Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | CP009273 | 4,601,044 | C→A | 31.0% | intergenic (+224/‑169) | prfC → / → osmY | peptide chain release factor RF‑3/periplasmic protein |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | CP009273 | 4,601,044 | 0 | C | A | 31.0% | 24.1 / 17.1 | 26 | intergenic (+224/‑169) | prfC/osmY | peptide chain release factor RF‑3/periplasmic protein |
Reads supporting (aligned to +/- strand): ref base C (10/8); new base A (4/4); total (14/12) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 5.79e-01 |
ATTCACTTTTGCTTATGTTTTCGCTGATATCCCGAGCGGTTTCAAAATTGTGATCTATATTTAACAAAGTGATGACATTTCTGACGGCGTTAAATACCGTTCAATGCGTAGATATCAGTATCTAAAGCCGTCGATTGTCATTCTACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCATCACTCATCGCTTTTGTGATGGCGACCATTGACTTCTGTAGAGGGTGAAGTCTCTCCCTATTCAGCAATGCAACCTCGTGTTGCCAGGCTCAAA > CP009273/4600902‑4601184 | aTTCACTTTTGCTTATGTTTTCGCTGATATCCCGAGCGGTTTCAAAATTGTGATCTATATTTAACAAAGTGATGACATTTCTGACGGCGTTAAATACCGTTCAATGCGTAGATATCAGTATCTAAAGCCGTCGATTGTCATTc < 1:423229/143‑1 (MQ=255) tATGTTTTCGCTGATATCCCGAGCGGTTTCAAAATTGTGATCTATATTTAACAAAGTGATGACATTTCTGACGGCGTTAAATACCGTTCAATGCGTAGATATCAGTATCTAAAGCCGTCGATTGTCATTCTACCGATATTAATAACTGa > 2:610986/1‑149 (MQ=255) tttCGCTTAAATGCCAAGCGTTTTTAAAATTGTAATCTATATTTAACAAAGTGATGACATTTCTGACGGCGTTAAATACCGTTCAATGCGTAGATATCAGTATCTAAAGCCGTCGATTGTCATTCTACCGATATTAATAACTg < 1:220036/143‑1 (MQ=255) cTGAAATCCCGAGCGTGTTCAAAATTGTGATCTATATTTAACAAAGGTATGACATTTCTGACGGCGTTAAATACCGTTCAAGGCGTAGATATCAGTATCTAAAGCCGTCGATTGTCATTATACCGATATTAATAACTGATTCa < 1:266792/143‑1 (MQ=255) ccGAGCGGTTTCAAAATTGTGATCTATATTTAACAAAGTGATGACATTTCTGACGGCGTTAAATACCGTTCAATGCGTAGATATCAGTATCTAAAGCCGTCGATTGTAATTCTACCGATATTAATAACTGATTCAGAGGCTGt > 1:313351/1‑143 (MQ=255) ttCAAAATTGTGATCTATATTTAACAAAGTGATGACATTTCTGACGGCGTTAAATACCGTTCAATGCGTAGATATCAGTATCTAAAGCCGTCGATTGTCATTCTACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATtca > 2:396365/1‑149 (MQ=255) tCAAAATTGTGATCTATATTTAACAAAGTGATGACATTTCTGACGGCGTTAAATACCGTTCAATGCGTAGATATCAGTATCTAAAGCCGTCGATTGTCATTCTACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATtcat > 2:327066/1‑149 (MQ=255) aTTGTGATCTATATTTAACAAAGTGATGACATTTCTGACGGCGTTAAATACCGTTCAATGCGTAGATATCAGTATCTAAAGCCGTCGATTGTCATTATACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATtca < 1:452487/143‑1 (MQ=255) aTCTATATTTAACAAAGTGATGACATTTCTGACGGCGTTAAATACCGTTCAATGCGTAGATATCAGTATCTAAAGCCGTCGATTGTCATTATACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCATCACTc > 1:187118/1‑143 (MQ=255) cTATATTTAACAAAGTGATGACATTTCTGACGGCGTTAAATACCGTTCAATGCGTAGCTATCCGTATCTAAAGCCGTCGATTGTCATTCTACCGATATTAATAACTGATTCAGAGGCGGTAATGGTCGTTATTCATCACTCATCGCttt > 2:486848/1‑149 (MQ=255) tttAACAAAGTGATGACATTTCTGACGGCGTTAAATACCGTTCAATGCGTAGATATCAGTATCTAAAGCCGTCGATTGTCATTCTACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCATCACTCATCGCTTTTGTGa > 2:606517/1‑149 (MQ=255) gTGATGACATTTCTGACGGCGTTAAATACCGTTCCGTGAGTAGCTCCAAGTCGCTAAAGCCGTCGATTGTCATTCTACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCATCACTCATCGCTTTTGTGATgg < 1:552594/143‑1 (MQ=255) ttttCTGACGGCCTTAAAGACCGTTCAATGCGTAGATATCACTATCTAAATCCGTCGATTGTCATTCTACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCTTCACTCTTCGCTTTAGTGATGGCGACCAtt < 1:385672/142‑1 (MQ=255) aTTTCTGACGGCGTTAAATACCGTTCAATGCGTAGATATCAGTATCTAAAGCCGTCGATTGTCATTCTACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCATCACTCATCGCTTTTGTGATGGCGACCAtt < 1:349233/143‑1 (MQ=255) cGGCGTTAAATACCGTTCAATGCGTAGATATCAGTATCTAAAGCCGTCGATTGTCATTCTACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCATCACTCATCGCTTTTGTGATGGCGACCATTGACTTCTGTAGAgg < 2:511672/149‑1 (MQ=255) ggCGTTAAATACCGTTCAATGCGTAGATATCAGTATCTAAAGCCGTCGATTGTCATTATACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTAATCACCACTCCCTTTTGTGATGGCGACCATTGACTTgtgt > 1:20790/1‑143 (MQ=255) ggCGTTAAATACCGTTCAATGCGTAGATATCAGTATCTAAAGCCGTCGATTGTAATTATACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCATCACTCATCGCTTTTGTGATGGCGACACTTTAATTCTGTAGAgga > 2:504666/1‑148 (MQ=255) gTTAAATACCGTTCAATGCGTAGATATCAGTATCTAAAGCCGTCGATTGTCATTATACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCATCACTCATCGCTTTTGTGATTGAGACCATTGACTTCTGTagc > 1:120247/1‑142 (MQ=255) aCCGTTCAATGCGTAGATATCAGTATCTAAAGCCGTCGATTGTCATTCTACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCATCACTCATCGCTTTTGTGATGGCGACCATTGACTTCTGTAGAGGGTGAAGtctct < 2:252082/149‑1 (MQ=255) aaTGCGTAGATATCAGGAGCTAAAGCCGTCGATTGTCATTATACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCATCACTCATCGCTTTTGTGATGGCGACCATTGACTTCTGTAGAGGGTGAAGtctctc < 1:284220/143‑1 (MQ=255) gCGTAGATATCAGTATCTAAAGCCGTCGATTGTCATTCTACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCATCACTCATCGCTTTTGTGATGGCGACCATTGACTTCTGTAGAGGGTGAAGTCTCTCCCt < 1:375987/143‑1 (MQ=255) cGTAGATATCAGTATCTAAAGCCGTCGATTGTCATTCTACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCATCACTCATCGCTTTTGTGATGGCGACCATTGACTTCTGTAGAGGGTGAAGTCTCTcccca > 1:229146/1‑141 (MQ=255) gTAGATATCAGTATCTAAAGCCGTCGATTGTCATTCTACCGATATGAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCATCACTCATCGCTTTTGTGATGGCGACCATTGACTTCTGTAGAGGGTGAAGTCTCTCCCTATTCAGCa < 2:356963/149‑1 (MQ=255) aGATATCAGTATCTAAAGCCGTCGATTGTCATTATACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCATCACTCATCGCTTTTGTGATGGCGACCATTGACTTCTGTAGAGGGTGAAGTCTCTCCCTATTCAGCAAt < 2:210225/149‑1 (MQ=255) tCTAAAGCCGTCGATTGTCATTCTACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCATCACTCATCGCTTTTGTGATGGAGAGCATTCACTTCTGTAGAGGGTGAAGGCTCGACCTATTAAGCAATGCAAc > 1:89918/1‑143 (MQ=255) tCGATTGTCATTCTACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCATCACTCATCGCTTTTGTGATGGCGACCATTGACTTCTGTAGAGGGTGAAGTCTCTCCCTATTCAGCAATGCAACCTCGTGTTGCCAGGCt > 2:574044/1‑149 (MQ=255) ttCTACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCATCACTCATCGCTTTTGTGATGGCGACCATTGACTTCTGTAGAGGGTGAAGTCTCTCCCTATTCAGCAATGCAACCTCGTGTTGCCAGGCTCaaa > 1:303005/1‑143 (MQ=255) | ATTCACTTTTGCTTATGTTTTCGCTGATATCCCGAGCGGTTTCAAAATTGTGATCTATATTTAACAAAGTGATGACATTTCTGACGGCGTTAAATACCGTTCAATGCGTAGATATCAGTATCTAAAGCCGTCGATTGTCATTCTACCGATATTAATAACTGATTCAGAGGCTGTAATGGTCGTTATTCATCACTCATCGCTTTTGTGATGGCGACCATTGACTTCTGTAGAGGGTGAAGTCTCTCCCTATTCAGCAATGCAACCTCGTGTTGCCAGGCTCAAA > CP009273/4600902‑4601184 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 13 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |