Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_002947 | 3,624,902 | A→G | 16.7% | L210P (CTG→CCG) ‡ | PP_3195 ← | hypothetical protein |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_002947 | 3,624,902 | 0 | A | G | 16.7% | 50.5 / 4.3 | 24 | L210P (CTG→CCG) ‡ | PP_3195 | hypothetical protein |
Reads supporting (aligned to +/- strand): ref base A (8/12); new base G (2/2); total (10/14) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 5.49e-01 |
TCAGCACGGGTTTCCAGCCAGTCCACTATGCGGCTGGCCCAGTGTTCGCTGTCATGGCGTGCCGTCATGCCGTGGAGGCGAAGCGCTTCGCCGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCTTGGTTGAATCCAGCCCGTTGACTTGCACCAGCAGCGGTGCCGGGCCACTCACGCCTTCTGCGCGCACCAGCAGTCCCGAGAGGTGCTTGCCTTCATACGGGATCT > NC_002947/3624764‑3625043 | tCAGCACGGGTTTCCAGCCAGTCCACTATGCGGCTGGCCCAGTGTTCGCTGTCATGGCGTGCCGTCATGCCGTGGAGGCGAAGCGCTTCGCCGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCT‑GCCTGGCTGGCcaggcgaggc < 2:611227/150‑6 (MQ=255) cACGGGTTTCCAGCCAGTCCACTATGCGGCTGGCCCAGTGTTCGCTGTCATGGCGTGCCGTCATGCCGTGGAGGCGAAGCGCTTCGCCGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCTGGCcaggcgagg > 1:600106/1‑142 (MQ=255) cACGGGTTTCCAGCCAGTCCACTATGCGGCTGGCCCAGTGTTCGCTGTCATGGCGTGCCGTCATGCCGTGGAGGCGAAGCGCTTCGCCGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCTGGCcaggcgagg < 2:600106/146‑5 (MQ=255) cACGGGTTTCCAGCCAGTCCACTATGCGGCTGGCCCAGTGTTCGCTGTCATGGCGTGCCGTCATGCCGTGGAGGCGAAGCGCTTCGCCGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCCAGCCaggcaggcaggc < 2:193507/150‑1 (MQ=255) ccACTATGCGGCTGGCCCAGTGTTCGCTGTCATGGCGTGCCGTCATGCCGTGGAGGCGAAGCGCTTCGCCGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTatttaattt > 2:525216/1‑150 (MQ=255) cTATGCGGCTGGTCCAGTGTTCGCGGTCATGGCGTGCCGTCATGCCGTGGAGGCGAAGCGCTTCGCCGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCt < 2:80266/150‑1 (MQ=255) aTGCGGCTGGCCCAGTGTTCGCTGTCATGGCGTGCCGTCATGCCGTGGAGGCGAAGCGCTTCGCCGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCTTg < 1:76872/150‑1 (MQ=255) tGCGGCTGGCCCAGTGTTCGCTGTCATGGCGTGCCGTCATGCCGTGGAGGCGAAGCGCTTCGCCGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCttag > 2:85000/1‑148 (MQ=255) gCGGCTGGCCCAGTGTTCGCTGTCATGGCGTGCCGTCATGCCGTGGAGGCGAAGCGCTTCGCCGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCTTGGt < 1:299399/150‑1 (MQ=255) cccAGTGTTCGCTGTCATGGCGTGCCGTCATGCCGTGGAGGCGAAGCGCTTCGCCGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGTCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTatttca < 1:457365/132‑1 (MQ=255) cccAGTGTTCGCTGTCATGGCGTGCCGTCATGCCGTGGAGGCGAAGCGCTTCGCCGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGTCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTatttca > 2:457365/1‑132 (MQ=255) gTCATGGCGTGCCGTCATGTCGTGGAGGCGAAGCGCTTCGCCGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCTTGGTTGAATCCAGCCCGTTGACTTg < 2:404453/150‑1 (MQ=255) gTGCCGTCATGCCGTGGAGGCGAAGCGCTTCGCCGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCTGTGTTGAATCCAGCCCGTTGACTTGCACcagca < 1:119508/150‑1 (MQ=255) tGCCGTGGAGGCGAAGCGCTTCGCCGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCTTGGTTGAATCCAGCCCGTTGACTTGCACCAGCAGCGGTGCCg > 2:346250/1‑150 (MQ=255) cGAAGCGCTTCGCCGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCTTGGTTGAATCCAGCCCGTTGACTTGCACCAGCAGCGGTGCCGGGCCACTCACg > 2:3720/1‑150 (MQ=255) aaGCGCTTCGCCGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCTTGGTTGAATCCAGCCCGTTGACTTGCACCAGCAGCGGTGCCGGGCCACTCACGcc < 1:369549/150‑1 (MQ=255) ccGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCTTGGTTGAATCCAGCCCGTTGACTTGCACCAGCAGCGGt < 2:253303/123‑1 (MQ=255) ccGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCTTGGTTGAATCCAGCCCGTTGACTTGCACCAGCAGCGGt > 1:253303/1‑123 (MQ=255) ccGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCTTGGTTGAATCCAGCCCGTTGACTTGCACCAGCAGCGGTGCCGGGCCACTCACGCCTTCTgcgcgc < 1:3720/150‑1 (MQ=255) cGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCTTGGTTGAATCCAGCCCGTTGACTTGCACCAGCAGCGGTGCCGGGCCACTCACGCCTTCTGCGCGCACcagca > 2:268219/1‑150 (MQ=255) gACAATCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCTTAGTTGAATCCAGCCCGTTGACTTGCACCAGCAGCGGTGCCGGGCCACTCACGCCTTCTGCGCGCACCAGCAGTCCCGagag < 1:85000/150‑1 (MQ=255) aaTCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCTTGGTTGAATCCAGCCCGTTGACTTGCACCAGCAGCGGTGCCg > 2:55790/1‑107 (MQ=255) aaTCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCTTGGTTGAATCCAGCCCGTTGACTTGCACCAGCAGCGGTGCCg < 1:55790/107‑1 (MQ=255) gcctGGCTGGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCTTGGTTGAATCCAGCCCGTTGACTTGCACCAGCAGCGGTGCCGGGCCACTCACGCCTTCTGCGCGCACCAGCAGTCCCGAGAGGTGCTTGCCTTCATACGGGAtct > 1:482922/1‑150 (MQ=255) | TCAGCACGGGTTTCCAGCCAGTCCACTATGCGGCTGGCCCAGTGTTCGCTGTCATGGCGTGCCGTCATGCCGTGGAGGCGAAGCGCTTCGCCGGTGCCGGGCTGGTCGACAATCAGCGACGACACGCCTCGCCTGGCCAGCCAGGCAGGCAGGCCGACGCGGTATTTCATTTCCTTGGTTGAATCCAGCCCGTTGACTTGCACCAGCAGCGGTGCCGGGCCACTCACGCCTTCTGCGCGCACCAGCAGTCCCGAGAGGTGCTTGCCTTCATACGGGATCT > NC_002947/3624764‑3625043 |
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: ‑ |