| Predicted mutation | ||||||
|---|---|---|---|---|---|---|
| evidence | seq id | position | mutation | annotation | gene | description |
| RA | NC_000913 | 1,809,808 | (A)5→6 | coding (429/669 nt) | hxpB → | hexitol phosphatase B |
| Read alignment evidence... | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
| * | NC_000913 | 1,809,803 | 1 | . | A | 100.0% | 58.8 / NA | 17 | E142K (GAA→AAA) | hxpB | hexitol phosphatase B |
| Reads supporting (aligned to +/- strand): ref base . (0/0); new base A (11/6); total (11/6) | |||||||||||
CGCGTCACCACTACATATGCTGGAAAAAGTGTTGACCATGTTTGACTTACGCGACAGTTTCGATGCCCTCGCCTCGGCCG‑AAAAACTGCCTTACAGCAAGCCGCATCCGCAAGTATATCTCGACTGCGCAGCAAAACTGGGCGTTGACCCT > NC_000913/1809724‑1809874 | cgcgTCACCACTACATATGCTGGAAAAAGTGTTGACCATGTTTGACTTACGCGACAGTTTCGATGCCCTCGCCTCGGCCG‑a < 2:290826/81‑1 (MQ=255) gcgTAACCAATAAATATGCTGGAAAAAGTGTTGACCATGTTTGACTTACGCGACAGTTTCGATGCCCTCGCCTCGGCCG‑aa < 1:290827/81‑1 (MQ=255) cATATGCTGGAAAAAGTGTTGACCATGTTTGACTTACGCGACAGTTTCGATGCCCTCGCCTCGGCCGAAAAAACTGCCtt < 2:290828/80‑1 (MQ=255) tGCTGGAAAAAGTGTTGACCATGTTTGACTTACGCGACAGTTTCGATGCCCTCGCCTCGGCCGAAAAAACTGCCTTACAg > 2:290868/1‑80 (MQ=255) tGCTGGAAAAAGTGTTGACCATGTTTGACTTACGCGACAGTTTCGATGCCCTCGCCTCGGCCGAAAAAACTGCCTTACAg > 2:290859/1‑80 (MQ=255) aaaaaGTGTTGACCATGTTTGACTTACGCGACAGTTTCGATGCCCTCGCCTCGGCCGAAAAAACTGCCTTACAGCAAGCCg > 2:290864/1‑81 (MQ=255) aaGTGTTGACCATGTTTGACTTACGCGACAGTTTCGATGCCCTCGCCTCGGCCGAAAAAACTGCCTTACAGCAAGCCGCAt > 2:290861/1‑81 (MQ=255) tGACCATGTTTGACTTACGCGACAGTTTCGATGCCCTCGCCTCGGCCGAAAAAACTGCCTTACAGCAAGCCGCATCCGc > 2:290860/1‑79 (MQ=255) gACTTACGCGACAGTTTCGATGCCCTCGCCTCGGCCGAAAAAACTGCCTTACAGCAAGCCGCATCCGCAAGTATATCTCg < 1:290830/80‑1 (MQ=255) gACTTACGCGACAGTTTCGATGCCCTCGCCTCGGCCGAAAAAACTGCCTTACAGCAAGCCGCATCCGCAAGTATATCTCg < 1:290831/80‑1 (MQ=255) gACTTACGCGACAGTTTCGATGCCCTCGCCTCGGCCGAAAAAACTGCCTTACAGCAAGCCGCATCCGCAAGTATATCTCGa > 2:290856/1‑81 (MQ=255) cTTACGCGACAGTTTCGATGCCCTCGCCTCGGCCGAAAAAACTGCCTTACAGCAAGCCGCATCCGCAAGTATATCTCGACt > 2:290863/1‑81 (MQ=255) gcgACAGTTTCGATGCCCTCGCCTCGGCCGAAAAAACTGCCTTACAGCAAGCCGCATCCGCAAGTATATCTCGACTgcg > 1:290867/1‑79 (MQ=255) aCAGTTTCGATGCCCTCGCCTCGGCCGAAAAAACTGCCTTACAGCAAGCCGCATCCGCAAGTATATCTCGACTGCgcagc > 2:290862/1‑80 (MQ=255) aGTTTCGATGCCCTCGCCTCGGCCGAAAAAACTGCCTTACAGCAAGCCGCATCCGCAAGTATATCTCGACTGCGCAGCaaa < 2:290832/81‑1 (MQ=255) gATGCCCTCGCCTCGGCCGAAAAAACTGCCTTACAGCAAGCCGCATCCGCAAGTATATCTCGACTGCGCAGCAAAACTggg < 1:290833/81‑1 (MQ=255) tGCCCTCGCCTCGGCCGAAAAAACTGCCTTACAGCAAGCCGCATCCGCAAGTATATCTCGACTGCGCAGCAAAACTGGGCg > 2:290865/1‑81 (MQ=255) cccTCGCCTCGGCCGAAAAAACTGCCTTACAGCAAGCCGCATCCGCAAGTATATCTCGACTGCGCAGCAAAACTGGGCGt < 1:290834/80‑1 (MQ=255) cctcgGCCGAAAAAACTGCCTTACAGCAAGCCGCATCCGCAAGTATATCTCGACTGCGCAGCAAAACTGGGCGTTGACCct > 2:290866/1‑81 (MQ=255) | CGCGTCACCACTACATATGCTGGAAAAAGTGTTGACCATGTTTGACTTACGCGACAGTTTCGATGCCCTCGCCTCGGCCG‑AAAAACTGCCTTACAGCAAGCCGCATCCGCAAGTATATCTCGACTGCGCAGCAAAACTGGGCGTTGACCCT > NC_000913/1809724‑1809874 |
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 22 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |