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Detailed information for vg0220869926:

Variant ID: vg0220869926 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 20869926
Reference Allele: GAlternative Allele: A
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.99, A: 0.01, others allele: 0.00, population size: 295. )

Flanking Sequence (100 bp) in Reference Genome:


TATGTCCTGAAACATTATCATCAGCTGAATCATCACATATTCAAATGAAAAAAATAATTTTGTAAACCATGACAAAATGCTAACACACCTTGAAGTAACT[G/A]
TTATCAAACTTCAACCATTCAACTGTCCATGATTGCCCTCCAGGTTCACCAGGCCCATCCTTCTGTAGACCACAATAATAGAAGCCACCTTTAAATGTCA

Reverse complement sequence

TGACATTTAAAGGTGGCTTCTATTATTGTGGTCTACAGAAGGATGGGCCTGGTGAACCTGGAGGGCAATCATGGACAGTTGAATGGTTGAAGTTTGATAA[C/T]
AGTTACTTCAAGGTGTGTTAGCATTTTGTCATGGTTTACAAAATTATTTTTTTCATTTGAATATGTGATGATTCAGCTGATGATAATGTTTCAGGACATA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: