Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | W3110S.gb | 599,692 | G→A | 20.0% | A586T (GCG→ACG) | cusA → | copper/silver efflux system, membrane component |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | W3110S.gb | 599,692 | 0 | G | A | 20.0% | 51.3 / 8.0 | 25 | A586T (GCG→ACG) | cusA | copper/silver efflux system, membrane component |
Reads supporting (aligned to +/- strand): ref base G (11/9); new base A (3/2); total (14/11) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.23e-01 |
ATCAATGAAGGCGACTTGTTGTATATGCCATCGACGCTGCCGGGGATTTCCGCAGCAGAGGCGGCGAGTATGCTGCAAAAAACCGACAAGCTAATTATGAGCGTACCTGAAGTGGCGCGGGTATTTGGCAAA > W3110S.gb/599629‑599760 | aTCAATGAAGGCGACTTGTTGTATATGCCATCGACGCTGCCGGGGATTTCCGCAGCAGAGGCGGCGAg < 1:2084736/68‑1 (MQ=255) cAATGAAGGCGACTTGTTGTATATGCCATCGACGCTGCCGGGGATTTCCGCAGCAGAGGCGGCGAGTAtgc > 1:2077495/1‑71 (MQ=255) cAATGAAGGCGACTTGTTGTATATGCCATCGACGCTGCCGGGGATTTCCGCAGCAGAGGCGGCGAGTAtgc > 1:3301779/1‑71 (MQ=255) aaGGCGACTTGTTGTATATGCCATCGACGCTGCCGGGGATTTCCGCAGCAGAGGCGACGAGTATGCTGCa > 1:969365/1‑70 (MQ=255) aCTTGTTGTATATGCCATCGACGCTGCCGGGGATTTCCGCAGCAGAGGCGACGAGTATGCTGCAAAAAAcc < 1:3862333/71‑1 (MQ=255) ttgttgTATATGCCATCGACGCTGCCGGGGATTTCCGCAGCAGAGGCGGCGAGTATGCTGCAAAAAACCGa > 1:1336326/1‑71 (MQ=255) ttgttgTATATGCCATCGACGCTGCCGGGGATTTCCGCAGCAGAGGCGGCGAGTATGCTGCAAAAAACCGa > 1:1398174/1‑71 (MQ=255) gttgtATATGCCATCGACGCTGCCGGTGATTTCCGCAGCAGAGGCGGCGAGTATGCTGCAAAAAACCGAc > 1:3795894/1‑70 (MQ=255) tGCCATCGACGCTGCCGGGGATTTCCGCAGCAGAGGCGGCGAGTATGCTGCAAAAAACCGACAAGCTAAt < 1:1162424/70‑1 (MQ=255) gCCATCGACGCTGCCGGGGATTTCCGCAGCAGAGGCGGCGAGTATGCTGCAAAAAACCGACAAGCTAATTa > 1:2127315/1‑71 (MQ=255) gCCATCGACGCTGCCGGGGATTTCCGCAGCAGAGGCGGCGAGTATGCTGCAAAAAACCGACAAGCTAATTa > 1:2480212/1‑71 (MQ=255) ccATCGACGCTGCCGGGGATTTCCGCAGCAGAGGCGGCGAGTATGCTGCAAAAAACCGACAAGCTAATTa < 1:1882551/70‑1 (MQ=255) ccATCGACGCTGCCGGGGATTTCCGCAGCAGAGGCGGCGAGTATGCTGCAAAAAACCGACAAGCTAATTa < 1:2120945/70‑1 (MQ=255) ccATCGACGCTGCCGGGGATTTCCGCAGCAGAGGCGGCGAGTATGCTGCAAAAAACCGACAAGCTAATTa < 1:2164137/70‑1 (MQ=255) tCGACGCTGCCGGGGATTTCCGCAGCAGAGGCGGCGAGTATGCTGCaaaa < 1:975694/50‑1 (MQ=255) tCGACGCTGCCGGGGATTTCCGCAGCAGAGGCGGCGAGTATGCTGCaaaa < 1:2819750/50‑1 (MQ=255) cGACGCTGCCGGGGATTTCCGCAGCAGAGGCGACGAGTATGCTGCAAAAAACCGACAAGCTAATTATGAGc > 1:3129063/1‑71 (MQ=255) cGACGCTGCCGGGGATTTCCGCAGCAGAGGCGACGAGTATGCTGCAAAAAACCGACAAGCTAATTATGAGc > 1:498798/1‑71 (MQ=255) gACGCTGCCGGGGATTTCCGCAGCAGAGGCGGCGAGTATGCTGCaaaaaa > 1:928851/1‑50 (MQ=255) gACGCTGCCGGGGATTTCCGCAGCAGAGGCGGCGAGTATGCTGCAAAAAACCGACAAGCTAATTATGAGCg > 1:3734474/1‑71 (MQ=255) gACGCTGCCGGGGATTTCCGCAGCAGAGACGGCGAGTATGCTGCAAAAAACCGACAAGCTAATTATGAGCg > 1:1074085/1‑71 (MQ=255) ccGGGGATTTCCGCAGCAGAGGCGGCGAGTATGCTGCAAAAAACCGACAAGCTAATTATGAGCGTACCTGa < 1:580375/71‑1 (MQ=255) gggATTTCCGCAGCAGAGGCGGCGAGTATGCTGCAAAAAACCGACAAGCTAATTATGAGCGTACCTGa < 1:3010346/68‑1 (MQ=255) ggATTTCCGCAGCAGAGGCGGCGAGTATGCTGCAAAAAACCGACAAGCTAATTATGAGCGTACCTGAAGTg > 1:1631845/1‑71 (MQ=255) cGCAGCAGAGGCGACGAGTATGCTGCAAAAAACCGACAAGCTAATTATGAGCGTACCTGAAGTGGCGCggg < 1:926374/71‑1 (MQ=255) gcggcgAGTATGCTGCAAAAAACCGACAAGCTAATTATGAGCGTACCTGAAGt > 1:169332/1‑53 (MQ=255) gcggcgAGTATGCTGCAAAAAACCGACAAGCTAATTATGAGCGTACCTGAAGTGGCGCGGGTATTTGGCaa < 1:722406/71‑1 (MQ=255) cggcgAGTATGCTGCAAAAAACCGACAAGCTAATTATGAGCGTACCTGAAGTGGCGCGGGTATTTGGCaaa < 1:949930/71‑1 (MQ=255) | ATCAATGAAGGCGACTTGTTGTATATGCCATCGACGCTGCCGGGGATTTCCGCAGCAGAGGCGGCGAGTATGCTGCAAAAAACCGACAAGCTAATTATGAGCGTACCTGAAGTGGCGCGGGTATTTGGCAAA > W3110S.gb/599629‑599760 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |