Predicted mutation | ||||||
---|---|---|---|---|---|---|
evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 431,286 | G→A | A243V (GCT→GTT) | tsx ← | nucleoside‑specific channel‑forming protein Tsx |
Read alignment evidence... | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 431,286 | 0 | G | A | 100.0% | 49.9 / NA | 20 | A243V (GCT→GTT) | tsx | nucleoside‑specific channel‑forming protein Tsx |
Reads supporting (aligned to +/- strand): ref base G (0/0); new base A (12/8); total (12/8) |
GTTTACGCCGCATCCGGCATGAACAAAGCACACGTTGTTAACAATCAGAAATGCCGGGAATAAATCCCGGCATTTTCATAATCAGAAGTTGTAACCTACTACCAGGTAACCACCCCAGCCGGTAGAGCGAACGTTGAAGTTGCCGTTGCCGAAGTTCAGTTCTGCATCGTCGTTCCACTGACCACCGTCGTGCCAGTAACGAGCTACGACAGAGTAGTGCCAGTGATCGTAGTTCAGAGCCAGAATATGGCTGGAAGCGATAGAGTTATTAGTACGGGTCTTAATACCGTTGATTGCGTTACCGCTGTCATCCCCTAAATCGGAACCCCAGTCGAAGTTGGTGAAGCCGATGTAGCTCAGCTGACCGCCCCACAGATCGGTAATCGGCACAAAGTATTTAATTTTGAAACGGTAACCGTCCCACTCGTTTTCGTTCGCTGCGCCATAGTTCTGCCACTGGTATTTCGCATAGACG > NC_000913/431048‑431522 | gTTTACGCCGCATCCGGCATGAACAAAGCACACGTTGTTAACAATCAGAAATGCCGGGAATAAATCCCGGCATTTTCATAATCAGAAGTTGTAACCTACTACCAGGTAACCACCCCAGCCGGTAGAGCGAACGTTGAAGTTGCCGTTGCCGAAGTTCAGTTCTGCATCGTCGTTCCACTGACCACCGTCGTGCCAGTAACGAGCTACGACAGAGTAGTGCCAGTGATCGTAGTTCAGAACCAGAATATggn < 1:102405/251‑2 (MQ=255) aaGCACACGTTGTTAACAATCAGAAATGCCGGGAATAAATCCCGGCATTTTCCTAATCAGAAGTTGTAACCTACTACCAGGTAACCACCCCAGCCGGTAGAGCGAACGTTGAAGTTGCCGTTGCCGAAGTTCAGTTCTGCATCGTCGTTACACTGACCACCGTCGTGCCAGTAACGAGCTACGACAGAGTAGTGCCAGTGATCGTAGTTAAGAACCAGAATATGGCTGGAAGCGATAGAGTTATTAGTACg > 1:235027/1‑251 (MQ=255) aGCACACGTTGGTAACAATCAGAAATGCCGGGAATAACTCCCGGCATTTTCATAATCAGAAGTTATAACCTACTACCAGGTAACCACCCCAGCCGGTAGAGCGAACGTTGAAGTTGCCGTTGCCGAAGTTCAGTTCTGCATCGTCGTTCCACTGACCACCGTCGTGCCAGTAACGAGCTACGACAGAGTAGTGCCAGTGATCGTAGTTCAGAACCAGAATATGGCTGACAGCGATAGCGTTATTAGTACgg > 1:259775/1‑251 (MQ=255) cAGAAATGCCGGGAATAAATCCCGGCATTTTCATAATCAGAAGTTGTAACCTACTACCAGGTAACCACCCCAGCCGGTAGAGCGAACGTTGAAGTTGCCGTTGCCGAAGTGCAGTTCTGCATCGTCGTTCCACTGACCACCGGCGTGCCAGTAACGAGGTACGACAGAGTAGTGCCAGTGATCGTAGGTCAGAACCAGAGTAGGGCTGGAAGCGATAGAGTTATTAGTACGGGTCTTAATACCGTTGATTg < 1:279650/251‑1 (MQ=255) aGAAATGCCGGGAATAAATCCCGGCATTTTCATAATCAGAAGTTGTAACCTACTACCAGGTAACCACCCCAGCCGGTAGAGCGAACGTTGAAGTTGCCGTTGCCGAAGTTCAGTTCTGCATCGTCGTTCCACTGACCACCGTCGTGCCAGTAACGAGCTACGACAGAGTAGTGCCAGTGATCGTAGTTCAGAACCAGAATATGGCTGGAAGCGATAGAGTTATTAGTACGGGTCTTAATACCGTTGATTgn < 1:406296/251‑2 (MQ=255) aTCCCGGCATTTTCATAATCAGAAGTTGTAACCTACTACCAGGTAACCACCCCAGCCGGTAGAGCGAACGTTGAAGTTGCCGTTGCCGAAGTTCAGTTCTGCATCGTCGTTCCACTGACCACCGTCGTGCCAGTAACGAGCTACGACAGAGTAGTGCCAGTGATCGTAGTTCAGAACCAGAATATGGCGGGAAGCGTTAGAGGTATTAGTACGGGTCTTAATACCGTTGATTGCGTTACCGCTGTCATccc < 1:466134/251‑1 (MQ=255) aaTCAGAAGTTGTAACCTACTACCAGGTAACCACCCCAGCCGGTAGAGCGAACGTTGAAGTTGCCGTTGCCGAAGTTCAGTTCTGCATCGTCGTTCCACTGACCACCGTCGTGCCAGTAACGAGCTACGACAGAGTAGTGCCAGTGATCGTAGTTCAGAACTAGAATATGGCTGGAAGCGATAGAGTTATTAGTACgg < 1:184932/198‑1 (MQ=255) ccccAGCCGGTAGAGCGAACGTTGAAGTTGCCGTTGCCGAAGTTCAGTTCTGCATCGTCGTTCCACTGACCACCGTCGTGCCAGTAACGAGCTACGACAGAGTAGTGCCAGTGATCGTAGTTCAGAACCAGAATATGGCTGGAAGCGATAGAGTTATTAGTACGGGTCTTAATACCGTTGATTGCGTTACCGCTGTCATCCCCTAAATCGGAACCCCAGTCGAAGTTGGTGAAGCCGATGTAGCTCAGCTg > 1:162695/1‑251 (MQ=255) gCGAACGTTGAAGTTGCCGTTGCCGAAGTTCAGTTCTGCATCGTCGTTCCACAGACCACCGTCGGGCCAGTAACGAGCTACGGCGAAGGAGTGTCAGTGATCGTAGTTGAGAACCAGAATATGGCTGGAAGCGATAGAGTGATTAGTACg < 1:277271/150‑1 (MQ=255) cgttgccgAAGTTCAGTTCTGNATCGTCGTTCCACTGACCACCGTCGTGCCATNANCGAGCTACGACAGAGTAGTGCCAGTGATCGTAGTTCAGAACCAGAATANGGCTGGAAGCNATANNGTTANTNGNACGGGACTTAATACCGTTGATTGCGTTACNGCTGTCATCCCCTAAATCGGAACNNCANNNGTNNTTggc < 2:365822/199‑2 (MQ=255) cgttgccgAAGTTCAGTTCTGCATCGTCGTTCCACTGCAAACCGTCGTGCAAGTAACGAGCTACGACAGAGTAGTGCCCGTGCTCGTAGTTCAGAACCAGAATATGGCTGGAAGCGATAGAGTTATTAGAAAGGGTCTTAATACCGTTGATTGCGTTACCGTTGTCATCCCCTAAATCGGAACCCCAGCCGAAGTTggc > 1:365822/1‑198 (MQ=255) agttcTGCATCGTCGTTCCACTGACCACCGTCGTGCCAGTAACGAGCTACGACAGAGTAGTGCCAGTGATCGTAGTTCAGAACCAGAATCTGGCTGGAAGCGATAGAGTTATTAGTACGGGTCTTAATAACGTTGATTGCGTTACCGCTGTCATCCCCTAAATCGGAACCCCAGTCGAAGTTGGTGAAGCCGATGTAGCTCAGCTGACCGCCCCACAGATCGGTAATCGGCACAAAGTATTTACTTTTGa > 1:201614/1‑250 (MQ=255) gtcgtTCCACTGACCACCGTCGTGCCAGTAACGAGCTCCGACAGAGTAGTGCCCGGGATCGTGGTTCAGAACCCGACTATGGCTGGAAGCGATAGAGTTATTCGTACGGGGCTTAATACCGTTGATTGCGTTACCGCTGTCATCCCCt > 1:224581/1‑148 (MQ=255) tcgtTCCACTGACCACCGTCGTGCCAGTAACGAGCTACGACAGAGTAGTGCCAGTGATCGTAGTTCAGAACCAGAATATGGCTGGAAGCGATAGAGTTATTAGTACGGGTCTTAATACCGTTGATTGCGTTACCGCTGTCATCCCCTAAATCGGAACCCCAGTCGAAGTTGGTGAAGCCGATGTAGCTCAGCTGACCGCCCCACAGATCGGTAATCGGCACAAAGTATTTAATTTTGAAACGGTAACCGTc > 1:436593/1‑251 (MQ=255) aCAGAGTAGTGACAGTGATCGTAGTTCAGAACCAGAATATGGCTGGAAGCGATAGAGTTATTAGTACGGGTCTTAATACCGTTGATTGCGTTACCGCTGTCATCCCCTAAATCGGAACCCCAGTCGAAGTTGGTGAAGCCGATGTAGCTCAGCTGAc > 1:164646/1‑157 (MQ=255) gCCAGTGATCGTAGTTCAGAACCAGAATATGGCTGGAAGCGATAGAGTTATTAGTACGGGTCTTAATACCGTTg > 1:189251/1‑74 (MQ=255) gTGATCGTAGTTCAGAACCAGAATATGGCTGGAAGCGATAGAGTTATTAGTACGGGTCTTAATACCGTTGATTGCGTTACCGCTGTCATCCCCTAAATCGGAACCCCAGTCGAAGTTGGTGAAGCCGATGTAGCTCAGCTGACCGCCCCACAGATCGGTAATCGGCACAAAGTATTTAATTTTGAAACGGTAACCGTCCCACTCGTTttcgttcg > 1:119647/1‑215 (MQ=255) naTCGTAGTTCAGAACCAGAATATGGCTGGAAGCGATAGAGGTATTAGTACGGGTCTTAATACCGTTGATTGCGTTACCGCTGTCATCCCCTAAATCGGAACCCCAGTCGAAGTTGGTGAAGCCGATGTAGCTCAGCTGACCGCCCCACAGATCGGTAATCGGCACAAAGTATTTAATTTTGAAACGGTAACCGTCCCACTCGTTTTCGTTCGCTGCGCCATAGTTCTGCCACTGGTATTTCGCATCGACg > 1:406305/2‑251 (MQ=255) aTCGTAGTTCAGAACCAGAATATGGCTGGAAGCGATAGAGTTATTAGTACGGGTCTTAATACCGTTGATTGCGTTACCGCTGTCATCCNNTAAATCNNa > 2:27808/1‑99 (MQ=255) tngtngTTCANAACCNGAATATGGCTGGAAGNGATAGAGTGATTAGTACGGNNCNTAATGNCGTTg < 2:189251/66‑1 (MQ=255) | GTTTACGCCGCATCCGGCATGAACAAAGCACACGTTGTTAACAATCAGAAATGCCGGGAATAAATCCCGGCATTTTCATAATCAGAAGTTGTAACCTACTACCAGGTAACCACCCCAGCCGGTAGAGCGAACGTTGAAGTTGCCGTTGCCGAAGTTCAGTTCTGCATCGTCGTTCCACTGACCACCGTCGTGCCAGTAACGAGCTACGACAGAGTAGTGCCAGTGATCGTAGTTCAGAGCCAGAATATGGCTGGAAGCGATAGAGTTATTAGTACGGGTCTTAATACCGTTGATTGCGTTACCGCTGTCATCCCCTAAATCGGAACCCCAGTCGAAGTTGGTGAAGCCGATGTAGCTCAGCTGACCGCCCCACAGATCGGTAATCGGCACAAAGTATTTAATTTTGAAACGGTAACCGTCCCACTCGTTTTCGTTCGCTGCGCCATAGTTCTGCCACTGGTATTTCGCATAGACG > NC_000913/431048‑431522 |
Alignment Legend |
---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 16 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |