| Predicted mutation | ||||||
|---|---|---|---|---|---|---|
| evidence | seq id | position | mutation | annotation | gene | description |
| JC JC | NC_000913 | 2,492,323 | IS1 (–) +9 bp | coding (924‑932/1251 nt) | frc ← | formyl‑CoA transferase, NAD(P)‑binding |
| New junction evidence | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| seq id | position | reads (cov) | reads (cov) | score | skew | freq | annotation | gene | product | ||
| * | ? | NC_000913 | 1978503 = | NA (NA) | 37 (0.800) | 30/296 | 0.3 | 97.2% | noncoding (768/768 nt) | IS1 | repeat region |
| ? | NC_000913 | = 2492331 | 1 (0.020) | coding (924/1251 nt) | frc | formyl‑CoA transferase, NAD(P)‑binding | |||||
| * | ? | NC_000913 | = 1979270 | NA (NA) | 46 (0.990) | 31/296 | 0.2 | 97.7% | noncoding (1/768 nt) | IS1 | repeat region |
| ? | NC_000913 | 2492323 = | 1 (0.020) | coding (932/1251 nt) | frc | formyl‑CoA transferase, NAD(P)‑binding | |||||
No reads uniquely aligned to region.