Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 2,077,132 | G→A | G7G (GGG→GGA) | cbeA → | CP4‑44 prophage; cytoskeleton bundling‑enhancing antitoxin CbeA |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 2,077,132 | 0 | G | A | 100.0% | 61.1 / NA | 18 | G7G (GGG→GGA) | cbeA | CP4‑44 prophage; cytoskeleton bundling‑enhancing antitoxin CbeA |
Reads supporting (aligned to +/- strand): ref base G (0/0); new base A (11/7); total (11/7) |
AGCAGAATTATCGCCACTACCGGACCATTCTTAGCCGATTTTCTGTAAGGATTTTATCGTGTCAGACACACTCCCCGGGACAACACTTCCCGACGACAATCACGACCGCCCCTGGTGGGGGCTGCCCTGCACCGTGACGCCCTGTTTCGG > NC_000913/2077054‑2077203 | aGCAGAATTATCGCCACTACCGGACCATTCTTAGCCGATTTTCTGTAAGGATTTTATCGTGTCAGACACACTCCCCGGAac < 1:368304/81‑1 (MQ=255) gCAGAATTATCGCCACTACCGGACCATTCTTAGCCGATTTTCTGTAAGGATTTTATCGTGTCAGACACACTCCCCGGAac > 1:368333/1‑80 (MQ=255) aaTTATCGCCACTACCGGACCATTCTTAGCCGATTTTCTGTAAGGATTTTATCGTGTCAGACACACTCCCCGGAACAacac > 2:368336/1‑81 (MQ=255) aTTATCGCCACTACCGGACCATTCTTAGCCGATTTTCTGTAAGGATTTTATCGTGTCAGACACACTCCCCGGAACAACACt > 2:368341/1‑81 (MQ=255) cTACCGGACCATTCTTAGCCGATTTTCTGTAAGGATTTTATCGTGTCAGACACACTCCCCGGAACAACACTTCCCgacgac < 1:368305/81‑1 (MQ=255) aCCGGACCATTCTTAGCCGATTTTCTGTAAGGATTTTATCGTGTCAGACACACTCCCCGGAACAACACTTCCCGACGACaa > 2:368340/1‑81 (MQ=255) ccATTCTTAGCCGATTTTCTGTAAGGATTTTATCGTGTCAGACACACTCCCCGGAACAACACTTCCCGACGACAATCACGa > 1:368339/1‑81 (MQ=255) tAGCCGATTTTCTGTAAGGATTTTATCGTGTCAGACACACTCCCCGGAACAACACTTCCCGACGACAATCACGACCGcccc > 1:368342/1‑81 (MQ=255) tAGCCGATTTTCTGTAAGGATTTTATCGTGTCAGACACACTCCCCGGAACAACACTTCCCGACGACAATCACGACCGcccc > 1:368344/1‑81 (MQ=255) cGATTTTCTGTAAGGATTTTATCGTGTCAGACACACTCCCCGGAACAACACTTCCCGACGACAATCACGACCGCCCCtggt < 2:368306/81‑1 (MQ=255) ttttCTGTAAGGATTTTATCGTGTCAGACACACTCCCCGGAACAACACTTCCCGACGACAATCACGACCGCCCCTGGTggg < 2:368307/81‑1 (MQ=255) tAAGGATTTTATCGTGTCAGACACACTCCCCGGAACAACACTTCCCGACGACAATCACGACCGCCCCTGGTGGGGGCt < 2:368308/78‑1 (MQ=255) aTTTTATCGTGTCAGACACACTCCCCGGAACAACACTTCCCGACGACAATCACGACCGCCCCTGGTGGGGGCTGCCCTGCa > 1:368345/1‑81 (MQ=255) ttATCGTGTCAGACACACTCCCCGGAACAACACTTCCCGACGACAATCACGACCGCCCCTGGTGGGGGCTGCCCTGCAcc < 1:368309/80‑1 (MQ=255) aTCGTGTCAGACACACTCCCCGGAACAACACTTCCCGACGACAATCACGACCGCCCCTGGTGGGGGCTGCCCTGCACCGt > 2:368349/1‑80 (MQ=255) cacacTCCCCGGAACAACACTTCCCGACGACAATCACGACCGCCCCTGGTTGGGGCTGCCCTTCACCGTGACGCCCTGttt > 1:368343/1‑81 (MQ=255) acacTCCCCGGAACAACACTTCCCGACGACAATCACGACCGCCCCTGGTGGGGGCTGCCCTGCACCGTGACGCCCTGTTTc < 2:368310/81‑1 (MQ=255) acTCCCCGGAACAACACTTACCGACGACAATCACGACCGCCAATGGTGGGGGCTGCCCTGCACCGTGACGCCCTGTTTCgg > 1:368350/1‑81 (MQ=255) | AGCAGAATTATCGCCACTACCGGACCATTCTTAGCCGATTTTCTGTAAGGATTTTATCGTGTCAGACACACTCCCCGGGACAACACTTCCCGACGACAATCACGACCGCCCCTGGTGGGGGCTGCCCTGCACCGTGACGCCCTGTTTCGG > NC_000913/2077054‑2077203 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 23 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |