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Detailed information for vg0216159752:

Variant ID: vg0216159752 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 16159752
Reference Allele: AAlternative Allele: G
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.96, A: 0.03, others allele: 0.00, population size: 291. )

Flanking Sequence (100 bp) in Reference Genome:


AGGACTTCACCAGGCAACCAGTGATGCGAAGAAGGATGCACCTGGTGGCAACTATGCACATTTTGTTCATATTAGATAGGTTTGTATAGCACTTATCCCT[A/G]
GTATTGTCATGTACTGAAGTTGAACAATGCACATGTCATGCCAAAAACTATGCCCTTTTGGATAGAACAGATAGGCCAACATGCCAATACTTCTGCTAGA

Reverse complement sequence

TCTAGCAGAAGTATTGGCATGTTGGCCTATCTGTTCTATCCAAAAGGGCATAGTTTTTGGCATGACATGTGCATTGTTCAACTTCAGTACATGACAATAC[T/C]
AGGGATAAGTGCTATACAAACCTATCTAATATGAACAAAATGTGCATAGTTGCCACCAGGTGCATCCTTCTTCGCATCACTGGTTGCCTGGTGAAGTCCT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: