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Detailed information for vg0235786272:

Variant ID: vg0235786272 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 35786272
Reference Allele: CAlternative Allele: T
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 1.00, others allele: 0.00, population size: 268. )

Flanking Sequence (100 bp) in Reference Genome:


AGTCCAATTGTTTTCCCTGAGTTGGAAATAAGGCATCTGCAAACAAATAAATTTTCTTTTAGAAAATCCATTACCAGAAGACAGATAATTTAGGCTAATG[C/T]
ACTGTGTGAGAATGACTGGGAGGCCCAATAAGTATAGGCAAAATTTTGAGGGGATCAGAGCCAAGGAGATAATTGATCATTTGATTTCCATTGACCTTTT

Reverse complement sequence

AAAAGGTCAATGGAAATCAAATGATCAATTATCTCCTTGGCTCTGATCCCCTCAAAATTTTGCCTATACTTATTGGGCCTCCCAGTCATTCTCACACAGT[G/A]
CATTAGCCTAAATTATCTGTCTTCTGGTAATGGATTTTCTAAAAGAAAATTTATTTGTTTGCAGATGCCTTATTTCCAACTCAGGGAAAACAATTGGACT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: