Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_002947 | 4,714,468 | C→A | 28.6% | L14L (CTG→CTT) | PP_4166 ← | hypothetical protein |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_002947 | 4,714,468 | 0 | C | A | 28.6% | 22.1 / 5.0 | 14 | L14L (CTG→CTT) | PP_4166 | hypothetical protein |
Reads supporting (aligned to +/- strand): ref base C (7/3); new base A (2/2); total (9/5) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 5.80e-01 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.44e-01 |
TGTTGCCTCGCAGCAGGGTCCAGCCCAGGGTTGTCGTTCACCTTGCGCATCAGGTGGTAAAGCTTGGCATCGGCCGATTCACGCAGCAGGCTGTATTGGGCGAAATCCAGCGAAGTACCTTGGTCAACCTGTTCCAGGGTGGGTTGCAGGTCCAGGGAGCGCAACAGTTCCAGCATTTCACCCCTCATTCGCCGTTCCCTGATGTTTGCCATGTGGCAACGCTAGCAAGCGGTGGTGAAGCGCGACAACTGACAAAAATGCCAGTTGCCT > NC_002947/4714334‑4714603 | tgttgCCTCGCAGCAGGGTCCAGCCCAGGGTTGTCGTTCACCTTGCGCATCAGGTGGTAAAGCTTGGCATCGGCCGATTCACGCAGCAGGCTGTATTGGGCGAAATCCAGCGAAGTACCTTGGTCAACCTGTTCCa > 2:3595/1‑136 (MQ=255) tGTCGTTCACCTTGCGCATCAGGTGGTAAAGCTTGGCATCGGCCGATTCACGCAGCAGGCTGTATTGGGCGAAATCCAGCGAAGTACCTTGGTCAACCTGTTCCAGGGTGGGTTGCAGGTCCAGGGAGCGCAACAg > 2:255723/1‑136 (MQ=255) ttCACCTTGCGCATCAGGTGGTAAAGCTTGGCATCGGCCGATTCACGCAGCAGGCTGTATTGGGCGAAATCCAGCGAAGTACCTTGGTCAACCTGTTCAAGGGTGGGTTGCAGGTCCAGGGAGCGCAACAGTTCCa > 1:291777/1‑136 (MQ=255) ttCACCTTGCGCATCAGGTGGTAAAGCTTGGCATCGGCCGATTCACGCAGCAGGCTGTATTGGGCGAAATCCAGCGAAGTACCTTGGTCAACCTGTTCAAGGGTGGGTTGCAGGTCCAGGGAGCGCAACAGTTCCa > 1:293888/1‑136 (MQ=255) gcATCAGGTGGTAAAGCTTAGCATCGGCCGATTCACGCAGCAGGCTGTATTGGGCGAAATCCAGCGAAGTACCTTGGTCAACCTGTTCCAGGGTGGGTTGCAGGTCCAGGGAGCGCAACAGTTCCAGCATTTCAcc > 2:207832/1‑136 (MQ=255) aTCAGGTGGTAAAGCTTGGCATCGGCCGATTCACGCAGCAGGCTGTATTGGGCGAAATCCAGCGAAGTACCTTGGTCAACCTGTTCCAGGGTGGGTTGCAGGTCCAGGGAGCGCAACAGTTCCAGCATTTCAcccc > 2:33826/1‑136 (MQ=255) tggtAAAGCTTGGCATCGGCCGATTCACGCAGCAGGCTGTATTGGGCGAAATCCAGCGAAGTACCTTGGTCAACCTGTTCCAGGGTGGGTTGCAGGTCCAGGGAGCGCAACAGTTCCAGCATTTCACCCCTCATTc < 1:3595/136‑1 (MQ=255) tggtAAAGCTTGGCATCGGCCGATTCACGCAGCAGGCTGTATTGGGCGAAATCCAGCGAAGTACCTTGGTCAACCTGTTCCAGGGTGGGTTGCAGGTCCAGGGAGCGCAACAGTTCCAGCATTTCACCCCTCATTc < 1:59946/136‑1 (MQ=255) tggtAAAGCTTGGCATCGGCCGATTCACGCAGCAGGCTGTATTGGGCGAAATCCAGCGAAGTACCTTGGTCAACCTGTTCAAGGGTGGGTTGCAGGTCCAGGGAGCGCAACAGTTCCAGCATTTCACCCCTCATTc < 2:291777/136‑1 (MQ=255) tggtAAAGCTTGGCATCGGCCGATTCACGCAGCAGGCTGTATTGGGCGAAATCCAGCGAAGTACCTTGGTCAACCTGTTCAAGGGTGGGTTGCAGGTCCAGGGAGCGCAACAGTTCCAGCATTTCACCCCTCATTc < 2:293888/136‑1 (MQ=255) ggtAAAGCTTGGCATCGGCCGATTCACGCAGCAGGCTGTATTGGGCGAAATCCAGCGAAGTACCTTGGTCAACCTGTTCCAGGGTGGGTTGCAGGTCCAGGGAGCGCAACAGTTCCAGCATTTCACCCCTCATTCg < 1:137065/136‑1 (MQ=255) ggCATCGGCCGATTCACGCAGCAGGCTGTATTGGGCGAAATCCAGCGAAGTACCTTGGTCAACCTGTTCCAGGGTGGGTTGCAGGTCCAGGGAGCGCAACAGTTCCAGCATTTCACCCCTCATTCGCCGTTCCCTg > 1:365035/1‑136 (MQ=255) cACGCAGCAGGCTGTATTGGGCGAAATCCAGCGAAGTACCTTGGTCAACCTGTTCCAGGGTGGGTTGCAGGTACAGGGAGCGCAACAGTTCCAGCATTTAACCCCTCATTCGCCGTTCACTGATGATTGCCAtgtg > 2:393398/1‑136 (MQ=255) aCCTGTTCCAGGGTGGGTTGCAGGTCCAGGGAGCGCAACAGTTCCAGCATTTCACACCTCATTCGCCGTTCCCTGATGTTTGCCATGTGGCAACGCTAGCAAGAGGTGGTGAAGCGCGACAACTCACAAAAATGcc > 2:293178/1‑136 (MQ=255) cAGGGTGGGTTGCAGGTCCAGGGAGCGCAACAGTTCCAGCATTTCACCCCTCATTCGCCGTTCCCTGATGTTTGCCATGTGGCAACGCTAGCAAGCGGTGGTGAAGCGCGACAACTGACAAAAATGCCAGTTGCCt < 1:393398/136‑1 (MQ=255) | TGTTGCCTCGCAGCAGGGTCCAGCCCAGGGTTGTCGTTCACCTTGCGCATCAGGTGGTAAAGCTTGGCATCGGCCGATTCACGCAGCAGGCTGTATTGGGCGAAATCCAGCGAAGTACCTTGGTCAACCTGTTCCAGGGTGGGTTGCAGGTCCAGGGAGCGCAACAGTTCCAGCATTTCACCCCTCATTCGCCGTTCCCTGATGTTTGCCATGTGGCAACGCTAGCAAGCGGTGGTGAAGCGCGACAACTGACAAAAATGCCAGTTGCCT > NC_002947/4714334‑4714603 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 21 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |