Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_002947 | 5,920,635 | G→C | 17.3% | D389H (GAC→CAC) | PP_5190 → | type II secretion system protein |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_002947 | 5,920,635 | 0 | G | C | 17.3% | 53.0 / 4.6 | 23 | D389H (GAC→CAC) | PP_5190 | type II secretion system protein |
Reads supporting (aligned to +/- strand): ref base G (9/10); new base C (2/2); total (11/12) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.99e-01 |
TCACCGGCCCCACCGGCTCCGGCAAGACCAGCACGCTGTACACCAGCCTCAAACTGCTGGCCACACCACAGGTCAACCTGTGCACCATCGAAGACCCGATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGTGCAGCCCGCGCTGGACCTGGGGTTTGCCAACGCGGTCAGGGCCATGCTGCGCCAAGACCCCGACATCATCATGATCGGCGAAATCCGCGACCGCGAAACCGCTCTGGTGGCGGTGCAGGCAGCGCTGACCGGGCACCTGGTGCTATCGA > NC_002947/5920486‑5920770 | TCACCGGCCCCACCGGCTCCGGCAAGACCAGCACGCTGTACACCAGCCTCGAACTGCTGGCCACACCACAGGTCAACCTGTGCACCATCGAAGACCCGATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGTGCAGCCCGCGCTgg < 1:70492‑M1/150‑1 (MQ=255) ccccACCGGCTCCGGCAAGACCAGCACGCTGTACACCAGCCTCAAACTGCTGGCCACACCACAGGTCAACCTGTGCACCATCGAAGACCCGATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGTCCATCGCGGGCTTCACCTgtg < 2:228915/150‑3 (MQ=255) acCAGCCTCAAACTGCTGGCCACACCACAGGTCAACCTGTGCACCATCGAAGACCCGATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGTGCAGCCCGCGCTGGACCTGGGGTTTGCCAACGCGGTCAGGGCCATGCTGCGCCaa < 1:12101/150‑1 (MQ=255) aaCTGCTGGCCACACCACAGGTCAACCTGTGCACCATCGAAGACCCGATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGTGCAGCCCGCGCTGGACCTGGGGTTTGCCAACGCGGTCAggg < 1:2100/126‑1 (MQ=255) aaCTGCTGGCCACACCACAGGTCAACCTGTGCACCATCGAAGACCCGATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGTGCAGCCCGCGCTGGACCTGGGGTTTGCCAACGCGGTCAggg > 2:2100/1‑126 (MQ=255) aCTGCTGGCCACACCACAGGTCAACCTGTGCACCATCGAAGACCCGATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGTGCAGCCCGCGCTGGACCTGGGGTTTGCCAACGCGGTCAGGGCCATGCTGCGCCAAGACCCCGAcat < 2:70492/150‑1 (MQ=255) tgctgGCCACACCACAGGTCAACCTGTGCACCATCGAAGACCCGATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGTGCAGCCCGCGCTGGACCTGGGGTTTGCCAACGCGGTCAGGGCCATGCTGCGCCAAGACCCCGAcatca < 2:249222/150‑1 (MQ=255) tgctgGCCACACCACAGGTCAACCTGTGCACCATCGAAGACCCGATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGTGCAGCCCGCGCTGGACCTGGGGTTTGCCAAAGCGTTCAGGGCCATGCTGCGCCAAGACCCCGAcatca < 1:217097/150‑1 (MQ=255) cacaccacaGGTCAACCTGTGCACCATCGAAGACCCGATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGTGCAGCCCGCGCTGGACCTGGGGTTTGCCAACGCGGTCAGGGCCATGCTGCGCCAAGACCCCGAcatcatca > 2:68537/1‑146 (MQ=255) cacaccacaGGTCAACCTGTGCACCATCGAAGACCCGATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGTGCAGCCCGCGCTGGACCTGGGGTTTGCCAACGCGGTCAGGGCCATGCTGCGCCAAGACCCCGAcatcatca < 1:68537/146‑1 (MQ=255) cacaccacaGGTCAACCTGTGCACCATCGAAGACCCGATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGCGCAGCCCGCGCTGGACCTGGGGTTTGCCAACGAGGTCAGGGCCATGCTGCGCCAAGACCCCGACATCATCATGAt > 1:99662/1‑150 (MQ=255) accacaGGTCAACCTGTGCACCATCGAAGACCCGATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGTGCAGCCCGCGCTGGACCTGGGGTTTGCCAACGCGGTCAGGGCCATGCTGCGCCAAGACCCCGACATCATCATGATCgg > 2:290433/1‑150 (MQ=255) aCCTGTGCACCATCGAAGACCCGATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGTCCAGCGCGGGCTGCACCt < 1:289851/79‑1 (MQ=37) aCCTGTGCACCATCGAAGACCCGATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGTCCAGCGCGGGCTGCACCt > 2:289851/1‑79 (MQ=37) ccTGTGCACCATCGAAGACCCGATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGTGCAGCCCGCGCTGGACCTGGGGTTTGCCAACGCGGTCAGGGCCATGCTGCGCCAAGACCCCGACATCATCATGATCGGCGAAATccgcga > 1:251165/1‑150 (MQ=255) cATCGAAGACCCGATCGAGCGCCGGGAGCCAGCCTTCAACCAGTTGCAGGTGCAGCCCGCGCTGGACCTGGGGTTTGCCAACGCGGTCAGGGCCATGCTGCGCCAAGACCCCGACATCATCATGATCGGCGAAATCGGCGACCGCGAAAc > 1:221550/1‑150 (MQ=255) gATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGTGCAGCCCGCGCTGGACCTGGGGTTTGCCAACGCGGTCAGGGCCATGCTGCGCCAAGACCCCGACATCATCATGATCGGCGAAATcc < 1:288096/125‑1 (MQ=255) gATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGTGCAGCCCGCGCTGGACCCGGGGTTTGCCAACGCGGTCAGGGCCATGCTGCGCCAAGACCCCGACATCATCATGATCGGCGAAATcc > 2:288096/1‑125 (MQ=255) gTTGCAGGTGCAGCCCGCGCTGGACCTGGGGTTTGCCAACGCGGTCAGGGCCATGCTGCGCCAAGACCCCGACATCATCATGATCGGCGAAATCCGCGACCGCGAAACCGCTCTGGTGGCGGTGCAGGCAGCGCTGACTGGGCACCTGGt < 2:75230/150‑1 (MQ=255) cAGGTGCAGCCCGCGCTGGACCTGGGGTTTGCCAACGCGGTCAGGGCCATGCTGCGCCAAGACCCCGACATCATCATGATCGGCGAAATCCGCGACCGCGAAACCGCTCTGGTGGCGGTGCAGGCAGCGCTGACCGGGCACCTGGTGCTa < 2:251165/150‑1 (MQ=255) cAGGTCCAGCGCGGGCTGCACCTGGGGTTTGCCAACGCGGTCAGGGCCATGCTGCGCCAAGACCCCGACATCATCATGATCGGCGAAATCCGCGACCGCGAAACCGCTCTGGTGGCGGTGCAGGCAGCGCTGACCGGGCACCTGGTGCTa > 1:227504/1‑150 (MQ=255) tGCAGCCCGCGCTGGACCTGGGGTTTGCCAACGCGGTCAGGGCCATGCTGCGCCAAGACCCCGACATCATCATGATCGGCGAAATCCGCGACCCCGAAACCGCTCTGGTGGCGGTGCAGGCAGCGCTGACCGGGCACCTGGTGCTATCGa > 1:359682/1‑150 (MQ=255) cccGCGCTGGACCTGGGGTTTGCCAACGCGGTCAGGGCCATGCTGCGCCAAGACCCCGACATCATCATGATCGGCGAAATCCGCGACCGCGAAACCGCTCTGGTGGCGGTGCAGGCCGCGCTGACCGGGCACCTGGTGCTAt < 2:152795/142‑1 (MQ=255) cccGCGCTGGACCTGGGGTTTGCCAACGCGGTCAGGGCCATGCTGCGCCAAGACCCCGACATCATCATGATCGGCGAAATCCGCGACCGCGAAACCGCTCTGGTGGCGGTGCAGGCAGCGCTGACCGGGCACCTGGTGCTAt > 1:152795/1‑142 (MQ=255) | TCACCGGCCCCACCGGCTCCGGCAAGACCAGCACGCTGTACACCAGCCTCAAACTGCTGGCCACACCACAGGTCAACCTGTGCACCATCGAAGACCCGATCGAGCGCCTGGAGCCAGCCTTCAACCAGTTGCAGGTGCAGCCCGCGCTGGACCTGGGGTTTGCCAACGCGGTCAGGGCCATGCTGCGCCAAGACCCCGACATCATCATGATCGGCGAAATCCGCGACCGCGAAACCGCTCTGGTGGCGGTGCAGGCAGCGCTGACCGGGCACCTGGTGCTATCGA > NC_002947/5920486‑5920770 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 22 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |