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Detailed information for vg0122456656:

Variant ID: vg0122456656 (JBrowse)Variation Type: SNP
Chromosome: chr01Position: 22456656
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.80, T: 0.20, others allele: 0.00, population size: 94. )

Flanking Sequence (100 bp) in Reference Genome:


TTATCAAAAACATCACATCGAATCTTTAGACACATATATGGAACATTAAATATAGATAAAAAGAAAAACCAATTGCACAGTTTGTATGTAAATCGCGAGA[C/T]
GAATCTTTTGAGCCTAATTAGGCCATGATTAGCCATAAGTGCTACGGTAACCCACACGTGTTAATGACGAATTAATTAGGTTCAAAAGATTCGTCTCGCG

Reverse complement sequence

CGCGAGACGAATCTTTTGAACCTAATTAATTCGTCATTAACACGTGTGGGTTACCGTAGCACTTATGGCTAATCATGGCCTAATTAGGCTCAAAAGATTC[G/A]
TCTCGCGATTTACATACAAACTGTGCAATTGGTTTTTCTTTTTATCTATATTTAATGTTCCATATATGTGTCTAAAGATTCGATGTGATGTTTTTGATAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: