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Detailed information for vg0223952998:

Variant ID: vg0223952998 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 23952998
Reference Allele: GAlternative Allele: A
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.92, A: 0.09, others allele: 0.00, population size: 82. )

Flanking Sequence (100 bp) in Reference Genome:


TGCTTTACCACTGTGCAGGTAGCTCGCCATGCTCGTAGCTTTGTTTGCGGCGTTAGTACTCCTCTGCTACTCAGCCGGCAACATCCACTGCGTCGTGGCG[G/A]
TCCATGGAAACGACTCCGACATGCTCGCGCTGCTCGAGTTCAAGGATGCCATCGGCGACGATCCGGCGGGCGTCCTGAGCTCCTGGAACAAAACCACCCC

Reverse complement sequence

GGGGTGGTTTTGTTCCAGGAGCTCAGGACGCCCGCCGGATCGTCGCCGATGGCATCCTTGAACTCGAGCAGCGCGAGCATGTCGGAGTCGTTTCCATGGA[C/T]
CGCCACGACGCAGTGGATGTTGCCGGCTGAGTAGCAGAGGAGTACTAACGCCGCAAACAAAGCTACGAGCATGGCGAGCTACCTGCACAGTGGTAAAGCA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: