Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | W3110S.gb | 1,135,828 | T→C | 71.4% | D150D (GAT→GAC) | flgF → | flagellar component of cell‑proximal portion of basal‑body rod |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | W3110S.gb | 1,135,828 | 0 | T | C | 71.4% | 17.3 / 6.0 | 14 | D150D (GAT→GAC) | flgF | flagellar component of cell‑proximal portion of basal‑body rod |
Reads supporting (aligned to +/- strand): ref base T (2/2); new base C (2/8); total (4/10) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 5.20e-01 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 7.96e-01 |
GCTGTGCCGGAAGGGGCGGAAATCACTATTGCTGCCGATGGCACAATCTCGGCGCTCAATCCGGGCGATCCGGCAAATACGGTTGCGCCAGTAGGGCGTCTTAAACTGGTGAAAGCCACGGGCAGCGAAG > W3110S.gb/1135760‑1135889 | gCTGTGCCGGAAGGGGCGGAAATCACTATTGCTGCCGATGGCACAATCTCGGCGCTCAATCCGGGCGAccc > 1:405169/1‑71 (MQ=255) gCTGTGCCGGAAGGGGCGGAAATCACTATTGCTGCCGATGGCACAATCTCGGCGCTCAATCCGGGCGAccc > 1:725202/1‑71 (MQ=255) ccGGAAGGGGCGGAAATCACTATTGCTGCCGATGGCACAATCTCGGCGCTCAATCCGGGCGACCCGGCaaa < 1:1731250/71‑1 (MQ=255) ggAAATCACTATTGCTGCCGATGGCACAATCTCGGCGCTCAATCCGGGCGACCCGGCAAATACGGTTgcgc < 1:910616/71‑1 (MQ=255) aTCACTATTGCTGCCGATGGCACAATCTCGGCGCTCAATCCGGGCGATCCGGCAAATACGGTTGCGCCAGt < 1:971759/71‑1 (MQ=255) tATTGCTGCCGATGGCACAATCTCGGCGCTCAATCCGGGCGACCCGGCAAATAc < 1:2078562/54‑1 (MQ=255) ttGCTGCCGATGGCACAATCTCGGCGCTCAATCCGGGCGATCCGGCAAATACGGt > 1:2354893/1‑55 (MQ=255) ttGCTGCCGATGGCACAATCTCGGCGCTCAATCCGGGCGACCCGGCAAATACGGTTGCGCCAGTAGGGCGt > 1:1209827/1‑71 (MQ=255) tgctgtCGATGGCACAATCTCGGCGCTCAATCCGGGCGACCCGGCAAATACGGTTGCGCCAGt < 1:2590864/63‑1 (MQ=255) ccGATGGCACAATCTCGGCGCTCAATCCGGGCGACCCGGCAAATACGGTTGCGCCAGTAGGGCGTCTTa < 1:1265357/69‑1 (MQ=255) ccGATGGCACAATCTCGGCGCTCAATCCGGGCGACCCGGCAAATACGGTTGCGCCAGTAGGGCGTCTTa < 1:1643676/69‑1 (MQ=255) aTGGCACAATCTCGGCGCTCAATCCGGGCGATCCGGCAAATACGGTTGCGCCAg < 1:307152/54‑1 (MQ=255) aTCTCGGCGCTCAATCCGGGCGACCCGGCAAATACGGTTGCGCCAGTAGGGCGTCTTAAACTGGTGAAAGc < 1:1678740/71‑1 (MQ=255) tcGGCGCTCAATCCGGGCGATCCGGCAAATACGGTTGCGCCAGTAGGGCGTCTTAAACTGGTGAAAGCCAc > 1:2578704/1‑71 (MQ=255) aaTCCGGGCGACCCGGCAAATACGGTTGCGCCAGTAGGGCGTCTTAAACTGGTGAAAGCCa > 1:376107/1‑61 (MQ=255) tCCGGGCGACCCGGCAAATACGGTTGCGCCAGTAGGGCGTCTTAAACTGGTGAAAGCCACGGGCAGCGAAg < 1:86441/71‑1 (MQ=255) | GCTGTGCCGGAAGGGGCGGAAATCACTATTGCTGCCGATGGCACAATCTCGGCGCTCAATCCGGGCGATCCGGCAAATACGGTTGCGCCAGTAGGGCGTCTTAAACTGGTGAAAGCCACGGGCAGCGAAG > W3110S.gb/1135760‑1135889 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |