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Detailed information for vg1124928261:

Variant ID: vg1124928261 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 24928261
Reference Allele: AAlternative Allele: T
Primary Allele: TSecondary Allele: A

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 0.67, A: 0.33, others allele: 0.00, population size: 89. )

Flanking Sequence (100 bp) in Reference Genome:


CTGTAGGTAAGTTTGGCGTGTTATCATCTTTTGTGTACACTCCCTGCATGATCGTAGAACTTCATGGATACTAACTAGCTCATCTTGAAGAATAGGAAAC[A/T]
GATAAAATGCTCTCTGCATCCTTTCTTTTGGAATCCACCATCATAGACGTTGGTTTCGACCTGTGGATCTGCACTCATCGACAGGCCTATGTGATCGCGT

Reverse complement sequence

ACGCGATCACATAGGCCTGTCGATGAGTGCAGATCCACAGGTCGAAACCAACGTCTATGATGGTGGATTCCAAAAGAAAGGATGCAGAGAGCATTTTATC[T/A]
GTTTCCTATTCTTCAAGATGAGCTAGTTAGTATCCATGAAGTTCTACGATCATGCAGGGAGTGTACACAAAAGATGATAACACGCCAAACTTACCTACAG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: