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Detailed information for vg1016851749:

Variant ID: vg1016851749 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 16851749
Reference Allele: AAlternative Allele: G
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.94, A: 0.06, others allele: 0.00, population size: 99. )

Flanking Sequence (100 bp) in Reference Genome:


AAAACTTTTGTGAAATATGTAAAATTATACGCCTACATCAAAATATATTTAACAATGAATCAAATGATAGGAAAAAGATTAATAATTACTTAAATTTTTT[A/G]
AATAAGACGAACGGTCAAACATGTGCTAAAAAGTTAACGGCGTCAAACATTTCGAAACGGAGGGAGTACTTCGAAACATGATTCCGCTAACTAGCAGCTG

Reverse complement sequence

CAGCTGCTAGTTAGCGGAATCATGTTTCGAAGTACTCCCTCCGTTTCGAAATGTTTGACGCCGTTAACTTTTTAGCACATGTTTGACCGTTCGTCTTATT[T/C]
AAAAAATTTAAGTAATTATTAATCTTTTTCCTATCATTTGATTCATTGTTAAATATATTTTGATGTAGGCGTATAATTTTACATATTTCACAAAAGTTTT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: