Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
MC JC | NC_000913 | 687,860 | Δ1,185 bp | IS5‑mediated | insH‑3 | insH‑3 |
Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_000913 | 687860 | 689044 | 1185 | 25 [0] | [0] 27 | insH‑3 | insH‑3 |
New junction evidence | |||||||||||
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seq id | position | reads (cov) | reads (cov) | score | skew | freq | annotation | gene | product | ||
* | ? | NC_000913 | = 687859 | 0 (0.000) | 24 (0.890) | 22/94 | 0.1 | 100% | noncoding (1187/1195 nt) | IS5 | repeat region |
? | NC_000913 | 689045 = | 0 (0.000) | noncoding (1/1195 nt) | IS5 | repeat region |
TATCGTCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCGAATAAGCGGGGAAATTCTTCTCGGCTGACTCAGTCATTTCAT > NC_000913/687811‑687902 | tATCGTCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGC > 1:724012‑M1/1‑49 (MQ=255) aTCGTCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCc > 1:1612562‑M1/1‑48 (MQ=255) cGTCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCct > 1:1600878‑M1/1‑46 (MQ=255) gTCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCctta < 1:1095482‑M1/49‑5 (MQ=255) gTCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCctt < 1:1276929‑M1/48‑4 (MQ=255) gTCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCctt < 1:573909‑M1/48‑4 (MQ=255) gTCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCct > 1:489746‑M1/1‑45 (MQ=255) tCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCcttag < 1:1177861‑M1/49‑6 (MQ=255) cTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCcttagg > 1:585098‑M1/1‑43 (MQ=255) cTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCcttagg > 1:1992725‑M1/1‑43 (MQ=255) tGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCcttagg > 1:213373‑M1/1‑42 (MQ=255) tATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCcttaggtaacattt < 1:687488‑M1/48‑15 (MQ=255) tgCAGTGTTGTGCCTGTTAGGGAAGGTGCcttaggtaacatttagtttg < 1:1026648‑M1/49‑21 (MQ=255) cAGTGTTGTGCCTGTTAGGGAAGGTGCcttaggtaacatttagtttggc > 1:624456‑M1/1‑27 (MQ=255) aGTGTTGTGCCTGTTAGGGAAGGTGCcttaggtaacatttagtttggc > 1:418699‑M1/1‑26 (MQ=255) tgttgtGCCTGTTAGGGAAGGTGCcttaggtaacatttagtttggcta > 1:1132030‑M1/1‑24 (MQ=255) tgCCTGTTAGGGAAGGTGCcttaggtaacatttagtttggctaaatgta < 1:866641‑M1/49‑31 (MQ=255) gCCTGTTAGGGAAGGTGCcttaggtaacatttagtttggctaaatgta > 1:1871609‑M1/1‑18 (MQ=255) cTGTTAGGGAAGGTGCcttaggtaacatttagtttggctaaatgtaaag < 1:1679333‑M1/49‑34 (MQ=255) tGTTAGGGAAGGTGCcttaggtaacatttagtttggctaaatgta > 1:1071217‑M1/1‑15 (MQ=255) gTTAGGGAAGGTGCcttaggtaacatttagtttggctaaatgtaaaga > 1:836117‑M1/1‑14 (MQ=255) ttAGGGAAGGTGCcttaggtaacatttagtttggctaaatgtaaaga < 1:1907091‑M1/47‑35 (MQ=255) gAAGGTGCcttaggtaacatttagtttggctaaatgtaaagatattgct < 1:87629‑M1/49‑42 (MQ=255) aaGGTGCcttaggtaacatttagtttggctaaatgtaaagatattgctg < 1:1097195‑M1/49‑43 (MQ=255) aGGTGCcttaggtaacatttagtttggctaaatgtaaagatattgctgt > 1:1535515‑M1/1‑6 (MQ=255) | TATCGTCTGCAACTTTATTGTGCAGTGTTGTGCCTGTTAGGGAAGGTGCGAATAAGCGGGGAAATTCTTCTCGGCTGACTCAGTCATTTCAT > NC_000913/687811‑687902 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |