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Detailed information for vg0217093461:

Variant ID: vg0217093461 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 17093461
Reference Allele: GAlternative Allele: A
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.84, A: 0.16, others allele: 0.00, population size: 86. )

Flanking Sequence (100 bp) in Reference Genome:


TGGACTCTAGTCTGCTCTTCTAATATTCTTTATTTTTTAATTCCGAATTTCAGCTATTTATAAATCTTTTTCTTTTCTCCAATTAATGTGAGAATTTTAG[G/A]
TCATGAGAGCGAACGTGGAGGCTCCTTTTTATTCCGAATTTTAGTTAGTTTTAAATTCTTATATGGACCCTATACTCTACTTCTAATATTCCTTATTTTT

Reverse complement sequence

AAAAATAAGGAATATTAGAAGTAGAGTATAGGGTCCATATAAGAATTTAAAACTAACTAAAATTCGGAATAAAAAGGAGCCTCCACGTTCGCTCTCATGA[C/T]
CTAAAATTCTCACATTAATTGGAGAAAAGAAAAAGATTTATAAATAGCTGAAATTCGGAATTAAAAAATAAAGAATATTAGAAGAGCAGACTAGAGTCCA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: