Search for Variation information by Variation ID:

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

Detailed information for vg0234905791:

Variant ID: vg0234905791 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 34905791
Reference Allele: AAlternative Allele: G
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele : A (evidence from allele frequency in Oryza rufipogon: A: 0.72, G: 0.27, others allele: 0.00, population size: 268. )

Flanking Sequence (100 bp) in Reference Genome:


TACTACAGTTATAGCTGGCGAAAGATATTGGGGAACTTTTCCATTGCGAAGCTGATTCATAGTTGATGTAGGCCTGTTTCATGTACCCCTAAGATGATTC[A/G]
CTTCAATCTGTTAAAGTGGAGCTCTGGTCATATCATCAGCCAAATGCAGAAGTCTATTACATCAAACTTGAAAACGAAATAAGTTTTCCCTGGTCTTGTT

Reverse complement sequence

AACAAGACCAGGGAAAACTTATTTCGTTTTCAAGTTTGATGTAATAGACTTCTGCATTTGGCTGATGATATGACCAGAGCTCCACTTTAACAGATTGAAG[T/C]
GAATCATCTTAGGGGTACATGAAACAGGCCTACATCAACTATGAATCAGCTTCGCAATGGAAAAGTTCCCCAATATCTTTCGCCAGCTATAACTGTAGTA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: