Search for Variation information by Variation ID:

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

Detailed information for vg0224963772:

Variant ID: vg0224963772 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 24963772
Reference Allele: AAlternative Allele: T
Primary Allele: ASecondary Allele: T

Inferred Ancestral Allele : A (evidence from allele frequency in Oryza rufipogon: A: 0.82, T: 0.18, others allele: 0.00, population size: 90. )

Flanking Sequence (100 bp) in Reference Genome:


TAATAAAAATGAATGGTCAAATGTTACAAGTAAAAAGTCAAAGCGACATTTATTATAAGACAGGGGTAGTAGTTATCAATGTCACGCATCCCAATCCCTT[A/T]
AAAAAATATATATTAAGAGCCTGCGAAACTCATTTATAGGCTAAAATGAGCCGTGGACCCACTTATTTTGAGCCATAAGCATCCCTTAGCTCCAAGGCTC

Reverse complement sequence

GAGCCTTGGAGCTAAGGGATGCTTATGGCTCAAAATAAGTGGGTCCACGGCTCATTTTAGCCTATAAATGAGTTTCGCAGGCTCTTAATATATATTTTTT[T/A]
AAGGGATTGGGATGCGTGACATTGATAACTACTACCCCTGTCTTATAATAAATGTCGCTTTGACTTTTTACTTGTAACATTTGACCATTCATTTTTATTA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: