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Detailed information for vg0212179937:

Variant ID: vg0212179937 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 12179937
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 1.00, others allele: 0.00, population size: 286. )

Flanking Sequence (100 bp) in Reference Genome:


ACATAAAGGGCAGATTTAACATGTCAATAAAACATATAGAGCAAATGTAGTTAAATCAGATAAGATCAGCTGAAATCCCGATACTACCCTAATCGGCAAC[C/T]
AGAAGGCAGGTTAGAGATTGATATTCCAAGCACGACTTAATAGATCAAACTCAACTAATGCGGCATTAAGTATGAAAAGAAGAACAATATCTAGATAATC

Reverse complement sequence

GATTATCTAGATATTGTTCTTCTTTTCATACTTAATGCCGCATTAGTTGAGTTTGATCTATTAAGTCGTGCTTGGAATATCAATCTCTAACCTGCCTTCT[G/A]
GTTGCCGATTAGGGTAGTATCGGGATTTCAGCTGATCTTATCTGATTTAACTACATTTGCTCTATATGTTTTATTGACATGTTAAATCTGCCCTTTATGT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: