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Detailed information for vg1013489724:

Variant ID: vg1013489724 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 13489724
Reference Allele: CAlternative Allele: T
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.92, T: 0.08, others allele: 0.00, population size: 104. )

Flanking Sequence (100 bp) in Reference Genome:


TGATTGATATACCCAAAAACCGAAAACTTTTAGCGGAAATAGAAGTTACCCTCGAAATCGACGGAAGTCGGTCTGACCGAGATTAATCTGCCGGTCTGAC[C/T]
GAAGCGTAGCCGCCGGTCTGACCGGTGTTGATCTTCTGGTTGGACTGCCCTGGAATCCCTGCCGCGCCTATTGTCGCCGCCGGTCTGACCGCAGGTCACC

Reverse complement sequence

GGTGACCTGCGGTCAGACCGGCGGCGACAATAGGCGCGGCAGGGATTCCAGGGCAGTCCAACCAGAAGATCAACACCGGTCAGACCGGCGGCTACGCTTC[G/A]
GTCAGACCGGCAGATTAATCTCGGTCAGACCGACTTCCGTCGATTTCGAGGGTAACTTCTATTTCCGCTAAAAGTTTTCGGTTTTTGGGTATATCAATCA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: