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Detailed information for vg1017130098:

Variant ID: vg1017130098 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 17130098
Reference Allele: CAlternative Allele: T
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.90, T: 0.10, others allele: 0.00, population size: 115. )

Flanking Sequence (100 bp) in Reference Genome:


GAAACTTTCTAACACAAAATTTGAATCCTTTCAAGTCAAGATTTGAAATCTTTTAAGTCAAAATTAAAAACTTTCAATTGTATATTTGTAAAGAGTTGTG[C/T]
GAAAGATTGAAAAAAATTGGAAAGAAGCGGCACCTGCCCTTTTTTATCCAATGTGGAATCGACGACCTATGTATAAAAAAAGGAGAAAGTTTTTGAAGAA

Reverse complement sequence

TTCTTCAAAAACTTTCTCCTTTTTTTATACATAGGTCGTCGATTCCACATTGGATAAAAAAGGGCAGGTGCCGCTTCTTTCCAATTTTTTTCAATCTTTC[G/A]
CACAACTCTTTACAAATATACAATTGAAAGTTTTTAATTTTGACTTAAAAGATTTCAAATCTTGACTTGAAAGGATTCAAATTTTGTGTTAGAAAGTTTC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: