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Detailed information for vg0112321732:

Variant ID: vg0112321732 (JBrowse)Variation Type: SNP
Chromosome: chr01Position: 12321732
Reference Allele: AAlternative Allele: G
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.96, A: 0.04, others allele: 0.00, population size: 100. )

Flanking Sequence (100 bp) in Reference Genome:


TTCATATTGTATTTTATATACATGTTAGTTATTAATTATTTTTAATATCAAATTTTAGTTATTTGTAAATTATATATATTCCTATATGGACTATAGACTC[A/G]
TCTTTTAATATTTCTTTTTTTTAATTCTGAATTTTTATTATTTCTAATTGTATTTCTATGTGGACTCTAAACTCATCTTTCAATATTCTTTAATTTTTAA

Reverse complement sequence

TTAAAAATTAAAGAATATTGAAAGATGAGTTTAGAGTCCACATAGAAATACAATTAGAAATAATAAAAATTCAGAATTAAAAAAAAGAAATATTAAAAGA[T/C]
GAGTCTATAGTCCATATAGGAATATATATAATTTACAAATAACTAAAATTTGATATTAAAAATAATTAATAACTAACATGTATATAAAATACAATATGAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: