Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 2,973,410 | A→G | G151G (GGT→GGC) | lplT ← | lysophospholipid transporter |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 2,973,410 | 0 | A | G | 95.8% | 155.7 / ‑2.4 | 48 | G151G (GGT→GGC) | lplT | lysophospholipid transporter |
Reads supporting (aligned to +/- strand): ref base A (1/1); new base G (24/22); total (25/23) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 2.18e-01 |
AGGACTGCCCCGGACGCGCCGCCGCCAGTTTGGGAATGTAGATATTGGCAACGACCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAACCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTAACTTACTACCCGTGGTTAATTCGCCGAGAATACCGTATTTCGCCGGTGAATAGGCTGCAGCACCAACACCCAC > NC_000913/2973277‑2973538 | aGGACTGCCCCGGACGCGCCGCCGCCAGTTTGGGAATGTAGATATTGGCAACGACCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAg > 1:10223/1‑139 (MQ=255) gCCCCGGACGCGCCGCCGCCAGTTTGGGAATGTAGATATTGGCAACGACCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAAt < 1:644867/139‑1 (MQ=255) gccgccgccAGTTTGGGAATGTGGATATTGGCAACGACCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATgg > 2:544046/1‑139 (MQ=255) gccgccgccAGTTTGGGAATGTAGATATTGGCAACGACCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATgg > 2:814600/1‑139 (MQ=255) ccgccgccAGTTTGGGAATGTAGATATTGGCAACGACCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGt > 1:803159/1‑139 (MQ=255) cAGTTTGGGAATGTAGATATTGGCAACGACCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCt < 1:814600/139‑1 (MQ=255) tAGGTATTGGCAACGACCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCACCGCt > 2:715297/1‑114 (MQ=255) tAGATATTGGCAACGACCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCACCGCt < 1:715297/114‑1 (MQ=255) atTGGCAACGACCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCt < 1:544046/139‑1 (MQ=255) atTGGCAACGACCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCt < 2:803159/139‑1 (MQ=255) gCAACGACCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCa > 1:67834/1‑139 (MQ=255) cAACGACCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCAc > 2:335438/1‑139 (MQ=255) cAACGACCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCAc < 2:265783/139‑1 (MQ=255) aaCGACCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACt < 2:577947/139‑1 (MQ=255) aaCGACCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACt < 2:67834/139‑1 (MQ=255) aCGACCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTa > 2:830661/1‑139 (MQ=255) aCCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATcgccgc > 2:921431/1‑98 (MQ=255) aCCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATcgccgc < 1:921431/98‑1 (MQ=255) caccacCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGTCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCa < 2:685539/129‑1 (MQ=255) caccacCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGACGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCa > 1:685539/1‑129 (MQ=255) ccGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTAACTTACTACCCg > 1:436531/1‑139 (MQ=255) gCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTAACTTACTACCCGTGGTTa > 2:804872/1‑139 (MQ=255) gTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCtt > 2:342342/1‑93 (MQ=255) gTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCtt < 1:342342/93‑1 (MQ=255) tGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTAACTTACTACCCGTGGTTAATTCg > 1:293300/1‑139 (MQ=255) tGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTAACTTACTACCCGTGGTTAATTCg > 2:290610/1‑139 (MQ=255) tGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTAACTTACTACCCGTGGTTAATTCg > 1:712524/1‑139 (MQ=255) cgcATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATcgc < 1:667935/73‑1 (MQ=255) cacATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATcgc > 2:667935/3‑73 (MQ=255) tGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTAACTTACTACCCGTGGTTAATTCGCCgaga < 2:343080/139‑1 (MQ=255) ggCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTAACTTACTACCCGTGGTTAATTCGCCGAGAATa < 2:293300/139‑1 (MQ=255) gaGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTAACTTACTACCCGTGGTTAATTCGCCGAGAATACCGTATTTCGcc < 2:997227/139‑1 (MQ=255) cATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAg < 1:494590/81‑1 (MQ=255) cATGCCAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAg > 2:494590/1‑81 (MQ=255) ccAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTaa > 2:264136/1‑87 (MQ=255) ccAGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTaa < 1:264136/87‑1 (MQ=255) aGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTAACTTACTACCCGTGGTTAATTCGcc < 2:16659/109‑1 (MQ=255) aGTCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTAACTTACTACCCGTGGTTAATTCGcc > 1:16659/1‑109 (MQ=255) tCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCtt < 2:328732/58‑1 (MQ=255) tCAGCCAGCACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCtt > 1:328732/1‑58 (MQ=255) gccagcACACCACCGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTAACTTACTACCCGTGGTTAATTCGCCGAGAATACCGTATTTCGCCGGTGAATAGGCTgcag > 1:859100/1‑139 (MQ=255) ccaccGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTAACTTACTACCCGTGGTTAATTCGCCGAGAATACCg > 2:77542/1‑105 (MQ=255) ccaccGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTAACTTACTACCCGTGGTTAATTCGCCGAGAATACCg < 1:77542/105‑1 (MQ=255) caccGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTAACTTACTACCCGTGGTTAATTCGCCGAGAATACCGTATTTCGCCGGTGAATAGGCTGCAGCAc > 2:276667/1‑132 (MQ=255) caccGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTAACTTACTACCCGTGGTTAATTCGCCGAGAATACCGTATTTCGCCGGTGAATAGGCTGCAGCAc < 1:276667/132‑1 (MQ=255) accGGCTACGGAACCGAGCAAAATCGCCGCTATGGTAg < 2:371464/38‑1 (MQ=255) accGGCTACGGAACCGAGCAAAATCGCCGCTATGGTAg > 1:371464/1‑38 (MQ=255) cGGCTACGGAGCCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTAACTTACTACCCGTGGTTAATTCGCCGAGAATACCGTATTTCGCCGGTGAATAGGCTGCAGCACCAAcacccac < 2:10223/139‑1 (MQ=255) | AGGACTGCCCCGGACGCGCCGCCGCCAGTTTGGGAATGTAGATATTGGCAACGACCGCACCACCGTAGGCCAGTGCGCATGCGGCCAGGGCGACGAGGACATGCCAGTCAGCCAGCACACCACCGGCTACGGAACCGAGCAAAATCGCCGCTATGGTAGAAGCTTCCATTAAACCGTTAGCTTTCACTAACTTACTACCCGTGGTTAATTCGCCGAGAATACCGTATTTCGCCGGTGAATAGGCTGCAGCACCAACACCCAC > NC_000913/2973277‑2973538 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |