| Predicted mutation | ||||||
|---|---|---|---|---|---|---|
| evidence | seq id | position | mutation | annotation | gene | description |
| RA | NC_000913 | 3,106,841 | C→T | G376G (GGC→GGT) | nupG → | nucleoside:H(+) symporter NupG |
| Read alignment evidence... | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
| * | NC_000913 | 3,106,841 | 0 | C | T | 100.0% | 20.8 / NA | 10 | G376G (GGC→GGT) | nupG | nucleoside:H(+) symporter NupG |
| Reads supporting (aligned to +/- strand): ref base C (0/0); new base T (4/6); total (4/6) | |||||||||||
CGATGATCGTTTACGGTTGCGCATTCGACTTCTTCAACATCTCTGGTTCGGTGTTTGTCGAAAAAGAAGTTAGCCCGGCAATTCGCGCCAGTGCACAAGGGATGTTCCTGATGATGACTAACGGCTTCGGCTGTATCCTCGGCGGCATCGTGAGCGGTAAAGTTGTTGAGATGTACACCCAAAACGGCATTACCGACTGGCAGACCGTATGGTTGATTTTCGCTGGTTACTCCGTGGTTCTGGCCTTCGCGTTCATGGCGATGTTCAAATATAAACACGTTCGTGTCCCGACAGGCACACAGACGGTTAGCCACTAATTACGCAAAGAAAAACGGGTCGCCAGAAGGTGACCCGTTTTTTTTATTCTTACTTCAACACATAACCGTACAACCGTTTCACGCCATCCGCATCGGTTTCGCTATAAAC > NC_000913/3106654‑3107079 | cGATGATCGTTTACGGTTGCGCATTCGACTTCTTCAACATCTCTGGTTCGGTGTTTGTCGAAAAAGAAGTTAGCCCGGCAATTCGCGCCAGTGCACAAGGGATGTTCCGGATGATGACTAACGGCTTCGGCTGGATCCCCGGCGGCATCGTGAGCGGTAAAGTTGGTGAGATGGACACCCAAAACGGTATTACCGACTGGCAGACCGTATGGTTGATTTTCGCTGGTTACTCCGTGGTTCTGGCCTTcgc < 1:64574/250‑1 (MQ=255) gatgatCGTTTACGGTTGCGCATTCGACTTCTTCAACATCTCTGGTTCGGTGTTAGTCGAAAAAGAAGTCAGCACGGCAATTAGCGCCAGTGCAAAAGGGATGTTCCTGATGATGACTAACGGCTTCGGCTGTATCCTCGGCGGCATCGTGAGCGGTAAAGTTGTTGAGATGTACACCCAAAACGGTATTACCGACTGGCAGACCGTATGGTTGATTTTCGCTGGTTACTCCGTGGTTCTGGCCTTCGCGt > 1:103053/1‑251 (MQ=255) cGTTTACGGTTGCGCATTCGACGTCTTCAACAGCGCTGGTTCGGTGTTTGTCGAAAAAGAAGTTAGCCCGGCAAGTCGCGCCAGTGCACAAGGTATGTTCCTGATGATGACTAACGGCTTCGGCTTGATCCTCGGCCGCCTCGTGAGCGGTAAAGTTGCTGAGATTTACACCCAAAACGGTATTACCGACTGGTAGATCGGATGGTTGATTTTCGCTGGTTACTCCGTGGTTCTGGCCTTCGCGTTCATgg < 1:204714/251‑1 (MQ=255) gTCGAAAAAGACGTTAGCCCGGCAATTCGCGCCAGTGCACAAGGGATGTTCCTGATGATGACTAACGGCTTCGGCTGTATCCTCGGCGGCATCGTGAGCGGTAAAGTTGTTGAGATGTACACCCAAAACGGTATTACCGACTGGCAGACCGTATGGTTGATTTTCGCTGGTTACTCCGTGGTTCTGGCCTTCGCGTTCATGGCGATGTTCAAATATAAACACGTTCGTGTCCCGACAGGCACACAGACGGt > 1:74935/1‑251 (MQ=255) gATGTTCCTGATGATTACTAACGGCTTCGGCTGTATCCGCGGCGGCAGCGTGAGCGGTAAAGTTGTTGAGATGTACACCCAAAACGGTATTACCGACTGGCAGACCTTATGGTTGATTTTCGCTGGTTACTCCGTGGTTCTGGCCTTCGGGTTCATGGCGATGGTCAAATATAAACACGGTCGTGTCCCGACAGGCACTCAGACGGTTATCCACTAATTACGCTAAGAAAAACTGGTCGCCAGAAGGTGAc < 1:140637/251‑1 (MQ=255) cGGTAAAGTTGTTGAGATGTACACCCAAAACGGTATTACCGACTGGCAGACCGTATGGTTGATTTTCGCTGGTTACTCCGTGGt < 1:95597/84‑1 (MQ=255) gagaTGTACACCCAAAACGGTATTACCGACTGGCAGACCGTATGGTTGATTTTCGCTGGTTACTCCGTGGTTCTGGCCTTCGCGTTCATGGCGATGTTCAAATATAAACACGTTCGTGTCCCGACAGGCACACAGACGGTTAGCCACTAATTACGCAAAGAAAAACGGGTCGCCAGAAGGTGACCCGTTTTTTTTATTCTTACTTCAACACATAACCGTACAACCGTTTCACGCCATCCGCATCGGTTTc < 1:74023/250‑1 (MQ=255) ncacCCAAAACGGTATTACCGACTGGCAGACCGTATGGTTGATTTTCGCTGGTTACTCCGTGGTTCTGGCCTTCGCGTTCATGGCGATGTTCAAATATAAACACGTTCGTGTCCCGACAGGCACACAGACGGTTAGCCACTAATTACGCAAAGAAAAACGGGTCGCCAGAAGGTGACCCGTTTTTTTTATTCTTACTTCAACACATAACCGTACAACCGTTTCACGCCATCCGCATCGGTTTCGCTATaa > 1:135030/2‑250 (MQ=255) cacCCAAAACGGTATTACCGACTGGCAGACCGTATGGTTGATTTTCGCTGGTTACTCCGTGGTTCTGGCCTTCGCGTTCATGGCGATGTTCAAATATAAACACGTTCGTGTCCCGACAGGCACACGGACGGTTAGCCACTAATTACGCAAAGAAAAACGGGTCGCCAGAAGGTGACCCGTTTTTTTTATTCTTACTTCAACACATAACCGTACAACCGTTTCACGCCATCCGCATCGGTTTCGCTATAAac < 1:14986/251‑1 (MQ=255) cAAAACGGTATTACCGACTGGCAGACCGTATGGTTGATTTTCGCTGGTTACTCCGTGGTTCTGGCCTTCGCGTTCATGGCGATGTTCAAATATAAACACGTTCGTGTCCCGACAGGCACACAGACGGTTAGCCACTAATTACGCAAAGAAAAACGGGTCGCCAGAAGGTGACCCGTTTTTTTTATTCTTACTTCAACACATAACCGTACAACCGTTTCACGCCATCCGCATCGGttt > 1:175886/1‑237 (MQ=255) | CGATGATCGTTTACGGTTGCGCATTCGACTTCTTCAACATCTCTGGTTCGGTGTTTGTCGAAAAAGAAGTTAGCCCGGCAATTCGCGCCAGTGCACAAGGGATGTTCCTGATGATGACTAACGGCTTCGGCTGTATCCTCGGCGGCATCGTGAGCGGTAAAGTTGTTGAGATGTACACCCAAAACGGCATTACCGACTGGCAGACCGTATGGTTGATTTTCGCTGGTTACTCCGTGGTTCTGGCCTTCGCGTTCATGGCGATGTTCAAATATAAACACGTTCGTGTCCCGACAGGCACACAGACGGTTAGCCACTAATTACGCAAAGAAAAACGGGTCGCCAGAAGGTGACCCGTTTTTTTTATTCTTACTTCAACACATAACCGTACAACCGTTTCACGCCATCCGCATCGGTTTCGCTATAAAC > NC_000913/3106654‑3107079 |
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 13 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |