Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | W3110S.gb | 2,964,217 | G→A | 22.6% | N159N (AAC→AAT) | lgt ← | phosphatidylglycerol‑prolipoprotein diacylglyceryl transferase |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | W3110S.gb | 2,964,217 | 0 | G | A | 22.6% | 60.0 / 13.3 | 31 | N159N (AAC→AAT) | lgt | phosphatidylglycerol‑prolipoprotein diacylglyceryl transferase |
Reads supporting (aligned to +/- strand): ref base G (16/8); new base A (5/2); total (21/10) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 1.00e+00 |
GGTTTGCAGCAGCAAAATATCTTCTGTACGGGAGCCAGGGAACAGCATGGCAAACGGGAAGTTCGGGTCAACGCGGCCCCACAATTCACCGTTAATAAAGTTGCCCAGACGCCCGGCACCAAGAC > W3110S.gb/2964157‑2964281 | ggttTGCAGCAGCAAAATATCTTCTGTACGGGAGCCAGGGAACAGCATGGCAAACGGGAAATTCGGGTc > 1:1473896/1‑69 (MQ=255) ttGCAGCAGCAAAATATCTTCTGTACGGGAGCCAGGGAACAGCATGGCAAACGGGAAGTTCGGGTCAAc > 1:1688403/1‑69 (MQ=255) ttGCAGCAGCAAAATATCTTCTGTACGGGAGCCAGGGAACAGCATGGCAAACGGGAAGTTCGGGTCAAc > 1:2919493/1‑69 (MQ=255) ttGCAGCAGCAAAATATCTTCTGTACGGGAGCCAGGCAACAGCATGGCAAACGGGAAGTTCGGGTCAAc > 1:1313960/1‑69 (MQ=255) aaaTATCTTCTGTACGGGAGCCAGGGAACAGCATGGCAAACGGGAAGTTCGGGTCACCGCGGCCCcaca > 1:2045316/1‑69 (MQ=255) aaaTATCTTCTGTACGGGAGCCAGGGAACAGCATGGCAAACGGGAAGTTCGGGTCAACGCGGCCCcaca > 1:71481/1‑69 (MQ=255) atCTTCTGTACGGGAGCCAGGGAACAGCATGGCAAACGGGAAGTTCGGGTCAACGCGGCCCCACAATTc < 1:1152700/69‑1 (MQ=255) tcttctGTACGGGAGCCAGGGAACAGCATGGCAAACGGGAAGTTc < 1:1648632/45‑1 (MQ=255) gTACGGGAGCCAGGGAACAGCATGGCAAACGGGAAGTTCGGGTCAACGCGGCCCCACAATTCACCGt < 1:3098380/67‑1 (MQ=255) aGCCAGGGAACAGCATGGCAAACGGGAAGTTCGGGTCAACGCGGCCCCACAATTCACCGt < 1:1092745/60‑1 (MQ=255) aaCAGCATGGCAAACGGGAAGTTCGGGTCAACGCGGCCCCACAATTCACCGTTAATAAAGTTGcc > 1:392812/1‑65 (MQ=255) aaCAGCATGGCAAACGGGAAGTTCGGGTCAACGCGGCCCCACAATTCACCGTTAATAAAGTTGcc > 1:3015506/1‑65 (MQ=255) aCAGCATGGCAAACGGGAAATTCGGGTCAACGCGGCCCCACAATTCACCGTTAATaaa < 1:1439072/58‑1 (MQ=255) gCATGGCAAACGGGAAGTTCGGGTCAACGCGGCCCCACAATTCACCGTtaataa > 1:2786541/1‑54 (MQ=255) gCATGGCAAACGGGAAGTTCGGGTCAACGCGGCCCCACAATTCACCGTtaataa > 1:142972/1‑54 (MQ=255) cATGGCAAACGGGAAGTTCGGGTCAACGCTGCCCCACAATTCACCGTTAATAAAGTTGCCCa < 1:649357/62‑1 (MQ=255) cATGGCAAACGGGAAGTTCGGGTCAACGCGGCCCCACAATTCACCGTTAATAAAGTTGCCCa < 1:97398/62‑1 (MQ=255) cATGGCAAACGGGAAGTTCGGGTCAACGCGGCCCCACAATTCACCGTTAATAAAGTTGCCCa < 1:2899169/62‑1 (MQ=255) cATGGCAAACGGGAAGTTCGGGTCAACGCGGCCCCACAATTCACCGTTAATAAAGTTGCCCAGACGccc > 1:1704513/1‑69 (MQ=255) cATGGCAAACGGGAAGTTCGGGTCAACGCGGCCCCACAATTCACCGTTAATAAAGTTGCCCAGACGccc > 1:251649/1‑69 (MQ=255) cATGGCAAACGGGAAATTCGGGTCAACGCGGCCCCACAATTCACCGTTAATAAAGTTGCCCAGACGccc < 1:1427279/69‑1 (MQ=255) tGGCAAACGGGAAGTTCGGGTCAACGCGGCCCCACAATTCACCGTtaata > 1:2928728/1‑50 (MQ=255) tGGCAAACGGGAAGTTCGGGTCAACGCGGCCCCACAATTCACCGTtaat > 1:1807417/1‑49 (MQ=255) ggCAAACGGGAAGTTCGGGTCAACGCGGCCCCACAATTCACCGTTAATAAAGTTGCCCAGACGCCCgg < 1:809149/68‑1 (MQ=255) gCAAACGGGAAGTTCGGGTCAACGCGGCCCCACAATTCACCGTTAATAAAGTTGCCCa > 1:3332610/1‑58 (MQ=255) gCAAACGGGAAATTCGGGTCAACGCGGCCCCACAATTCACCGTTAATAAAGTTGCCCa > 1:413473/1‑58 (MQ=255) gCAAACGGGAAATTCGGGTCAACGCGGCCCCACAATTCACCGTTAATAAAGTTGCCCa > 1:858554/1‑58 (MQ=255) aCGGGAAGTTCGGGTCAACGCGGCCCCACAATTCACCGTTAATAAAGTTGCCCAGACGCCCGGCACCaa > 1:718486/1‑69 (MQ=255) cGGGAAATTCGGGTCAACGCGGCCCCACAATTCACCGTTAATAAAGTTGCCCa > 1:2297999/1‑53 (MQ=255) cGGGAAATTCGGGTCAACGCGGCCCCACAATTCACCGTTAATAAAGTTGCCCa > 1:2441490/1‑53 (MQ=255) gAAGTTCGGGTCAACGCGGCCCCACAATTCACCGTTAATAAAGTTGCCCAGACGCCCGGCACCAAGAc > 1:3168536/1‑68 (MQ=255) | GGTTTGCAGCAGCAAAATATCTTCTGTACGGGAGCCAGGGAACAGCATGGCAAACGGGAAGTTCGGGTCAACGCGGCCCCACAATTCACCGTTAATAAAGTTGCCCAGACGCCCGGCACCAAGAC > W3110S.gb/2964157‑2964281 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |