Predicted mutation | |||||||
---|---|---|---|---|---|---|---|
evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_002947 | 3,723,352 | C→T | 24.4% | A189V (GCC→GTC) | PP_3288 → | universal stress protein family protein |
Read alignment evidence... | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_002947 | 3,723,352 | 0 | C | T | 24.4% | 18.6 / 5.5 | 17 | A189V (GCC→GTC) | PP_3288 | universal stress protein family protein |
Reads supporting (aligned to +/- strand): ref base C (7/4); new base T (2/2); total (10/7) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 6.46e-01 |
ACCCTTGCACCTGGTACACAAGGCCAGCCATGCGTTGCCACGCAGGGTTCTGGCGGCGGTGGACCTGTCCAGGCCGGAGGATCAGTTTGAAGGCTTCAACGACCAGATCATCAGCGAAGCGCTGAAGCTGACATTGCAGTGCAATGCCCAGATCGAGTTGCTGTACGCCTACGATTTGGGTTCCATGTACCTGGACGCCGGCGGCAGCCGGGAACATTCGTTCCTGTTCGATTCAAACGATGCCCAGACCTTGCATGACGCTCAA > NC_002947/3723206‑3723470 | aCCCTTGCACCTGGTACACAAGGCCAGCCATGCGTTGCCACGCAGGGTTCTGGCGGCGGTGGACCTGTCCAGGCCGGAGGATCAGTTTGAAGGCTTCAACGACCAGATCATCAGCGAAGCGCTGAAGCTGACATTGCAGTGCAATGCCCa > 1:393333/1‑150 (MQ=255) tGGTACACAAGGCCAGCCATGCGTTGCCACGCAGGGTTCTGGCGGCGGTGGACCTGTCCAGGCCGGAGGATAAGTTTGAAGGCTTCAACGACCAGACCATCAGCGAAGCGCTGAAGCTGACATTACAGTGCAATGCCCAGATCGAGTTGc > 2:247730/1‑150 (MQ=255) ccagccaTGCGTTGCCACGCAGGGTTCTGGCGGCGGTGGACCTGTCCAGGCCGGAGGATCAGTTTGAAGGCTTCAACGACCAGATCATCAGCGAAGCGCTGAAGCTGACATTGCAGTGCAATGACCAGATCGAGTTGCTGTACGCCTACg > 1:288059/1‑150 (MQ=255) tGGACCTGTCCAGGCCGGAGGATCAGTTTGAAGGCTTCAACGACCAGATCATCAGCGAAGCGCTGAAGCTGACATTGCAGTGCAATGCCCAGATCGAGTTGCTGTACGCCTACGATTTGGGTTCCAGGTACCTGGACGCCGGCGGCAGcc > 2:143421/1‑150 (MQ=255) aCCTGTCCAGGCCGGAGGATCAGTTTGAAGGCTTCAACGACCAGATCATCAGCGAAGCGCTGAAGCTGACATTGCAGTGCAATGCCCAGATCGAGTTGCTGTACGCCTACGATTTGGGTTCCATGTAc > 2:71404/1‑128 (MQ=255) aCCTGTCCAGGCCGGAGGATCAGTTTGAAGGCTTCAACGACCAGATCATCAGCGAAGCGCTGAAGCTGACATTGCAGTGCAATGCCCAGATCGAGTTGCTGTACGCCTACGATTTGGGTTCCATGTAc < 1:71404/128‑1 (MQ=255) ccGGAGGATCAGTTTGAAGGCTTCAACGACCAGATCATCAGCGAAGCGCTGAAGCTGACATTGCAGTGCAATGCCCAGATCGAGTTGCTGTACGCCTACGATTTGGGTTCCATGTACCTGGACGCCGGCGGCAGCCGGGAACATTCGTTc < 2:393333/150‑1 (MQ=255) tttGAAGGCTTCAACGACCAGATCATCAGCGAAGCGCTGAAGCTGACATTGCAGTGCAATGCCCAGATCGAGTTGCTGTACGCCTACGATTTGGGTTCCATGTACCTGGACGCCGGCGGCAGCCGGGAACATTCGTTCCTGTTCGATTCa > 2:390457/1‑150 (MQ=255) aGGCTTCAACGACCAGATCATCAGCGAAGCGCTGAAGCTGACATTGCAGTGCAATGCCCAGATCGAGTTGCTGTACGCCTACGATTTGGGTTCCATGTACCTGGACGCCGGCGGCAGCCGGGAACATTCGTTCCTGTTCGATTCAAACGa < 1:127912/150‑1 (MQ=255) atcaGCGAAGCGCTGAAGCTGACATTGCAGTGCAATGACCAGATCGAGTTGCTGTACGCCTACGATTTGGGTTCCATGTACCTGGACGCCGGCGGCAGCCGGGAACATTCGTTCCTGTTCGATTCAAACGATGCCCAGACCTTGCATGAc < 2:288059/150‑1 (MQ=255) tcaGCGAAGCGCTGAAGCTGACATTGCAGTGCAATGCCCAGATCGAGTTGCTGTACGCCTACGATTTGGGTTCCATGTACCTGGACGCCGGCTGCCGCCggcgt < 1:315602/104‑4 (MQ=255) tcaGCGAAGCGCTGAAGCTGACATTGCAGTGCAATGCCCAGATCGAGTTGCTGTACGCCTACGATTTGGGTTCCATGTACCTGGACGCCGGCTGCCGCCggcgt > 2:315602/1‑101 (MQ=255) gAAGCGCTGAAGCTGACATTGCAGTGCAATGCCCAGATCGAGTTGCTGTACGCCTACGATTTGGGTTCCATGTACCTGGACGCCGGCGGCAGCCGGGAACATTCGTTCCTGTTCGATTCAAACGATGCCCAGACCTTGCATGACGCTCaa > 1:253293/1‑150 (MQ=255) actGCAATGTCCAGATCGAGTTGCTGTACGCCTACGATTTGGGTTCCATGTACCTGGACGCCGGCGGCAGCCGGGAACATTCGt > 1:231930/3‑84 (MQ=255) actGCAATGTCCAGATCGAGTTGCTGTACGCCTACGATTTGGGTTCCATGTACCTGGACGCCGGCGGCAGCCGGGAACATTCGt < 2:231895/82‑1 (MQ=255) actGCAATGTCCAGATCGAGTTGCTGTACGCCTACGATTTGGGTTCCATGTACCTGGACGCCGGCGGCAGCCGGGAACATTCGt < 2:231930/82‑1 (MQ=255) actGCAATGTCCAGATCGAGTTGCTGTACGCCTACGATTTGGGTTCCATGTACCTGGACGCCGGCGGCAGCCGGGAACATTCGt > 1:231895/3‑84 (MQ=255) | ACCCTTGCACCTGGTACACAAGGCCAGCCATGCGTTGCCACGCAGGGTTCTGGCGGCGGTGGACCTGTCCAGGCCGGAGGATCAGTTTGAAGGCTTCAACGACCAGATCATCAGCGAAGCGCTGAAGCTGACATTGCAGTGCAATGCCCAGATCGAGTTGCTGTACGCCTACGATTTGGGTTCCATGTACCTGGACGCCGGCGGCAGCCGGGAACATTCGTTCCTGTTCGATTCAAACGATGCCCAGACCTTGCATGACGCTCAA > NC_002947/3723206‑3723470 |
Alignment Legend |
---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |