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Detailed information for vg1006382038:

Variant ID: vg1006382038 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 6382038
Reference Allele: AAlternative Allele: G
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.89, A: 0.11, others allele: 0.00, population size: 227. )

Flanking Sequence (100 bp) in Reference Genome:


TTGTTCTCAGATGCCTTCAACTAAATCTGATACCACTTGATGTGCACTAGGGTTCCCGATCTTCTGAAAGGTTCTGATAAACAACGATTTGGGTGGAGTC[A/G]
CGACACAAATTGATCCGGCTTGTTGAACGTGCACGCTCTTGAGCCCCGCAATCGCAGCACCATGTCTCCTCTGGTTATCAACCGTGCCGAAACCCAGTTG

Reverse complement sequence

CAACTGGGTTTCGGCACGGTTGATAACCAGAGGAGACATGGTGCTGCGATTGCGGGGCTCAAGAGCGTGCACGTTCAACAAGCCGGATCAATTTGTGTCG[T/C]
GACTCCACCCAAATCGTTGTTTATCAGAACCTTTCAGAAGATCGGGAACCCTAGTGCACATCAAGTGGTATCAGATTTAGTTGAAGGCATCTGAGAACAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: