Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 2,700,633 | T→C | V122V (GTA→GTG) | acpS ← | holo‑[acyl‑carrier‑protein] synthase |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 2,700,633 | 0 | T | C | 100.0% | 61.4 / NA | 18 | V122V (GTA→GTG) | acpS | holo‑[acyl‑carrier‑protein] synthase |
Reads supporting (aligned to +/- strand): ref base T (0/0); new base C (12/6); total (12/6) |
AACCCCCGTTCCTTACCAGTTCGGGGGTTTTACTTTTTAAAGAGAACGGTATTATTTTTAACTTTCAATAATTACCGTGGCACAAGCATAGTGCCGCTCATCTGCCAGCGTTACATGCATATTTGCAACGCCCAGCTTTTCCGCCAGT > NC_000913/2700561‑2700708 | aaCCCCCGTTCCTTACCAGTTCGGGGGTTTTACTTTTTAAAGAGAACGGCATTATTTTTAACTTTCAATAATCACCGTgg > 2:482130/1‑80 (MQ=255) ccTTACCAGTTCGGGGGTTTTACTTTTTAAAGAGAACGGTATTATTTTTAACTTTCAATAATCACCGTGGCACAAGCATAg > 2:482134/1‑81 (MQ=255) gggTTTTACTTTTTAAAGAGAACGGTATTATTTTTAACTTTCAATAATCACCGTGGCACAAGCATAGTGCCGCTCATCTGc > 1:482139/1‑81 (MQ=255) ttACTTTTTAAAGAGAACGGTATTATTTTTAACTTTCAATAATCACCGTGGCACAAGCATAGTGCCGCTCATCTGCCAGc < 1:482115/80‑1 (MQ=255) ttACTTTTTAAAGAGAACGGTATTATTTTTAACTTTCAATAATCACCGTGGCACAAGCATAGTGCCGCTCATCTGCCAGc < 1:482114/80‑1 (MQ=255) tACTTTTTAAAGAGAACGGTATTATTTTTAACTTTCAATAATCACCGTGGCACAAGCATAGTGCCGCTCATCTGCCAGCg < 1:482116/80‑1 (MQ=255) ttAAAGAGAACGGTATTATTTTTAACTTTCAATAATCACCGTGGCACAAGCATAGTGCCGCTCATCTGCCAGCGTTACATg > 2:482147/1‑81 (MQ=255) cGGTATTATTTTTAACTTTCAATAATCACCGTGGCACAAGCATAGTGCCGCTCATCTGCCAGCGTTACATGCATATTTGCa < 1:482117/81‑1 (MQ=255) ggTATTATTTTTAACTTTCAATAATCACCGTGGCACAAGCATAGTGCCGCTCATCTGCCAGCGTTACATGCATATTTGCaa < 1:482118/81‑1 (MQ=255) ttattTTTAACTTTCAATAATCACCGTGGCACAAGCATAGTGCCGCTCATCTGCCAGCGTTACATGCATATTTGCAACGcc > 1:482153/1‑81 (MQ=255) ttattTTTAACTTTCAATAATCACCGTGGCACAAGCATAGTGCCGCTCATCTGCCAGCGTTACATGCATATTTGCAACGc < 1:482119/80‑1 (MQ=255) attTTTAACTTTCAATAATCACCGTGGCACAAGCATAGTGCCGCTCATCTGCCAGCGTTACATGCATATTTGCAACGcc > 1:482143/1‑79 (MQ=255) ttAACTTTCAATAATCACCGTGGCACAAGCATAGTGCCGCTCATCTGCCAGCGTTACATGCATATTTGCAACGCCCAGCtt > 2:482146/1‑81 (MQ=255) aaCTTTCAATAATCACCGTGGCACAAGCATAGTGCCGCTCATCTGCCAGCGTTACATGCATATTTGCAACGCCCAGCtttt > 1:482149/1‑81 (MQ=255) aCTTTCAATAATCACCGTGGCACAAGCATAGTGCCGCTCATCTGCCAGCGTTACATGCATATTTGCAACGCCCAGCTTTTc > 2:482156/1‑81 (MQ=255) aataatCACCGTGGCACAAGCATAGTGCCGCTCATCTGCCAGCGTTACATGCATATTTGCAACGCCCAGCTTTTCCGCCAg > 1:482150/1‑81 (MQ=255) aataatCACCGTGGCACAAGCATAGTGCCGCTCATCTGCCAGCGTTACATGCATATTTGCAACGCCCAGCTTTTCCGCCAg > 1:482145/1‑81 (MQ=255) ataatCACCGTGGCACAAGCATAGTGCCGCTCATCTGCCAGCGTTACATGCATATTTGCAACGCCCAGCTTTTCCGCCAGt > 1:482136/1‑81 (MQ=255) | AACCCCCGTTCCTTACCAGTTCGGGGGTTTTACTTTTTAAAGAGAACGGTATTATTTTTAACTTTCAATAATTACCGTGGCACAAGCATAGTGCCGCTCATCTGCCAGCGTTACATGCATATTTGCAACGCCCAGCTTTTCCGCCAGT > NC_000913/2700561‑2700708 |
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 < 38 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |