Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | USA300TCH1516_ALE | 496,458 | C→A | 17.0% | S220I (AGC→ATC) | gltC ← | HTH‑type transcriptional regulator GltC |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | USA300TCH1516_ALE | 496,458 | 0 | C | A | 17.0% | 74.5 / 6.8 | 28 | S220I (AGC→ATC) | gltC | HTH‑type transcriptional regulator GltC |
Reads supporting (aligned to +/- strand): ref base C (13/10); new base A (2/3); total (15/13) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 6.39e-01 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.14e-01 |
AGCACATATCGTTCTTTTTAATTCAGTATGATCTAATTTTATATCTATCCATGATTTAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTGTTTTTTTACAGTTTCGGCAAATGGTGCCAAGCAATAAATATGACTATGCTCAAACTGAATTAATGGTGGGTGTGTCGCCATCGTAATTGGATCGTC > USA300TCH1516_ALE/496322‑496597 | aGCACATATCGTTCTTTTTAATTCAGTATGATCTAATTTTATATCTATCCATGATTTAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACt > 2:130915/1‑141 (MQ=255) aGCACATATCGTTCTTTTTAATTCAGTATGATCTAATTTTATATCTATCCATGATTTAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACt > 2:108927/1‑141 (MQ=255) cGTTCTTTTTAATTCAGTATGATCTAATTTTATATCTATCCATGATTTAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACTGATAGTGta > 2:240054/1‑141 (MQ=255) tttAATTCAGTATGATCTAATTTTATATCTATCCATGATTTAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACTGATTGTGTATACATCt > 1:105668/1‑141 (MQ=255) tCAGTATGATCTAATTTTATATCTATCCATGATTTAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACGTATTGTGTATACATCTGATTTa < 2:377540/141‑1 (MQ=255) cAGTATGATCTAATTTTATATCTATCCATGATTTAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACTGATTGTGTATACATCTGATTTAg > 1:101530/1‑141 (MQ=255) cAGTATGATCTAATTTTATATCTATCCATGATTTAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGATACTGATTGTGTATACATCTGATTTAg < 2:157511/141‑1 (MQ=255) aTGATCTAATTTTATATCTATCCATGATTTAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTCGTTGGCTACTGATTGTGTATACATCTGATTTAGTAAt < 1:272498/141‑1 (MQ=255) aaTTTTATATCTATCCATGATTTAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAAACTTCTTTTTGCCAAAGGAGATACTGCGCAAGTGGTTGGCTACTGCTTGTGTATACATCTGATTTAGTAATCTTgcgc > 1:93542/1‑141 (MQ=255) ttttATATCTATCCATGATTTAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCaa > 2:197490/1‑141 (MQ=255) tataTCTATCCATGATTTAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTg < 1:59843/141‑1 (MQ=255) atatCTATCCATGATTTAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGATACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTGt < 2:162806/141‑1 (MQ=255) tctatcCATGATTTAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTGtttt > 1:32310/1‑141 (MQ=255) ctatcCATGATTTAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTGttttt > 2:212817/1‑141 (MQ=255) tatcCATGATTTAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTGtttttt > 2:157434/1‑141 (MQ=255) tcCATGATTTAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTGTTTTTTTa < 1:346592/141‑1 (MQ=255) tttAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTGTTTTTTTACAGTTTc > 1:19050/1‑141 (MQ=255) cTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACTGATTGTGTATACATCTGATCTAGTAATCTTGCGCAATTGTTTTTTTACAGTTTCGGCAAATg > 2:360784/1‑141 (MQ=255) tgatgTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTGTTTTTTTACAGTTTCGGCAAATGGTGCCAAGCAATAAATATGACTATGCt < 1:77310/141‑1 (MQ=255) gatgTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGATACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTGTTTTTTTACAGTTTCGGCAAATGGTGCCAAGCAATAAATATGACTATGCTc < 2:24354/141‑1 (MQ=255) atgTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTGTTTTTTTACAGTTTCGGCAAATGGTGCCAAGCAATAAATATGACTATGCTCa < 1:303651/141‑1 (MQ=255) tAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTGTTTTTTTACAGTTTCGGCAAATGGTGCCAAGCAATAAATATGACTATGCTCAAAc > 1:89351/1‑141 (MQ=255) ttttGACGAAGGAGATACTGCGCAAGTGGTTGGCTACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTGTTTTTTTACAGTTTCGGCAAATGGTGCCAAGCAATAAATATGACTATGCTCAAACTGAATTAAt < 1:333537/141‑1 (MQ=255) gagaTACTGCGCAAGTGGTTGGCTACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTGTTTTTTTACAGTTTCGGCAAATGGTGCCAAGCAATAAATATGACTATGCTCAAACTGAATTAATGGTGGgtgtgt < 1:108927/141‑1 (MQ=255) cTGCGCAAGTGGTTGGCTACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTGTTTTTTTACAGTTTCGGCAAATGGTGCCAAGCAATAAATATGACTATGCTCAAACTGAATTAATGGTGGGTGTGTCGCCAt < 2:37589/141‑1 (MQ=255) ttGGATACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTGTTTTTTTACAGTTTCGGCAAATGGTGCCAAGCAATAAATATGACTATGCTCAAACTGAATTCATGGTGGGTGTGTCGCCATCGTAATTGGATc > 2:128021/1‑141 (MQ=255) ttGGATACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTGTTTTTTTACAGTTTCGGCAAATGGTGCCAAGCAATAAATATGACTATGCTCAAACTGAATTAATGGTGGGTGTGTCGCCATCGTAATTGGATc > 2:151792/1‑141 (MQ=255) gCTACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTGTTTTTTTACAGTTTCGGCAAATGGTGCCAAGCAATAAATATGACTATGCTCAAACTGAATTAATGGTGGGTGTGTCGCCATCGTAATTGGATCGTc < 1:360784/141‑1 (MQ=255) | AGCACATATCGTTCTTTTTAATTCAGTATGATCTAATTTTATATCTATCCATGATTTAGATTCTGGTAAATGTATATTTTGTGATGAAATGATGTAACCTTCTTTTTGACGAAGGAGATACTGCGCAAGTGGTTGGCTACTGATTGTGTATACATCTGATTTAGTAATCTTGCGCAATTGTTTTTTTACAGTTTCGGCAAATGGTGCCAAGCAATAAATATGACTATGCTCAAACTGAATTAATGGTGGGTGTGTCGCCATCGTAATTGGATCGTC > USA300TCH1516_ALE/496322‑496597 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 22 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |