Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
JC | NC_002947 | 5,912,986 | Δ42 bp | 12.1% | coding (199‑240/1377 nt) | spuI → | glutamylpolyamine synthetase |
New junction evidence | |||||||||||
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seq id | position | reads (cov) | reads (cov) | score | skew | freq | annotation | gene | product | ||
* | ? | NC_002947 | = 5912985 | 71 (0.800) | 9 (0.110) | 8/226 | NT | 12.1% | coding (198/1377 nt) | spuI | glutamylpolyamine synthetase |
? | NC_002947 | 5913028 = | 66 (0.810) | coding (241/1377 nt) | spuI | glutamylpolyamine synthetase |
ACGCGTTCCTTAAGGAACATCCTGAGGTTCTCTACGTTGACCTTCTGATTGCAGATATGAATGGTGTGGTGCGTGGCAAGCGCATAGAGCGCACCAGCCTCCACAAGGTTTACGAGAAAGGCATCAATCTGCCGGCCTCCCTCTTTGCCCTGGACATC‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑ > NC_002947/5912828‑5912985 ‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑cctggacatcGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGTAACGAGCCATGGCAAAAGCGCCCCACCGCCCAGCTGCTGATGACCATGCACGAGCTGGAAGGCGAGCCGTTCTTCGCCGACCCGCGCGAAGTGCTGCGTCAGG > NC_002947/5913028‑5913175 ggatGTTCCTTAAGGAACATCCTGAGGTTCTCTACGTTGACCTTCTGATTGCAGATATGAATGGTGTGGTGCGTGGCAAGCGCATAGAGCGCACCAGCCTCCACAAGGTTTACGAGAAAGGCATCAATCTGCCGGCCTCCCTCTTTGCCC > 1:699666/5‑150 CCTTAAGGAACATCCTGAGGTTCTCTACGTTGACCTTCTGATTGCAGATATGAATGGTGTGGTGCGTGGCAAGCGCATAGAGCGCACCAGCCTCCACAAGGTTTACGAGAAAGGCATCAATCTGCCGGCCTCCCTCTTTGCCCTGGACAT < 1:131915/150‑1 CTTAAGGAACATCCTGAGGTTCTCTACGTTGACCTTCTGATTGCAGATATGAATGGTGTGGTGCGTGGCAAGCGCATAGAGCGCACCAGCCTCCACAAGGTTTACGAGAAAGGCATCAATCTGCCGGCCTCCCTCTTTGCCCTGGACATC > 1:2021793/1‑150 CTTAAGGAACATCCTGAGGTTCTCTACGTTGACCTTCTGATTGCAGATATGAATGGTGTGGTGCGTGGCAAGCGCATAGAGCGCACCAGCCTCCACAAGGTTTACGAGAAAGGCATCAATCTGCCGGCCTCCCTCTTTGCC > 2:1979181/1‑141 CTTAAGGAACATCCTGAGGTTCTCTACGTTGACCTTCTGATTGCAGATATGAATGGTGTGGTGCGTGGCAAGCGCATAGAGCGCACCAGCCTCCACAAGGTTTACGAGAAAGGCATCAATCTGCCGGCCTCCCTCTTTGCC < 1:1979181/141‑1 TCTACGTTGACCTTCTGATTGCAGATATGAATGGTGTGGTGCGTGGCAAGCGCATAGAGCGCACCAGCCTCCACAAGGTTTACGAGAAAGGCATCAATCTGCCGGCCTCCCTCTTTGCCCT > 1:1597588/1‑121 TCTACGTTGACCTTCTGATTGCAGATATGAATGGTGTGGTGCGTGGCAAGCGCATAGAGCGCACCAGCCTCCACAAGGTTTACGAGAAAGGCATCAATCTGCCGGCCTCCCTCTTTGCCCT < 2:1597588/121‑1 GAATGGTGTGGTGCGTGGCAAGCGCATAGAGCGCACCAGCCTCCACAAGGTTTACGAGAAAGGCATCAATCTGCCGGCCTCCCTCTTTGCCCTGGACATCGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGTAACGA < 2:303707/150‑1 GCACCAGCCTCCACAAGGTTTACGAGAAAGGCATCAATCTGCCGGCCTCCCTCTTTGCCCTGGACATCGGCGATGCTGACCGCATCTGCTATCCAACCCCCGACACGCTCTGTAACGAACAATGGCAAAAGCGCCCCACCGCGCAGCTtc < 2:1353862/150‑3 ACCAGCCTCCACAAGGTTTACGAGAAAGGCATCAATCTGCCGGCCTCCCTCTTTGCCCTGGACATCGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGTAACGAGCCATGGCAAAAGCGCCCCACCGCCCAGCTGCTG > 2:807968/1‑150 CCACAAGGTTTACGAGAAAGGCATCAATCTGCCGGCCTCCCTCTTTGCCCTGGACATCGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGTAA > 1:1862830/1‑105 CCACAAGGTTTACGAGAAAGGCATCAATCTGCCGGCCTCCCTCTTTGCCCTGGACATCGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGTAA < 2:1862830/105‑1 GTTTACGAGAAAGGCATCAATCTGCCGGCCTCCCTCTTTGCCCTGGACATCGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGTAACGAGCCATGGCAAAAGCGCCCCACCGCCCAGCTGCTGATGACCATGCACGAG > 1:1035941/1‑150 AAAGGCATCAATTTGCCGGCCTCCCTCTTTGCCCTGGACATCGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGTAACGAGCCATGGCAAAAGCGCCCCACCGCCCAGCTGCTGATGACCATGCACGAGCTGGAAGGC > 2:411278/1‑150 TCAATCTGCCGGCCTCCCTCTTTGCCCTGGACATCGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGTAACGAGCCATGGCAAAAGCGCCCCACCGCCCAGCTGCTGATGACCATGCACGAGCTGGAAGGCGAGCCGT > 2:205766/1‑150 TCTTTGCCCTGGACATCGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGTAACGAGCCATGGCAAAAGCGCCCCACCGCCCAGCTGCTGATGACCATGCACGAGCTGGAAGGCGAGCCGTTCTTCGCCGACCCGCGCG > 2:1144376/1‑150 CTGGACATCGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGTAACGAGCCATGGCAAAAGCGCCCCACCGCCCAGCTGCTGATGACCATGCACGAGCTGGAAGGCGAGCCGTTCTTCGCCGACCCGCGCGAAG > 2:185945/1‑145 CTGGACATCGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGTAACGAGCCATGGCAAAAGCGCCCCACCGCCCAGCTGCTGATGACCATGCACGAGCTGGAAGGCGAGCCGTTCTTCGCCGACCCGCGCGAAG < 1:185945/145‑1 CTGGACATCGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGT > 1:336832/1‑54 CTGGACATCGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGT < 2:336832/54‑1 TGGACATCGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGTAACGAGCCATGGCAAAAGCGCCCCCCCGACCAACTGATGCTGCACATGTATTTTTTGGAAGGCGAGCTGTTCTTCGCCGACCCGCGCGAAGTGCTGC < 1:1253883/150‑1 TGGACATCGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGTAACGAGCCATGGCAAAAGCGCCCCACCGCCCAGCTGCTGATGACCATGCACGAGCTGGAAGGCGAGC > 2:1909703/1‑120 TGGACATCGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGTAACGAGCCATGGCAAAAGCGCCCCACCGCCCAGCTGCTGATGACCATGCACGAGCTGGAAGGCGAGC < 1:1909703/120‑1 CATCGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGTAACGAGCCATGGCAAAAGCGCCCCACCGCCCAGCTGCTGATGACCATGCACGAGCTGGAAGGCGAGCCGTTCTTCGCCGACCCGCGCGAAGTGCTGCGTCA > 2:896660/1‑150 TCGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGTAACGAGCCATGGCAAAAGCGCCCCACCGCCCAGCTGCTGATGACCATGCACGAGCTGGAAGGCGAGCCGTTCTTCGCCGACCCGCGCGAAGTGCTGCGTCAGG < 2:877277/150‑1 ACGCGTTCCTTAAGGAACATCCTGAGGTTCTCTACGTTGACCTTCTGATTGCAGATATGAATGGTGTGGTGCGTGGCAAGCGCATAGAGCGCACCAGCCTCCACAAGGTTTACGAGAAAGGCATCAATCTGCCGGCCTCCCTCTTTGCCCTGGACATC‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑ > NC_002947/5912828‑5912985 ‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑cctggacatcGGCGATGCTGACCGCATCTGCTATCCAATCCCCGACACGCTCTGTAACGAGCCATGGCAAAAGCGCCCCACCGCCCAGCTGCTGATGACCATGCACGAGCTGGAAGGCGAGCCGTTCTTCGCCGACCCGCGCGAAGTGCTGCGTCAGG > NC_002947/5913028‑5913175 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 37 ≤ 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. |