Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_002947 | 3,489,707 | G→T | 19.7% | P576Q (CCG→CAG) | clpV ← | protein ClpV1 |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_002947 | 3,489,707 | 0 | G | T | 19.7% | 55.0 / 5.9 | 26 | P576Q (CCG→CAG) | clpV | protein ClpV1 |
Reads supporting (aligned to +/- strand): ref base G (11/9); new base T (2/3); total (13/13) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 6.45e-01 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.80e-01 |
TCTTGCCGACGCCGCTGGGGCCGAGCAGCAGGAACACGCCAATCGGTTTGTTCGGGTCTTCCATGCGCGCTCGGGAAATCTTGATGCGCTTGCCGATCTCATGCAGGGCGTGGTCCTGGCCCAGCACGCGCTCACCAAGCAGGGCCGGCAGGCGCTGCACGGTATCGATTTCGTCACGCAGCATCTTGCCCAGCGGGATGCCGGTCCAGCCACTGATGACCTGGGCGATGGCGCCGCTGTCGACCAGCGCGTGGACCAGTGGCTGGTCGCC > NC_002947/3489561‑3489831 | tCTTGCCGACGCCGCTGGGGCCGAGCAGCAGGAACACGCCAATCGGTTTGTTCGGGTCTTCCATGCGCGCTCTGGAAATCTTGATGCGCTTGCCGATCTCATGCAGGACGTGGTCCTGCCCCAGCACGCGCTCACCAAACAGGGCCGGCa > 2:386013/1‑150 (MQ=255) ccGACGCCGCTGGGGCCGAGCAGCAGGAACACGCCAATCGGTTTGTTCGGGTCTTCCATGCGCGCTCGGGAAATCTTGATGCGCTTGCCGATCTCATGCAGGGCGTGGTCCTGGCCCAGCACGCGCTCACCAAGCAGGGCCGGCAGgcgc < 2:250251/150‑1 (MQ=255) gACGCCGCTGGGGCCGAGCAGCAGGAACACGCCAATCGGTTTGTTCGGGTCTTCCATGCGCGCTCGGGAAATCTTGATGCGCTTGCCGATCTCATGCAGGGCGTGGTCCTGGCCCAGCACGCGCTCACCAAGCAGGGCCGGCAGGCGCTg > 2:373494/1‑150 (MQ=255) cgccgcTGGGGCCGAGCAGCAGGAACACGCCAATCGGTTTGTTCGGGTCTTCCATGCGCGCTCGGGAAATCTTGATGCGCTTGCCGATCTCATGCAGGGCGTGGTCCTGGCCCAGCACGCGCTCACCAAGCAGCGCCTGCCGGCCCTGct < 2:588610/150‑2 (MQ=255) gccgcTGGGGCCGAGCAGCAGGAACACGCCAATCGGTTTGTTCGGGTCTTCCATGCGCGCTCGGGAAATCTTGATGCGCTTGCCGATCTCATGCAGGGCGTGGTCCTGGCCCAGCACGCGCTCACCAAGCAGGGCCGGCAGGCGCTGCAc > 2:510791/1‑150 (MQ=255) ggCCGAGCAGCAGGAACACGCCAATCGGTTTGTTCGGGTCTTCCATGCGCGCTCGGGAAATCTTGATGCGCTTGCCGATCTCATGCAGGGCGTGGTCCTGGCCCAGCACGCGCTCACCAAGCAGGGCCGGCAGGCGCTGCACGGTATCGa < 1:541746/150‑1 (MQ=255) cGAGCAGCAGGAACACGCCAATCGGTTTGTTCGGGTCTTCCATGCGCGCGCGGGAAATCTTGATGCGCTTGCCGATCTCATGCAGGGCGTGGTCCTGGACCAGCACGCGCTCATCAAGCAGGGCCAGCAGGCGCTGCACGGTATCGAttt < 1:117489/150‑1 (MQ=255) gCCAATCGGTTTGTTCGGGTCTTCCATGCGCGCTCGGGAAATCTTGATGCGCGTGCCGATCTCATGCAGGGCGTGGTCCTGGCCCAGCACGCGCTCACCAAGCAGGGCCGGCAGGCGCTGCACGGTATCGATTTCGTCACGCAGCATCtt > 1:66627/1‑150 (MQ=255) cTTCCATGCGCGCTCGGGAAATCTTGATGCGCTTGCCGATCTCATGCAGGGCGTGGTCCTGGCCCAGCACGCGCTCACCAAGCAGGGCCGGCAGGCGCTGCACGGTATCGATTTCGTCACGCAGCATCTTGCCCAGCGGGATGCCGGTcc < 2:230323/150‑1 (MQ=255) ttCCATGCGCGCTCGGGAAATCTTGATGCGCTTGCCGATCTCATGCAGGGCGTGGTCCTGGCCCAGCACGCGCTCACCGTGCAGCGCCTGCCGGCCCTGcttggt > 2:530826/1‑100 (MQ=37) ttCCATGCGCGCTCGGGAAATCTTGATGCGCTTGCCGATCTCATGCAGGGCGTGGTCCTGGCCCAGCACGCGCTCACCGTGCAGCGCCTGCCGGCCCTGcttggt < 1:530826/105‑6 (MQ=37) aaTCTTGATGCGCTTGCCGATCTCATGCAGGGCGTGGTCCTGGCCCAGCACGCGCTCACCAAGCAGGGCCGGCAGGCGCTGCACGGTATCGATTTCGTCACGCAGCATCTTGCCCAGCGGGATGCCGGTCCAGCCACTGATGACCTGGGc < 1:373494/150‑1 (MQ=255) gcTTGCCGATCTCATGCAGGGCGTGGTCCTGGCCCAGCACGCGTTCGCCAAGCAGCGCCTGCCGGCCCTGcttg < 1:478468/74‑4 (MQ=25) gcTTGCCGATCTCATGCAGGGCGTGGTCCTGGCCCAGCACGCGCTCACCAAGCAGCGCCTGCCGGCCCTGcttg > 2:478468/1‑71 (MQ=25) ttGCCGATCTCATGCAGGGCGTGGTCCTGGCCCAGCACGCGCTCACCAAGCAGGGCCGGCAGGCGCTGCACGGTATCGATTTCGTCACGCAGCATCTTGCCCAGCGGGATGCCGGTCCAGCCACTGATGACCTGGGCGATGGCGCCGCTg > 2:93543/1‑150 (MQ=255) gATCTCATGCAGGGCGTGGTCCTGGCCCAGCACGCGCTCACCAAGCAGGGCCGGCAGGCGCTGCACGGTATCGATTTCGTCACGCAGCATCTTGCCCAACGGGATGCCGGTCCAGCCACTGATGACCTGGGCGATGGCGCCGCTGTCGAc > 1:32883/1‑150 (MQ=255) aTGCAGGGCGTGGTCCTGGCCCAGCACGCGCTCACCAAGCAGGGCCGGCAGGCGCTGCACGGTATCGATTTCGTCACGCAGCATCTTGCCCAGCGGGATGCCGGTCCAGCCACTGATGACCTGGGCGATGGCGCCGCTGTCGACCAgcgc > 1:249552/1‑150 (MQ=255) cAGGGCGTGGTCCTGGCCCAGCACGCGCTCACCAAGCAGGGCCGGCAGGCGCTGCACGGTATCGATTTCGTCACGCAGCATCTTGCCCAGCGGGATGCCGGTCCAGCCACTGATGACCTGGGCGATGGCGCCGCTGTCGACCAGCGCGTg < 1:386013/150‑1 (MQ=255) tCCTGGCCCAGCACGCGCTCACCAAGCAGGGCCGGCAGGCGCTGCACGGTATCGATTTCGTCACGCAGCATCTTGCCCAGCGGGATGCAGGTCCAGCCACTGATGACCTGGGCGATGGCGCCGCTGTCGACCAGCGCGTGGACCAGTGGc > 2:140051/1‑150 (MQ=255) gCCCAGCACGCGCTCACCAAGCAGGGCCGGCAGGCGCTGCACGGTATCGATTTCGTCACGCAGCATCTTGCCCAGCGGGATGCCGGTCCAGCCACTGATGACCTGGGCGATGGCGCCGCTGTCGACCAGCGCGTGGACCAGTGGCTGGTc < 2:125606/150‑1 (MQ=255) cAGCACGCGCTCACCAAGCAGGGCCGGCAGGCGCTGCACGGTATCGATTTCGTCACGCAGCATCTTGCCCAGCGGGATGCCGGTCCAGCCACTGATGACCTGGGCGATGGCGCCGCTGTCGACCAGCGCGTGGACCAGTGGCTGGTCGcc > 2:40120/1‑150 (MQ=255) cAGCACGCGCTCACCAAGCAGGGCCGGCAGGCGCTGCACGGTATCGATTTCGTCACGCAGCATCTTGCCCAGCGGGATGCCGGTCCAGCCACTGATGACCTGGGCGATGGCGCCGCTGTCGACCAGCGCGTGGACCAGCCACTGGTccac < 2:370517/150‑4 (MQ=255) aCCAAGCAGGGCCGGCAGGCGCTGCACGGTATCGATTTCGTCACGCAGCATCTTGCCCAGCGGGATg < 2:337433/67‑1 (MQ=255) aCCAAGCAGGGCCGGCAGGCGCTGCACGGTATCGATTTCGTCACGCAGCATCTTGCCCAGCGGGATg > 1:337433/1‑67 (MQ=255) aaGCAGGGCCGGCAGGCGCTGCACGGTATCGATTTCGTCACGCAGCATCTTGCCCAGCGGGATGc < 1:79206/65‑1 (MQ=255) aaGCAGGGCCGGCAGGCGCTGCACGGTATCGATTTCGTCACGCAGCATCTTGCCCAGCGGGATGc > 2:79206/1‑65 (MQ=255) | TCTTGCCGACGCCGCTGGGGCCGAGCAGCAGGAACACGCCAATCGGTTTGTTCGGGTCTTCCATGCGCGCTCGGGAAATCTTGATGCGCTTGCCGATCTCATGCAGGGCGTGGTCCTGGCCCAGCACGCGCTCACCAAGCAGGGCCGGCAGGCGCTGCACGGTATCGATTTCGTCACGCAGCATCTTGCCCAGCGGGATGCCGGTCCAGCCACTGATGACCTGGGCGATGGCGCCGCTGTCGACCAGCGCGTGGACCAGTGGCTGGTCGCC > NC_002947/3489561‑3489831 |
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: ‑ |