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Detailed information for vg1202159597:

Variant ID: vg1202159597 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 2159597
Reference Allele: AAlternative Allele: G
Primary Allele: ASecondary Allele: G

Inferred Ancestral Allele : A (evidence from allele frequency in Oryza rufipogon: A: 1.00, G: 0.00, others allele: 0.00, population size: 286. )

Flanking Sequence (100 bp) in Reference Genome:


CCGTTCTTTGATGACACATAGTAAGATGGGCTCCAACAGAATAAGAGAGCACAACGCCAACGGGTGTGCAGTGTCCTGAGAGCAAGTATAATAGAGGGCT[A/G]
TAAGAAGGCTGAATGCTGATGTGGATGAGAGAGGAGAGGAGAGAGATGAGAAGCGAGCTATAAGTTTACAGCCGGCTTAGGCACAAGAACCAATAAAATC

Reverse complement sequence

GATTTTATTGGTTCTTGTGCCTAAGCCGGCTGTAAACTTATAGCTCGCTTCTCATCTCTCTCCTCTCCTCTCTCATCCACATCAGCATTCAGCCTTCTTA[T/C]
AGCCCTCTATTATACTTGCTCTCAGGACACTGCACACCCGTTGGCGTTGTGCTCTCTTATTCTGTTGGAGCCCATCTTACTATGTGTCATCAAAGAACGG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: