Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | CP000730 | 947951 | 948007 | 57 | 2 [1] | [1] 2 | mnhA2 | CPA3 family monovalent cation:proton (H+) antiporter‑3 subunit A |
CCATCAAGATATAAATCAAAGTTCATACCAAAATGAGGCATCCAATTTAAGGTTTTCATTACAGTATTACCTGACATCGTCGTTTTAATTAATGTAAGCATATAAATAAATATGACGATAGGGACAGGTAATACGAACCATCCTAAATGTATACGTTT > CP000730/947810‑947967 | ccATCAAGATATAAATCAAAGTTCATACCAAAATGAGGCATCCAATTTAAGGTTTTCATTACAGTATTACCTGACATCGTCGTTTTAATTAATGTAAGCATATAAATAAATATGACGATAGGGACAGGTAATACGAACCAt < 2:10537/141‑1 (MQ=255) aaaGTTCATACCAAAATGAGGCATCCAATTTAAGGTTTTCATTACAGTATTACCTGACATCGTCGTTTTAATTAATGTAAGCATATAAATAAATATGACGATAGGGACAGGTAATACGAACCATCCTAAATGTATACGttt < 2:52284/141‑1 (MQ=255) | CCATCAAGATATAAATCAAAGTTCATACCAAAATGAGGCATCCAATTTAAGGTTTTCATTACAGTATTACCTGACATCGTCGTTTTAATTAATGTAAGCATATAAATAAATATGACGATAGGGACAGGTAATACGAACCATCCTAAATGTATACGTTT > CP000730/947810‑947967 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |