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Detailed information for vg1016625606:

Variant ID: vg1016625606 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 16625606
Reference Allele: TAlternative Allele: G
Primary Allele: GSecondary Allele: T

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 0.72, G: 0.29, others allele: 0.00, population size: 200. )

Flanking Sequence (100 bp) in Reference Genome:


CCACAATTGGCTGAGACAAGTGGTGGCATGCATGGCCATTTGTTGCGTCGGATGCTTCATCCTTGTGTGATCTAACCAACCAATGCAACGCTCTCTCCCT[T/G]
TGGATGCAACAGCATGCATGTTTTTAGCTAAAAGTCTTGTGTAAATATGTTATGTTTCTTAATTCTTACGTGTTTTCAGCTAGCATAAAGACAATGACTT

Reverse complement sequence

AAGTCATTGTCTTTATGCTAGCTGAAAACACGTAAGAATTAAGAAACATAACATATTTACACAAGACTTTTAGCTAAAAACATGCATGCTGTTGCATCCA[A/C]
AGGGAGAGAGCGTTGCATTGGTTGGTTAGATCACACAAGGATGAAGCATCCGACGCAACAAATGGCCATGCATGCCACCACTTGTCTCAGCCAATTGTGG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: