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Detailed information for vg1017847198:

Variant ID: vg1017847198 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 17847198
Reference Allele: TAlternative Allele: A
Primary Allele: ASecondary Allele: T

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 0.80, A: 0.20, others allele: 0.00, population size: 104. )

Flanking Sequence (100 bp) in Reference Genome:


TATCACTAATGGTTGATTGCTTCCCCAGTGAGATCTCAAACAGCCCGATTTTTTTAAAAAAAAATGAGATATCGGTGAGAGTTTTTATATTTTAGAATGG[T/A]
CACGAAAAGTTGTTACTATATTATTCTGGAACGGAGGGACTACATGTAGTGCCACCAGGGGATCGAGCACAAATTAAGGTGACCAGCCAGCATGCAAGGA

Reverse complement sequence

TCCTTGCATGCTGGCTGGTCACCTTAATTTGTGCTCGATCCCCTGGTGGCACTACATGTAGTCCCTCCGTTCCAGAATAATATAGTAACAACTTTTCGTG[A/T]
CCATTCTAAAATATAAAAACTCTCACCGATATCTCATTTTTTTTTAAAAAAATCGGGCTGTTTGAGATCTCACTGGGGAAGCAATCAACCATTAGTGATA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: