| Predicted mutation | ||||||
|---|---|---|---|---|---|---|
| evidence | seq id | position | mutation | annotation | gene | description |
| RA | NC_000913 | 1,183,061 | G→A | A187V (GCG→GTG) | potC ← | spermidine preferential ABC transporter membrane subunit PotC |
| Read alignment evidence... | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
| * | NC_000913 | 1,183,061 | 0 | G | A | 100.0% | 71.1 / NA | 21 | A187V (GCG→GTG) | potC | spermidine preferential ABC transporter membrane subunit PotC |
| Reads supporting (aligned to +/- strand): ref base G (0/0); new base A (10/11); total (10/11) | |||||||||||
TCATAACTTGGTCCGGTGACGAACGAAGAAACTACCACATCGTCCATCGACAGGGTAAAGCTTAACACCCAGCCCGCCGCCACCGCTGGCATTGCCAGTGGCAGAATGATTTTTCGCAGAATGGTAAATTCGCTGGCACCGAGATCTTTCGCC > NC_000913/1182986‑1183138 | tCATAACTTGGTCCGGTGACGAACGAAGAAACTACCACATCGTCCATCGACAGGGTAAAGCTTAACACCCAGCCcaccgc < 2:215062/80‑1 (MQ=255) tGGTCCGGTGACGAACGAAGAAACTACCACATCGTCCATCGACAGGGTAAAGCTTAACACCCAGCCCACCGCCACCGCTgg > 2:215090/1‑81 (MQ=255) cGGTGACGAACGAAGAAACTACCACATCGTCCATCGACAGGGTAAAGCTTAACACCCAGCCCACCGCCACCGCTGGCAtt < 1:215063/80‑1 (MQ=255) tGACGAACGAAGAAACTACCACATCGTCCATCGACAGGGTAAAGCTTAACACCCAGCCCACCGCCACCGCTGGCATTGCCa < 1:215064/81‑1 (MQ=255) acgaacgaAGAAACTACCACATCGTCCATCGACAGGGTAAAGCTTAACACCCAGCCCACCGCCACCGCTGGCATTGCCAGt < 2:215065/81‑1 (MQ=255) cgaacgaaGAAACTACCACATCGTCCATCGACAGGGTAAAGCTTAACACCCAGCCCACCGCCACCGCTGGCATTGCCAGTg < 1:215066/81‑1 (MQ=255) gaacgaaGAAACTACCACATCGTCCATCGACAGGGTAAAGCTTAACACCCAGCCCACCGCCACCGCTGGCATTGCCAGTgg > 1:215092/1‑81 (MQ=255) agaaACTACCACATCGTCCATCGACAGGGTAAAGCTTAACACCCAGCCCACCGCCACCGCTGGCATTGCCAGTGGCAGAAt < 1:215067/81‑1 (MQ=255) aCTACCACATCGTCCATCGACAGGGTAAAGCTTAACACCCAGCCCACCGCCACCGCTGGCATTGCCAGTGGCAGAATGAtt < 1:215068/81‑1 (MQ=255) cacaTCGTCCATCGACAGGGTAAAGCTTAACACCCAGCCCACCGCCACCGCTGGCATTGCCAGTGGCAGAATGATTTTTCg > 2:215094/1‑81 (MQ=255) aTCGTCCATCGACAGGGTAAAGCTTAACACCCAGCCCACCGCCACCGCTGGCATTGCCAGTGGCAGAATGATTTTTCg > 2:215102/1‑78 (MQ=255) aTCGTCCATCGACAGGGTAAAGCTTAACACCCAGCCCACCGCCACCGCTGGCATTGCCAGTGGCAGAATGATTTTTCGCAg < 2:215069/81‑1 (MQ=255) gTCCATCGACAGGGTAAAGCTTAACACCCAGCCCACCGCCACCGCTGGCATTGCCAGTGGCAGAATGATTTTTCGCAGAAt > 1:215091/1‑81 (MQ=255) aTCGACAGGGTAAAGCTTAACACCCAGCCCACCGCCACCGCTGGCATTGCCAGTGGCAGAATGATTTTTCGCAGAATGGTa < 1:215070/81‑1 (MQ=255) aaCACCCAGCCCACCGCCACCGCTGGCATTGCCAGTGGCAGAATGATTTTTCGCAGAATGGTAAATTCGCTGGCAcc > 1:215093/1‑77 (MQ=255) acacCCAGCCCACCGCCACCGCTGGCATTGCCAGTGGCAGAATGATTTTTCGCAGAATGGTAAATTCGCTGGCAcc > 1:215101/1‑76 (MQ=255) cccAGCCCACCGCCACCGCTGGCATTGCCAGTGGCAGAATGATTTTTCGCAGAATGGTAAATTCGCTGGCACCGAGATCtt < 2:215071/81‑1 (MQ=255) cccAGCCCACCGCCACCGCTGGCATTGCCAGTGGCAGAATGATTTTTCGCAGAATGGTAAATTCGCTGGCACCGAGATCtt > 2:215096/1‑81 (MQ=255) cAGCCCACCGCCACCGCTGGCATTGCCAGTGGCAGAATGATTTTTCGCAGAATGGTAAATTCGCTGGCACCGAGATCTTTc > 1:215105/1‑81 (MQ=255) cAGCCCACCGCCACCGCTGGCATTGCCAGTGGCAGAATGATTTTTCGCAGAATGGTAAATTCGCTGGCACCGAGATCTTTc < 2:215072/81‑1 (MQ=255) cccACCGCCACCGCTGGCATTGCCAGTGGCAGAATGATTTTTCGCAGAATGGTAAATTCGCTGGCACCGAGATCTTTcgcc < 1:215073/81‑1 (MQ=255) cccACCGCCACCGCTGGCATTGCCAGTGGCAGAATGATTTTTCGCAGAATGGTAAATTCGCTGGCACCGAGATCTTTcgcc > 2:215104/1‑81 (MQ=255) | TCATAACTTGGTCCGGTGACGAACGAAGAAACTACCACATCGTCCATCGACAGGGTAAAGCTTAACACCCAGCCCGCCGCCACCGCTGGCATTGCCAGTGGCAGAATGATTTTTCGCAGAATGGTAAATTCGCTGGCACCGAGATCTTTCGCC > NC_000913/1182986‑1183138 |
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 31 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |