Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_000913 | 3,427,068 | Δ1 bp | 100% | intergenic (‑35/+8) | alaU ← / ← ileU | tRNA‑Ala/tRNA‑Ile |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 3,427,068 | 0 | T | . | 60.0% | ‑6.5 / 4.8 | 5 | intergenic (‑35/+8) | alaU/ileU | tRNA‑Ala/tRNA‑Ile |
Reads supporting (aligned to +/- strand): ref base T (0/0); major base . (0/3); minor base G (0/2); total (0/5) | |||||||||||
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 |
CGAACCGCAGACCTCCTGCGTGCAAAGCAGGCGCTCTCCCAGCTGAGCTATAGCCCCATAACATGTAGTTAAAACCTCTTCAAATTTGC‑CGTGCAAATTTGGTAG > NC_000913/3426977‑3427081 | cGAACCGCAGACCTCCTGCGTGCAAAGCAGGCGCTCTCCCAGCTGAGCTATAGCCCCATAACATGTAGTTAAAACCTCTTCAAATTTGCACG‑GCAAAttt < 1:3341829/100‑1 (MQ=1) cGAACCGCAGACCTCCTGCGTGCAAAGCAGGCGCTCTCCCAGCTGAGCTATAGCCCCATAACATGTAGTTAAAACCTCTTCAAATTTGCACG‑GCAAAttt < 2:1635714/100‑1 (MQ=1) cGAACCGCAGACCTCCTGCGTGCAAAGCAGGCGCTCTCCCAGCTGAGCTATAGCCCCATAACATGTAGTTAAAACCTCTTCAAATTTGCACG‑GCAAAttt < 2:4004250/100‑1 (MQ=1) agcctcAGACCTCTTGCGGGCAAAGCAGGCGCTCTCCCAGCTGAGCTATAGACGCATAACATGTAGTTAAAACCTCTTCAAATTTGC‑ACGGCAAATTTg < 1:220575/94‑1 (MQ=1) cggaGACGTGCTGCGTGCAAAGCAGGCGCTCTCCCAGCTGAGCTAGAGCCCCATAACATGTAGTTAAAACCTCGTCAAATTTGC‑ACGGCAAATTTgaaga < 1:1837425/97‑5 (MQ=1) | CGAACCGCAGACCTCCTGCGTGCAAAGCAGGCGCTCTCCCAGCTGAGCTATAGCCCCATAACATGTAGTTAAAACCTCTTCAAATTTGC‑CGTGCAAATTTGGTAG > NC_000913/3426977‑3427081 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 22 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |