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Detailed information for vg0205559811:

Variant ID: vg0205559811 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 5559811
Reference Allele: AAlternative Allele: T
Primary Allele: TSecondary Allele: A

Inferred Ancestral Allele : A (evidence from allele frequency in Oryza rufipogon: A: 0.89, T: 0.11, others allele: 0.00, population size: 104. )

Flanking Sequence (100 bp) in Reference Genome:


AGATCCCGGGTGAAATAACCGGGAGTAAAAATCCATTTTTAGTCACGGTTGGTGTCATCAACCGGGACTAAAAATAGAACATTTTTAGTCCCGGTTGGTA[A/T]
CAAGATAGAGCTAGGCTAGCTAGATCCGGTTGCTCTATTATTCTATTCTTTTCTTCATTGTTTTTAATATATTGATTTCACTCCATCCCCATCCCAAAAT

Reverse complement sequence

ATTTTGGGATGGGGATGGAGTGAAATCAATATATTAAAAACAATGAAGAAAAGAATAGAATAATAGAGCAACCGGATCTAGCTAGCCTAGCTCTATCTTG[T/A]
TACCAACCGGGACTAAAAATGTTCTATTTTTAGTCCCGGTTGATGACACCAACCGTGACTAAAAATGGATTTTTACTCCCGGTTATTTCACCCGGGATCT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: