Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_002947 | 1,035,788 | G→A | 14.8% | A132A (GCC→GCT) | PP_0894 ← | hypothetical protein |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_002947 | 1,035,788 | 0 | G | A | 14.8% | 55.3 / 4.1 | 27 | A132A (GCC→GCT) | PP_0894 | hypothetical protein |
Reads supporting (aligned to +/- strand): ref base G (12/11); new base A (2/2); total (14/13) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 7.25e-01 |
ACATCGCGGTGGACCAGGCGCATGTGGATGGCAACCTGGTGACCGCACCGGCATGGCCCGCGCACCCGGCCTGGCTGGCGGCGTTCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCAGCGGGTTGCTTCAGGCAACCTGCTCCACCCAGTCATTGAGGTTGTAGTAGTTGGTGACCCGGGCAATCTTGCCACAGTGAATATAGAAGAACGCCCCTGCCGGCAGCACATAGGTCTGGCCGTTTGCTGTCGGCAACCCTTCGTCATCGGCCAGGTATTGG > NC_002947/1035639‑1035935 | aCATCGCGGTGGACCAGGCGCATGTGGATGGCAACCTGGTGACCGCACCGGCATGGCCCGCGCCCCCGGATTGTCTGGCGGCGTTCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCAGCGGGTTGCTTCAg < 2:699950/150‑1 (MQ=255) aCATCGCGGTGGACCAGGCGCATGTGGATGGCAACCTGGTGACCGCACCGGCATGGCCCGCGCACCCGGCCTGGCTGGCGGCGTTCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCAGCGGGTTGCTTCAg < 1:733734/150‑1 (MQ=255) cgGTGGACCAGGCGCATGTGGATGGCAACCTGGTGACCGCACCGGCATGGCCCGCGCACCCGGCCTGGCTGGCGACTGGCCTTAAAGTGCTGGGGACGCGTAGTGTCTGACAGGCTTGATTGAGTTGGCAGCGGGTTGCTTCAGGCAAcc > 1:270682/1‑150 (MQ=255) ggTGGACCAGGCGCATGTGGATGGCAACCTGGTGACCGCACCGGCATGGCCCGCGCACCCGGCCTGGCTGGCGGCGTTCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCAGCGGGTTGCTTCAGGCAACCt < 2:692419/150‑1 (MQ=255) gTGGACCAGGCGCATGTGGATGGCAACCTGGTGACCGCACCGGCATGGCCCGCGCACCCGGCCTGGCTGGCGGCGTTCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCAGCGGGTTGCTTCAGGCAACCTg < 1:480488/150‑1 (MQ=255) aCCAGGCGCATGTGGATGGCAACCTGGTGACCGCACCGGCATGGCCCGCGCACCCGGCCTGGCTGGCGGCGTTCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCAGCGGGTTGCTTCAGGCAACCTGCTcc < 2:137035/150‑1 (MQ=255) cAGGCGCATGTGGATGGCAACCTGGTGACCGCACCGGCATGGCCCGCGCACCCGGCCTGGCTGGCGGCGTTCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCAGCGGGTTGCTTCAGGCAACCTGCTCTAc < 1:877342/150‑1 (MQ=255) cAGGCGCATGTGGATGGCAACCTGGTGACCGCACCGGCATGGCCCGCGCACCCGGCCTGGCTGGCGGCGTTCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCAGCAGGTTGCCTGAAGCAACCCGCt < 1:44585/146‑1 (MQ=255) cAGGCGCATGTGGATGGCAACCTGGTGACCGCACCGGCATGGCCCGCGCACCCGGCCTGGCTGGCGGCGTTCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCAGCAGGTTGCCTGAAGCAACCCGCt > 2:44585/1‑146 (MQ=255) gcgcATGTGGATGGCAACCTGGTGACCGCACCGGCATGGCCCGCGCACCCGGCCTGGCTGGCGGCGTTCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCAGCGGGTTGCTTCAGGCAACCTGCTCCACCCa > 1:398958/1‑150 (MQ=255) cATGTGGATGGCAACCTGGTGACCGCACCGGCATGGCCCGCGCACCCGGCCTGGCTGGCGGCGTTCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCGGCGGGTTGCTTCAGGCAACCTGCTCCACCCAGTc > 1:873658/1‑150 (MQ=255) tGACCGCACCGGCATGGCCCGCGCACCCGGCCTGGCTGGCGGCGTTCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCAGCGGGTTGCTTCAGGCAACCTGCTCCACCCAGTCATTGAGGTTGTAGTAGTTg < 2:398958/150‑1 (MQ=255) ggCCCGCGCACCCGGCCTGGCTGGCGGCGTTCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCAGCGGGTTGCTTCAGGCAACCTGCTCCACCCAGTCATTGAGGTTGTAGTAGTTGGTGACCCGGGCAATc < 2:843906/150‑1 (MQ=255) ccGGCCTGGCTGGCGGCGTTCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCAGCGGGTTGCTTCAGGCAACCTGCTCCACCCAGTCATTGAGGTTGTAGTAGTTGGTGACCCGGGCAATCTTg > 1:426541/1‑142 (MQ=255) ccGGCCTGGCTGGCGGCGTTCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCAGCGGGTTGCTTCAGGCAACCTGCTCCACCCAGTCATTGAGGTTGTAGTAGTTGGTGACCCGGGCAATCTTg < 2:426541/142‑1 (MQ=255) cgTTCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCAGCGGGTTGCTTCAGGCAACCTGCTCCACCCAGTCATTGAGGTTGTAGTAGTTGGTGACCCGGGCAATCTTGCCACAGTGAATATAGAAGAACGcc < 1:1133923/150‑1 (MQ=255) gTTCCTTAAAGTGCTGGGCACGCGGATTGTCTGACAGGCTTGAGTGAGTTGGCAGCGGGTTGCTTCAGGCAACCTGCTCCACCCAGTCATTGAGGTTGTAGTAGTTGGTGACCCGGGCAATCTTGCCACAGTGAATATAGAAGAACGccc > 1:1118612/1‑150 (MQ=255) ttCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCAGCGGGTTGCCTGAAGCAAcccgc > 2:942666/1‑73 (MQ=255) ttCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGACAGCGGGTTGCCTGAAGCAACCCGc < 1:942666/76‑1 (MQ=38) tGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCAGCGGGTTGCTTCAGGCAACCTGCTCGACCCAGTCATTGAGGTTGTAGTAGTTGGTGACCCGGGCAATCTTGCCACAGTGAATATAGAAGAACGCCCCTGCCGGCAGcaca < 1:746273/150‑1 (MQ=255) gACAGGCTTGATTGAGTTGGCAGCGGGTTGCTTCAGGCAACCTGCTCCACCCAGTCATTGAGGTTGTAGTAGTTGATGATTGTCGAACTGGTGCCACAGTGAATATAGAAGAACGACCCAGACCACATTACGTAGTTCTGGCCGTTTGCt > 1:327707/1‑150 (MQ=255) gACAGGCTTCATTGAGTTGGCAGCGGGTTGCTTCAGGCAACCAGCTGCACCGAGTCACAACGATCGCAGTAATAAGGCGCCCGCGCTGATGTGCCTCGGTGTGGATAGATTAACGCCCCTGCCGGCAGCACCTAGGTCTGGCCGTTTGCt > 2:1041780/1‑150 (MQ=255) aGGCTTGATTGAGTTGGCAGCGGGTTGCTTCAGGCAACCTGCTCCACCCAGTCATTGAGGTTGTAGTAGTTGGTGACCCGGGCAATCTTGCCACAGTGAATATAGAAGAACGCCCCTGCCGGCAGCACATAGGTCTGGCCGTTTGCTGTc < 1:121102/150‑1 (MQ=255) attgaGTTGGCAGCGGGTTGCTTCAGGCAACCTGCTCCACCCAGTCAGTGAGGTTGTAGTAGTTGGTGACCCGGGCAAACTTGCCACAGTGAATATAGAAGACCGCCCCTGCCGGCCGCACATATGTCTGGCCGTTTGCGATGGGCAAcc > 1:566413/1‑150 (MQ=255) gTTGGCAGCGGGTTGCTTCAGGCAACCTGCTCCACCCAGTCATTGAGGTTGTAGTAGTTGGTGACCCGGGCAATCTTGCCACAGTGAATATAGAAGAACGCCCCTGCCGGCAGCACATAGGTCTGGCCGTTTGCTGTCGGCAACCCTTCg > 1:502455/1‑150 (MQ=255) ttGGCAGCGGGTTGCTTCAGGCAACCTGCTCCACCCAGTCATTGAGGTTGTAGTAGTTGGTGACCCGGGCAATCTTGCCACAGTGAATATAGAAGAACGCCCCTGCCGGCAGCACATAGGTCTGGCCGTTTGCTGTCGGCAACCCTTCGt > 2:573625/1‑150 (MQ=255) cTTCAGGCAACCTGCTCCACCCAGTCATTGAGGTTGTAGTAGTTGGTGACCCGGGCAATCTTGCCACAGTGAATATAGAAGAACGCCCCTGCCGGCAGCACATAGGTCTGGCCGTTTGCTGTCGGCAACCCTTCGTCATCGGCCaatacc > 1:1016961/1‑145 (MQ=255) cTTCAGGCAACCTGCTCCACCCAGTCATTGAGGTTGTAGTAGTTGGTGACCCGGGCAATCTTGCCACAGTGAATATAGAAGAACGCCCCTGCCGGCAGCACATAGGTCTGGCCGTTTGCTGTCGGCAACCCTTCGTCATCGGCCAGGTAt > 1:460490/1‑150 (MQ=255) cAGGCAACCTGCTCCACCCAGTCATTGAGGTTGTAGTAGTTGGTGACCCGGGCAATCTTGCCACAGTGAATATAGAAGAACGCCCCTGCCGGCAGCACATAGGTCTGGCCGTTTGCTGTCGGCAACCCTTCGTCATCGGCCAGGTATTgg < 1:104810/150‑1 (MQ=255) | ACATCGCGGTGGACCAGGCGCATGTGGATGGCAACCTGGTGACCGCACCGGCATGGCCCGCGCACCCGGCCTGGCTGGCGGCGTTCCTTAAAGTGCTGGGCACGCGTATTGTCTGACAGGCTTGATTGAGTTGGCAGCGGGTTGCTTCAGGCAACCTGCTCCACCCAGTCATTGAGGTTGTAGTAGTTGGTGACCCGGGCAATCTTGCCACAGTGAATATAGAAGAACGCCCCTGCCGGCAGCACATAGGTCTGGCCGTTTGCTGTCGGCAACCCTTCGTCATCGGCCAGGTATTGG > NC_002947/1035639‑1035935 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 22 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |