTGTCGGCACCCAGCGAGAGGATCTTGTCCTCGACCTCGGc < 2:614884/93‑1 (MQ=255) aaTGATCACCCCGCCCGAGCCCATGATCGGCTCGGCGAAGAATGCCGCCACGTTGTCGGCACCCAGCGAGAGGATCTTGTCCTCGAACTCGGc > 1:614884/1‑93 (MQ=255) | GTGATGATGTCTGGGGTGACGCCAAACAGTTCCTCGCTGGCGAAGAAGGTGCCCAGGCGCCCGAACGAGGTCACCACTTCGTCGGCGACGAACAGGATGTCGTAGGTCTGGCACAGCTGCCACATGCGCTGGAAGTAGCCCTCGGGCGGAATGATCACCCCGCCCGAGCCCATGATCGGCTCGGCGAAGAATGCCGCCACGTTGTCGGCACCCAGCGAGAGGATCTTGTCCTCGAACTCGGCCACCAGGAAGTCGAGGAACTCCGCCTCGTCCATGTCGTCTGGCGCGCGG > NC_002947/4240868‑4241158 |
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |