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Detailed information for vg0216649351:

Variant ID: vg0216649351 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 16649351
Reference Allele: GAlternative Allele: A
Primary Allele: ASecondary Allele: G

Inferred Ancestral Allele : A (evidence from allele frequency in Oryza rufipogon: A: 0.98, G: 0.02, others allele: 0.00, population size: 123. )

Flanking Sequence (100 bp) in Reference Genome:


GCATGCACCCATTCGGACCAAAATAATTTTGGTAGATAAGTAGTAATCTCAGTCATAAACAGGCAGTCCCCAAAATTTAGGCTTAACTTCAGTTTCAATG[G/A]
CACATCACTACTAGAAAAAGCATTTTTCCCATAGTAGGGGTCTCATTTTCGCAGGCGGACATGACTCTTAAAGCCAAATGACCGTCACCAAAAATATAAA

Reverse complement sequence

TTTATATTTTTGGTGACGGTCATTTGGCTTTAAGAGTCATGTCCGCCTGCGAAAATGAGACCCCTACTATGGGAAAAATGCTTTTTCTAGTAGTGATGTG[C/T]
CATTGAAACTGAAGTTAAGCCTAAATTTTGGGGACTGCCTGTTTATGACTGAGATTACTACTTATCTACCAAAATTATTTTGGTCCGAATGGGTGCATGC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: