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Detailed information for vg1001449111:

Variant ID: vg1001449111 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 1449111
Reference Allele: AAlternative Allele: G
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 1.00, others allele: 0.00, population size: 300. )

Flanking Sequence (100 bp) in Reference Genome:


AGTAGGACAATAGTGGCATTTCTTTTTCTAGAACAATAGTGGAAATTCATCGGAGATAAAGCGTAACTCACAGGAAGCATCATAGGAGGAAGTTCCTCAC[A/G]
AACAGGCGACAGTGTAGGATGTTCAATTCGGGCACGAGATATTTTTCTTGACAAAGTGCGCCCTTCATCTTTGAAAGACTCCTGCTTCTTTATTTTACAC

Reverse complement sequence

GTGTAAAATAAAGAAGCAGGAGTCTTTCAAAGATGAAGGGCGCACTTTGTCAAGAAAAATATCTCGTGCCCGAATTGAACATCCTACACTGTCGCCTGTT[T/C]
GTGAGGAACTTCCTCCTATGATGCTTCCTGTGAGTTACGCTTTATCTCCGATGAATTTCCACTATTGTTCTAGAAAAAGAAATGCCACTATTGTCCTACT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: