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Detailed information for vg1005826161:

Variant ID: vg1005826161 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 5826161
Reference Allele: TAlternative Allele: G
Primary Allele: TSecondary Allele: G

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 0.99, G: 0.01, others allele: 0.00, population size: 309. )

Flanking Sequence (100 bp) in Reference Genome:


GATAATTAACTTAAGTAATAGTGTATTAGGCCCCTTTCCAAACACCCTTGGGGCCATTGCCTGGAAACATAGAATGGTCACACGATATATATGATGCATC[T/G]
ATTTGTTGCAGCTGGTCCAAGATCATACTCCTACGAGGAATTGTACACTGCAACAAATGGTTTTTCAGATGAACGAAAGTTGGGCCAGGGTGCGTTTGGT

Reverse complement sequence

ACCAAACGCACCCTGGCCCAACTTTCGTTCATCTGAAAAACCATTTGTTGCAGTGTACAATTCCTCGTAGGAGTATGATCTTGGACCAGCTGCAACAAAT[A/C]
GATGCATCATATATATCGTGTGACCATTCTATGTTTCCAGGCAATGGCCCCAAGGGTGTTTGGAAAGGGGCCTAATACACTATTACTTAAGTTAATTATC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: