Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 1,941,326 | C→T | D104N (GAT→AAT) | mepM ← | peptidoglycan DD‑endopeptidase MepM |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 1,941,326 | 0 | C | T | 96.4% | 72.9 / NA | 28 | D104N (GAT→AAT) | mepM | peptidoglycan DD‑endopeptidase MepM |
Reads supporting (aligned to +/- strand): ref base C (0/0); major base T (14/13); minor base G (1/0); total (15/13) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.89e-01 |
GTTCGCCGTCCGCGGTTAATGTCCAGGAGAGTTGTTGACCGATTTTCAGGTTACGCAATTCTTTGTCGGCCGCAGCCAGTTGGGTGATATCACCCATATCAATACCATACTGATTGAGAATGCTGCTTAGCGTATCGCCAGTGGAAACAACATATTCATGCACGCCCGCTTCACCGGCGATTTTGTCATCCAGTTCGTCCTGGGGAATGGCTTCATCTTCTTGTGCAGCTTGATCAATCGGCTCACTGGCTTCAGGTAAGAGCGAACGAATTTCG > NC_000913/1941191‑1941465 | tttCGCCGTCCGCGGTTAATGTCCAGGAGTGTTGTTGACCGATTTTTAGGTTATGCAATTCTTTGTCGGCCGCAGCCAGTTGGGTGATATCACCCATATCAATACCATACTGATTGAGAATGCTGCTTAGCGTATTGCCAGTg < 2:247684/142‑1 (MQ=255) ttCGCCGTCCGCGGTTAATGTCCAGGAGAGTTGTTGACCGATTTTCAGGTTACGCAATTCTTTGTCGGCCGCAGCCAGTTGGGTGATATCACCCATATCAATACCATACTGATTGAGAATGCTGCTTAGCGTATTGCCAGTgg > 1:297488/1‑143 (MQ=255) gCCGTCCGCGGTTAATGTCCAGGAGAGTTGTTGACCGATTTTCAGGTTACGCAATTCTTTGTCGGCCGCAGCCAGTTGGGTGATATCACCCATATCAATACCATACTGATTGAGAATGCTGCTTAGCGTATTGCCAGTGGaaa > 2:241199/1‑143 (MQ=255) ttAATGTCCAGGAGAGTTGTTGACCGATTTTCAGGTTACGCAATTCTTTGTCGGCCGCAGCCAGTTGGGTGATATCACCCATATCAATACCATACTGATTGCGAATGATGCTTAGCGTATTGCCAATGTAAACAACATATTCa > 2:103463/1‑143 (MQ=255) ctGTCCAGCAGAGTTGTTGACCGATTTACAGGTTACGCAATTCCTTGTCGGCCGCCGCCAGATCAAACATATCACCCATATCAATGCCATACTGATTGAGAATGCTGCTTAGCGTATTGCCAGTGGAAACAACATATTCATGc < 2:188620/142‑1 (MQ=255) cAGGAGAGTTGTTGACCGATTTTCAGGTTACGCAATTCTTTGTCGGCCGCAGCCAGTTGGGTGATATCACCCATATCAATACCATACTGATTGAGAATGCTGCTTAGCGTATTGCTAGTGGAAACAACATATTCATGCACGcc < 2:76941/143‑1 (MQ=255) tgttgACCGATTTTCAGGTTACGCAATTCTTTGTCGGCCGCAGCCAGTTGGGTGATATCACCCATATCAATACCATACTGATTGAGAATGCTGCTTAGCGTATTGCCAGTGGAAACAACATATTCATGCACGCCCGCTTCAcc < 1:355368/143‑1 (MQ=255) aCCGATTTTCAGGTTACGCAATTCTTTGTCGGCCGCAGCCAGTTGGGTGATATCACCCATACCACTACCCTACTGATTGAGAATGCTGCTTAGCGTATTGCCAGGGGAAACCCCATATGTTTGCAGCCCCGCTTCGCCGGGGa > 2:127165/1‑143 (MQ=255) cGATTTTCAGGTTACGCAATTCTTTGTCGGCCGCAGCCAGTTGGGTGATATCACCCATATCAATACCATACTGATTGAGAATGCTGCTTAGCGTATTGCCAGTGGACACAACATATTCATGCACGCCCGCTTCACCggagctt > 1:578208/1‑138 (MQ=255) gATTTTCAGGTTACGCAATTCTTTGTCGGCCGCAGCCAGTTGGGTGATATCACCCATATCAATACCATACTGATTGAGAATGCTGCTTAGCGTATTGCCAGTGGAAACAACATATTCATGCACGCCCGCTTCACCGGCGAttt > 1:89661/1‑143 (MQ=255) ttCAGGTTACGCAATTCTTTGTCGGCCGCAGCCAGTTGGGTGATATCACCCATATCAATACCATACTGATTGAGAATGCTGCTTAGCGTATTGCCAGTGGAAACAACATATTCATGCACGCCCGCTTCACCGGCGATTTTGTc > 2:617197/1‑143 (MQ=255) aGGTTATGGTATTCTTTGTCGTCCGCATCCAGTTGGTTCATATCACCCATATCAATACCATACTGATTGAGAATGCTGCTTAGCGTATTGCCAGTGGAAACAACATATTCATGCACGCCCGCTTCACCGGCGATTTTGTCATc < 2:556657/143‑1 (MQ=255) cGCAATTCTTTGTCGGCCGCAGCCAGTTGGGTGATATCACCCATATCAATACCATACTGATTGAGAATGCTGCTTAGCGTATTGCCAGTGGAAACAACATATTCATGCACGCCCGCTTCACCGGCGATTTTGTCATCCAGTTc > 2:262112/1‑143 (MQ=255) aaTTCTTTGTCGGCCGCAGCCAGTTGGGTGATATCACCCATATCAATACCATACTGATTGAGAATGCTGCTTAGCGTATGGCCAGTGGAAACAACATATTCATGCACGGCCGCTTCACCGGCGAGCTTGTCATCGACTTCgac > 2:295126/1‑141 (MQ=255) gCCAGTTGGGTGATATCACCCATATCAATACCATACTGATTGAGAATGCTGCTTAGCGTATTGCCAGTGGAAACAACATATTCATGCACGCCCGCTTCACCGGCGATTTTGTCATCCAGTTCGTCCTGGGGAATGGCTTCAtc < 1:105596/143‑1 (MQ=255) aGTTGGGTGACATCACCCATATCGATACCATACTGATTGAGAATGCTGCTTAGCGCATTGCGAGTGGAGCCAACATATTCATGCACGCCCGCTTCACCGGCGATTTTGTAATCCAGTTCGTCCTGGCGAATGGCTTCAtcttc < 2:509405/143‑1 (MQ=255) ttGGGTGGTTTCGCCTCTATCAATACCATACTGTTTTAGACTGCTGCTTTGCGTATTGCCAGTTGTATCAACATATTCTTGCTCGCTCGCTTCACCGGCGATTTTGTCATCCAGTTCGTCCTGGTGATTGGCTTCATcttctt < 2:404704/143‑1 (MQ=255) gTGATATCACCCATATCAATACCATACTGATTGAGAATGCTGCTTAGCGTATTGCCAGTGGAAACAACATATTCATGCACGCCCGCTTCACCGGCGATTTTGTCATCCAGTTCGTCCTGGGGAATGGCTTCATCTTCTTGTGc > 2:230576/1‑143 (MQ=255) tCAGCCATATCAATACCATACTGAGTGAGAATGCTGCTTAGCGTATTGCCAGTGGAAACAACATATTCATGCACGCCCGCTTCACCGGCGATTTTGTCATCCAGTTCGTCCTGGGGAATGGCTTCATCTTCTTGTGCAGCTTg < 2:194897/143‑1 (MQ=255) atatCAATACCATACTGATTGAGAATGCTGCTTAGCGTATTGCCAGTGGAAACAACATATTCATGCACGCCCGCTTCACCGGCGATTTTGTCATCCAGTTCGTCCTGGGGAATGGCTTCATCTTCTTGTGCAGCTTGATCAAt > 1:294336/1‑143 (MQ=255) atatCAATACCATACTGATTGAGAATGCTGCTTAGCGTATTGCCAGTGGAAACAACATATTCATGCACGCCCGCTTCACCGGCGATTTTGTCATCCAGTTCGTCCTGGGGAATGGCTTCATCTTCTTGTGCAGCTTCGTCAAt > 1:109389/1‑143 (MQ=255) tagcAATACCATACTGATTGAGAATGCTGCTTAGCGTATTGCCAGTGGAAACAACATATTCATGCACGCCCGCTTCACCGGCGATTTTGTCATCCAGTTCGTCCTGGGGAATGGCTTCATCTTCTTGTGCAGCTTGATCAATc < 1:241199/140‑1 (MQ=255) atCAATAGCATACTGATTGAGAATGCTGCTTAGCGTAGTGCCAGTGGAAACAACATATTCAGGCACGCCCGCTTCACCGGCGATTTTGTCATCCAGTTCGTCCTGGGGAATGGCTTCATCTTCTTGTGCAGCTTGATCAATCg < 1:117629/143‑1 (MQ=255) tCAATACCATACTGATTGAGAATGCTGCTTAGCGTATTGCCAGTGGAAACAACATATTCATGCACGCCCGCTTCACCGGCGATTTTGTCATCCAGTTCGTCCTGGGGAATGGCTTCATCTTCTTGTGCAGCTTGATCAATCgg < 1:105001/143‑1 (MQ=255) cAACACCATACTGATTGATACTGCTGCTTAGCGTATTGCCAGTGGAAACAACATATTCATGCACGCCCGCTTCACCCGCGATTTTGTCATTCAGTTCGTCCTGGGGAATGGCTTCATCTTCTTGTGCAGCTTGATCAATCGGc < 1:94826/143‑1 (MQ=255) tgctTAGCGTATTGCCAGTGGAAACAACATATTCATGCACGCCCGCTTCACCGGCGATTTTGTCATCCAGTTCGTCCTGGGGAATGGCTTCATCTTCTTGTGCAGCTTGATCAATCGGCTCACTGGCTTCAGGTAAGAGcgaa > 1:223158/1‑143 (MQ=255) cGTATTGCCAGTGGAAACAACATATTCATGCACGCCCGCTTCACCGGCGATTTTGTCATCCAGTTCGTCCCGGGGAATGGCTTCATCTTCAAGCGCAGCTCGATCAATCGGCGCACTGGCTCCCGGCACCAGcgaacgaaaac > 2:409570/1‑140 (MQ=255) tATTGCCAGTGGAAACAACATATTCATGCACGCCCGCTTCACCGGCGATTTTGTCATCCAGTTCGTCCTGGGGAATGGCTTCATCTTCTTGTGCAGCTTGATCAATCGGCTCACTGGCTTCAGGTAAGAGCGAACGAATTTCg > 1:612303/1‑143 (MQ=255) | GTTCGCCGTCCGCGGTTAATGTCCAGGAGAGTTGTTGACCGATTTTCAGGTTACGCAATTCTTTGTCGGCCGCAGCCAGTTGGGTGATATCACCCATATCAATACCATACTGATTGAGAATGCTGCTTAGCGTATCGCCAGTGGAAACAACATATTCATGCACGCCCGCTTCACCGGCGATTTTGTCATCCAGTTCGTCCTGGGGAATGGCTTCATCTTCTTGTGCAGCTTGATCAATCGGCTCACTGGCTTCAGGTAAGAGCGAACGAATTTCG > NC_000913/1941191‑1941465 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 13 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |