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Detailed information for vg1116856270:

Variant ID: vg1116856270 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 16856270
Reference Allele: TAlternative Allele: A
Primary Allele: ASecondary Allele: T

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 0.83, A: 0.17, others allele: 0.00, population size: 92. )

Flanking Sequence (100 bp) in Reference Genome:


TTATAGTAAAAACTAAATGTCACAGTCATGTTTGCTCCTAAGTCCCAAGCAAAGTATACATAAAGATTGTATTCTTGGTACTGCACAAGGATAGGAAGAA[T/A]
TCTGTCAAGCCGTCAGCTGTTAGCTTTGATTTTCACTGATAAAAATGAGTTGTCTTGCTTAAAACATTTGCTGACCCAGCTGCAGACATTTAAGCAGCTG

Reverse complement sequence

CAGCTGCTTAAATGTCTGCAGCTGGGTCAGCAAATGTTTTAAGCAAGACAACTCATTTTTATCAGTGAAAATCAAAGCTAACAGCTGACGGCTTGACAGA[A/T]
TTCTTCCTATCCTTGTGCAGTACCAAGAATACAATCTTTATGTATACTTTGCTTGGGACTTAGGAGCAAACATGACTGTGACATTTAGTTTTTACTATAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: