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Detailed information for vg1002291312:

Variant ID: vg1002291312 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 2291312
Reference Allele: TAlternative Allele: C
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 0.91, C: 0.08, others allele: 0.00, population size: 200. )

Flanking Sequence (100 bp) in Reference Genome:


AAGATAAATATATGTAAACTGAATAAAATTCTAAAAGGAAGCAATATTCCTCCAAACAGTATATTCATAAACCTTGTAACTAGGGGGTGCATAAGTTATC[T/C]
AAAATTATTCTGTGCAAGTAATCACTAGTATGTAAATGGACTAGAGTAATACATCCTGAAGCTAACATAATCTAGTAAAAAATAGAACTTCATTGACCAA

Reverse complement sequence

TTGGTCAATGAAGTTCTATTTTTTACTAGATTATGTTAGCTTCAGGATGTATTACTCTAGTCCATTTACATACTAGTGATTACTTGCACAGAATAATTTT[A/G]
GATAACTTATGCACCCCCTAGTTACAAGGTTTATGAATATACTGTTTGGAGGAATATTGCTTCCTTTTAGAATTTTATTCAGTTTACATATATTTATCTT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: