Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_000913 | 3,041,634 | A→C | 100% | T108P (ACC→CCC) | ygfZ → | folate‑binding protein |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 3,041,634 | 0 | A | C | 100.0% | 38.2 / NA | 16 | T108P (ACC→CCC) | ygfZ | folate‑binding protein |
Reads supporting (aligned to +/- strand): ref base A (0/0); new base C (4/12); total (4/12) | |||||||||||
Rejected as polymorphism: Frequency below/above cutoff threshold. | |||||||||||
Rejected as polymorphism: Variant not supported by required number of reads on each strand. |
CCATTGCGACGCCAAAGGTAAAATGTGGAGCAATTTACGTCTGTTCCGCGACGGCGATGGCTTTGCATGGATTGAACGGCGCAGCGTGCGTGAACCGCAGCTGACTGAACTGAAAAAATATGCGGTATTCTCTAAAGTGACCATCGCGCCAGACGACGAGCGTGTGCTGCTTGGTGTTGCCGGTTTTCAGGCGCGCGCCGCGCTGGCAAATCTCTTTAGCGAACTGCCTTCGAAAGAAAAACAGGTAGTCAAAGAAGGCGCGACCACTTTGCTATG > NC_000913/3041495‑3041770 | ccATTGCGACGCCAAAGGTAAAATGTGGAGCAATTTACGTCTGTTCCGCGACGGCGATGGCTTTGAATGGATTGAACGGCGCAGCGTGCGTGAACCGCAGCTGACTGAACTGAAAAAATATGCGGTATTCTCTAAAGTGCCCa < 1:232119/143‑1 (MQ=255) aTTGCGACGCGAAAGGTAAAATGTGGAGCAATATACGTCTGTTCCGCGACGGCGATGGCTTTGCATGGATTGAACTGCGCAGCGTGCGTGAACCGCAGCTGACTGAACTGAAAAAATATGCGGTATTCTCTAAAGTGCCCATc < 2:87182/143‑1 (MQ=255) cGCCAATGTTAATATGTGGAGCAATTTACGTCTGTTCCGCGACGGCGATGGCTTTGCATGGATTGAACGGCGCAGCGCGAGTGAACCGCAGTGGACTGAACTGAAAAAATATGCGGTATTCTCTAAAGTGCCCATCGCGCCAg < 1:125795/143‑1 (MQ=255) ccAAAGGTAAAATGTGGAGCAATTTACGTCTGTTCCGCGACGGCGATGGCTTTGCATGGATTGAACGGCGCAGCGTGCGTGAACCGCAGCTGACTGCTCTGACAAAATATGCGGTATTCAATAAAGTGCCCATCACGCAAgac > 1:198492/1‑143 (MQ=255) gcTGGTCCGCAACGGCGATGGCTTTGCATGGATTGAACGGCGCAGCTTGCGTGAACCGCAGCTGAATGCTCGGATTAAATATGCGGTTTTCTCTTATTTGCCCATCGCGCCAGACGACGAGCGTGTGCTGCTTGGTGTTGCCg < 2:265127/142‑1 (MQ=255) gcgACGGCGATGGCTTTGCATGGATTGAACGGCGCAGCGTGCGTGAACCGCAGCTGACTGAACTGAAAAAATATGCGGTATTCTCTAAAGTGCCCATCGCGCCAGACGACGAGCGTGTGCTGCTTGGTGTTGCCGGTTTTCAg < 1:57317/143‑1 (MQ=255) gcgACGGCGATGGCTTTGCATGGATTGAACGGCGCAGCGTGCGTGAACCGCAGCTGACTGAACTGAAAAAATATGCGGTATTCTCTAAAGTGCCCATCGCGCCAGACGACGAGCGTGTGCTGCTTGGTGTTGCCGGTTTTCAg < 1:60414/143‑1 (MQ=255) aTGGCTTTGCATGGATTGAACGGCGCAGCGTGCGTGAACCGCAGCTGACTGAACTGAAAAAATATGCGGTATTCTCTAAAGTGCCCATCGCGCCAGACGACGAGCGTGTGCTGCTTGGTGTTGCCGGTTTTCAGGCGcgcgcc > 2:254469/1‑143 (MQ=255) tttGCATGGATGGATCGGTGCAGCGTGCGTGAACCGCAGCTGACTGAACTGAAAAAATATGCGGTATTCTCTGAAGTGCCCATCGCGCCAGACGGCTAGTGTTTTCTGCTTGGTGTTGCCGGTTTTCAGGCGCGCGCCGCGCt < 2:164562/143‑1 (MQ=255) tGCATGGATTGAACGGCGCAGCGTGCGTGAACCGCAGCTGACTGAACTGAAAAAATATGCGGTATTCTCTAAAGTGCCCATCGCGCCAGACGACGAGCGTGTGCTGCTTGGTGTTGCCGGTTTTCAGGCGCGCGCCGCGCTgg < 1:224256/143‑1 (MQ=255) gATTGAACGGCGCAGCGTGCGTGAACCGCAGCTGACTGAACTGAAAAAATATGCGGTATTCTCTAAAGTGCCCATCGCGCCAGACGACGAGCGTGTGCTGCTTGGTGTTGCCGGTTTTCAGGCGCGCGCCGCCCTGGCACAtc > 1:130469/1‑143 (MQ=255) aCGGCGCAGCGTGCGTGAACCGCAGCTGACTGAACTGAAAAAATATGCGGTTTTTTCTTATGTGCCCATCGCGCCAGACGACGAGCGTGTGCTGCTTGGTGTTGCCGGTTTTCAGGCGCGCGCCGCGCTGGCAAATCTCTTTa < 1:126407/143‑1 (MQ=255) gcAGCGTGCGTGAACCGCAGCGGACTGAACTGAAAAAATATGCGGTATTCTCTAAAGTGCCCATCGCGCCAGACGACGAGCGTGTGCTGCTTGGTGTTGCCGGTTTTCAGGCGCGCGCCGCGCTGGCAAATCTCTTTAGCGaa < 2:35976/143‑1 (MQ=255) cAGCGTGCGTGAACCGCAGCTGACTGAACTGAAAAAATATGCGGTATTCTCTACAGTGCCCATCGCGCCAGACGACGAGCGCGTGCTGCTTGGCGTTGCCGGTTTTCCGGCGCGCGCCGCGCGGGCCAACCTCCTTCGCGCAc > 2:237753/1‑143 (MQ=255) gcctcgcgtgAACCGCGGCCGACTGAACTGCAAAACTATGCGGTACTCTCTAAAGTGCCCATCGCGCTAGACGCCGCGCGAGTGCTCCTTGGTGTTGCCGGTTTTCAGGCGCGCCCCGCGCTGTCAAATCTCTTTAGCGAACt < 2:305658/138‑1 (MQ=255) aatgTGCCCACCGCGCCAGCAGACGAGCGTGTGCTGCCTGGTGCTGCCGGTTTTCCGGCGCGCGCCGCGCTGGCAAATCTCTTTAGCGATCTGCCTTCGAAAGAAAAACAGGTAGTCAAAGAAGGCGCGACCACTTTGCTATg < 1:14129/140‑1 (MQ=255) | CCATTGCGACGCCAAAGGTAAAATGTGGAGCAATTTACGTCTGTTCCGCGACGGCGATGGCTTTGCATGGATTGAACGGCGCAGCGTGCGTGAACCGCAGCTGACTGAACTGAAAAAATATGCGGTATTCTCTAAAGTGACCATCGCGCCAGACGACGAGCGTGTGCTGCTTGGTGTTGCCGGTTTTCAGGCGCGCGCCGCGCTGGCAAATCTCTTTAGCGAACTGCCTTCGAAAGAAAAACAGGTAGTCAAAGAAGGCGCGACCACTTTGCTATG > NC_000913/3041495‑3041770 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 8 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 22 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |