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Detailed information for vg1007689790:

Variant ID: vg1007689790 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 7689790
Reference Allele: CAlternative Allele: A
Primary Allele: CSecondary Allele: A

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.99, A: 0.01, others allele: 0.00, population size: 268. )

Flanking Sequence (100 bp) in Reference Genome:


AGGTAGCTCTACTCTTCCATAACCAAATGAAATATTGCGGTGGCTGCAGGGCACTAAAGTTTAAAGCATAAAACTTCTAAGATGAATATTTCAAATTCCC[C/A]
AGATATAAGCCCATGTATCATATTCCTATGAGATGTTTACCTCTTCTAACATCTGAGATAAAGACTGATACTCTTCAAAAGCTTGCTGAGAAAGAGGCAA

Reverse complement sequence

TTGCCTCTTTCTCAGCAAGCTTTTGAAGAGTATCAGTCTTTATCTCAGATGTTAGAAGAGGTAAACATCTCATAGGAATATGATACATGGGCTTATATCT[G/T]
GGGAATTTGAAATATTCATCTTAGAAGTTTTATGCTTTAAACTTTAGTGCCCTGCAGCCACCGCAATATTTCATTTGGTTATGGAAGAGTAGAGCTACCT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: