Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 4,184,542 | C→A | P1100Q (CCG→CAG) | rpoB → | RNA polymerase, beta subunit |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 4,184,542 | 0 | C | A | 100.0% | 39.7 / NA | 17 | P1100Q (CCG→CAG) | rpoB | RNA polymerase, beta subunit |
Reads supporting (aligned to +/- strand): ref base C (0/0); new base A (6/11); total (6/11) |
TCTGGCGGTTAAACGCCGTATCCAGCCTGGTGACAAGATGGCAGGTCGTCACGGTAACAAGGGTGTAATTTCTAAGATCAACCCGATCGAAGATATGCCTTACGATGAAAACGGTACGCCGGTAGACATCGTACTGAACCCGCTGGGCGTACCGTCTCGTATGAACATCGGTCAGATCCTCGAAACCCACCTGGGTATGGCTGCGAAAGGTATCGGCGACAAGATCAACGCCATGCTGAAACAGCAGCAAGAAGTCGCGAAACTGCGCGAATTC > NC_000913/4184402‑4184675 | ttttgcttttAAACGCCGTAGCCAGCCTGGTGCCAAGAGGGGAGGTCGTCACGGTAACAAGGGTGTAATTTCTAAGATCAACCCGATCCAAGATATGCCTTACGATGAAAACGGTACGCCGGTAGACATCGTACTGAACCAGc < 1:44019/135‑1 (MQ=255) tAAATGCGGTATTGATCCTGGGGACATGAGGGCAGGGTGTCACTGTAACGAGGGGGTACTTTCTAAGATCGACTCGCGCGAAGATATGCCTTACGATGAAAACGGTACGCCGGTAGACATCGTACTGAACCAGCTGGGCGTAc < 2:90389/143‑1 (MQ=255) ccGTATCCAGCCTGGTGACAAGATGGCAGGTCGTCACGGTAACAAGGGTGTAATTTCTAAGATCAACCCGATCGAAGATATGCCTTACGATGAAAACGGTACGCCGGTAGACATCGTACTGAACCAGCTGGGCGTACCGtctc > 2:89479/1‑143 (MQ=255) gTATCCATCCTGGTGACAAGATTGCAGGTCGTCACGGTAACAAGCGTGTATTTTCTATGATCAACCCGATCGAAGATATGCTTTACGATGAAAACGGTACGCCGGTAGACATCGTACTGAACCAGCTGGGCGTACCGTCTCGt < 1:48895/143‑1 (MQ=255) cAGCCTGGTGACAAGATGGCAGGTCGTCCCGGTATCACGGCCGTAATTTCTAAGATCAACCCGATCGAAGATATGCCTTACGATGAAAACGGTACGCCGGTAGACATCGTACTGAACCAGCTGGGCGTACCGTCTCGTATGaa < 2:175365/143‑1 (MQ=255) gTGACAAGATGGCAGGTCGTCACGGTAACAAGGGTGTAATTTCTAAGATCAACCCGATCGAAGATATGCCTTACGATAAAAACGGTACGCCAGTAGACATCGTACTGAACCAGCTGGGCGTACCGTCTCGTATGAACATCGGt > 1:67456/1‑143 (MQ=255) tGACAAGCTGGCAGGTCGTCACGGTAACAAGGGTGTAATTTCTAAGATCAACCCGATCGAAGCTATGCCTTACGATGAAAACGGTACGCCGGTAGACATCGTACTGAACCAGCTGGGCGTACCGTCTCGTATGAACATCGGTc < 2:229466/143‑1 (MQ=255) aCAAGATTGCAGGTCGTCACGGTATCAAGGGTGTAATTTCTAAGATCAACCCGATCGAAGATATGCCTTACGATGAAATCGGTACGCCGGTAGACATCGTACTGAACCAGCTGGGCGTACCGTCTCGTATGAACATCGGTCAg < 2:62446/143‑1 (MQ=255) aaGATGGCAGGTCGTCACGGTAACAAGGGTGTAATTTCTAAGATGAACCCGATCGAAGATATGACTTCCGGTGAAAACGGTACGCCGGGAGAAACGGTACTGAAGCAGCTGGGGGGACCGGCTAGTACGAACATCGGTCAGAt > 2:254843/1‑143 (MQ=255) aaGATGGCAGGTCGTCACGGTAACAAGGGTGTAATTTCTAAGATCAACCCGATCGAAGATATGCCTTACGATGAAAACGGTACGCCGGTAGACATCGTACTGAACCAGCTGGGCGTACCGTCTCGGATGAACATCGGTCAGAt > 2:380712/1‑143 (MQ=255) gggTGTAATTTCTAAGATCAACCCGATCGAAGATATGCCTTACGATGAAAACGGTACGCCGGTAGACATCGTACTGAACCAGCTGGGCGTACCGTCTCGTATGAACATCGGTCAGATCCTCGAAACCCACCTGGGTATGGCTg < 1:199728/143‑1 (MQ=255) tgtAATTTCTAAGATAAACCCGATCGAAGATATGCCTTACGATGAAAACGGTACGCCGGTAGACAACGTACTAAACCAGCTGGGCGTAACGTATCGTATGAACATAGGTAAGATCCTAGAAACCCACCTAGGTATGGCTGCGa > 1:109267/1‑143 (MQ=255) gtAATTGCTAAGTTCAACCTGATCGATGATATGCTTTTCTATTTTTACGTTACGTCGTTAGACATCGTACGGAACCAGCTGGGCGTACCGTCTCGTATGAACATCGGTCAGATCCTCGAAACCCACCTGGGTATGGCTGCGaa < 1:53478/143‑1 (MQ=255) tctttCTAAGATCGTCTCTCTCGAAGATATTCCTTACGATGGAAACGTTACGCCGGTAGACATCGTACTGAACCAGCTGGGCGTACCGTCTCGTATGAGCTTCTGTCAGATCCTCGATACCCACCTGTGTATGGCTGCGAAAg < 2:202800/141‑1 (MQ=255) aaGATCAGCCCGATGGAAGATATGCCTTACGATGAAAACGGTACGCCGGTAGACATCGTACTGAACCAGCTGGGCGTACCGTCTCGTATGAACATCGGACAGATCCTCGAAACCCACCTGGGTATGGCTGCGAAAGGTATCgg < 2:305249/143‑1 (MQ=255) aaGATCACCCCGATCGAAGATATGTCTTATGATGATAACGGTACGCCGGTAGACACCGTACTCAACCAGCTGGGCGTACCGTCTCGTATGAACATCGGTCAGATCCTCGAATCCCACCTGGGTATGGCTGCGAAAGGTATCgg < 2:265006/143‑1 (MQ=255) tACTGAACCAGCTGGGCGTACCGTCTCGTATGAACATCGGTCAGATCCTCGAAACCCACCTGGGTATGGCTGCGTTAGGTATCGGCGACTAGATAAACGCCATGCTGAAAAAGCAGAAAGAAGTCGCGAAACTGAGCGAATTc > 1:41109/1‑143 (MQ=255) | TCTGGCGGTTAAACGCCGTATCCAGCCTGGTGACAAGATGGCAGGTCGTCACGGTAACAAGGGTGTAATTTCTAAGATCAACCCGATCGAAGATATGCCTTACGATGAAAACGGTACGCCGGTAGACATCGTACTGAACCCGCTGGGCGTACCGTCTCGTATGAACATCGGTCAGATCCTCGAAACCCACCTGGGTATGGCTGCGAAAGGTATCGGCGACAAGATCAACGCCATGCTGAAACAGCAGCAAGAAGTCGCGAAACTGCGCGAATTC > NC_000913/4184402‑4184675 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 8 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 22 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |