| Predicted mutation | |||||||
|---|---|---|---|---|---|---|---|
| evidence | seq id | position | mutation | freq | annotation | gene | description |
| RA | NC_002947 | 3,212,321 | A→T | 13.8% | *189R (TGA→AGA) ‡ | PP_2816 ← | transcriptional regulator NfxB |
| Read alignment evidence... | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
| * | NC_002947 | 3,212,321 | 0 | A | T | 13.8% | 77.0 / 5.8 | 29 | *189R (TGA→AGA) ‡ | PP_2816 | transcriptional regulator NfxB |
| Reads supporting (aligned to +/- strand): ref base A (13/12); new base T (2/2); total (15/14) | |||||||||||
| Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
| Kolmogorov-Smirnov test that lower quality scores support variant p-value = 5.82e-01 | |||||||||||
TCCCGCTTGCCGACCATCGCATCCAGATCGCCGCTGCCCTTGAGCTGGTGATCTGGAGCACGCCGCTCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATAGGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGCTCTCCAGCACCGTTGCACACTCTCTTGGCGCGCGCCCCCGTTGGCGGGCGTCGACCATGCCATGCAACAGCGATACGAACATCTCGGTCAGCAACG > NC_002947/3212175‑3212455 | tCCCGCTTGCCGACCATCGCATCCAGATCGCCGCTGCCCTTGAGCTGGTGATCTGGAGCACGCCGCTCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATa < 2:233867/150‑1 (MQ=255) ccGCTTGCCGACCATCGCATCCAGATCGCCGCTGCCCTTGAGCTGGTGATCTGGAGCACGCCGCTCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATAgg < 1:442185/150‑1 (MQ=255) aCCATCGCATCCAGATCGCCGCTGCCCTTGAGCTGGTGATCTGGAGCACGCCGCTCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCCCTATTGAGCGCCcgcgc > 2:669902/1‑149 (MQ=255) ccATCGCATCCAGATCGCCGCTGCCCTTGAGCTGGTGATCTGGAGCACGCCGCTCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCCCTATTGAGCGCCcgcgca < 1:669902/150‑3 (MQ=255) gCATCCAGATCGCCGCTGCCCTTGAGCTGGTGATCTGGAGCACGCCGCTCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCCCAATAGGGCGCCCGCGTGGCAAt < 1:369392/150‑1 (MQ=255) cAGATCGCCGCTGCCCTTGAGCTGGTGATCTGGAGCACGCCGCTCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTACGCGGGCGCCCTATTGAGCGCCcgcgcag > 1:204937/1‑138 (MQ=255) cAGATCGCCGCTGCCCTTGAGCTGGTGATCTGGAGCACGCCGCTCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTACGCGGGCGCCCTATTGAGCGCCcgcgcag < 2:204937/141‑4 (MQ=255) aGATCGCCGCTGCCCTTGAGCTGGTGATCTGGAGCACGCCGCTCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATAGGGCGCCCGCGTGGCAATGCCCTg < 1:35949/150‑1 (MQ=255) cTTGAGCTGGTGATCTGGAGCACGCCGCTCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATAGGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGctct > 1:167137/1‑150 (MQ=255) ttGAGCTGGTGATCTGGAGCACGCCGCTCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATAGGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGCtctc > 1:98692/1‑150 (MQ=255) ggTGATCTGGAGCACGCCGCTCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATAg > 2:82489/1‑105 (MQ=255) ggTGATCTGGAGCACGCCGCTCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATAg < 1:82489/105‑1 (MQ=255) gATCTGGAGCACGCCGCTCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATAGGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGCTCTCCAGCACCGtt < 2:80663/150‑1 (MQ=255) tCTGGAGCACGCCGCTCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATATGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGCTCTCCAGCACCGTTGc > 2:60713/1‑150 (MQ=255) gAGCACGCCGCTCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATAGGgc > 2:404729/1‑99 (MQ=255) gAGCACGCCGCTCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATAGGgc < 1:404729/99‑1 (MQ=255) tCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATAGGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGCTCTCCAGCACCGTTGCACACTCTCTTGgcgc < 2:98692/150‑1 (MQ=255) gATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATAGGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGct < 1:672070/118‑1 (MQ=255) gATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATAGGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGct > 2:672070/1‑118 (MQ=255) aaTAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATGGGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGCTCTCCAGCACCGTTGCACACTCTCTTGGCGCGCGCCCCCGTTggcg > 1:308913/1‑150 (MQ=255) ccttTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATAGGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGCTCTCCAGCACCGTTGCACACTCTCTTGGCGCGCGCCCCCGTTGGCGGGCGTCGAccatgccatg > 2:702953/1‑150 (MQ=255) gTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATAGGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGCTCTCCAGCACCGTTGCACACTCTCTTGGCGCGCGCCCCCGTTGGCGGGCGTCGACCATGCCATGCAACAGCGATACGaa < 2:456090/150‑1 (MQ=255) ttCACGGCTGTTGCCCTGCGCGGGCGCTCAATAGGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGCTCTCCAGCACCGTTGCACACTCTCTTGGCGCGCGCCCCCGTTGGCGGGCGTCGACCATGCCATGCAACAGCGATACGAACAt > 2:452403/1‑150 (MQ=255) aCGGCTGTTGCCCTGCGCGGGCGCTCAATAGGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGCTCTCCAGCa < 2:390522/74‑1 (MQ=255) aCGGCTGTTGCCCTGCGCGGGCGCTCAATAGGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGCTCTCCAGCa > 1:390522/1‑74 (MQ=255) cccTGCGCGGGCGCTCAATAGGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGCTCTCCAGCACCGTTGCACACTCTCTTGGCGCGCGCCCCCGTTGGCGGGCGTCGACCATGCCATGCAACAGCGATACGAACATCTCGGTCAGCAAc > 1:672739/1‑150 (MQ=255) ccTGCGCGGGCGCTCAATAGGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGCTCTCCAGCACCGTTGCACACTCTCTTGGCGCGCGCCCCCGTTGGCGGGCGTCGACCATGCCATGCAACAGCGATACGAACATCTCGGTCAGCAAcg > 2:469141/1‑150 (MQ=255) tCAATAGGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGCTCTCCAGCACCGTTGCACACTCTCTTGGCGCGCGCCCCCGTTGGCGGGCGTCGACcatgccatgc > 2:634693/1‑106 (MQ=255) tCAATAGGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGCTCTCCAGCACCGTTGCACACTCTCTTGGCGCGCGCCCCCGTTGGCGGGCGTCGACcatgccatgc < 1:634693/106‑1 (MQ=255) | TCCCGCTTGCCGACCATCGCATCCAGATCGCCGCTGCCCTTGAGCTGGTGATCTGGAGCACGCCGCTCGATGACGCCGAGCAATAGCGTTCATTCCCTTCCTTTGACGCAATAGGTCTTCACGGCTGTTGCCCTGCGCGGGCGCTCAATAGGGCGCCCGCGTGGCAATGCCCTGTAGAAACGCGCTCTCCAGCACCGTTGCACACTCTCTTGGCGCGCGCCCCCGTTGGCGGGCGTCGACCATGCCATGCAACAGCGATACGAACATCTCGGTCAGCAACG > NC_002947/3212175‑3212455 |
| 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: ‑ |