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Detailed information for vg1001229450:

Variant ID: vg1001229450 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 1229450
Reference Allele: AAlternative Allele: T
Primary Allele: ASecondary Allele: T

Inferred Ancestral Allele : A (evidence from allele frequency in Oryza rufipogon: A: 0.99, T: 0.01, others allele: 0.00, population size: 127. )

Flanking Sequence (100 bp) in Reference Genome:


TTACATAACGTTTGACCATTCGTTTTATTCATAAATATATAAAGTATAAGCATGTGAAATTACAAGTTAAGATTATAGTTTTTTTATTACAGTATAAAAT[A/T]
AGTTATAATATATATTTTGAATAAGATGAATGATCAACGTCAAAGTCAGCGAAGTCATTACTTTTGAAAACGGAGGTAGTACTACTAGCTTATACAAACA

Reverse complement sequence

TGTTTGTATAAGCTAGTAGTACTACCTCCGTTTTCAAAAGTAATGACTTCGCTGACTTTGACGTTGATCATTCATCTTATTCAAAATATATATTATAACT[T/A]
ATTTTATACTGTAATAAAAAAACTATAATCTTAACTTGTAATTTCACATGCTTATACTTTATATATTTATGAATAAAACGAATGGTCAAACGTTATGTAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: