Predicted mutation | |||||||
---|---|---|---|---|---|---|---|
evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | CP009273 | 3,365,908 | G→A | 100% | P9L (CCG→CTG) | nanT ← | sialic acid transporter |
Read alignment evidence... | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | CP009273 | 3,365,908 | 0 | G | A | 100.0% | 28.8 / NA | 11 | P9L (CCG→CTG) | nanT | sialic acid transporter |
Reads supporting (aligned to +/- strand): ref base G (0/0); new base A (5/6); total (5/6) | |||||||||||
Rejected as polymorphism: Frequency below/above cutoff threshold. | |||||||||||
Rejected as polymorphism: Variant not supported by required number of reads on each strand. |
GAGAAGAGAACGATGCTGGTGACCATTGCCAGACGACGCCCGTAGCGGTCACCCATAGCGCCGAGCATCAGGCCGCCGAACCAGCGAGAGATAAAGGCTGCAGAGATCAGACTTGCCGCCTGCACCGTCGTCAGCCCGAATTCACCTTGTACTTCGGTGAGTACCAGGGCGATTAAAACGAAATCAAAACCGTCAAGCAGATATCCCAACCAGGCAGCGGAAAATGCGCGCCATTGTGCACGGTTGAGATGGCGATACCACGGGATATTCTGGGTTGTAGTACTCATTGTGAGTCTCCCGCGGTGGGCGATGCCCACACGCTTTGGTATGAAAATTGTAGGGTACAGATGCGTTTATTTCCCCTCACCCGGTAGGGGCGAGCGAGGGGAAACAACTCACCCGCGCTCTTGCATCAACTGCTGGGCCAGCGCCTTCAGTTCTGGCA > CP009273/3365647‑3366091 | gagaagagaaCGATGCTGGTGACCATTGCCAAAGGACGCCCGTAGCGGTCACCCATAGCGCCGAGCATCCGGCCGCCGAACCAGCGAGAGATAAAGGCTGCAGAGATCAGACTTGCCGCCTGCACCGTCGTCAGCCCGAATTCACCTTGTACTTCGGTGAGTACCAGTGCGATTAAAACGAAATCAAAACCGTCAAGCAGATATCCCAACCAGGCAGCGGAAAATGCGCGCCATTGTGCACGGTTGAGATGGCGATACCACAGGATATTCTggg < 1:70631/274‑1 (MQ=255) gagaagagaaAAAACATGGTGACACTTGCCACACGCGGCCCGTAGAGGTCACCCATAGCGCCGAGCATCAGGCCGCCGAACAAGCGAGAGATAAAGGCTGCAGAGATCAGACTTGCAGCCTGCACCGTCGTCAGCCCGAATTCACCTTGTACTTCGGTGAGTACCAGGGCGATTAAAACGAAATCAAAACCGTCAAGCAGATATCCCAACCAGGCAGCGGAAAATGCGCGCCATTGTGCACGGTTGAGATGGCGATACCACAGGATATTCTggg < 2:400902/274‑1 (MQ=255) cATTGCCAGACGACGCCCGTAGCGGTCACCCATAGCGCCGAGCATCAGGCCGCCGAACCAGCGAGAGATAAAGGCTGCAGAGATCAGACTTGCCGCCTGCACCGTCGTCAGCCCGAATTCACCTTGTACTTCGGTGAGTACCAGGGCGATTAAAACGAAATCAAAACCGTCAAGCAGATATCCCAACCAGGCAGCGGAAAATGCGCGCAATTGTGCACGGATGAGATGGCGATACCACAGGACATTCTGGGTTGAAGTACTAATGGTGAGTcccc > 1:123354/1‑275 (MQ=255) gccACCCCTGGCGCCGACCCACAGTCCGCCGAACCAGCGCCGGAGCAAGGCTGCAGAGATCAGCCTTGCCGCCTGCACCGTCGTCAGCCCGAATTCACCTGGTACTTCGGTAAGTACCAGGGCGCTTAAAACGAAATCCAAACCGTCAAGCAGATATCCCAACCAGGCCGCGGAAAATGCGCGCCATTGTGCACGGTTGAGATGGCGATACCACAGGCTATTCTGGGTTGTAGTACTCATTGTGAGTCTCCCGCGGTGGGCGATGCCCACACGCt < 2:210140/273‑1 (MQ=255) gTACTTCGGTGAGTACCAGGGCGATTAAAACGAAATCAAAACCGTCAAGCAGATATCCCAACCAGGCAGCGGAAAATGCGCGCCATTGTGCACGGTTGAGATGGCGATACCACAGGATATTCTGGGTTGTAGTACTCATTGTGAGTCTCCCGCGGTg > 1:157333/1‑157 (MQ=255) ttCGGTGAGTACCAGGGCGATTAAAACGAAATCAAAACCGTCAAGCAGATATCCCAACCAGGCAGCGGAAAATGCGCGCCATTGTGCACGGTTGAGATGGCGATACCACAGGATATTCTGGGTTGTAGTACTCATTGTGAGTCTCCCGCGGTGGGCg < 2:157332/157‑1 (MQ=255) aTTAAAACGAAATCAAAACCGTCAAGCAGATATCCCAACCAGGCAGCGGAAAATGCGCGCCATTGTGCACGGTTGAGATGGCGATACCACAGGATATTCTGGGTTGTAGTACTCATTGTGAGTCTCCCGCGGTGGGCGATGCCCACACGCTTTGGTATGAAAATTGTAGGGTACAGATGCGTTTATTTCCCCTCACCCGGTAGGGGCGAGCGAGGGGAAACAACTCACTCGCGCTCTTGCATCAACTGCTGGGCCCGCGCCTTCAGTTCTGGCa > 1:28466/1‑274 (MQ=255) cccAACCAGGCAGCGGAAAATGCGCGCCATTGTGCACGGTTGAGATGGCGATACCACagg < 1:238282/60‑1 (MQ=255) cGGAAAATGCGCGCCATTGTGCACGGTTGAGATGGCGATACCACagg < 2:138767/47‑1 (MQ=255) tgtgCACGGTTGAGATGGCGATACCACAGGATATTc > 1:48870/1‑36 (MQ=255) cACGGTTGAGATGGCGATACCACAGGATATTCTggg < 2:48870/36‑1 (MQ=255) gATACCACAGGATATTCTGGGTTGTAGTACTCATtgt > 2:148690/1‑37 (MQ=255) ccACAGGATATTCTGGGTTGTAGTACTCATTGTGAGt < 1:148691/37‑1 (MQ=255) | GAGAAGAGAACGATGCTGGTGACCATTGCCAGACGACGCCCGTAGCGGTCACCCATAGCGCCGAGCATCAGGCCGCCGAACCAGCGAGAGATAAAGGCTGCAGAGATCAGACTTGCCGCCTGCACCGTCGTCAGCCCGAATTCACCTTGTACTTCGGTGAGTACCAGGGCGATTAAAACGAAATCAAAACCGTCAAGCAGATATCCCAACCAGGCAGCGGAAAATGCGCGCCATTGTGCACGGTTGAGATGGCGATACCACGGGATATTCTGGGTTGTAGTACTCATTGTGAGTCTCCCGCGGTGGGCGATGCCCACACGCTTTGGTATGAAAATTGTAGGGTACAGATGCGTTTATTTCCCCTCACCCGGTAGGGGCGAGCGAGGGGAAACAACTCACCCGCGCTCTTGCATCAACTGCTGGGCCAGCGCCTTCAGTTCTGGCA > CP009273/3365647‑3366091 |
Alignment Legend |
---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 9 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |