Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 4,499,998 | G→C | intergenic (+498/‑1262) | insD6 → / → yjgZ | IS2 insertion element protein InsB/uncharacterized protein YjgZ |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 4,499,998 | 0 | G | C | 100.0% | 26.4 / NA | 11 | intergenic (+498/‑1262) | insD6/yjgZ | IS2 insertion element protein InsB/uncharacterized protein YjgZ |
Reads supporting (aligned to +/- strand): ref base G (0/0); new base C (5/6); total (5/6) |
GCACTGATTTTTCTACTGACGGGCTGATGAGACGTTATGTCACTGGCGGTAATAATCAGTGGCACACTGTAGCCTCCCTGCACATGACCATAATGATGAACAGGATTGGCACTGTCGCTGACCGACAGCCCAAGGCCAGAAAAGTAAAGCATGGCGAAATGACGTGAGTACCGGCGAAGGATACCATCAAGCTGGCCAAGAAAGTTATCCAGTTTACTGATGCTGGCGAGGTAACAGGCAATTTTTCGGGGATACTGCTCCAGGTAATTATTCGGCTAGGAGTTAAGGCTGTCACACGGATTTGGATGAGAACCCATCATGTGCAGGAAAATTATCTTCGGAGAGGATGTATCCGCCAGCGCACGTTCTGTTTCCTGTAACAACAGTTTGTCATCTGTTTTACGGGAAGCGAAGCTGCCTTTCTTGAGGAAAGT > NC_000913/4499768‑4500201 | gCACTGATTTTTCTACTGACGGGCTGATGAGACGTTATGTCACTGGCGGTAATAATCAGTGGCACACTGTAGCCTCCCTGCACATGACCATAATGAGGAACAGGATTGGCACTGTCGCTGACCGACAGCCCAAGGCCAGAAAAGGAAAGCATGGCGAAATGACGTGAGTACCGGCGAAGGATACCATCAAGCTGGCCAAGAAAGTTATCCAGTTTACTGATGCTGGCGAGCTAACAgn < 1:37670/238‑2 (MQ=255) tCTACTGACGGGCTGATGAGACGTTATGTCACTGGCGGTAATAATCAGTTGCACACTGGAGCCTCCCCGCACATTACCATAATGATGAACAGGAATGGCAATGTCGCTGACCGAAAGCCCAAGGCCAGAAAAATAAAACATGTCGAAATGACGTGCGTACCGGCGAAGGATACCATCAAGCCGGCCAAGAAAGTTATCCCGGTTAATGATGCTGGAGAGCTAACAGGCAATTTTTCGGGGATACTGCTcc > 1:8015/1‑250 (MQ=255) gatgaGACGTTATGGCACTGGCGGTAATAATCAGTGGCACACTGTAGCCTCCCTGCACATGACCATAATGATGAACAGGATTGGCACTGTCGCTGACCGACAGCCCAAGGCCAGAAAAGTAAAGCATGGCGAAATGACGTGAGTACCGGCGAAGGATAGCATCAAGCTGGCCAAGAAAGTTATCCAGTTTACTGATGCGTTCGAGCTAACAGGCAATTGTTCGTG‑ATACTGCCCCAGGTAATTATTCGGc < 1:318701/250‑1 (MQ=255) ggTAATAATCAGTGGCACACTGTAGCCTCCCTGCACATGACCATAATGATGAACAGGATTGGCACTGTCGCTGACCGACAGCCCAAGGCCAGAAAAGTAAAGCATGGCGAAATGACGTGAGTACCGGCGAAGGTTACCATCAAGCTGGCCAAGAAAGGTATCCAGTTTACTGATGCTGGCGAGCTAACAGGCAATTTTTCGGGGATACTGCTCCAGGTAATTAGGCGGCTAGGAGTTAAGGCt < 1:127161/243‑1 (MQ=255) gCTGACCGACAGCCCAAGGCCAGAAAAGTAAAGCATGGCGCAATGACGTGAGTACCGGCGAAGGATACCATCAAGCTGGCCAAGAAAGTTATCCAGTTCACTGATGCTGGCGAGCTAACAGGCAATTTTTCGGGGATACTGCTCCAGGTAATTATTCGGCTAGGAGTTAAGGCTGTCACACGGATTTGGATGCGAAcc > 1:334091/1‑198 (MQ=255) cTGACCGACAGCCCAAGGCCAGAAAAGTAAAGCATGGCGAAATGACGTGAGTACCGGCGAAGGATACCATCAAGCTGGCCAAGAAAGTTATCCAGTTTACTGATGCTGGCGAGCTAACAGGCACTTTTTCGGGGATACTGCTCCAGGTAATTATTCGGCTAg > 1:56731/1‑162 (MQ=255) aGAAAAGTAAAGCATGGCGAAATGACGTGAGTACCGGCGAAGGATACCATCAAGCTGGCCAAGAAAGTTATCCAGTTTACTGATGCTGGCGAGCTAACAGGCAATTTTTCGGGGATACTGCTCCAGGTAATTATTCg > 1:139588/1‑137 (MQ=255) gACGTGAGTACCGGCGAAGGATACCATCAAGCTGGCCAAGAAAGTTATCCAGTTTACTGATGCTGGCGAGCTAACAGGCAATTTGTCGGGGATACTGCTCCAGGTAATTATTCGGCTAGGAGTTAAGGCTGTCACACGGATTTGGATGAGAACCCATCATGTGCAGGAAAATTATCTTCGGAGAGGATGTATCCGCCAGCGCACGTTCTGTTTCCTGTAACAACAGTTTGTCATCTGTTTTACGGgaagc < 1:106769/250‑1 (MQ=255) tCAAGCTGGCCAAGAAAGTTATCCAGTTTACTGATGCTGGCGAGCTAACAGGCAATTTTTCGGGGATACTGCTCCAGGTAATTATTCGGCTAGGAGTTAAGGCTGTCACACGGATTTGGATGAGAACCCATCATGTGCAGGAAAATTATCTTCGGAGAGGATGTATCCGCCAGCGCACGTTCTGTTTCCTGTAACAACAGTTTGTCATCTGTTTTACGGGAAGCGAAGCTGCCTTTCTTGAGGAAAGt < 1:119030/248‑1 (MQ=255) gCCAAGAAAGTTATCCAGTTTACTGATGCTGGCGAGCTAACAGGCAATTTTTGAGGGATACTGCTGCTGGTACTTATTCGGCTAGGAGTTACGGCTGTCACACGGATTTGGATGAGAACCCATCCTGTGCAGGGATATTATCTTCGGAGAGGATGTATCCGCCAGCGCACGTTCTGTTTCCTGTAACAACAGTTTGTCATCTGt > 1:352458/1‑204 (MQ=255) tnNCTGATGNNGGCGAGCTAACAGGCAATTTTTCGGGGATACTGCTCCAGGTAATTATTCGGCTAGGAGTTAAGGCTGTCACACGGATTTGGATGAGaa < 2:8015/99‑1 (MQ=255) | GCACTGATTTTTCTACTGACGGGCTGATGAGACGTTATGTCACTGGCGGTAATAATCAGTGGCACACTGTAGCCTCCCTGCACATGACCATAATGATGAACAGGATTGGCACTGTCGCTGACCGACAGCCCAAGGCCAGAAAAGTAAAGCATGGCGAAATGACGTGAGTACCGGCGAAGGATACCATCAAGCTGGCCAAGAAAGTTATCCAGTTTACTGATGCTGGCGAGGTAACAGGCAATTTTTCGGGGATACTGCTCCAGGTAATTATTCGGCTAGGAGTTAAGGCTGTCACACGGATTTGGATGAGAACCCATCATGTGCAGGAAAATTATCTTCGGAGAGGATGTATCCGCCAGCGCACGTTCTGTTTCCTGTAACAACAGTTTGTCATCTGTTTTACGGGAAGCGAAGCTGCCTTTCTTGAGGAAAGT > NC_000913/4499768‑4500201 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 31 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |