| Predicted mutation | ||||||
|---|---|---|---|---|---|---|
| evidence | seq id | position | mutation | annotation | gene | description |
| RA | NC_000913 | 1,730,552 | C→T | A489V (GCC→GTC) | lhr → | ATP‑dependent helicase Lhr |
| Read alignment evidence... | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
| * | NC_000913 | 1,730,552 | 0 | C | T | 90.9% | 18.0 / NA | 11 | A489V (GCC→GTC) | lhr | ATP‑dependent helicase Lhr |
| Reads supporting (aligned to +/- strand): ref base C (0/0); major base T (3/7); minor base G (0/1); total (3/8) | |||||||||||
| Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
| Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.82e-01 | |||||||||||
GGGTTACAACGCATTGGTCGCGCCGGACATCAGGTTGGCGGTGTATCTAAAGGGCTGTTTTTCCCCCGTACCCGGCGTGATTTAGTCGATTCCGCAGTCATTGTAGAGTGTATGTTCGCAGGCAGGCTGGAAAACCTGACACCACCGCATAATCCTCTCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGGATGCATTACAGGTAGACGAATGGTACTCCCGCGTACGCCGTGCCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGCTTTCCGGGCGCTATCCCTCTGGCGATTTTTCTGCTTTTCGCCCCAAACTGGTCTGGAACAGGGAGACCGGGATATTGACCGCCCGACCTGGCGCTCAATTGTTGGCGGTTACCAGCGGCGGCACCATTCCGGATC > NC_000913/1730311‑1730740 | gggTTACAACGCATTGGTCGCGCCGGACATCAGGTTGGCGGTGTATCTAAAGGGCTGTTTTTCCCCCGTACCCGGCGTGATTTAGTCGATTCCGCAGTCATTGTAGAGTGTATGTTCGCAGGCAGGCTGGAAAACCTGACACCACCGCATAATCCTCTCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGGAGGCATTACAGGTAGACGAATGGTACTCCCGCGTACGCCGTGTCGCACCGTg < 1:104578/251‑1 (MQ=255) ccGGACATCAGGTTGGCGGTGTATCTAAAGGGCTGTTTTTCCCCCGTACCCGGCGTGATTTAGTCGATTCCGCAGTCATTGTAGAGTGTATGTTCGCAGGCAGGCTGGAAAACCTGACACCACCGCATAATCCTCTCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGGATGCATTACAGGAAGACGAATGGTACTCCCGCGTACGCCGTGTCGCACCGTGGAAAGATc > 1:60941/1‑237 (MQ=255) aaaGGGCTGTTTTTCCCCCGTACCCGGCGTGATTTAGTCGATTCCGCAGTCATTGTAGAGTGTATGTTCGCAGGCAGGCTGGAAAACCTGACACCACCACATAATCCTCTCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGTATGCATTACAGGGAGACGGATGGTACTCCCGCGTACGCCGTGGCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGc < 1:221781/247‑1 (MQ=255) ggCTGTTTTTCCCCCGTACCCGGCGTGATTTAGTCGATTCCCCCGTCATTGTAGAGTGTATGTTCCCAGGCACGCTGGAAAAACTGACAACACCGCCTAATCCTCTCGAAGTCCTTGCGCGGCCAACCGTTGCCGCCGCGGAGATGGATGCATTACAGGTAGACGGATGGGACTCCCGCGTAAGCCGTGTCGCCCCGTGGAAAGATCTGCCACGCCGTGTTTTTGACGCCCCGCTGGATATGTTTTCCggg > 1:98415/1‑251 (MQ=255) tttCCCCCGTACCCGGCGTGATTTAGTCGATTCCGCAGTCATTGTAGAGTGTATGTTCGCAGGCAGGCTGGAAAACCTGACACCACCGCATAATCCTCTCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGGATGCATTACAGGTAGACGAATGGTACTCCCGCGTACGCCGTGTCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGc < 1:108677/236‑1 (MQ=255) gTCGATTCCGCAGTCATTGTAGAGTGTATGTTCGCAGGCAGGCTGGAAAACCTGACACCACCGCATAATCCTCTCTACGTCCTGGCGCAGCAAACCGGTGCCGCCGCGGCGAGGGGTGCAGGACAGGTAGACTAATGGTACTCCCGCGTACGCCGTGTCGCACCGTGGaa < 1:202812/170‑1 (MQ=255) aggcTGGAAAACCTGACACCACCGCATAATCCTCTCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGGATGCATTACAGGTAGACGAATGGTACTCCCGCGTACGCCGTGTCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGCTTTCCGGGCGCTATCCCTCTGGCGATTTTTCTGCTTTTCGCCCCAAACTGGTCTGGAACAGGGAGACCGGGATATTGAc < 1:62394/251‑1 (MQ=255) ggAAAACCTGACACCACCGCATAATCCTCTCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGGATGCATTACAGGTAGACGAATGGTACTCCCGCGTACGCCGTGTCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGCTTTCCGGGCGCTATCCCTCTGGCGATTTTTCTGCTTTTCGCCCCAAACTGGTCTGGAACAGGGAGACCGGGATATTGACCGccc > 1:115433/1‑251 (MQ=255) ggAAAACCTGACACCACCGCATAAGCCTCGCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGGAAGCATTACAGGTAGACGAATGGTACTCCCGCGTACGGCGTGTCGCACCGGGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGCTTTCCGGGCGCTATCCCTCTGGCGATTTTTCTGCTTTTCGCCCCAAACTGGTCTGGAACAGGGAGACCGGGATATTGACCga < 1:118731/249‑2 (MQ=255) gACACCACCGCATAATCCT‑TCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGGATGCATTACAGGTAGACGAATGGTACTCCCGCGTACGCCGTGTCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGCTTGCCGGGCGCTATCCCACTGGCGATTTTTCGGCTTTTCGCCCCAAACTGGTCTTGAACAGGGAGACCGGGATATTGACCGCCCGACCTGgcn < 1:40651/250‑2 (MQ=255) cGTTGCCGCCGCGGCGATGGATGCATTACAGGTAGACGAATGGTACTCCCGCGTACGCCGTGTCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGCTTTCCGGGCGCTATCCCTCTGGCGATTTTTCTGCTTTTCGCCCCAAACTGGTCTGGAACAGGGAGACCGGGATATTGACCGCCCGACCTGGCGCTCAATTGTTGGCGGTTACCAGCGGCGGCACCATTCCGGAtn < 1:135010/251‑2 (MQ=255) | GGGTTACAACGCATTGGTCGCGCCGGACATCAGGTTGGCGGTGTATCTAAAGGGCTGTTTTTCCCCCGTACCCGGCGTGATTTAGTCGATTCCGCAGTCATTGTAGAGTGTATGTTCGCAGGCAGGCTGGAAAACCTGACACCACCGCATAATCCTCTCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGGATGCATTACAGGTAGACGAATGGTACTCCCGCGTACGCCGTGCCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGCTTTCCGGGCGCTATCCCTCTGGCGATTTTTCTGCTTTTCGCCCCAAACTGGTCTGGAACAGGGAGACCGGGATATTGACCGCCCGACCTGGCGCTCAATTGTTGGCGGTTACCAGCGGCGGCACCATTCCGGATC > NC_000913/1730311‑1730740 |
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |