Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | ACB122 | 2,856,886 | T→G | S297A (TCG→GCG) | hdfR_4 → | HTH‑type transcriptional regulator HdfR |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | ACB122 | 2,856,886 | 0 | T | G | 100.0% | 11.3 / NA | 11 | S297A (TCG→GCG) | hdfR_4 | HTH‑type transcriptional regulator HdfR |
Reads supporting (aligned to +/- strand): ref base T (0/0); new base G (1/10); total (1/10) |
ACCTGGTGGGCGAGCCGCTCATCAACGAGGAAATGGTGGTGCTGGCCCGTCGGGGGCACCCGCTGTTGCACACTCACCTGACGCTCAAGGGCGTGCACCAGGCGCGCTGGGTGTTGCCGCGGGCCGGCTCGCCGGCCCGTCAGCTGCTCGACAACTGCTTCGCCGCCGCGGGCCTGACAGCGCCGTGGCCGGTGGTGGAAAGCGCTGATCTGGCGGTTATCCGTGGCCTACTGGTGCGTTCGGACATGCTGGCGG > ACB122/2856758‑2857012 | aCCTGGTGGGCGAGCCGCTCATCAACGAGGAAATGGTGGTGCTGGCCCGTCGGGGGCACCCGCTGTTGCACACTCACCTGACGCTCAAGGGCGTGCACCAGGCGCGCTGGGTGTTGCCGCGGGGCGGCGCGCCGGc > 8:1377/1‑136 (MQ=255) gggggcCACCGGCGGTTGCACACTCCCCGCCCGCGCACGGGGGTGCCCCAGGCGCGGTGGGTGTGGCCGCGGGCGGGCGCGCGGGCCCGTCAGCTGCTCGACAACTGCTTCGCCGCCGCGGGCCTGACAGCGCCGt < 7:1377/135‑1 (MQ=255) gggggCCCCGGCTATTCCACCCAATCCAGACGCGCACGGGCGAGCCCCGGGCGCGGTGTGGGTTGCGGGGGGCCGGCGCGCCGGCCCGTCAGCTGCTCGACAACTGCTTCGCCGCCGCGGGCCTGACAGCGCCGt < 6:212959/135‑1 (MQ=255) cGCTGTCCCACCCTCACCTCCCGCTCCCGGGCGGGCACCCGGCGGGGGGGGGGTGGCCGGGGGCCGGCGCGCCGGCCCGTCAGCTGCTCGACAACTGCTTCGCCGCCGCGGGCCTGACAGCGCCGTGGCCggtggt < 1:26796/136‑1 (MQ=255) tgccGCTCCGGGGCGGGCCCCTGGCGGGGTGGGTGTGGCGGGGGGCGGGCGCGCGGGCCCGTCAGCTGCTCGACAACTGCTTCGCCGCCGCGGGCCTGACAGCGCCGTGGCCGGTGGTGGAAAGCGCTGATCTgg < 6:10435/132‑1 (MQ=255) tCACGGGGGTGCACCAGGGGCGGGGGGTGTTGCGGCGGGCGGGCGCGCGGGCCCGTCAGCTGCTCGACAACTGCTTCGCCGCCGCGGGCCTGACAGCGCCGTGGCCGGTGGTGGAAAGCGCTGATCTGGCGGTTAt < 2:144208/136‑1 (MQ=255) gcaggggcgggcCCCTGGGGCGCGGGGTGGGGCGGGGGGCCGGGGCGCGGGCCGGTCAGCTGCTCGACAACTGCTTCGCCGCCGCGGGCCTGACAGCGCCGTGGCCGGTGGTGGAAAGCGCTGATCTGGCGGTTAt < 3:87519/132‑1 (MQ=255) cccgggCGTGCCCCCGGCGCGGGGGGGGTGGCCGCGGGCGGGCGCGCCGGCCCGTCAGCTGCTCGACAACTGCTTCGCCGCCGCGGGCCTGACAGCGCCGTGGCCGGTGGTGGAAAGCGCTGATCTGGCGGTTAt < 5:114665/132‑1 (MQ=255) acgggCGCGCACCAGGCGGGCTGGGTGTTGCCGGGGGCGGGCGCGCCGGCCCCTCAGCTGCTCGACAACTGCTTCGCCGCCGCGGGCCTGACAGCGCCGTGGCCGGTGGTGGAAAGCGCTGATCTGGCGGTTAt < 3:89587/132‑1 (MQ=255) gggcgggcACCAGGCGCGGGGGGTGTTGCCGCGGGCCGGCGCGCCGGCCCGTCAGCTGCTCGACAACTGCTTCGCCGCCGCGGGCCTGACAGCGCCGTGGCCGGTGGTGGAAAGCGCTGATCTGGCGGTTATCCGt < 3:78052/136‑1 (MQ=255) ggggCCGGCGCGCCGGCCCGTCAGCTGCTCGACAACTGCTTCGCCGCCGCGGGCCTGACAGCGCCGTGGCCGGTGGTGGAAAGCGCTGATCTGGCGGTTATCCGTGGCCTACTGGTGCGTTCGGACATGCTggcgg < 3:61311/135‑1 (MQ=255) | ACCTGGTGGGCGAGCCGCTCATCAACGAGGAAATGGTGGTGCTGGCCCGTCGGGGGCACCCGCTGTTGCACACTCACCTGACGCTCAAGGGCGTGCACCAGGCGCGCTGGGTGTTGCCGCGGGCCGGCTCGCCGGCCCGTCAGCTGCTCGACAACTGCTTCGCCGCCGCGGGCCTGACAGCGCCGTGGCCGGTGGTGGAAAGCGCTGATCTGGCGGTTATCCGTGGCCTACTGGTGCGTTCGGACATGCTGGCGG > ACB122/2856758‑2857012 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |