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Detailed information for vg1124469615:

Variant ID: vg1124469615 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 24469615
Reference Allele: GAlternative Allele: A
Primary Allele: ASecondary Allele: G

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.97, A: 0.03, others allele: 0.00, population size: 63. )

Flanking Sequence (100 bp) in Reference Genome:


CCTCCCCCTCCGCGGTAGCACGGGCCAGCTCCCGCCGCCGGTTGCCGCCTTGCCTCGTCGCGCCGCCGCCTAGGGTTTGCAAATAGGGAGCGGCGCGAGG[G/A]
AGCCGAGCTATGGAGGGATGGGTCACGGAGGGAGAGCGAGAGGGCGCCGTCTGGTAGAGTGGTGGCTAAGTGGGTCAACTGATGTCTGATGGGTCACGAC

Reverse complement sequence

GTCGTGACCCATCAGACATCAGTTGACCCACTTAGCCACCACTCTACCAGACGGCGCCCTCTCGCTCTCCCTCCGTGACCCATCCCTCCATAGCTCGGCT[C/T]
CCTCGCGCCGCTCCCTATTTGCAAACCCTAGGCGGCGGCGCGACGAGGCAAGGCGGCAACCGGCGGCGGGAGCTGGCCCGTGCTACCGCGGAGGGGGAGG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: