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Detailed information for vg1009948618:

Variant ID: vg1009948618 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 9948618
Reference Allele: AAlternative Allele: T
Primary Allele: TSecondary Allele: A

Inferred Ancestral Allele : A (evidence from allele frequency in Oryza rufipogon: A: 0.76, T: 0.25, others allele: 0.00, population size: 218. )

Flanking Sequence (100 bp) in Reference Genome:


GCCAGTGGAATTCTGATCAGGTTTACCGATTTTCATATAGGGAAAGAGCATGCAGAATTTTCCATACCATCCATGTGATTAAAATGGTTGCATCAAGCGA[A/T]
TTGATTCCTAACTGAACTTATGCAAGTATAACTCTGATTAGGAATTGAAATATGCAAAAAACGTATAGTTGGTACGAAACAAGGGAGTTATTTACTTGCA

Reverse complement sequence

TGCAAGTAAATAACTCCCTTGTTTCGTACCAACTATACGTTTTTTGCATATTTCAATTCCTAATCAGAGTTATACTTGCATAAGTTCAGTTAGGAATCAA[T/A]
TCGCTTGATGCAACCATTTTAATCACATGGATGGTATGGAAAATTCTGCATGCTCTTTCCCTATATGAAAATCGGTAAACCTGATCAGAATTCCACTGGC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: