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Detailed information for vg1000757961:

Variant ID: vg1000757961 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 757961
Reference Allele: AAlternative Allele: G
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.76, A: 0.24, others allele: 0.00, population size: 85. )

Flanking Sequence (100 bp) in Reference Genome:


TTGTGGGCTATCTCCGCCCAATGTCTCTGCTATCTTGGCATGTGCATACGGCATGACATGCATGCAGTGTTCTCCCTCTTTACTATCAATGGCCATATAT[A/G]
TATGGCACGTATATTTTCCAGCCACATATGAAACGTGGATCACTATAGTTCAATTTGCACTCTAATTACCATCTAAACATAGATTAATGTAATTTGTCTG

Reverse complement sequence

CAGACAAATTACATTAATCTATGTTTAGATGGTAATTAGAGTGCAAATTGAACTATAGTGATCCACGTTTCATATGTGGCTGGAAAATATACGTGCCATA[T/C]
ATATATGGCCATTGATAGTAAAGAGGGAGAACACTGCATGCATGTCATGCCGTATGCACATGCCAAGATAGCAGAGACATTGGGCGGAGATAGCCCACAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: