Search for Variation information by Variation ID:

Please input a variation ID (e.g., vg0722097923 , STR0500036000 ).

Detailed information for vg0216569039:

Variant ID: vg0216569039 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 16569039
Reference Allele: TAlternative Allele: G
Primary Allele: TSecondary Allele: G

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 0.97, G: 0.02, others allele: 0.00, population size: 245. )

Flanking Sequence (100 bp) in Reference Genome:


ATTTATACATAGCAGGAGCAGCGTTCAAGCATTATTTGAATTGCATACACAACTTTAGGGATATAATGAGATGTATTGAAGATTAGTAGAAGAGAATTAA[T/G]
TACCATCACTTGTTCGTAACTAAAAGGAAAAATCGACCGCTAAAGTATCAACTATATTGCCAGATAATTTTGTTGTGTGGTGTATAAAACTTGTCTGAAA

Reverse complement sequence

TTTCAGACAAGTTTTATACACCACACAACAAAATTATCTGGCAATATAGTTGATACTTTAGCGGTCGATTTTTCCTTTTAGTTACGAACAAGTGATGGTA[A/C]
TTAATTCTCTTCTACTAATCTTCAATACATCTCATTATATCCCTAAAGTTGTGTATGCAATTCAAATAATGCTTGAACGCTGCTCCTGCTATGTATAAAT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: