Search for Variation information by Variation ID:

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

Detailed information for vg0216784769:

Variant ID: vg0216784769 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 16784769
Reference Allele: TAlternative Allele: C
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 0.90, C: 0.10, others allele: 0.00, population size: 62. )

Flanking Sequence (100 bp) in Reference Genome:


ACGAACTCTAGAGGCAGTCGTGAATCTCGACGGATGCACGATCAGCCCAAGCACGAGGGTATTTGTTCCTGCAAGCAATCGAGAACCAGCAAGAACAAGA[T/C]
GAACAAGCAAATAAATTTGCAAATCAAAGATGTTGGATTGAATCAATAGAAGTAACAAGTGGGGTTCAATAACAAGCAATCTAGCGATCTAATCGATCAC

Reverse complement sequence

GTGATCGATTAGATCGCTAGATTGCTTGTTATTGAACCCCACTTGTTACTTCTATTGATTCAATCCAACATCTTTGATTTGCAAATTTATTTGCTTGTTC[A/G]
TCTTGTTCTTGCTGGTTCTCGATTGCTTGCAGGAACAAATACCCTCGTGCTTGGGCTGATCGTGCATCCGTCGAGATTCACGACTGCCTCTAGAGTTCGT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: