| Predicted mutation | ||||||
|---|---|---|---|---|---|---|
| evidence | seq id | position | mutation | annotation | gene | description |
| RA | NC_000913 | 2,250,928 | C→T | A30V (GCC→GTC) | nfo → | endonuclease IV |
| Read alignment evidence... | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
| * | NC_000913 | 2,250,928 | 0 | C | T | 100.0% | 27.7 / NA | 11 | A30V (GCC→GTC) | nfo | endonuclease IV |
| Reads supporting (aligned to +/- strand): ref base C (0/0); new base T (6/5); total (6/5) | |||||||||||
GCTGATGGCACTGGTACTGTTTGCCTGGCTGATTGTTGGTGGTGGTGCGATTAACTATGTGATTCAAAGCGTCATCGCATAAACCACTACATCTTGCTCCTGTTAACCCGCTATCATTACCGTTTTCCTCCAGCGGGTTTAACAGGAGTCCTCGCATGAAATACATTGGAGCGCACGTTAGTGCTGCTGGCGGTCTGGCAAATGCCGCAATTCGCGCCGCCGAAATCGACGCAACCGCGTTTGCCTTGTTCACCAAAAACCAACGTCAGTGGCGTGCCGCACCGCTCACGACGCAAACCATCGATGAATTCAAAGCCGCCTGTGAAAAATATCACTACACATCGGCGCAAATTCTTCCCCACGACAGTTATCTGATTAACCTCGGACATCCGGTCACTGAAGCTCTGGAAAAATCGCGCGATGCCTTTATAGATGAAATGCAGCGTTGCGAACA > NC_000913/2250685‑2251138 | nctgATGGCACTGGTACTGTTTGCCTGGCTGATTGTTGGTGGTGGTGCGATTAACTATGTGATTCAAAGCGTCATCGCATAAACCACTACATCTTGCTCCTGTTAACCCGCTATCATTACCGTTTTCCTCCAGCGGGTTTAACAGGAGTCCTCGCATGAAATACATTGGAGCGCACGATAGTGCTGCTGGCGGTCTGGCAAATGCCGCAATTCGCGCCGCCGAAATCGACGCAACCGCGTTTGTCTTGTTc > 1:127581/2‑251 (MQ=255) aaCCCGCTATCATTACCGTTTTCCTCCAGCGGGTTTAACAGGAGTCCTAGCATGAAATACATTGGAGCGCACGTTAGTGCTGCTGGCGGTCTGGCAAATGCCGCAATTCGCGCCGCCGAAATCGACGCCACCGCGTTTGTCTTGTTCACCAAAAACCAACGTCAGTGGCGTGCCGCACCGCTCACGACGCAAACCATCGATGAATTCAAAg > 1:183090/1‑211 (MQ=255) gggTTTAACAGGAGTCCTCGCATGAAATACATTGGAGCGCACGTTAGTGCTGCTGGCGGTCTGGCAAATGCCGCAATTCGCGCCGCCGAAATCGACGCAACCGCGTTTGTCTTGTTCACCAAAAACCAACGTCAGTGGCGTGCCGCACCGCTCACGACGCAAACCATCGATGAATTCAAAGCCGCCTGTGAAAAATATCACTACACATCGGCGCAAATTCTTCCCCACGACAGTTATCTGATTAACCTCgn < 1:135534/251‑2 (MQ=255) gTTTAACAGGAGTCCTCGCATGAAATACATTGGAGCGCACGTTAGTTCTGCTGTCGGTCTGGCAAATGCCGCAATTCGTGCCGCCGAAATCGACGCAACCGCGTTTGTCTTGTTCACCAAAAACCAACGTCAGTGGCGTGCCGCACCGCTCACGACGCAAACCATCGATGAATTCAAAGCCTCCTGTGAAAAATATCACTACACATCGGCGCAAATTCTTCCCCACGACAGTTATCTGATTAACCTCGGAc < 1:142721/251‑1 (MQ=255) ntCTGGCAAATGCCGCAATTCGCGCCGCCGAAATCGACGAAACCGCGTTTGTCTTGTTCACAAAAAACCAACGTCAGTGGAGTGCAGCACCGCTCACGACGCAAACCATCGATGAATTCAAAGACGCCTGTGAAAAATATCACTACACATCGGCGCAAATTCTTCCCCACGACAGTTATCTGATTAACCTCGGACATACGGTCACTGAAGCTCTGGAAAAATCGCGCGATGCCTTTATAGATGAAATGc > 1:20844/2‑249 (MQ=255) ncGCAATTCGCGCCGCCGAAATCGACGCAACCGCGTTTGTCTTGTTCACCAAAAACCAACGTCAGTGGCGTGCCGCACCGCTCACGACGCAAACCATCGATGAATTCAAAGCCGCCTGTGAAAAATATCACTACACATAGGCGCAAATTCTTCCCCACGACAGTTATCTGATTAACCTCGGACATCCGGTCACTGAAGCTCTGGAAAAATCGCGCGATGCCTTTATAGATGAAATGCAGCGTTGCGAACa > 1:38383/2‑250 (MQ=255) ccGCAATTCGCGCCGCCGAAATCGACGCAACCGCGTTTGTCTTGTTCACCAAAAACCAACGTCAGTGGCGTGCCGCACCGCTCACGACGCAAACCATCGATGAATTCAAAGCCGCCTGTGAAAAATATCACTACACATCGGCGCAAATTCTTCCCCACGACAGTTATc > 1:119735/1‑168 (MQ=255) nnnnnnnnnngcnnnnNAAANCGCCGCAACCGCGTTTGTCTTGTTCACCAAAAACCAACGTCAGTGGCGTGCCGCACCGCTCACGACGCAAACCATCGATGAATTCAAACCCGCCTGTGAAAAACATCACTCCACATCGGCGCAAATTCTTccc < 2:127581/144‑1 (MQ=255) gccgaatacGNCNCAACCGCGTTTTTCTTGTTCACCAAAAACCAACGTCAGTGGCGTGCCGNACCGCTCACGNCCCNNACCANCNANGAATTCAAAGCCGTCTGGGAAAAATATCANTACACATCGGCGCAAATCCTTCCNNACNNNATNNATCTg < 2:158894/148‑1 (MQ=255) gTTTGTCTTGTTCACCAAAAACCAACGTCAGTGGCGTGACGCACCGCTAACGACACAAACCATCGAAGAATTCAAAGCCGACTGAGAAAAATATCACTACACCTCGGCGCAACttc > 1:150642/1‑116 (MQ=255) gTTTGTCTTGTTCACCAAAAACCAACGNCAGNGGCGNGCNGCACCGCTCACGACGNAAACCATCGATGAATTCAAAGCCGCCTGTGAAAAATATCACTACNNANNNGNGCAAAttc < 2:150642/116‑1 (MQ=255) | GCTGATGGCACTGGTACTGTTTGCCTGGCTGATTGTTGGTGGTGGTGCGATTAACTATGTGATTCAAAGCGTCATCGCATAAACCACTACATCTTGCTCCTGTTAACCCGCTATCATTACCGTTTTCCTCCAGCGGGTTTAACAGGAGTCCTCGCATGAAATACATTGGAGCGCACGTTAGTGCTGCTGGCGGTCTGGCAAATGCCGCAATTCGCGCCGCCGAAATCGACGCAACCGCGTTTGCCTTGTTCACCAAAAACCAACGTCAGTGGCGTGCCGCACCGCTCACGACGCAAACCATCGATGAATTCAAAGCCGCCTGTGAAAAATATCACTACACATCGGCGCAAATTCTTCCCCACGACAGTTATCTGATTAACCTCGGACATCCGGTCACTGAAGCTCTGGAAAAATCGCGCGATGCCTTTATAGATGAAATGCAGCGTTGCGAACA > NC_000913/2250685‑2251138 |
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 30 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |