Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 1,969,794 | 0 | A | C | 57.1% | 22.2 / 37.5 | 28 | G397G (GGT→GGG) | tap | methyl‑accepting protein IV |
Reads supporting (aligned to +/- strand): ref base A (10/2); new base C (0/16); total (10/18) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 5.03e-06 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 7.31e-05 |
GGGTCACCGAACTGACAATATCGATCATGGTCGCGGCGGCGTTATTCACCAGTTTCGAACCCTGCTGGACACGATTGACTGACTCTTCGATCAGCCCTTTGATCTCTTTTGCTGCCTGCGCGCTACGGCTGGCAAG‑ATTGCGCACTT‑CACCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAATATTGGTCTGGAAAGCAATTCCGTCGATAACGCTGATAATGTCGCCAATTTTTTGCGAGCTGGTGGCGATCT > NC_000913/1969646‑1969939 | gggTCACCGAACTGACAATATCGATCATGGTCGCGGCGGCGTTATTCACCAGTTTCGAACCCTGCTGGACACGATTGACTGACTCTTCGATCAGCCCTTTGATCTCTTTTGCTGCCTGCGCGCTACGGCTGGCAAG‑ATTGCGCACTT‑CAcc > 2:307275/1‑151 (MQ=255) cACCGAACTGACAATATCGATCATGGTCGCGGCGGCGTTATTCACCAGTTTCGAACCCTGCTGGACACGATTGACTGACTCTTCGATCAGCCCTTTGATCTCTTTTGCTGCCTGCGCGCTACGGCTGGCAAG‑ATTGCGCACTT‑CACCTGcc > 1:338574/1‑151 (MQ=255) ggttCGCGGGGGCGTTATTCCCCAGTTCCAACCCCGGCGGGACGCGTTGGGGTGACTTTCCGACCACCCCTTGGCTCTTTTTTGCTCCCGGCGCATTCCGGCT‑GCAAGTTTTGGCCACTT‑CCCCTGCCACTACCGCAAAACCACGCCCCt < 1:465689/147‑1 (MQ=255) gcggcggctTTATTCCCCATTTTCGACCCCTGCTGGACACGATTGACTGACTCTTCGATCAGCCCTTTGATCTCTTTTGCTGCCTGCGCGCTACGGCGGGCAAG‑ATTGCGCACTT‑CACCTGCCACTACCGCAAAACCACGCCCCTGctc < 1:544594/149‑1 (MQ=255) gcggcggcgTTATTCACCAGTTTCGAACCCTGCTGGACACGATTGACTGACTCTTCGATCAGCCCTTTGATCTCTTTTGCTGCCTGCGCGCTACGGCTGGCAAG‑ATTGCGCACTT‑CACCTGCCACTACCGCAAAACCACGCCCCTGCtctc > 1:250299/1‑151 (MQ=255) cggcggcgTTATTCACCAGTTTCGAACCCTGCTGGACACGATTGACTGACTCTTCGATCAGCCCTTTGATCTCTTTTGCTGCCTGCGCGCTACGGCTGGCAAG‑ATTGCGCACTT‑CACCTGCCACTACCGCAAAACCACGCCCCTGCTCTcc > 2:392513/1‑151 (MQ=255) ttCCCCAGTTTCGACCCCTGCTGGACACGATTGACTGACTCTTCGACCAGCCTTTTGATCTTTTTTGCTGCCTGCGCGCTCCGGCTGGAAAG‑ATTGCGCACTT‑CCCCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGcc < 2:259459/150‑1 (MQ=255) aGTTTCGAACCCTGCTGGACACGATTGACTGACTCTTCGATCAGCCCTTTGATCTCTTTTGCTGCCTGCGCGCTACGGCTGGCAAG‑ATTGCGCACTT‑CACCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTcc > 2:141497/1‑150 (MQ=255) ccTGCTGGACACGATTGACTGACTCTTCGATCAGCCCTTTGATCTCTTTTGCTGCCTGCGCGCTACGGCTGGCAAG‑ATTGCGCACTT‑CACCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCAtt > 1:424595/1‑151 (MQ=255) ggctgAACCCGTTTGACTGCCTCTCCGACCGCCCTTTTGTTCCCTTTCGCCCCCGCCGCGCTCCGGTGGACAAG‑GTTGCCCCCTC‑CCCCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCAtt < 1:432972/148‑1 (MQ=255) ggACACGTTTGACTGCCTCTTCGACCACCCTTTTGTTCTTTTTTGCTCCCTGCGCGCTCCGGCTGGAAAG‑TTTGCGCCCTT‑CCCCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAgg < 2:199922/149‑1 (MQ=255) ttGCCTTACTCTCCGACCCCCCCTTTGTTCTTTTTTCCTGCCTGCGCGCTCCGGCGGGCAAG‑TTGGCCCACTC‑CCCCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAat < 1:508227/149‑1 (MQ=21) ttGACTGACTCTTCGATCAGCCCTTTGATCTCTTTTGCTGCCTGCGCGCTACGGCTGGCAAG‑ATTGCGCACTT‑CACCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAatat > 1:27149/1‑151 (MQ=255) ttGACTGACTCTTCGATCAGCCCTTTGATCTCTTTTGCTGCCTGCGCGCTACGGCTGGCAAG‑ATTGCGCACTT‑CACCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAatat > 2:232635/1‑151 (MQ=255) ttCGACCAGCCTTTTGTTCTTTTTTGCGGCCGGCGCGCTACGGCGGGAAAG‑ATTGCGCCCTC‑CCCCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAATATTGGTCt < 2:52359/146‑1 (MQ=25) cAGCCTTTTGTTCTTTTTTGCTCCCGGCGCGCTCGGGCGGGAAAG‑ATTGCCCCCTC‑CCCCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAATATTGGTCTGGAAAGCaa < 2:577218/149‑1 (MQ=21) cccTTTGATCTTTTTTGCTCCCTGCGCGCTGCGGCGGGCAAG‑ATTGCGCCCTC‑CCCCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAATATTGGTCTGGAAAGCAATTc < 2:289443/149‑1 (MQ=25) ttttttGCTCCCTGCGCGCTCCGGCTGGCAAG‑TTTGCGCCCTT‑CCCCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAATATTGGTCTGGAAAGCAATTCCGTCGATa < 2:225040/145‑1 (MQ=37) ttttGCTGCCTGCGCGCTCCGGCAGGAAAG‑TTGGCCCACTT‑CACCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAATATTGGTCTGGAAAGCAATTCCGTCGATAACGCt < 2:478052/150‑1 (MQ=37) ttttGCCCCCTGCGGGCGCCGTCGGGAAAG‑TTTGCGCACTC‑CCCCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAATATTGGTCTGGAAAGCAATTCCGTCGATAACg < 2:188705/148‑1 (MQ=21) tttCCTGCCTCCGGGCTGCGGCTGCAAAG‑ATGGCGCTCTT‑CCCCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAATATTGGTCTGGAAAGCAATTCCGTCGATAACGCTg < 2:499842/150‑1 (MQ=25) ctccctgcGCGCTACGGCTGGAAAG‑ATTGCCCCCTC‑CCCCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAATATTGGTCTGGAAAGCAATTCCGTCGATAACGCTGATaa < 2:20539/147‑1 (MQ=37) cctgcGCGCTCGGGCTGCCGAG‑TGTGCGCCCTC‑CCCCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAATATTGGTCTGGAAAGCAATTCCGTCGATAACGCTGATaa < 1:456326/147‑1 (MQ=25) accggcggGCAAG‑‑TTGCCCCCTTCCCCCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAATATTGGTCTGGAAAGCAATTCCGTCGATAACGCTGATAATGTCGCCAAtttt < 2:209516/149‑1 (MQ=25) ggCTGGAAAG‑TTTGCCCCTTT‑CCCCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAATATTGGTCTGGAAAGCAATTCCGTCGATAACGCTGATAATGTCGCCAAtttttt < 2:485963/150‑1 (MQ=25) ggCGGGCAAG‑ATTGCCCCCTC‑CCCCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAATATTGGTCTGGAAAGCAATTCCGTCGATAACGCTGATAATGTCGCCAAtt < 2:321773/146‑1 (MQ=255) tGCGCACTT‑CACCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAATATTGGTCTGGAAAGCAATTCCGTCGATAACGCTGATAATGTCGCCAATTTTTTGCGAGCTGGTGGc > 2:288318/1‑151 (MQ=255) aCTT‑CACCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAATATTGGTCTGGAAAGCAATTCCGTCGATAACGCTGATAATGTCGCCAATTTTTTGCGAGCTGGTGGCGAtct > 2:127758/1‑151 (MQ=255) | GGGTCACCGAACTGACAATATCGATCATGGTCGCGGCGGCGTTATTCACCAGTTTCGAACCCTGCTGGACACGATTGACTGACTCTTCGATCAGCCCTTTGATCTCTTTTGCTGCCTGCGCGCTACGGCTGGCAAG‑ATTGCGCACTT‑CACCTGCCACTACCGCAAAACCACGCCCCTGCTCTCCGGCGCGAGCCGCTTCCACTGCCGCATTCAGGGCCAGAATATTGGTCTGGAAAGCAATTCCGTCGATAACGCTGATAATGTCGCCAATTTTTTGCGAGCTGGTGGCGATCT > NC_000913/1969646‑1969939 |
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 < 33 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |