| Predicted mutation | ||||||
|---|---|---|---|---|---|---|
| evidence | seq id | position | mutation | annotation | gene | description |
| RA | NC_000913 | 834,538 | C→T | S490F (TCC→TTC) | dinG → | ATP‑dependent DNA helicase DinG |
| Read alignment evidence... | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
| * | NC_000913 | 834,538 | 0 | C | T | 100.0% | 23.7 / NA | 10 | S490F (TCC→TTC) | dinG | ATP‑dependent DNA helicase DinG |
| Reads supporting (aligned to +/- strand): ref base C (0/0); new base T (4/6); total (4/6) | |||||||||||
GGCGACGCGGGAAGAGCGCGAAGGGCAGCTACACCTCTGGTTTCACTGCGTGGGAATACGTGTCAGCGATCAGCTGGAAAGGCTGCTGTGGCGCAGTATTCCGCACATTATTGTCACCTCCGCAACCTTGCGTTCGCTGAACAGTTTTTCGCGTTTGCAGGAGATGAGTGGTCTGAAAGAGAAAGCGGGCGACCGTTTTGTGGCGCTGGATTCCCCCTTTAACCACTGCGAACAGGGCAAAATTGTTATTCCCCGGATGCGCGTTGAGCCTTCCATCGACAACGAAGAGCAGCATATTGCCGAAATGGCGGCCTTTTTCCGTAAGCAGGTGGAGAGCAAAAAACATCTCGGTATGTTGGTACTGTTTGCCAGCGGACGGGCGATGCAGCGCTTTCTCGACTATGTGACGGATTTACG > NC_000913/834326‑834742 | ggCGACGCGGGAAGAGCGCGAAGGGCAGCTACACCTCTGGTTTCACTGCGTGGGAATACGTGTCAGCGATCAGCTGGAAAGGCTGCTGTGGCGCAGTATTCCGCACATTATTGTCACCTCCGCAACCTTGCGTTCGCTGAACAGTTTTTCGCGTTTGCAGGAGATGAGTGGTCTGAAAGAGAAAGCGGGCGGCCGTTTTGTGGCGCTGGATTTCCGCTTTAACCACTGCGAACAGGGCAAAATTGTTATTc < 1:208120/251‑1 (MQ=255) cGACGCGGGAAGAGCGCGAAGGGCAGCTACACCTCTGGTTTCACTGCGTGGGAATACGTGTCAGCGATCAGCTGGAAAGGCTGCTGTGGCGCAGTATTCCGCACATTATTGTCACCTCCGCAACCTTGCGTTCGCTGAACAGTTTTTCGCGTTTGCAGGAGATGAGTGGTCTGAAAGAGAAAGCGGGCGACCGTTTTGTGGCGCTGGATTTCCCCTTTAACCACTGCGAACAGGGCAAAATTGTTATTccc > 1:237272/1‑251 (MQ=255) ccGCACATTATGGTCACCGCCGCAACCGTGCGTTCGCTGAACAGTTTTTCGCGTTTGCAGTAGATGAGTGGTCTGAAAGAGAAAGCGGGCGACCGTTTTGTGGTGCTGGATTTCCCCTTTAACCACTGGGAACATGGCAAAATTTTTATTCCCCGGATGCGCGTTGAGCCTGCCACCGTGAACGAAGAGCGGTATATTTCCGAAATTGCGGCCTTTTTCCGTAAGCAGGTGGAGAGCAAAAAACATCTCg < 1:193531/250‑1 (MQ=255) cgcgTTTGCAGGAGATGAGTGGTCTGAAAGAGAAAGCGGGCGACCGTTTTGTGGCGCTGGATTTCCCCTTTAACCACTGCGAACAGGGCAAAATTGTTATTCCCCGGATGCGCGTTGAGCCTTCCATCGACAACGAAGAGCAGCATATTGCCGAAATGGCGGCCTTTTTcc > 1:3721/1‑171 (MQ=255) gCAGGAGATGAGTGGTCTGAAAGAGAAAGCGGGCGACCGTTTTGTGGCGCTGGATTTCCCCTTTAACCACTGCGAACAGGGAAAACTTGTTATTCCCCGGATGCGCGTTGAGCCTTCCATCGACAACGCAGAGCAGCATATTGCCGAAATGGCGGCCTTTTTCCGTAAGCAGGTGGCGAGCACAAAACATCTCGGTATGTTGGTACTGTTTGCCAGCGGACGGGCGATGCAGCGCTTTCTCGACTAtgtg > 1:112298/1‑250 (MQ=255) aGTGGTCTGAAAGAGAAAGCGGGCGACCGTTTTGTGGCGCTGGATGTCCCCTTTAACCACTGCGAACAGGGCAAAATTGTTATTCCCCGGATGCGCGTTGAGCCTTCCATCGACAACGAAGAGCAGCATATTGCCGAAATGGCGGCCTTTTTCCGTAAGCAGGTGGAGAGCAAAAAACATCGCGGTATGTTGGTACTGGTTGCCAGCGGACGGGCGATGCAGCGCTTTCTCGACTAGGTGACGGATTTACg < 1:160956/251‑1 (MQ=255) nannNCNNNCGACCNTTTTGTGGCGCNGGATTTCCCCTTTAACCACTGCGAACAGNGCAAAATTGtc < 2:36146/66‑2 (MQ=255) gaAAGCGGGCGACCGTTTTGTGGCGCTGGATTTCCCCTTTAACCACTGCGAACAGGGCAAAATTGtc > 1:36146/1‑66 (MQ=255) tttttGTGTCGCTGGATTTCCCCTTTAATCACTGCGAACAGGGCAAAATTTTTATTCCCCGGATTCGCGTTGAGCCTTCCATCGACAACGAAGAGCAGCATATTGCCGAAATggcgg < 1:181734/116‑1 (MQ=255) gTTTTGTGGCGCTGGATTTCCCCTTTAACCACTGCGAACAGGGCAAAATTGTTATTCCCCGTATGCACGTTGAGCCTTCCATCGACAACGAAGAGCAGCATATTGCCGAAATggcgn < 1:55576/117‑2 (MQ=255) | GGCGACGCGGGAAGAGCGCGAAGGGCAGCTACACCTCTGGTTTCACTGCGTGGGAATACGTGTCAGCGATCAGCTGGAAAGGCTGCTGTGGCGCAGTATTCCGCACATTATTGTCACCTCCGCAACCTTGCGTTCGCTGAACAGTTTTTCGCGTTTGCAGGAGATGAGTGGTCTGAAAGAGAAAGCGGGCGACCGTTTTGTGGCGCTGGATTCCCCCTTTAACCACTGCGAACAGGGCAAAATTGTTATTCCCCGGATGCGCGTTGAGCCTTCCATCGACAACGAAGAGCAGCATATTGCCGAAATGGCGGCCTTTTTCCGTAAGCAGGTGGAGAGCAAAAAACATCTCGGTATGTTGGTACTGTTTGCCAGCGGACGGGCGATGCAGCGCTTTCTCGACTATGTGACGGATTTACG > NC_000913/834326‑834742 |
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 13 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 30 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |