| Predicted mutation | ||||||
|---|---|---|---|---|---|---|
| evidence | seq id | position | mutation | annotation | gene | description |
| RA | NC_000913 | 3,711,620 | G→A | P130S (CCG→TCG) | yhjX ← | putative transporter YhjX |
| Read alignment evidence... | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
| * | NC_000913 | 3,711,620 | 0 | G | A | 91.7% | 27.5 / ‑6.0 | 12 | P130S (CCG→TCG) | yhjX | putative transporter YhjX |
| Reads supporting (aligned to +/- strand): ref base G (1/0); new base A (5/6); total (6/6) | |||||||||||
| 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 | |||||||||||
GTGCGTCTTTCATTAACGTTGCGCCGAAAACAATCATCAACAGCGCAATCGCTCCCCAAATCACAAAGGTTTTTTCCAGACCGACCGTTTCCAGCAGCTGCGTGTCGATAAATTTGAAACCCAGGCTACCCAGACCATAAGAACCGATAGCGAACGCGGAGATCAGACCTTTACGCTCCGGGAACCACTTCACACAGTTAGAGAGCGTCAGCAGATAACCCGCGCCATCTGCCAGTCCCACCAGCACACCGGCGCTTAACCACAGCATCATCAGGTTGTCAGAATGCGCTGTCAGGAAGAAGCCTAATCCCAGCAAAATGCCGGAAGCCATGGTGACGCGTTTAACGCCAAAACGTTCCTGTAATTTGCCCGCAACAGAAGACGAAATTGCCAGCCCCAGACTTAAC > NC_000913/3711440‑3711846 | gTGCGTCTTTCATTAACGTTGCGCCGAAAACAATCATCAACAGCGCAATCGCTCCCCAAATCCCAAAGGTTTTTTCCAGACCGACCGTCTCCAGCAGCTGCGTGTCGATAAATTTGAAACCCAGGCTCCCCCGACCATAAGAACCGCTAGCGAACGCGGAGATCAGACCTTTACGCTCCGAGAACCACTTCACACAGTTag > 1:230892/1‑201 (MQ=255) aCAATCATCAACAGCGCAATCGCTCCCCAAATCACAAAGGTTTTTTCCAGACCGACCGTTTCCAGCAGCTGCGTGTCGATAAATTTGAAACCCAGGCTACCCAGACCATAAGAACCGATAGCGAACGCGGAGATCAGACCTTTACGCTCCGAGAAc < 1:298210/156‑1 (MQ=255) cAATCACTCCCCAAATCACAAAGGATTTTTCCAGACCGACCGTTTCCAGCCGGTGCGTGTCGCTAAATTTGAAACCCCGGCTACCCAGACCATCAGCACCGATAGCGAACGCGGAGATCAGACCTTTACGCTCCGGGAACCACCACACACAGTTAGAGAGCGTCAGCAGATAAccc > 1:56934/1‑176 (MQ=255) ccAAATCACAAAGGTTTTTTCCAGACCGACCGTTTCCAGCAGCTGCGTGTCGATAAATTTGAAACCCAGGCTACCCAGACCATAAGAACCGATAGCGAACGCGGAGATCAGACCTTTACGCTCCGAGAACCACTTCACACAGTTAGAGAGCGTCAGCGGAt > 1:132057/1‑161 (MQ=255) caagtCACAAAGGTTTTTTCCAGACCGACCGTTTCCAGCAGCTGCGTGTCGATAAATTTGAAACCCAGGCTACCCAGACCATAAGAACCGATAGCGAACGCGGAGATCAGACCTTTACGCTCCGAGAACCACTTCACACAGt < 1:11664/138‑1 (MQ=255) cTGCGTGTCGATAAATTTGAAACCCAGGCTACCCAGACCATAAGAACCGATAGCGAACGCGGAGATCAGACCTTTACGCTCCGAGAACCACTTCACACAGTTAGAGAGCGTCAGCAGATAACCCTCTCCATCTGc < 1:270883/135‑1 (MQ=255) cGATAAATTTGAAACC‑AGGCTACCCAGACCATAAGAACCGATAGCGAACGCGGAGATCAGACCTTTACGCTCCGAGAACCACTTCACACAGTTAGAGAGCGTCAGCAGATAACCCGCGCCATCTGCCAGTccc > 1:263236/1‑133 (MQ=255) aCCCAGGCTACCCAGACCATAAGAACCGATAGCGAACGCGGAGATCAGACCTTTACGCTCCGAGAACCACTTCACACAGTTAGAGAGCGTCAGCAGATAACCCGCGCCATCTGCCAGTCCCACCAGCACACCGGCGCGTAACCACAGCATCATCAGGTTGTCAGAATGCGCTGTCAGGAAGAAGCCTAATCCCAGCAAAATGCCGGAAGCCAGGGTGACGCGTTTAACGCCAAAACGTTCCTGTAATTTGc < 1:236496/251‑1 (MQ=255) ccATAAGAACCGATAGCGAACGCGGAGATCAGACCTTTACGCTCCGAGAACCACTTCACACAGTTAGAGAGCGTCAGCAGATAACCCGCGCCATCTGCCAGTCCCACCAGCACACCGGCGCTTAACCACAGCATCATCAGGTTGTCAGAATGCGCTGTCAGGAAGAAGCCTAATCCCAGCAAAATGCCGGAAGCCATGGTGACGCGTTTAACGCCAAAACGTTCCTGTAATTTGCCCGCAACAGAAGACg > 1:110741/1‑250 (MQ=255) aaNGCGGANATCANACCTTTACGCTCCGANAACCACTTCACACAGTTAGNNANCGTCANCGGAt < 2:132057/64‑1 (MQ=255) cgGAGATCAGACCTTTACGCTCCGAGAACCACTTCACACAGTTAGAGAGCGTCAGCAGATAACCCGCGCCATCTGCCAGTCCCACCAGCACACCGGCGCTTAACCACAGCATCATCAGGTTGTCAGAATGCGCTGTCAGGAAGAAGCCTAATCCCAGCAAAATGCCGGAAGCCATGGTGACGCGTTTAACGCCAAAACGTTCCTGTAATTTGCCCGCAACAGACGACGAACTTGCCAGCCCCAGACTTAAc > 1:238638/1‑251 (MQ=255) cTCCGAGAACCACTTCACACAGTGAGAGAGCGTCAGCAGATAACCCGCGCCATCTGCCAGTCCCACCAGCACCCCGGCGCTTAACCACAGCATCATCAGGTTGTCAGAATGCGCTGTCAGGAAGAAGCCTAATcc < 1:251572/135‑1 (MQ=255) | GTGCGTCTTTCATTAACGTTGCGCCGAAAACAATCATCAACAGCGCAATCGCTCCCCAAATCACAAAGGTTTTTTCCAGACCGACCGTTTCCAGCAGCTGCGTGTCGATAAATTTGAAACCCAGGCTACCCAGACCATAAGAACCGATAGCGAACGCGGAGATCAGACCTTTACGCTCCGGGAACCACTTCACACAGTTAGAGAGCGTCAGCAGATAACCCGCGCCATCTGCCAGTCCCACCAGCACACCGGCGCTTAACCACAGCATCATCAGGTTGTCAGAATGCGCTGTCAGGAAGAAGCCTAATCCCAGCAAAATGCCGGAAGCCATGGTGACGCGTTTAACGCCAAAACGTTCCTGTAATTTGCCCGCAACAGAAGACGAAATTGCCAGCCCCAGACTTAAC > NC_000913/3711440‑3711846 |
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 13 ≤ ATCG/ATCG < 16 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |