Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_002947 | 3,116,213 | T→C | 18.6% | L303P (CTG→CCG) | PP_2732 → | hypothetical protein |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_002947 | 3,116,213 | 0 | T | C | 18.6% | 52.1 / 6.0 | 27 | L303P (CTG→CCG) | PP_2732 | hypothetical protein |
Reads supporting (aligned to +/- strand): ref base T (10/12); new base C (2/3); total (12/15) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.35e-01 |
CGAGCCGTACCTGTTTCATGCGCGCATCAGTGCGGCGCTCAACATCGGCCTTCTGGATGTGCGTCGTCTGTGCGACGACGTCGACAAAGCCTGGCGCGAGGGGCGGGTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGCGTGAGTACGTGCGTGGCATCTATTGGCAGCGCATGCCGGCATATGCCGGGCTCAATCACCTGAACAATCACCGGGCGCTGCCAGAATTCTACTGGACCGGGCGCACCCGCATGCGCTGCATGGCGCAAGCCAT > NC_002947/3116070‑3116357 | cGAGCCGTACCTGTTTCATGCGCGCATCAGTGCGGCGCTCAACATCGGCCTTCTGGATGTGCGTCGTCTGTGCGACGACGTCGACAAAGCCTGGCGCGAGGGGCGGGTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCgg > 2:781204/1‑150 (MQ=255) cGTACCTGTTTCATGCGCGCATCAGTGCGGCGCTCAACATCGGCCTTCTGGATGTGCGTCGTCTGTGCGACGACGTCGACAAAGCCTGGCGCGAGGGGCGGGTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGc < 1:367865/150‑1 (MQ=255) cGTACCTGTTTCATGCGCGCATCAGTGCGGCGCTCAACATCGGCCTTCTGGATGTGCGTCGTCTGTGCGACGACGTCGACAAAGCCTGGCGCGAGGGGCGGGTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGc < 1:375947/150‑1 (MQ=255) cGTACCTGTTTCATGCCCGCATCAGTGCGGCGCTCAACATCGGCCTTCTGGATGTGCGTCGTCTGTGCGACGACGTCGACAAAGCTTGGCGCGAGGGGCGGGTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGc < 1:38379/150‑1 (MQ=255) tACCTGTCCCATGCGCGCATGCGGCAGTCGCTCACCATCGGCCTTCGTGATGTGCGGCGTCTGTGCGACGACGTCGACAAAGCCTGGCGCGAGGGGGGGGGGCCGCGCAATGCAGCCGAAGGCTTCAGTCGCCAGCTGATCGGCTGGCGt < 2:822388/150‑1 (MQ=255) ccTGTTTCATGCGCGCATCAGTGCGGCGGTCAGCGTCTGCCTTCTGGATGTGCGTCGTCTGTGCGAAAAGGAGGACAAAGCCTGGCGCGAGGGGCGGGTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGCGTGa < 1:787210/150‑1 (MQ=255) ccTGTTTCATGCGCGCATCAGTGCGGCGCTCAACATCGGCCTTCTGGATGTGCGTCGTCTGTGCGACGACGTCGACAAAGCCTGGCGCGAGGGGCGGGTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCCGATCAGCTGGCgaat < 1:229296/150‑4 (MQ=255) cTGTTTCATGCGCGCATCAGTGCGGCGCTCAACATCGGCCTTCTGGATGTGCGTCGTCTGTGCGACGACGTCGACAAAGCCTGGCGCGAGGGGCGGGTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGCGTGAg > 2:803585/1‑150 (MQ=255) aTGCGCGCATCAGTGCGGCGCTCAACATCGGCCTTCTGGATGTGCGTCGTCTGTGCGACGACGTCGACAAAGCCTGGCGCGAGGGGCGGGTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCCGATCAGCTGGCgaatgaa > 1:639329/1‑139 (MQ=255) aTGCGCGCATCAGTGCGGCGCTCAACATCGGCCTTCTGGATGTGCGTCGTCTGTGCGACGACGTCGACAAAGCCTGGCGCGAGGGGCGGGTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCCGATCAGCTGGCgaatgaa < 2:639329/145‑7 (MQ=255) tGCGCGCATCAGTGCGGCGCTCAACATCGGCCTTCTGGATGTGCGTCGTCTGTGCGACGCCGTCGACACAGCCTTGCGCGAGGGGCGGGTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGCGTGAGTAcgtgcg > 2:570193/1‑150 (MQ=255) gcgcgcATCAGTGCGGCGCTCAACATCGGCCTTCTCGAGGTGCGTCGTCTGTGCGACGACGTCGACAAAGCCTGGCGCGAGGGGCGGGTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGCGTGAGTAcgtgcgt > 1:496074/1‑150 (MQ=255) tGCGGCGCTCAACATCGGCCTTCTGGATGTGCGTCGTCTGTGCGACGACGTCGACAAAGCCTGGCGCGAGGGGCGGGTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGCGTGAGTACGTGCGTGGCATCTATTg < 1:462220/150‑1 (MQ=255) ggATGTGCGTCGTCTGTGCGACGACGTCGACAAAGCCTGGCGCGAGGGGCGTGTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGCGTGAGTACGTGCGTGGCATCTATTGGCAGCGCATGCCGGCATATGCCgg < 2:359780/150‑1 (MQ=255) aCAAAGCCTGGCGCGAGGGGCGGGTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGCGTGAGTACGTGCGTGGCATCTATTGGCAGCGCATGCCGGCATATGCCGGGCTCAATCACCTGAACAATCACCGGgcgc > 2:131524/1‑150 (MQ=255) aaGCCTGGCGCGAGGGGCGGGTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGCGTGAGTACGTGCGTGGCATCTATTGGCAGCGCATGCCGGCATATGCCGGGCTCAATCACCTGAACAATCACCGGGCGCTGc < 1:803585/150‑1 (MQ=255) aaGCCTGGCGCGAGGGGCGGGTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGCGTGAGTACGTGCGTGGCATCTATTGGCAGCGCATGCCGGCATATGCCGGGCTCAATCACCTGAACAATCACCGGGCGCTGc < 1:211030/150‑1 (MQ=255) gTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGCGTGAGTACGTGCGTGGCATCTATTGGCAGCGCATGCCGGCATATGCCGGGCTCAATCACCTGAACAATCACCGGGCGCTGCCAGAATTCTACTGGACCggg > 1:705038/1‑150 (MQ=255) tGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGCGTGAGTACGTGCGTGGCATCTATTGGCAGCGCATGCCGGCATATGCCGGGCTCAATCACCTGAACAATCACCGGGCGCTGCCAGAATTCTACTGGACCGGgc < 2:496074/150‑1 (MQ=255) tGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGCGTGAGTACGTGCGTGGCATCTATTGCCAGCGCATGCCGGCATATGCCGGGCTCAATCACCTGAACAATCACCGGGCGCTGCCAGAATTCTACTGGACCGGgc < 1:781204/150‑1 (MQ=255) gctggcgaaTGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGCGTGAGTACGTGCGTGGCATCTATTGGCAGCGCATGCCGGCATATGCCGGGCTCAATCACCTGAACAATCACCGGGCGCTGCCAGAATTCTACTGGACCGGgcg > 2:644580/8‑150 (MQ=255) cGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGCGTGAGTACGTGCGTGGCATCTATTGGCAGCGCATGCCGGCATATGCCGGGCTCAATCACCTGAACAATCACCGGGCGCTGCCAGAATTCTACTGGACCGGGCGCa > 1:63449/1‑150 (MQ=255) cTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGCGTGAGTAcgtgcgt > 1:801519/1‑57 (MQ=255) cTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGCGTGAGTAcgtgcgt < 2:801519/57‑1 (MQ=255) tcacGCCAGCCGATCAGCTGGCGTGAGTACGTGCGTGGCATCTATTGGCAGCGCATGCCGGCATATGCCGGGCTCAATCACCTGAACAATCACCGGGCGCTGCCAGAATTc > 2:146519/4‑111 (MQ=255) tcacGCCAGCCGATCAGCTGGCGTGAGTACGTGCGTGGCATCTATTGGCAGCGCATGCCGGCATATGCCGGGCTCAATCACCTGAACAATCACCGGGCGCTGCCAGAATTc < 1:146519/108‑1 (MQ=255) ccAGCTGATCGGCTGGCGTGAGTACGTGCGTGGCATCTATTGGCAGCGCATGCCGGCATATGCCGGGCTCAATCACCTGAACAATCACCGGGCGCTGCCAGAATTCTACTGGACCGGGCGCACCCGCATGCGCTGCATGGCGCAAGCCAt > 1:384138/1‑150 (MQ=255) | CGAGCCGTACCTGTTTCATGCGCGCATCAGTGCGGCGCTCAACATCGGCCTTCTGGATGTGCGTCGTCTGTGCGACGACGTCGACAAAGCCTGGCGCGAGGGGCGGGTGCCGCTCAATGCAGCCGAAGGCTTCATTCGCCAGCTGATCGGCTGGCGTGAGTACGTGCGTGGCATCTATTGGCAGCGCATGCCGGCATATGCCGGGCTCAATCACCTGAACAATCACCGGGCGCTGCCAGAATTCTACTGGACCGGGCGCACCCGCATGCGCTGCATGGCGCAAGCCAT > NC_002947/3116070‑3116357 |
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: ‑ |