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Detailed information for vg1013156252:

Variant ID: vg1013156252 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 13156252
Reference Allele: GAlternative Allele: A
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.67, A: 0.33, others allele: 0.00, population size: 88. )

Flanking Sequence (100 bp) in Reference Genome:


AAGGGTAAAATTGTCATTTCATTCATACTGCTGCATGCGAGGATGACTTAGCATGCTCACGTGGTATTTTTATGGGTCCAAGGACTATATTAACCCAAAT[G/A]
ATTAATTTGGGGGACTTGTTTGGATGATTTGAAACCTCAATGACCAAGCTGAGCCCGAAACGAAACTCAAGAACCATATGAGCTATTCACCCAAATTTAA

Reverse complement sequence

TTAAATTTGGGTGAATAGCTCATATGGTTCTTGAGTTTCGTTTCGGGCTCAGCTTGGTCATTGAGGTTTCAAATCATCCAAACAAGTCCCCCAAATTAAT[C/T]
ATTTGGGTTAATATAGTCCTTGGACCCATAAAAATACCACGTGAGCATGCTAAGTCATCCTCGCATGCAGCAGTATGAATGAAATGACAATTTTACCCTT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: