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Detailed information for vg1006612280:

Variant ID: vg1006612280 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 6612280
Reference Allele: AAlternative Allele: T
Primary Allele: TSecondary Allele: A

Inferred Ancestral Allele : A (evidence from allele frequency in Oryza rufipogon: A: 0.93, T: 0.07, others allele: 0.00, population size: 86. )

Flanking Sequence (100 bp) in Reference Genome:


CAATACTTTTGACAAGATCATGAACTCCCAATGTCCGCATCATCCAAATTCCAATCATGCGGCCAAAGATTGCTTCGTCTACAAACAGTTTGCAGAACAA[A/T]
ACACCAAGAATGCACGAAAGGCCTCCGACGGAGATCAAAGCATGTCAAAAAAGAAGGACGATGACGACGATGCCCCGATAGGTTTTCGAGACCGTCGTAA

Reverse complement sequence

TTACGACGGTCTCGAAAACCTATCGGGGCATCGTCGTCATCGTCCTTCTTTTTTGACATGCTTTGATCTCCGTCGGAGGCCTTTCGTGCATTCTTGGTGT[T/A]
TTGTTCTGCAAACTGTTTGTAGACGAAGCAATCTTTGGCCGCATGATTGGAATTTGGATGATGCGGACATTGGGAGTTCATGATCTTGTCAAAAGTATTG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: