Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NZ_CP009273 | 2,247,045 | C→T | A194T (GCA→ACA) | nupX ← | NupC/NupG family nucleoside CNT transporter |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NZ_CP009273 | 2,247,045 | 0 | C | T | 100.0% | 76.0 / NA | 21 | A194T (GCA→ACA) | nupX | NupC/NupG family nucleoside CNT transporter |
Reads supporting (aligned to +/- strand): ref base C (0/0); new base T (12/9); total (12/9) |
TCGGTGAAAGAGAGGTTATTAAAGGAAACCTGCGAAGATTCCGTTGCCGGGCTTAACAGGCGGGCAAACAAGATCCCGCCAGGGATCGCCATTAATGATGCCGCCAGCAGATATTCCACAGGCACGCCCAGTGCGGCGTAACCAATCATTGTCGAACCAGCAATCGAGGCCATGCCACTACAAATCGCTGTAAATAATTCATTGCGATTCAGACGATCGATAAAGGGTTTGACGATTGCCGGAATTTCGTTTTGCCCGAG > NZ_CP009273/2246912‑2247171 | tCGGTGAAAGAGAGGTTATTAAAGGAAACCTGCGAAGATTCCGTTGCCGGGCTTAACAGGCGGGCAAACAAGATCCCGCCAGGGATCGCCATTAATGATGCCGCCAGCAGATATTCCACAGGCACGCCCAGTgtggcg < 2:367322/138‑1 (MQ=255) aaGGAAACCTGCGAAGATTCCGTTGCCGGGCTTAACAGGCGGGCAAACAAGATCCCGCCAGGGATCGCCATTAATGATGCCGCCAGCAGATATTCCACAGGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAg < 1:478993/139‑1 (MQ=255) aaGGAAACCTGCGAAGATTCCGTTGCCGGGCTTAACAGGCGGGCAAACAAGATCCCGCCAGGGATCGCCATTAATGATGCCGCCAGCAGATATTCCACAGGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAg < 1:592221/139‑1 (MQ=255) aaaCCTGCGAAGATTCCGTTGCTGGGCTTAACAGGCGGGCAAACAAGATCCCGCCAGGGATCGCCATTAATGATGCCGCCAGCAGATATTCCACAGGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAg > 2:621408/1‑135 (MQ=255) aaaCCTGCGAAGATTCCGTTGCTGGGCTTAACAGGCGGGCAAACAAGATCCCGCCAGGGATCGCCATTAATGATGCCGCCAGCAGATATTCCACAGGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAg < 1:621408/135‑1 (MQ=255) aaCCTGCGGAGATTCCGTTGCCGAGCTTAACAGGCGGGCAAACAAGATCCCGCAAGGGAACGCCATTACTGATTCCGCCAGCAGATATTCCACACGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAGCAATc > 2:125238/1‑139 (MQ=255) ccTGCGAAGATTCCGTTGCCGGGCTTAACAGGCGGGCAAACAAGATCCCGCCAGGGATCGCCATTAATGATGCCGCCAGCAGATATTCCACAGGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAGCAATc > 2:489943/1‑137 (MQ=255) tCCGTTGCCGGGCTTAACAGGCGGGCAAACAAGATCCCGCCAGGGATCGCCATTAATGATGCCGCCAGCAGATATTCCACAGGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAg > 2:129944/1‑121 (MQ=255) tCCGTTGCCGGGCTTAACAGGCGGGCAAACAAGATCCCGCCAGGGATCGCCATTAATGATGCCGCCAGCAGATATTCCACAGGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAg < 1:129944/121‑1 (MQ=255) ggCAAACAAGATCCCGCCAGGGATCGCCATTAATGATGCCGCCAGCAGATATTCCACAGGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAGCAATCGAGGCCATGCCACTACAAATCGCTGTAAATAATTCa > 2:1951/1‑139 (MQ=255) aaaCAAGATCCCGCCAGGGATCGCCATTAATGATGCCGCCAGCAGATATTCCACAGGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAGCAATCGAGGCCATGCCACTACAAATCGCTGTAAATAATTCATTg < 1:333400/139‑1 (MQ=255) tCCCGCCAGGGATCGCCATTAATGATGCCGCCAGCAGATATTCCACAGGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAGCAATCGAGGCCATGCCACTACAAATCGCTGTAAATAATTCATTGCGAtt > 2:460607/1‑136 (MQ=255) ccGCCAGGGATCGCCATTAATGATGCCGCCAGCAGATATTCCACAGGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAGCAATCGAGGCCATGCCACTACAAATCGCTGTAAATAATTCATTGCGATTCAGAc < 1:460607/139‑1 (MQ=255) gCCATTAATGATGCCGCCAGCAGATATTCCACAGGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAGCAATCGAGGCCATGCCACTACAAATCGCTGTAAATAATTCATTGCGATTCAGACGATCGATAAAgg > 2:600212/1‑139 (MQ=255) tgCCGCCAGCAGATATTCCACAGGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAGCAATCGAGGCCATGCCACTACAAATCGCTGTAAATAATTCATTGCGATTCAGACGATCGATAAAGGGTTTGACGAtt > 2:576712/1‑139 (MQ=255) gccgccAGCAGATATTCCACAGGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAGCAATCGAGGCCATGCCACTACAAATCGCTGTAAATAATTCAtt < 1:575558/104‑1 (MQ=255) gccgccAGCAGATATTCCACAGGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAGCAATCGAGGCCATGCCACTACAAATCGCTGTAAATAATTCAtt > 2:575558/1‑104 (MQ=255) gccgccAGCAGATATTCCACAGGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAGCAATCGAGGCCATGCCACTACAAATCGCTGTAAATAATTCATTGCGATTCAGACGATCGATAAAGGGTTTGACGATTg > 1:422252/1‑139 (MQ=255) gccgccAGCAGATATTCCACAGGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAGCAATCGAGGCCATGCCACTACAAATCGCTGTAAATAATTCATTGCGATTCAGACGATCGATAAAGGGTTTGACGATTg > 2:481724/1‑139 (MQ=255) gccgccAGCAGATATTCCACAGGCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAGCAATCGAGGCCATGCCACTACAAATCGCTGTAAATAATTCATTGCGATTCAGACGATCGATAAAGGGTTTGACGATTg > 2:508731/1‑139 (MQ=255) caGGCACGCCCAGTGTGGCGTAACAAATCATTGTCGAACCAGCAATCGAGGCCATGCGACTACAAATCGGTGTAAATAATTCATTGCGATTCAGACGATCGATAAAGGGTTTGACGATTGTGGGAATTTCGTTTTGccc < 1:125238/139‑1 (MQ=255) gCACGCCCAGTGTGGCGTAACCAATCATTGTCGAACCAGCAATCGAGGCCATGCCACTACAAATCGCTGTAAATAATTCATTGCGATTCAGACGATCGATAAAGGGTTTGACGATTGCCGGAATTTCGTTTTGCCCGAg < 1:508731/139‑1 (MQ=255) | TCGGTGAAAGAGAGGTTATTAAAGGAAACCTGCGAAGATTCCGTTGCCGGGCTTAACAGGCGGGCAAACAAGATCCCGCCAGGGATCGCCATTAATGATGCCGCCAGCAGATATTCCACAGGCACGCCCAGTGCGGCGTAACCAATCATTGTCGAACCAGCAATCGAGGCCATGCCACTACAAATCGCTGTAAATAATTCATTGCGATTCAGACGATCGATAAAGGGTTTGACGATTGCCGGAATTTCGTTTTGCCCGAG > NZ_CP009273/2246912‑2247171 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |