Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | CP000730 | 944782 | 944869 | 88 | 2 [1] | [1] 2 | mnhD2 | CPA3 family monovalent cation:proton (H+) antiporter‑3 subunit D |
GCACTGAATATGTCTAATACAAAGACAATACTGTATGGTGCTTTCCATGAACCTAGCTCTACGCGTATTGGTCCATGTTTAACAACATTTGCTAAATTGATAATTGCCGCGACCAAGGTTAATAATGTACCGCCTAGTGCGACATAA > CP000730/944641‑944787 | gCACTGAATATGTCTAATACAAAGACAATACTGTATGGTGCTTTCCATGAACCTAGCTCTACGCGTATTGGTCCATGTTTAACAACATTTGCTAAATTGATAATTGCCGCGACCAAGGTTAATAATGTACCGCCTAGTGCg < 1:7194/141‑1 (MQ=255) aaTATGTCTAATACAAAGACAATACTGTATGGTGCTTTCCATGAACCTAGCTCTACGCGTATTGGTCCATGTTTAACAACATTTGCTAAATTGATAATTGCCGCGACCAAGGTTAATAATGTACCGCCTAGTGCGACATaa < 1:27299/141‑1 (MQ=255) | GCACTGAATATGTCTAATACAAAGACAATACTGTATGGTGCTTTCCATGAACCTAGCTCTACGCGTATTGGTCCATGTTTAACAACATTTGCTAAATTGATAATTGCCGCGACCAAGGTTAATAATGTACCGCCTAGTGCGACATAA > CP000730/944641‑944787 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |