Read alignment evidence... | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 4,111,747 | 0 | G | T | 56.0% | 10.9 / 36.1 | 25 | N156K (AAC→AAA) | yiiQ | DUF1454 family putative periplasmic protein |
Reads supporting (aligned to +/- strand): ref base G (11/0); new base T (0/14); total (11/14) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 2.24e-07 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 4.98e-04 |
ATTTATTCAAACCTTCAAGCGATTCAGATAGCGCCAGCTTAATCGGTTC‑AACAGCGAAGGTCAGCCCCTTTTCG‑CC‑G‑TTGTCCGCGACAACATAACGCAGTGCACCTTCTGTCTCGGTGTAATAACGTTTGTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATCACCGCTGCCATGTATTCCTGAGCTTTCGCTTTCGCGGCTTTTTGCTCTGGCCCCTGGATGGGTAGCC > NC_000913/4111617‑4111892 | ttttttcaaccccTCCAAGCGATCCAGATGGCCCCATCTTATTCGGTTC‑AACAGCTAAGGTCACCCCTTTTTCG‑CC‑G‑TTGTCCGCGACACCAAAACGCAGTGCCCCTTCTTTCTGGGTGTAATACCTTTTTTTTTTCCCCGCCGTtagtag < 2:189918/140‑1 (MQ=255) gATTCAGATAGCGCCAGCTTAATCGGTTC‑AACAGCGAAGGTCAGCCCCTTTTCG‑CC‑G‑TTGTCCGCGACAACATAACGCAGTGCACCTTCTGTCTCGGTGTAATAACGTTTGTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTgg > 2:201869/1‑150 (MQ=255) ccattttaacGGTTCAAACAGCGAGGGCCACCCCTTTTTCG‑CG‑T‑TTGCCCGCAACAACATACCGCGGTCCCCTTTCTTTCTGGGTGTAATAAGTTTTTTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGt < 2:159040/142‑1 (MQ=255) aGCTTAATCGGTTC‑AACAGCGAAGGTCAGCCCCTTTTCG‑CC‑G‑TTGTCCGCGACAACATAACGCAGTGCACCTTCTGTCTCGGTGTAATAACGTTTGTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCa > 2:114744/1‑151 (MQ=255) gCTTAATCGGTTC‑AACAGCGAAGGTCAGCCCCTTTTCG‑CC‑G‑TTGTCCGCGACAACATAACGCAGTGCACCTTCTGTCTCGGTGTAATAACGTTTGTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCAt > 2:53840/1‑151 (MQ=255) tAATGGGTCA‑AACGGCGAGGGTCAGCCCTTTTTCC‑CC‑T‑TTGCCCCCAACAATATAACGCGGTCCTCCTTTTTTCTCGGTGTAATATCGTTTTTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTaa < 2:188357/151‑1 (MQ=255) gtac‑AACAGCGGGGGTCCCCCCTTTTTCC‑CT‑T‑TTGCCCGCGAAACTATACCGCGGTGCTCCTTCTGTTTGGGTTTAATATTGTTTTTTTTCCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATgggg < 2:131210/147‑1 (MQ=255) gtac‑AACAGAAAGGGTCA‑CCCCCTTTCG‑CCTG‑TTCCCGGCAACAACATAACGAAGTGCCCCTGTTGGTTCGTTGTATTACCGTTTTTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATgggg < 1:217520/147‑1 (MQ=255) atcaaaCAGCGAAGCTCAGCCCTTTTTGC‑CG‑G‑TTGTCCGCAACAACATAACGCAGTGCCCTTTCTGTCTGGGTTTAATATCTTTTTTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATgggg < 1:168955/146‑1 (MQ=255) c‑AACAGCGAAGGTCA‑CCCCTTTTCGCCC‑T‑TTGCCCGCGAAAAAATACCGCGGTGCCCCTTTTTTCTGGGTGTAATAACTTTTTTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAg < 2:399370/151‑1 (MQ=255) aaGGTCAGCCCTTTTCCG‑CC‑G‑TTGTCCGCAACAACATACCGCAGTGCACCTTCTGTCTCGGTGTAATAGTGTTTTTTTTCCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGa < 1:36110/151‑1 (MQ=255) gcccccccTTTTTC‑CC‑GTTTGCCCGCAACAACAAAACGCGTTGCCCCTTCTTTCTCGGTGTAATATCTTTTTTTTTTCGCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATc < 2:373468/146‑1 (MQ=255) tttGTCCGCAGAAACAAAACACGGTGGCCTTTGTGTCTGGGTTAAATGGGGTTTTTTTTCCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGATTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATCACCGCTGCCATGTATTcc < 2:11942/150‑1 (MQ=255) gTCCGCGACAACATAACGCAGTGCACCTTCTGTCTCGGTGTAATAACGTTTGTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATCACCGCTGCCATGTATTCCTGa > 1:325473/1‑151 (MQ=255) ccGCAAAAAAATACCGCTGTGCCCTTTCTTTCTGGTTGTAATATCTTTTTTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATCACCGCTGCCATGTATTCCTGAgc < 1:58634/151‑1 (MQ=255) acaTAACGCAGTGCACCTTCTGTCTCGGTGTAATAACGTTTGTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATCACCGCTGCCATGTATTCCTGAgctttcgctt > 2:135731/1‑151 (MQ=255) acaTAACGCAGTGCACCTTCTGTCTCGGTGTAATAACGTTTGTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATCACCGCTGCCATGTATTCCTGAgctttcgctt > 1:364662/1‑151 (MQ=255) acaTAACGCAGTGCACCTTCTGTCTCGGTGTAATAACGTTTGTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATCACCGCTGCCATGTATTCCTGAgctttcgctt > 1:123800/1‑151 (MQ=255) caTAACGCAGTGCACCTTCTGTCTCGGTGTAATAACGTTTGTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATCACCGCTGCCATGTATTCCTGAgctttcgcttt > 2:368224/1‑151 (MQ=255) gTGCACCTTCTGTCTCGGTGTAATAACGTTTGTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATCACCGCTGCCATGTATTCCTGAGCTTTCGCTTTCGCGGCttt > 1:3800/1‑151 (MQ=255) ttgggtgtattatttttttttttTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATCACCGCTGCCATGTATTCCTGAGCTTTCGCTTTCGCGGCTTTTTGCTCTGGcccc < 2:134289/136‑1 (MQ=255) gtttattatctttttttttTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATCACCGCTGCCATGTATTCCTGAGCTTTCGCTTTCGCGGCTTTTTGCTCTGGCCCCTgg < 2:394836/139‑1 (MQ=255) gtgtAATAACGTTTGTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATCACCGCTGCCATGTATTCCTGAGCTTTCGCTTTCGCGGCTTTTTGCTCTGGCCCCTGGa > 1:19077/1‑151 (MQ=255) tgtAATATCTTTTTTTTTCCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATCACCGCTGCCATGTATTCCTGAGCTTTCGCTTTCGCGGCTTTTTGCTCTGGCCCCTGGAt < 1:408620/151‑1 (MQ=255) tgtAATAGTGTTTTTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATCACCGCTGCCATGTATTCCTGAGCTTTCGCTTTCGCGGCTTTTTGCTCTGGCCCCTGGAt < 1:376632/151‑1 (MQ=255) gtAATAACGTTTGTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATCACCGCTGCCATGTATTCCTGAGCTTTCGCTTTCGCGGCTTTTTGCTCTGGCCCCTGGATg > 1:210103/1‑151 (MQ=255) atgagtttttttttCCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATCCCCGCTGCCATGTATTCCTGAGCTTTCGCTTTCGCGGCTTTTTGCTCTGGCCCCTGGATGGGt < 1:43421/145‑1 (MQ=255) cGTTTTTTTTCCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATCACCGCTGCCATGTATTCCTGAGCTTTCGCTTTCGCGGCTTTTTGCTCTGGCCCCTGGATGGGTAGcc < 2:212121/151‑1 (MQ=255) | ATTTATTCAAACCTTCAAGCGATTCAGATAGCGCCAGCTTAATCGGTTC‑AACAGCGAAGGTCAGCCCCTTTTCG‑CC‑G‑TTGTCCGCGACAACATAACGCAGTGCACCTTCTGTCTCGGTGTAATAACGTTTGTTTTTCCCCGCCGTTAGTAGCGACTGCAGTTTTTTCTGGCTTTGTGTTTTGGTCATTAATGGGGTGAGTGTGCGGATCACCGCTGCCATGTATTCCTGAGCTTTCGCTTTCGCGGCTTTTTGCTCTGGCCCCTGGATGGGTAGCC > NC_000913/4111617‑4111892 |
Alignment Legend |
---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 30 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |