Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 4,293,898 | A→G | Y119C (TAC→TGC) | nrfG → | heme lyase (NrfEFG) for insertion of heme into c552, subunit NrfG |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 4,293,898 | 0 | A | G | 100.0% | 116.4 / NA | 31 | Y119C (TAC→TGC) | nrfG | heme lyase (NrfEFG) for insertion of heme into c552, subunit NrfG |
Reads supporting (aligned to +/- strand): ref base A (0/0); new base G (13/18); total (13/18) |
GAACAGTGGGCGTTACTGGGCGAGTACTATCTGTGGCAAAACGATTACAGCAATTCGTTGCTGGCGTACCGTCAGGCGTTGCAACTACGTGGTGAGAACGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTACCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTCGCGCTGGACAGTAATGAAATCACCGCCCTGATGCTGCTGGCTTCCGATGCGTTTATGCAGGCGAACTACGCGCA > NC_000913/4293762‑4294027 | gAACAGTGGGCGTTACTGGGCGAGTACTATCTGTGGCAAAACGATTACAGCAATTCGTTGCTGGCGTACCGTCAGGCGTTGCAACTACGTGGTGAGAACGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGcc < 1:507667/139‑1 (MQ=255) gTGGGCGTTACTGGGCGAGTACTATCTGTGGCAAAACGATTACAGCAATTCGTTGCTGGCGTACCGTCAGGCGTTGCAACTACGTGGTGAGAACGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGgcc < 1:7755/139‑1 (MQ=255) ggCGTTACTGGGCGAGTACTATCTGTGGCAAAACGATTACAGCAATTCGTTGCTGGCGTACCGTCAGGCGTTGCAACTACGTGGTGAGAACGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGgccagc < 2:843743/139‑1 (MQ=255) tGGGCGAGTACTATCTGTGGCAAAACGATTACAGTAATTCGTTGCTGGCGTACCGTCAGGCGTTGCAACTACGTGGTGAGAACGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCatat < 2:718970/139‑1 (MQ=255) ggCGAGTACTATCTGTGGCAAAACGATTACAGCAATTCGTTGCTGGCGTACCGTCAGGCGTTGCAACTACGTGGTGAGAACGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGa < 2:877413/139‑1 (MQ=255) tCTGTGGCAAAACGATTACAGCAATTCGTTGCTGGCGTACCGTCAGGCGTTGCAACTACGTGGTGAGAACGCTGAACTGTATGCGGCGCTGGCGACGGTGATTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACt < 2:1119027/139‑1 (MQ=255) ggCAAAACGATTACAGCAATTCGTTGCTGGCGTACCGTCAGGCGTTGCAACTACGTGGTGAGAACGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACt > 2:354019/1‑134 (MQ=255) ggCAAAACGATTACAGCAATTCGTTGCTGGCGTACCGTCAGGCGTTGCAACTACGTGGTGAGAACGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACt < 1:354019/134‑1 (MQ=255) gTCAGGCGTTGCAACTACGTGGTGAGAACGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTCGCGCTGGACAGTAATGa < 2:265147/139‑1 (MQ=255) cGTTGCAACTACGTGGTGAGAACGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTCGCGCTGGACAGTAATGAAATCAc < 2:1007679/139‑1 (MQ=255) gCAACTACGTGGTGAGAACGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTCGCGCTGGACAGTAATGAAATCACCGcc > 1:1039276/1‑139 (MQ=255) cGTGGTGAGAACGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTCGCGCTGGACAGTAATGAAATCACCGCCCTGAtgc > 2:176441/1‑139 (MQ=255) cGTGGTGAGAACGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTCGCGCTGGACAGTAATGAAATCACCGCCCTGAtgc > 2:119190/1‑139 (MQ=255) cGTGGTGAGAACGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAACCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTCGCGCTGGACAGTAATGAAATCACCGCCCTGAtgc > 2:769184/1‑139 (MQ=255) tggtgAGAACGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTCGCGCTGGACAGTAATGAAATCACCGCCCTGAtgctg < 2:1042397/139‑1 (MQ=255) gtgAGAACGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTCGCGCTGGACAGTAATGAAATCACCGCCCTGATgctgct > 2:21677/1‑139 (MQ=255) gaACGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATCATCGACAAAGCCCTCGCGCTGGACAGTAATGAAATCACCGCCCTGATGCTGCTGGCt > 1:659933/1‑139 (MQ=255) aaCGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTcgcg < 2:814070/99‑1 (MQ=255) aaCGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTcgcg > 1:814070/1‑99 (MQ=255) aaCGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTCGCGCTGGa < 1:578610/104‑1 (MQ=255) aaCGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTCGCGCTGGa > 2:578610/1‑104 (MQ=255) cTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAACCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTCGCGCTGGACAGTAATGAAATCACCGCCCTGATGCTGCTGGCTTCCGa < 1:769184/139‑1 (MQ=255) aTGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGa > 2:69606/1‑69 (MQ=255) aTGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGa < 1:69606/69‑1 (MQ=255) aTGCGGCGCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTCGCGCTGGACAGTAATGAAATCACCGCCCTGATGCTGCTGGCTTCCGATGCGTTTAt > 2:100958/1‑139 (MQ=255) ggcgCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTcg < 2:713748/80‑1 (MQ=255) ggcgCTGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTcg > 1:713748/1‑80 (MQ=255) tGGCGACGGTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTCGCGCTGGACAGTAATGAAATCACCGCCCTGATGCTGCTGGCTTCCGATGCGTTTATGCAGGCGaa > 1:282522/1‑139 (MQ=255) ggTGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTCGCGCTGGACAGTAATGAAATCACCGCCCTGATGCTGCTGGCTTCCGATGCGTTTATGCAGGCGAACTAcgcg < 2:33664/139‑1 (MQ=255) tGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTCGCGCTGGACAGTAATGAAATCACCGCCCTGATGCTGCTGGCTTCCGATGCGTTTATGCAGGCGAACTACGCGCa < 1:517435/139‑1 (MQ=255) tGCTTTATTGCCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTCGCGCTGGACAGTAATGAAATCACCGCCCTGATGCTGCTGGCTTCCGATGCGTTTATGCAGGCGAACTACGCGCa < 2:282522/139‑1 (MQ=255) | GAACAGTGGGCGTTACTGGGCGAGTACTATCTGTGGCAAAACGATTACAGCAATTCGTTGCTGGCGTACCGTCAGGCGTTGCAACTACGTGGTGAGAACGCTGAACTGTATGCGGCGCTGGCGACGGTGCTTTATTACCAGGCCAGCCAGCATATGACCGCCCAGACTCGCGCAATGATCGACAAAGCCCTCGCGCTGGACAGTAATGAAATCACCGCCCTGATGCTGCTGGCTTCCGATGCGTTTATGCAGGCGAACTACGCGCA > NC_000913/4293762‑4294027 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 28 ≤ ATCG/ATCG < 35 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |