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Detailed information for vg1124410475:

Variant ID: vg1124410475 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 24410475
Reference Allele: TAlternative Allele: C
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 0.84, C: 0.16, others allele: 0.00, population size: 62. )

Flanking Sequence (100 bp) in Reference Genome:


AGTTTATTTTTTTTAAAAAAAGACATGCATGAAAATTTGATCAGTTAATTTTTGCCATGTTTGATGTGGCTCAGATCCACTTACTTCGTGCCACACCCAT[T/C]
ATCTCCATCAGTCATCCCCAAATCCAACCAGAGCTCGAGCTCGCCACGGATGACCCACCACCACCACCCATGCACGCATGGATGACGACAAGCTCGCCCT

Reverse complement sequence

AGGGCGAGCTTGTCGTCATCCATGCGTGCATGGGTGGTGGTGGTGGGTCATCCGTGGCGAGCTCGAGCTCTGGTTGGATTTGGGGATGACTGATGGAGAT[A/G]
ATGGGTGTGGCACGAAGTAAGTGGATCTGAGCCACATCAAACATGGCAAAAATTAACTGATCAAATTTTCATGCATGTCTTTTTTTAAAAAAAATAAACT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: