Predicted mutation | ||||||
---|---|---|---|---|---|---|
evidence | seq id | position | mutation | annotation | gene | description |
MC JC | NC_000913 | 3,909,311 | Δ774 bp | [pstA]–[pstC] | [pstA], [pstC] |
Missing coverage evidence... | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_000913 | 3909311 | 3910084 | 774 | 13 [0] | [2] 15 | [pstA]–[pstC] | [pstA], [pstC] |
New junction evidence | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
seq id | position | reads (cov) | reads (cov) | score | skew | freq | annotation | gene | product | ||
* | ? | NC_000913 | = 3909310 | 0 (0.000) | 11 (0.550) | 11/270 | 0.6 | 91.7% | coding (129/891 nt) | pstA | phosphate ABC transporter permease |
? | NC_000913 | 3910085 = | 2 (0.100) | coding (313/960 nt) | pstC | phosphate ABC transporter permease |
ATATTGCCGACCGGCTCCTGAAAGTAAACGGCGAACAGCGGCGCAAAGATAAACAGGCCCCACATGCCGTAAACGATACTTGGAATGGCTGCCAGCAGCTCAATGGCGATACCCAGCGGGCGTTTCAGCCAGCCAGGCGCAAGCTCAGTCAGGAACAGGGCGATACCGAAACTCACCGGGACGGCGATCAGCAGCGCGATAAACGAAGTCACCAACGTACCGTAGATCGGCACCAGCGCCCCGTAGATATCGTTCGGTGCATCCCACTCTTTGGT > NC_000913/3909949‑3910223 | cagcccgctacccgccagagcgttcgccagaccaccacctgccgtattgggcggcggcgtcattccagtgaacagcgccagcgacataccgtcgataccgcgcgtgatggtggacattaaaatccagatcagccagGCGCAAg > 2:115479‑M2/137‑143 (MQ=255) caagtgcgttcgccccaccaccaccttccttattggtcggcggcgtcatttcagtgaacagcgccagcgacataccgtcgataccgcgagtgatggtggacattaaaatccagatcagccagGCGCAAGCTCAGTCAGGAACa < 2:68055‑M2/21‑1 (MQ=255) cttccgtattgggcggcggcgtcatttcagtgaacagcgccagcgacataccgtcgataccgcgagtgatggtggacataaaaatccagatcagccagGCGCAAGCTCAGTCAGGAACAGGGCGATACCGAAACTCACCGGGa > 1:223257‑M2/99‑143 (MQ=255) atttggctgcggcgtcatttctgtgaatttcttttgcgacatagcttcgataccgcgagagatggtggacattaaaagccagatcagccagGCGCAAGCTCAGTCAGGAACAGGGCGATACCGAAACTCACCGGGACGGCGAt < 1:259294‑M2/52‑1 (MQ=255) gcggcggcgtcatttcagtgaacagcgccagcgacattccgtctataccgcgagtgattgtggacattaaaggccagatcagccagGCGCAAGCTCAGTCAGGAACAGGGCGATACCGAAACTCACCGGGACGGCGATcagca < 1:181820‑M2/57‑1 (MQ=255) gcgtcgtttcagtgaacagcgccagcgacataccgtcgataccgcgagtggtggtggacattaaaatcccgatcagccagGCGCAAGCTCAGTCAGGTACAGGGCGATCCCGAAACTCACCGGGACGGCGATCAGCAGCGCGa < 1:106724‑M2/63‑1 (MQ=255) cgccagcgacataccgtcgataccgcgagtgatggtggacattaaaatccagatcagccagGCGCAAGCTCAGTCAGGCACAGGCCGATACCGAAACTCAACGGGACAGCGATCAACAGCGCGATAAAAGAAGTAACAaacaa > 1:165598‑M2/62‑141 (MQ=255) accgtcgataccgcgagtgatggtggacattaaaatccagctcagccagGCGCACGCTCAGTCAGGAACAGGGCGATACCGAAACTCACCGAAACGGCAATCAGCAGCGCGATAAACGAAGTCAACAACGTACCGTAGATCgg > 1:36128‑M2/50‑143 (MQ=255) ccgtcgataccgcgagtgatggtggacattaaaatccagatcagccagGCGCAAGCTCAGTCAGGAACAGGGCGATACCGAAACTCACCGGGACGGCCAACACCAACACGATAAACAAAGAAACCAAAGTAACGTAAATCGGc > 1:81225‑M2/49‑143 (MQ=255) ccgcgagtgatggtggacattaaaatccagatcagccagGCGCAAGCTCAGTCAGGAACAGGGCGATACCGAAACTCACCGGGACGGCGATCAGCAGCGCGATAAACGAAGTCACCGCAGGATCGTAGATCGGCACCAGCGcc < 2:227981‑M2/104‑1 (MQ=255) gatggtcgacattaatattcatatcagctagTCTCAATCTCATTCTTGAACAGGGCGATACCGAAACTAACCGGGACGGCGATCAGCAGCGCGATAAACGAAGTCACCAACGTACCGTAGATCGGCACCAGCGCCCCGTAGat < 1:44341‑M2/112‑1 (MQ=255) ccAGCGGGCGTTTCAGCCAGCCAGGCGCAAGCTCAGTCAGGAACAGGGCGATACCGAAACTCACCGGGACGGCGCTCAGCAGCGCGATAAACGAAGTCACCAACGTACCGTAGATCGGCACCAGCGCCCCGTAGATATCGtcc > 2:347211/1‑141 (MQ=255) gcagccagGCGCGAGCTCAGTCAGGAACAGGGCGATACCGAAACTCACCGGGACGGCGATCAGCAGCGCGATAAACGAAGTCACCAACGTACCGTAGATCGGCACCAGCGCCCCGTAGATATCGTTCGGTGCATCCCACTCtt < 1:385806‑M2/135‑1 (MQ=255) ccagccagGCGCAAGCTCAGTCAGGAACAGGGCGATACAGAAACTCACCGGGTCGGCGATCAGCAGCGCGATAAACGAAGTCACCAACGTACCGTAGATCGGCACCAGCGCCCCGTAGATATCGTTCGGTGCATCCCACTCtt < 1:285731/143‑1 (MQ=255) ccagGCGCAAGCTCAGTCAGGAACAGGGCGATACCGAAACTCACCGGGACGGCGATCAGCAGCGCGATAAACGCAGTCACCAACGTACCGTAGATCGGCACCAGCGCCCCGTAGATATAGATCGGTACATCACACCCTTTGGt > 1:211945‑M2/5‑143 (MQ=255) | ATATTGCCGACCGGCTCCTGAAAGTAAACGGCGAACAGCGGCGCAAAGATAAACAGGCCCCACATGCCGTAAACGATACTTGGAATGGCTGCCAGCAGCTCAATGGCGATACCCAGCGGGCGTTTCAGCCAGCCAGGCGCAAGCTCAGTCAGGAACAGGGCGATACCGAAACTCACCGGGACGGCGATCAGCAGCGCGATAAACGAAGTCACCAACGTACCGTAGATCGGCACCAGCGCCCCGTAGATATCGTTCGGTGCATCCCACTCTTTGGT > NC_000913/3909949‑3910223 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 13 ≤ ATCG/ATCG < 22 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |
Reads not counted as support for junction |
read_name Not counted due to insufficient overlap past the breakpoint. |
read_name Not counted due to not crossing MOB target site duplication. |