Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 1,941,784 | A→G | V267A (GTC→GCC) | znuA ← | Zn(2(+)) ABC transporter periplasmic binding protein |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 1,941,784 | 0 | A | G | 100.0% | 41.9 / NA | 12 | V267A (GTC→GCC) | znuA | Zn(2(+)) ABC transporter periplasmic binding protein |
Reads supporting (aligned to +/- strand): ref base A (0/0); new base G (7/5); total (7/5) |
AGGGGATCCAACGTTCCCATACGAACGGATGTCCCTCGTGCGACGCTCTCAACGACCGCTGGCCTGAACTGTGGCTCAGCAAAAAC > NC_000913/1941742‑1941827 | aGGGGATCCAACGTTCCCATACGAACGGATGTCCCTCGTGCGGCGctct > 1:2153250/1‑49 (MQ=255) ggATCCAACGTTCCCATACGAACGGATGTCCCTCGTGCGGCGCTCTCaa > 1:220235/1‑49 (MQ=255) ccAACGTTCCCATACGAACGGATGTCCCTCGTGCGGCGCTCTCAACGAc > 1:1633617/1‑49 (MQ=255) aCGTTCCCATACGAACGGATGTCCCTCGTGCGGCGCTCTCAACGACCGc > 1:1060514/1‑49 (MQ=255) ccATACGAACGGATGTCCCTCGTGCGGCGCTCTCAACGACCGCTGGCCt > 1:1637716/1‑49 (MQ=255) gAACGGATGTCCCTCGTGCGGCGCTCTCAACGACCGCTGGCCTGAACtg > 1:823294/1‑49 (MQ=255) ggATGTCCCTCGTGCGGCGCTCTCAACGACCGCTGGCCTGAACTGTGGc < 1:509974/49‑1 (MQ=255) tCCCTCGTGCGGCGCTCTCAACGACCGCTGGCCTGAACTGTGGCTCAg < 1:703503/48‑1 (MQ=255) cccTCGTGCGGCGCTCTCAACGACCGCTGGCCTGAACTGTGGCTCAGc > 1:759226/1‑48 (MQ=255) cTCGTGCGGCGCTCTCAACGACCGCTGGCCTGAACTGTGGCTCAGCaaa < 1:253791/49‑1 (MQ=255) cTCGTGCGGCGCTCTCAACGACCGCTGGCCTGAACTGTGGCTCAGCaaa < 1:532345/49‑1 (MQ=255) gTGCGGCGCTCTCAACGACCGCTGGCCTGAACTGTGGCTCAGCAAAAAc < 1:334760/49‑1 (MQ=255) | AGGGGATCCAACGTTCCCATACGAACGGATGTCCCTCGTGCGACGCTCTCAACGACCGCTGGCCTGAACTGTGGCTCAGCAAAAAC > NC_000913/1941742‑1941827 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |