| Predicted mutation | ||||||
|---|---|---|---|---|---|---|
| evidence | seq id | position | mutation | annotation | gene | description |
| RA | NC_000913 | 1,716,945 | G→A | T93I (ACC→ATC) | tyrS ← | tyrosine‑‑tRNA ligase |
| Read alignment evidence... | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
| * | NC_000913 | 1,716,945 | 0 | G | A | 91.7% | 24.1 / NA | 12 | T93I (ACC→ATC) | tyrS | tyrosine‑‑tRNA ligase |
| Reads supporting (aligned to +/- strand): ref base G (0/0); major base A (7/4); minor base C (1/0); total (8/4) | |||||||||||
| Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
| Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.85e-01 | |||||||||||
GAACGAAATCCCCTGATCTTCACGGTTGAGACGCTGCTTAACCGCTTCTTTGTTGATCATCTGGTTAACGGAGAAGTGTTTGCCAATATCGCGCAGGAAGGTCAGCACATTCATATTGCCGAACCAGTCATAGTTGTTCGCCGCGATAGCAGAGTTTTCTCCACAGTCGAAATCGAGGAACGGGGCAACCTGCTTACGGATTTTGTCCACCCACTCCTGAACAGTTTCTTCGGTGTTCAGCTTACGCTCGGCAGCTTTGAAGCTCGGGTCGCCAATCAGACCCGTCGCGCCGCCTACCAGCGCAACCGGCTTGTGGCCCGCCTGCTGGAAGCGTTTCAGGCATAACAATGGAACAAGATGCCCCAAATGCAAGCTGTCAGCGGTAGGATCGAAGCCGCAATAGAGCGCGATCGGGC > NC_000913/1716713‑1717128 | naaCGAAATCCCCTGATCTTCACGGTTGAGACGCTGCTTAACCGCTTCTTTGTTGATCATCTGGTTAACGGAGAAGTGTTTGCCAATATCGCGCAGGAAGGTCAGCACATTCATATTGCCGAACCAGTCATAGTTGTTCGCCGCGATAGCAGAGTTTTCTCCACAGTCGAAATCGAGGAACGGGGCAACCTGCTTACGGATTTTGTCCACCCACTCCTGAACAGTTTCTTCGATGTTCAGCTTACGCTCgg > 1:156921/2‑251 (MQ=255) cgcAGGAAGGTCAGCACATTCATATTGCCGAACCAGTCATAGTTGGTCGCCGCGATAGCAGAGTTTTCTCCACAGTCGAAATCGAGGAACGGGGCAACCTGCTTACGGATTTTGTCCACCCACTCCTGAACAGTTTCTTCGATGTTCAGCTTACGCACGGCAGCTTTGAAGCTCGTGTCGCCAATCAGTCCCGTCGCGCCGCCTACCAGCGCAACCGGCTTGTGGCCCGCCTGCTGGAAGCGTTTCAGGCa < 1:220837/251‑1 (MQ=255) ggAAGGTCAGCACATTCATATTGCCGAACCAGTCATAGTTGTTCGCCGCGATAGCAGAGTTTTCTCCACAGTCGAAATCGAGGAACGGGGCAACCTGCTTACGGATTTTGTCCACCCCCTCCTGAACAGTTTCTTCGATGTTCAGc > 1:131680/1‑146 (MQ=255) cacaTTCATATTGCCGAACCAGTCATAGTTGTTCGCCGCGATAGCAGAGTTTTCTCCACAGTCGAAATCGAGGAACGGGGCAACCTGCTTACGGATTTTGTCCACCCACTCCTGAACAGTTTCTTCGATGTTCAGCTTa > 1:82208/1‑139 (MQ=255) ncGAACCAGTCATAGTTGTTCGCCGCGATAGCAGAGTTTTCTCCACAGTCGAAATCGAGGAACGGGGCAACCTGCTTACGGATTTTGTCCACCCACTCCTGAACAGTTTCTTCGATGTTCAGCTTACGCTCg > 1:53222/2‑132 (MQ=255) gcgATAGCAGAGTTTTCTCCACAGTCGAAATCGAGGAACGGGGCAACCTGCTTACGGATTTTGTCCACCCACTCCTGAACAGTTTCTTCGATGTTCAGCTTACGCTCGGCAGCTTTGAAGCTCGGGTCGCCAATCAGACCCGTCGCGCCGCCTACCAGCGCAACCGGCTTGTGGCCCGc > 1:14437/1‑179 (MQ=255) nnnnnnnnnnacNNNNNACGNGGCAACCTGCTTTCGGATTTTGGCCCCCCCCTCCTGAACAGTTTCTTCGATGTTCAGCTTACGCTCGGCAGCTTTGAAGCTCGGGGCGCCAAACAGGCCCGTCGCGCCGCCTACCAACGCAACCGGCTTGTgg < 2:156921/143‑1 (MQ=255) aGTCGAAATCGAGGAACGGGGCAACCTGCTTACGGATTTTGTCCACCCACTCCTGAACAGTTTCTTCGATGTTCAGCTTACGCTCGGCAGCTTTAAAGCTCGGGTCGCCAAGCAGACCCGTCGCGCCGCCTACCAGCGCAACCGGCTTGTGGCCCGCCTGCTGGAAGCGGTTCAGGCATAACAATGGAACAAGATGCCCCAAATGCAAGCTGTCAGCGGTAGGATCGAAGCCGCAATAGAgcg < 1:249362/243‑1 (MQ=255) aaTCGAGGAACGGGGCAACCTGCTTACGGATTTTGTCCACCCACTCCTCAACAGCTTCTTCGCTGTTCAGCTTACGCTCGGCAGCTTTGAAGCTCGGGTCGCCAATCAGACCCGTCGCGCCGCCTACCAGCGCAACCGGCTTGTGGACCGCCTGCTGGAAGCGTTTCAGGCATAACAATGGACCAAGATGCCCCAAATGCAAGCTGTCAGCGGGAGGATCGAAGCCGCAATAGAGCGCGATCGGGc > 1:130818/1‑246 (MQ=255) gTCCANCCACCNCNNGACAGTTGCTTCGATGTTCNGCTTACGCTCGGCAGNTTTGNAGCTCngtnc > 2:98166/1‑63 (MQ=255) ccacccacTCCTGAACAGTTTCTTCGATGTTCAGCTTACGCTCGGCAGCTTTGAAGCTCGGGTCGCCAATCAGACCCGTCgcgc > 1:35026/1‑84 (MQ=255) cacccacTCCTGAACAGTTTCTTCGATGTTCAGCTTACGCTCGGCAGCTTTGAAGCTCGGGTCGCCAATCAGACCCGTCGCGCCGCCTACCAGCGCAACCGGCTTGTGGcc < 1:224217/111‑1 (MQ=255) | GAACGAAATCCCCTGATCTTCACGGTTGAGACGCTGCTTAACCGCTTCTTTGTTGATCATCTGGTTAACGGAGAAGTGTTTGCCAATATCGCGCAGGAAGGTCAGCACATTCATATTGCCGAACCAGTCATAGTTGTTCGCCGCGATAGCAGAGTTTTCTCCACAGTCGAAATCGAGGAACGGGGCAACCTGCTTACGGATTTTGTCCACCCACTCCTGAACAGTTTCTTCGGTGTTCAGCTTACGCTCGGCAGCTTTGAAGCTCGGGTCGCCAATCAGACCCGTCGCGCCGCCTACCAGCGCAACCGGCTTGTGGCCCGCCTGCTGGAAGCGTTTCAGGCATAACAATGGAACAAGATGCCCCAAATGCAAGCTGTCAGCGGTAGGATCGAAGCCGCAATAGAGCGCGATCGGGC > NC_000913/1716713‑1717128 |
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 13 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |