| Predicted mutation | |||||||
|---|---|---|---|---|---|---|---|
| evidence | seq id | position | mutation | freq | annotation | gene | description |
| RA | NC_002947 | 4,316,702 | C→T | 23.5% | H247H (CAC→CAT) | PP_3788 → | non‑ribosomal peptide synthetase |
| Read alignment evidence... | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
| * | NC_002947 | 4,316,702 | 0 | C | T | 23.5% | 24.6 / 5.2 | 17 | H247H (CAC→CAT) | PP_3788 | non‑ribosomal peptide synthetase |
| Reads supporting (aligned to +/- strand): ref base C (7/6); new base T (2/2); total (9/8) | |||||||||||
| Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
| Kolmogorov-Smirnov test that lower quality scores support variant p-value = 8.65e-01 | |||||||||||
AAACCCAGGCCTCGTTCGACCCCTCGATCCAGGAGGCCGTGCTGCCTTTTTTTTCCGCCGGCGCCGTGTTCGTGCCTGACCACAACCGAGTCAACTTTCCCAATTACCTGTCGGCCTGCATCGCTGAGCACGGTGTCACCATGCTCATCATGGTACCCAGCCACCTGCAGCATCTTCTCGCCAGCCCGGCAATCAATGCCTGCCAGCACCTCAGGCATATCGTTTGCTGCGGAGAACCTTGGGGAGTTGAGTTGATCAGTGCGC > NC_002947/4316572‑4316835 | aaaCCCAGGCCTCGTTCGACCCCTCGATCCAGGAGGCCGTGCTGCCTTTTTTTTCCGCCGGCGCCGTGTTCGTGCCTGACCACAACCGAGTCAACTTTCCCAATTACCTGTCGGCCTGCATCGCTGAGCACGGTGTCACCATGCtcatca > 1:151645/1‑150 (MQ=255) cAGGCCTCGTTCGACCCCTCGATCCAGGAGGCCGTGCTGCCTTTTTTTTCCGCCGGCGCCGTGTTCGTGCCTGACCACAACCGAGTCAACTTTCCCAATTACCTGTCGGCCTGCATCGCTGAGCACGGTGTCACCATGCTCATCATGGTa < 1:23165/150‑1 (MQ=255) aGGCCTCGTTCGACCCCTCGATCCAGGAGGCCGTGCTGCCTTTTTTTTCCGCCGGCGCCGTGTTCGTGCCTGACCACAACCGAGTCAACTTTCCCAATTACCTGTCGGACTCAATCGCTCAGCACGGTGTCACCATGCTCATCATGGTAc > 1:26574/1‑150 (MQ=255) cTCGATCCAGGAGGCCGTGCTGCCTTTTTTTTCCGCCGGCGCCGTGTTCGTGCCTGACCACAACCGAGTCAACTTTCCCAATTACCTGTCGGCCTGCATCGCTGAGCACGGTGTCACCATGCTCATCATGGTACCCAGCCACCTgcagca > 1:7516/1‑150 (MQ=255) tttCCGCCGGCGCCGGGTCCGTGCCTGAACACAACCAAGTCAACGTTCCCACTTACCTGTCGGCCTGCATCGCTGAGCACGGTGTCACCATGCTCATCATGGTACCCAGCCACCTGCAGCATCTTCTCGCCAGCCCGGCAATCAAtgccg < 1:198632/150‑2 (MQ=255) gcCGTGTTCGTGCCTGACCACAACCGAGTCAACTTTCCCAATTACCTGTCGGCCTGCATCGCTGAGCATGGTGACAcc < 1:245508/78‑1 (MQ=255) gcCGTGTTCGTGCCTGACCACAACCGAGTCAACTTTCCCAATTACCTGTCGGCCTGCATCGCTGAGCATGGTGACAcc > 2:245508/1‑78 (MQ=255) gTGCCTGACCACAACCGAGTCAACTTTCCCAATTACCTGTCGGCCTGCATCGCTGAGCACGGTGTCACCATGCTCATCATGGTACCCAGCCACCTGCAGCATCTTCTCGCCAGCCCGGCAATCAATGCCTGCCAGCACCTCAGGCATATc > 1:60380/1‑150 (MQ=255) ccTGACCACAACCGAGTCAACTTTCCCAATTACCTGTCGGCCTGCATCGCTGAGCACGGTGTCACCATGCTCATCATGGTACCCAGCAACCTGCAGCATCTTCTCGCCAGCCCGGCAATCAATGCCTGCCAGCCCCTCAGGCATATCGtt < 2:151645/150‑1 (MQ=255) tGACCACAACCGAGTCAACTTTCCCAATTACCTGTCGGCCTGCATCGCTGAGCACGGTGTCACCATGCTCATCATGGTACCCAGCCACCTGCAGCATCTTCTCGCCAGCCCGGCAATCAATGCCTGCCAGCACCTCAGGCATATCGTTtg < 2:7516/150‑1 (MQ=255) cacaACCGAGTCAACTTTCCCAATTACCTGTCGGCCTGCATCGCTGAGCATGGTGTCACCATGCTCATCATg < 1:45705/72‑1 (MQ=255) cacaACCGAGTCAACTTTCCCAATTACCTGTCGGCCTGCATCGCTGAGCATGGTGTCACCATGCTCATCATg > 2:45705/1‑72 (MQ=255) acaACCGAGTCAACTTTCCCAATTACCTGTCGGCCTGCATCGCTGAGCACGGTGTCACCATGCTCATCATGGTACCCAGCCACCTGCAGCATCTTCTCGCCAGCCCGGCAATCAATGCCTGCCAGCACCTCAGGCATATCGTTTGCTGCg > 1:502472/1‑150 (MQ=255) aCTTTCCCAATTACCTGTCGGCCTGCATCGCTGAGCACGGTGTCACCATGCTCATCATGGTACCCAGCCACCTGCAGCATCTTCTCGCCAGCCCGGCAATCAATGCCTGCCAGCACCTCAGGCATATCGTTTGCTGCGGAGAACCTTggg < 2:60380/150‑1 (MQ=255) tCCCAATTACCTGTCGGCCTGCATCGCTGAGCACGGTGTCACCATGCTCATCATGGTACCCAGCCACCTGCAGCATCTTCTCGCCAGCCCGGCAATCAAtgcct > 1:435283/1‑104 (MQ=255) tCCCAATTACCTGTCGGCCTGCATCGCTGAGCACGGTGTCACCATGCTCATCATGGTACCCAGCCACCTGCAGCATCTTCTCGCCAGCCCGGCAATCAAtgcct < 2:435283/104‑1 (MQ=255) ccTGCATCGCTGAGCACGGTGTCACCATGCTCATCATGGTACCCAGCCACCTGCAGCATCTTCTCGCCAGCCCGGCAATCAATGCCTGCCAGCACCTCAGGCATATCGTTTGCTGCGGAGAACCTTGGGGAGTTGAGTTGATCAGTgcgc > 1:234664/1‑150 (MQ=255) | AAACCCAGGCCTCGTTCGACCCCTCGATCCAGGAGGCCGTGCTGCCTTTTTTTTCCGCCGGCGCCGTGTTCGTGCCTGACCACAACCGAGTCAACTTTCCCAATTACCTGTCGGCCTGCATCGCTGAGCACGGTGTCACCATGCTCATCATGGTACCCAGCCACCTGCAGCATCTTCTCGCCAGCCCGGCAATCAATGCCTGCCAGCACCTCAGGCATATCGTTTGCTGCGGAGAACCTTGGGGAGTTGAGTTGATCAGTGCGC > NC_002947/4316572‑4316835 |
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 22 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |