Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 1,792,782 | T→C | intergenic (‑51/+27) | nlpC ← / ← btuD | NlpC/P60 family lipoprotein NlpC/vitamin B12 ABC transporter ATP binding subunit |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 1,792,782 | 0 | T | C | 96.2% | 82.6 / NA | 26 | intergenic (‑51/+27) | nlpC/btuD | NlpC/P60 family lipoprotein NlpC/vitamin B12 ABC transporter ATP binding subunit |
Reads supporting (aligned to +/- strand): ref base T (1/0); new base C (17/8); total (18/8) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 1.00e+00 |
GAAAGTCTGGCATTTGGCGGCGGTGCTTTATGGTGGCTACACCCGGCCAGAAGCAGTGCTGTGATCAAAATAAGGCAGAAACGCATTCCGTACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATTACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCATTCTGTGACCTTCGATATCCAGACGGCGAAAATTCATCCCATAGGCCTGCGCCAGATTTGGCGGCGTGAGCACCTCTTCCCTGCGTCCA > NC_000913/1792646‑1792917 | gAAAGTCTGGCATTTGGCGGCGGTGCTTTATGGTGGCTACACCCGGCCAGAAGCAGTGCTGTGATCAAAATAAGGCAGAAACGCATTCCGTACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATCAcc < 1:720127/140‑1 (MQ=255) aaaGTCTGGCATTTGGCGGCGGTGCTTTATGGTGGCTACACCCGGCCAGAAGCAGTGCTGTGATCAAAATAAGGCAGAAACGCATTCCGTACGGTTCCTCTGCTTTTTATGCTTGCAGTAATTTAGCGTCGTAATCAccc > 1:280975/1‑140 (MQ=255) tggCTACACCCGGCCAGAAGCAGTGCTGTGATCAAAATAAGGCAGAAACGCATTCCGTACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTc > 1:534459/1‑140 (MQ=255) gCTACACCCGGCCAGAAGCAGTGCTGTGATCAAAATAAGGCAGAAACGCATTCCGTACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGa > 2:631405/1‑140 (MQ=255) gCTACACCCGGCCAGAAGCAGTGCTGTGATCAAAATAAGGCAGAAACGCATTCCGTACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAACGTCGTAAACACGCGACTTTCAAGATACTATTGAAATCACATGGTCGa > 2:462228/1‑140 (MQ=255) ccGGCCAGAAGCAGTGCTGTGATCAAAATAAGGCATAAACGCATTCCGTACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGc < 2:79822/140‑1 (MQ=255) gCCAGAAGCAGTGCTGTGATCAAAATAAGGCAGAAACGCATTCCGTACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATTACCCGATTATCAAGATACTAATGAAGTCAGATGGTCGAAATCAGCAtt > 2:339517/1‑140 (MQ=255) gCCAGAAGCAGTGCTGTGATCAAAATAAGGCAGAAACGCATTCCGTACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCAtt > 1:859601/1‑140 (MQ=255) gCCAGAAGCAGTGCTGTGATCAAAATAAGGCAGAAACGCATTCCGTACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCAtt > 2:43598/1‑140 (MQ=255) gCCAGAAGCAGTGCTGTGATCAAAATAAGGCAGAAACGCATTCCGTACGGTTCCTATGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCAtt > 2:825188/1‑140 (MQ=255) gCAGTGCTGTGATCAAAATAAGGCAGAAACGCATTCCGTACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCATTCTGTGAc < 1:703506/140‑1 (MQ=255) tgATCAAAATAAGGCAGAAACGCATTCCGTACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCATTCTGTGACCTTCGatat > 2:862856/1‑140 (MQ=255) ggCAGAAACGCATTCCGTACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATTAGATGGTCGAAAGCAGGCTTCTGTGACCTTCGATATCCAGACGGCGaa > 2:482711/1‑140 (MQ=255) ggCAGAAACGCATTCCGTACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATGAGATGGTCAAAAACAGCATTCTGTGACCTTAGATATCCAGACGGCGaa > 2:478075/1‑140 (MQ=255) aaCGCATTCCGTACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCATTCTGTGACCTTCGATATCCAGACGGCGAAAATTCa < 2:679007/140‑1 (MQ=255) aaCGCATTCCGTACGGTTCCTAGGTTTTTCATTCTTGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCATTCTGTGACCTTCGATATCCAGACGGCGAAAATTCa < 1:368516/140‑1 (MQ=255) gTACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCATTCTGTGACCTTCGATATCCAGACGGCGAAAATTCATCCCATAGGc < 1:892512/140‑1 (MQ=255) gTACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCATTCTGTGACCTTCGATATCCAGACGGCGAAAATTCATCCCATAGGc > 2:680489/1‑140 (MQ=255) tACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCATTCTGTGACCTTCGATATCCAGACGGCGAAAATTCATCCCATAGGcc > 2:769417/1‑140 (MQ=255) tACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCATTCTGTGACCTTCGATATCCAGACGGCGAAAATTCATCCCATAGGcc > 1:130740/1‑140 (MQ=255) tCTTGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCATTCTGTGACCTTCGATATCCAGACGGCGAAAATTCATCCCATAGGCCTGCGCCAGATTTGGCGGCGTg < 2:534459/140‑1 (MQ=255) tCTTGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCATTCTGTGACCTTCGATATCCAGACGGCGAAAAATCAAGCCATAGGACTGCCACAGATTTGGCGGCGTg > 2:487816/1‑140 (MQ=255) ttGCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCATTCTGTGACCTTCGATATCCAGACGGCGAAAATTCATCCCATAGGCCTGCGCCAGATTTGGCGGCGTGAg < 2:809417/140‑1 (MQ=255) gCATTAATTTAGCGTCGTAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCATTCTGTGACCTTCGATATCCAGACGGCGAAAATTCATCCCATAGGCCTGCGCCAGATTTGGCGGCGTGAGCa < 1:862856/140‑1 (MQ=255) gtAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCATTCTGTGACCTTCGATATCCAGACGGCGAAAATTCATCCCATAGGCCTGCGCCAGATTTGGCGGCGTGAGCACCTCTTCCCTGCGTcc > 1:193979/1‑140 (MQ=255) gtAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCATTCTGTGACCTTCGATATCCAGACGGCGAAAATTCATCCCATAGGCCTGCGCCAGATTAGGCGGCGTGAGCAACTCTTCCCTGCGTcc > 1:275853/1‑140 (MQ=255) tAATCACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCATTCTGTGACCTTCGATATCCAGACGGCGAAAATTCATCCCATAGGCCTGCGCCAGATTTGGCGGCGTGAGCACCTCTTCCCTGCGTCCa > 1:113360/1‑140 (MQ=255) | GAAAGTCTGGCATTTGGCGGCGGTGCTTTATGGTGGCTACACCCGGCCAGAAGCAGTGCTGTGATCAAAATAAGGCAGAAACGCATTCCGTACGGTTCCTCTGTTTTTTATTCTTGCATTAATTTAGCGTCGTAATTACCCGATTTTCAAGATACTAATGAAATCAGATGGTCGAAATCAGCATTCTGTGACCTTCGATATCCAGACGGCGAAAATTCATCCCATAGGCCTGCGCCAGATTTGGCGGCGTGAGCACCTCTTCCCTGCGTCCA > NC_000913/1792646‑1792917 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |