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Detailed information for vg0118996593:

Variant ID: vg0118996593 (JBrowse)Variation Type: SNP
Chromosome: chr01Position: 18996593
Reference Allele: AAlternative Allele: T
Primary Allele: TSecondary Allele: A

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 0.99, A: 0.01, others allele: 0.00, population size: 115. )

Flanking Sequence (100 bp) in Reference Genome:


CATGCCGGAGCACGAAGCGTCCACCGCTGCGTCGTACACCTCCTACGAGAGGCGGAGCCTTGCACCGCCGCCGCAAGAACACTCCATTCTCGAGTGGGAG[A/T]
TCTCGTTGCCGCTCCCAGGCGTGGCAGCAACCGCCGTCGAGAGAGAATATAGAGAGAGATGAGAAGAGAGATACGAGATAGAGCTGACATGTGGGCACAA

Reverse complement sequence

TTGTGCCCACATGTCAGCTCTATCTCGTATCTCTCTTCTCATCTCTCTCTATATTCTCTCTCGACGGCGGTTGCTGCCACGCCTGGGAGCGGCAACGAGA[T/A]
CTCCCACTCGAGAATGGAGTGTTCTTGCGGCGGCGGTGCAAGGCTCCGCCTCTCGTAGGAGGTGTACGACGCAGCGGTGGACGCTTCGTGCTCCGGCATG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: