Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_002947 | 2,185,374 | C→A | 17.2% | A760S (GCA→TCA) | PP_1936 ← | membrane protein |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_002947 | 2,185,374 | 0 | C | A | 17.2% | 49.4 / 3.2 | 24 | A760S (GCA→TCA) | PP_1936 | membrane protein |
Reads supporting (aligned to +/- strand): ref base C (11/8); new base A (2/2); total (13/11) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.29e-01 |
TTTCATGAGTAAGTAAGAGTCCAGTAGTGTCAAAGTTTTCGTCAGGAATCGCGTCTACAGTGTCATAAAAGTTGATTTTTTTGTCAATGTGCTCGGCTTTGAATTTGGCAAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGCCAGTCTGCTTATAACTCCTGAGGTTGCTGCATTCGGGTGATCGACCACAATGAGCGCCTTTTGAAGATTGTAAAGTTGTCCTTTACGATCAGCCGAACATTGGAGTCGTAGAAGCATTAGATCATTCCAACCCAGCGCACCTC > NC_002947/2185227‑2185517 | tttCATGAGTAAGTAAGAGTCCAGTAGTGTCGAAGTTTTCGTCAGGAATCGCGTCTACAGTGTCATAAAAGTTGATTTTTTTGTCAATGTGCTCGGCTTTGAATTTGGCAAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGCCa > 2:604930/1‑150 (MQ=255) aagAGTCCAGTAGTGTCAAAGTTTTCGTCAGGAATCGCGTCTACAGTGTCATAAAAGTTGATTTTTTTGTCAATGTGCTCGGCTTTGAATTTGGCAAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGACAGTCTGCTta > 2:512466/1‑145 (MQ=255) aagAGTCCAGTAGTGTCAAAGTTTTCGTCAGGAATCGCGTCTACAGTGTCATAAAAGTTGATTTTTTTGTCAATGTGCTCGGCTTTGAATTTGGCAAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGACAGTCTGCTta > 2:512071/1‑145 (MQ=255) aagAGTCCAGTAGTGTCAAAGTTTTCGTCAGGAATCGCGTCTACAGTGTCATAAAAGTTGATTTTTTTGTCAATGTGCTCGGCTTTGAATTTGGCAAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGACAGTCTGCTta < 1:512466/145‑1 (MQ=255) aagAGTCCAGTAGTGTCAAAGTTTTCGTCAGGAATCGCGTCTACAGTGTCATAAAAGTTGATTTTTTTGTCAATGTGCTCGGCTTTGAATTTGGCAAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGACAGTCTGCTta < 1:512071/145‑1 (MQ=255) tCCAGTAGTGTCAAAGTTTTCGTCAGGAATCGCGTCTACAGTGTCATAAAAGTTGATTTTTTTGTCAATGTGCTCGGCTTTGAATTTGGCAAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGCCAGTCTGCTTATAACTCCTGa < 1:739147/150‑1 (MQ=255) tgtCAAAGTTTTCGTCAGGAATCGCGTCTACAGTGTCATAAAAGTTGATTTTTTTGTCAATGTTCTCGGCTTTGAATTTGGCAAAGACTATTTGGAAGATTCTTCTCATGCCCATAATTGCCAGTCTGCTTATAACTCCTGAGGTtgctg > 2:164259/1‑150 (MQ=255) ttCGTCAGGAATCGCGTCTACAGTGTCATAAAAGTTGATTTTTTTGTCAATGTGCTCGGCTTTGAATTTGGCAAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGCCAGTCTGCTTATAACTCCTGAGGTTGCTGCATTCGGGTg < 1:604930/150‑1 (MQ=255) gcgTCTACAGTGTCATAAAAGTTGATTTTTATATGGCGCGCCTCTTTTTTGAATTTGGCAAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGCCAGTCTGCTTATAACTCCTGAGGTTGCTGCATTCAGGTGATCGACCACAATg > 2:590582/1‑150 (MQ=255) aCAGTGTCATAAAAGTTGATTTTTTTGTCAATGTGCTCGGCTTTGAATTTGGCAAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGCCAGTCTGCTTATAACTCCTGAGGTTGCTGCATTCGGGTGATCGACCACAATGAGCGcc > 1:455920/1‑150 (MQ=255) ctAAAAGTTGATTTTTTTGTCTTTGTGCTGGGCTTTGAATTTGGCAAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGCCAGTCTGCTTATAACTCCTGAGGTTGCTGCATTCGGGTGATCGACCACAATGAGCGCCTTTTGAAg > 2:402416/2‑150 (MQ=255) tAAAAGTTGATTTTTTTGTCAATGTGCTCGGCTTTGAATTTGGCAAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGCCAGTCTGCTTATAACTCCTGAGGTTGCTGCATTCgg > 2:194802/1‑119 (MQ=255) tAAAAGTTGATTTTTTTGTCAATGTGCTCGGCTTTGAATTTGGCAAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGCCAGTCTGCTTATAACTCCTGAGGTTGCTGCATTCgg < 1:194802/119‑1 (MQ=255) tGATTTTTTTGTCAATGTGCTCGGCTTTGAATTTGGCGAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGCCAGTCTGCTTATAACTCCTGAGGTTGCTGCATTCGGGTGATCGACCACAATGAGCGCCTTTTGAAGATTGTaaa > 1:370073/1‑150 (MQ=255) tttttttGTCAATGTGCTCGGCTTTGAATTTGGCAAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGCCAGTCTGCTTATAACTCCTGAGGTTGCTGCATTCGGGTGATCGACCACAATGAGCGCCTTTTGAAGATTGTAAAGtt > 1:250716/1‑150 (MQ=255) ttGTCAATGTGCTCGGCTTTGAATTTGGCGAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGCCAGTCTGCTTATAACTCCTGAGGTTGCTGCATTCGGGTGATCGACCACAATGAGCGCCTTTTGAAGATTGTAAAGTTGTCCt < 2:370073/150‑1 (MQ=255) gCTTTGAATTTGGCAAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGCCAGTCTGCTTATAACTCCTGAGGTTGCTGCATTCGGGTGATCGACCACAATGAGCGCCTTTTGAAGATTGTAAAGTTGTCCTTTACGATCAGCCGaa < 2:455920/150‑1 (MQ=255) tGGCAAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGCCAGTCTGCTTATAACTCCTGAGGTTGCTGCATTCGGGTGATCGACCACAATGAGCGCCTTTTGAAGATTGTAAAGTTGTCCTTTACGATCAGCCGAACATTGGAGTc < 1:34427/150‑1 (MQ=255) aCTAGTTGGGAGATTCTTCTCATGCCCATAATTGCCAGTCTGCTTATAACTCCTGAGGTTGCTGCATTCGGGTGATCGACCACAATGAGCGCCTTTTGAAGATTGTAAAGTTGTCCTTTACGATCAGCCGAACATTGGAGTCGTAGAAGc > 2:349554/1‑150 (MQ=255) ctcATGCCCATAATTGCCAGTCTGCTTATAACTCCTGAGGTTGCTTCATTCGGGTGATCGTCCACAATGAGCGCCTTTTGAAGATGGTAAAGTTGTCTTTTACGATCAGCCGAACATTGGAGTCGTAGAAGCATTAGATCATTccctgac < 1:590582/150‑6 (MQ=255) tcATGCCCATAATTGCCAGTCTGCTTATAACTCCTGAGGTTGCTGCATTCGGGTGATCGACCACAATGAGCGCCTTTTGAAGATTGTAAAGTTGTCCTTTACGATCAGCCGAAc < 2:131733/114‑1 (MQ=255) tcATGCCCATAATTGCCAGTCTGCTTATAACTCCTGAGGTTGCTGCATTCGGGTGATCGACCACAATGAGCGCCTTTTGAAGATTGTAAAGTTGTCCTTTACGATCAGCCGAAc > 1:131733/1‑114 (MQ=255) tcATGCACATAGTTCTCTGCCTGCTTATAACTCCTGAGGTTGCTGCATTCGGGTGATCGACCAAATTCAGCGGTTTTTGAAGATTGTAAAGTTGTCCTTTACGATCAGCCGAACATTGGAGTCGTAGAAGCATTAGATCATTCCAACCCa < 1:402416/150‑1 (MQ=255) tAATTGCCAGTCTGCTTATAACTCCTGAGGTTGCTGCATTCGGGTGATCGACCACAATGAGCGCCTTTTGAAGATTGTAAAGTTGTCCTTTACGATCAGCCGAACATTGGAGTCGTAGAAGCATTAGATCATTCCAACCCAGCGCACCTc > 1:603002/1‑150 (MQ=255) | TTTCATGAGTAAGTAAGAGTCCAGTAGTGTCAAAGTTTTCGTCAGGAATCGCGTCTACAGTGTCATAAAAGTTGATTTTTTTGTCAATGTGCTCGGCTTTGAATTTGGCAAAGACTAGTTGGGAGATTCTTCTCATGCCCATAATTGCCAGTCTGCTTATAACTCCTGAGGTTGCTGCATTCGGGTGATCGACCACAATGAGCGCCTTTTGAAGATTGTAAAGTTGTCCTTTACGATCAGCCGAACATTGGAGTCGTAGAAGCATTAGATCATTCCAACCCAGCGCACCTC > NC_002947/2185227‑2185517 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |