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Detailed information for vg1013528269:

Variant ID: vg1013528269 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 13528269
Reference Allele: CAlternative Allele: A
Primary Allele: CSecondary Allele: A

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.97, A: 0.04, others allele: 0.00, population size: 117. )

Flanking Sequence (100 bp) in Reference Genome:


TTCTACTAACTTATATAGTGTAGTATCATAAAATTTATATTTTGATTCACTTTTAGAAATACTTCTATAACATATAATTCACATGTTATTAAACTATATA[C/A]
CGATTTTTAAAATTTAATGACTAAAAGTAGATACATTTAATTTAAAATAAACCTAAAATAATTTGAAACCGATCGACAAAATACATGATTCAGTCCGAGA

Reverse complement sequence

TCTCGGACTGAATCATGTATTTTGTCGATCGGTTTCAAATTATTTTAGGTTTATTTTAAATTAAATGTATCTACTTTTAGTCATTAAATTTTAAAAATCG[G/T]
TATATAGTTTAATAACATGTGAATTATATGTTATAGAAGTATTTCTAAAAGTGAATCAAAATATAAATTTTATGATACTACACTATATAAGTTAGTAGAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: