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Detailed information for vg1008769988:

Variant ID: vg1008769988 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 8769988
Reference Allele: CAlternative Allele: T
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.74, T: 0.25, others allele: 0.00, population size: 232. )

Flanking Sequence (100 bp) in Reference Genome:


ATATCTTTGTGTTGTGGTAAGTCTTTTCTCTCCATTCCTCAAGTTCAGCGATCTGCATTTTTCTCCATTCTCCTGCTCCCTCAAAATCCATGTTCCAGTT[C/T]
CTGATGGCCAAGTATGCTCTGTGCTCAAGTTCTACAGGGAGTCGACATGGCTTCCCGTAAACTATCTGATGTGGGGACATTCTAATGGGTGTCTTGTATG

Reverse complement sequence

CATACAAGACACCCATTAGAATGTCCCCACATCAGATAGTTTACGGGAAGCCATGTCGACTCCCTGTAGAACTTGAGCACAGAGCATACTTGGCCATCAG[G/A]
AACTGGAACATGGATTTTGAGGGAGCAGGAGAATGGAGAAAAATGCAGATCGCTGAACTTGAGGAATGGAGAGAAAAGACTTACCACAACACAAAGATAT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: