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Detailed information for vg1004766552:

Variant ID: vg1004766552 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 4766552
Reference Allele: AAlternative Allele: G
Primary Allele: ASecondary Allele: G

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.99, A: 0.01, others allele: 0.00, population size: 93. )

Flanking Sequence (100 bp) in Reference Genome:


CTGCATTTATGTAAGACTTTTATGATGTTTGTAAGACGTGGATCTGGATGTCAACATTGTCGTTTGTGTACCCCGGCCGGTCCTGGACGGGGATTTTAAT[A/G]
CACATTCTGCTTGAAATTCTATTCGGGAATTTCTGGGCGTGACAAGTTGGTATCAGAGCCGACCTTGACCGTAGGACAAGCCAAACGGAAAAAAAAACCT

Reverse complement sequence

AGGTTTTTTTTTCCGTTTGGCTTGTCCTACGGTCAAGGTCGGCTCTGATACCAACTTGTCACGCCCAGAAATTCCCGAATAGAATTTCAAGCAGAATGTG[T/C]
ATTAAAATCCCCGTCCAGGACCGGCCGGGGTACACAAACGACAATGTTGACATCCAGATCCACGTCTTACAAACATCATAAAAGTCTTACATAAATGCAG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: