Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | minE | 1,458,605 | G→A | 52.2% | pseudogene (3350/4605 nt) pseudogene (3350/4104 nt) |
yfaS ← yfaS ← |
ECK2220:JW2222+JW2221:b4500; hypothetical protein ECK2220:JW2222:b2228; hypothetical protein, N‑ter fragment |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | minE | 1,458,605 | 0 | G | A | 52.2% | ‑5.1 / 16.9 | 23 | pseudogene (3350/4605 nt) pseudogene (3350/4104 nt) | yfaS yfaS | ECK2220:JW2222+JW2221:b4500; hypothetical protein ECK2220:JW2222:b2228; hypothetical protein, N‑ter fragment |
Reads supporting (aligned to +/- strand): ref base G (7/4); new base A (5/7); total (12/11) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 4.14e-01 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.23e-01 |
ATGCCCATGCCGTAAGGAAGGCGTCACCATTGCCATCTTCACCCCACCAGGTAAAGCGCGCTCCGGGCCCCGCCAGTTGCATCAGCCGCAGACGGTTATCCTGAATCATCTGACGAATGTCGTT > minE/1458546‑1458669 | atgcccatgccTTGAGGAAGGCGTCGCCATTGCCATCTTCACCCCACCAGGTAAAGCGCACTCCGGGcc < 1:691474/69‑1 (MQ=255) atgcccatgccGTGAGGAAGGCGTCGCCATTGCCATCTTCACCCCACCAGGTAAAGCGCACTCCGGGcc < 1:1637416/69‑1 (MQ=255) atgcccatgccGTGAGGAAGGCGTCGCCATTGCCATCTTCACCCCACCAGGTAAAGCGCACTCCGGGcc < 1:1945024/69‑1 (MQ=255) atgcccatgccGTGAGGAAGGCGTCGCCATTGCCATCTTCACCCCACCAGGTAAAGCGCACTCCGGGcc < 1:1987051/69‑1 (MQ=255) atgcccatgccGTGAGGAAGGCGTCGCCATTGCCATCTTCACCCCACCAGGTAAAGCGCACTCCGGGcc < 1:2869734/69‑1 (MQ=255) atgcccatgccGTGAGGAAGGCGTCGCCATTGCCATCTTCACCCCACCAGGTAAAGCGCACTCCGGGcc < 1:2704278/69‑1 (MQ=255) atgcccatgccGTAAGGAAGGCGTCACCATTGCCATCTTCACCCCACCAGGTAAAGCGCGCTCCGGGc < 1:687114/68‑1 (MQ=255) atgcccataccGTGAGGAAGGCGTCGCCATTGCCATCTTCACCCCACCAGGTAAAGCGCACTACGGGcc < 1:1308139/69‑1 (MQ=255) gccGTGAGGAAGGCGTCGCCATTGCCATCTTCACCCCACCAGGTAAAGCGCACTCCgg > 1:2196791/1‑58 (MQ=255) gccGTGAGGAAGGCGTCGCCATTGCCATCTTCACCCCACCAGGTAAAGCGCACTCCGGGc > 1:1214899/1‑60 (MQ=255) gccGTGAGGAAGGCGTCGCCATTGCCATCTTCACCCCACCAGGTAAAGCGCACTCCGGGc > 1:3434234/1‑60 (MQ=255) gccGTGAGGAAGGCGTCGCCATTGCCATCTTCACCCCACCAGGTAAAGCGCACTCCGGGc > 1:522200/1‑60 (MQ=255) gccGTGAGGAAGGCGTCGCCATTGCCATCTTCACCCCACCAGGTAAAGCGCACTCCGGGc > 1:1326567/1‑60 (MQ=255) aCCATTGCCATCTTCACCCCACCAGGTAAAGCGCGCTCCGGGCCCCGCCAGTTGCATCAGCCGCAg > 1:2226407/1‑66 (MQ=255) aCCATTGCCATCTTCACCCCACCAGGTAAAGCGCGCTCCGGGCCCCGCCAGTTGCATCAGCCGCAGACg > 1:922468/1‑69 (MQ=255) aCCATTGCCATCTTCACCCCACCAGGTAAAGCGCGCTCCGGGCCCCGCCAGTTGCATCAGCCGCAGACg > 1:2273580/1‑69 (MQ=255) aCCATTGCCATCTTCACCCCACCAGGTAAAGCGCGCTCCGGGCCCCGCCAGTTGCATCAGCCGCAGACg > 1:1133598/1‑69 (MQ=255) aCCATTGCCATCTTCACCCCACCAGGTAAAGCGCGCTCCGGGCCCCGCCAGTTGCATCAGCCGCAGACg > 1:3085351/1‑69 (MQ=255) ttCACCCCACCAGGTAAAGCGCGCTCCGGGCCCCGCCAGTTGCATCAGCCGCAGACGGTTATCCTGAat > 1:511329/1‑69 (MQ=255) ttCACCCCACCAGGTAAAGCGCGCTCCGGGCCCCGCCAGTTGCATCAGCCGCAGACGGTTATCCTGAat > 1:937614/1‑69 (MQ=255) ccccACCAGGTAAAGCGCGCTCCGGGCCCCGCCAGTTGCATCAGCCGCAGACGGTTATCCTGAatca < 1:456730/67‑1 (MQ=255) ccccACCAGGTAAAGCGCGCTCCGGGCCCCGCCAGTTGCATCAGCCGCAGACGGTTATCCTGAatca < 1:3056700/67‑1 (MQ=255) ccaGGTAAAGCGCGCTCCGGGCCCCGCCAGTTGCATCAGCCGCAGACGGTTATCCTGAATCATCTGACg < 1:408929/69‑1 (MQ=255) gcgcgcTCCGGGCCCCGCCAGTTGCATCAGCCGCAGACGGTTATCCTGAATCATCTGACGAATGTCGtt > 1:3175150/1‑69 (MQ=255) gcgcgcTCCGGGCCCCGCCAGTTGCATCAGCCGCAGACGGTTATCCTGAATCATCTGACGAATGTCGtt < 1:3142969/69‑1 (MQ=255) gcgcgcTCCGGGCCCCGCCAGTTGCATCAGCCGCAGACGGTTATCCTGAATCATCTGACGAATGTCGtt > 1:2903472/1‑69 (MQ=255) gcgcgcTCCGGGCCCCGCCAGTTGCATCAGCCGCAGACGGTTATCCTGAATCATCTGACGAATGTCGtt < 1:908381/69‑1 (MQ=255) gcgcgcTCCGGGCCCCGCCAGTTGCATCAGCCGCAGACGGTTATCCTGAATCATCTGACGAATGTCGtt > 1:2399353/1‑69 (MQ=255) gcgcgcTCCGGGCCCCGCCAGTTGCATCAGCCGCAGACGGTTATCCTGAATCATCTGACGAATGTCGtt > 1:1786403/1‑69 (MQ=255) gcgcgcTCCGGGCCCCGCCAGTTGCATCAGCCGCAGACGGTTATCCTGAATCATCTGACGAATGTCGt > 1:901431/1‑68 (MQ=255) | ATGCCCATGCCGTAAGGAAGGCGTCACCATTGCCATCTTCACCCCACCAGGTAAAGCGCGCTCCGGGCCCCGCCAGTTGCATCAGCCGCAGACGGTTATCCTGAATCATCTGACGAATGTCGTT > minE/1458546‑1458669 |
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: ‑ |