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Detailed information for vg1117619488:

Variant ID: vg1117619488 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 17619488
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 1.00, others allele: 0.00, population size: 107. )

Flanking Sequence (100 bp) in Reference Genome:


CCTCCACCGCCAGCGTCTCCGACGGCACGAACACCGGGTGCCGGGTCATCACCTTCCACGCCGGCGTCTCCTCGATCTTCAGCTCCCGCGCGATCACCCG[C/T]
GTCGCAATGTCCTGCAGATTGATCGATTGATTGATTGATTGTTCGTATCTTTTACATACAGAGAAGGGGAAATTAAGCGTATATATTCATGTTGCCACAT

Reverse complement sequence

ATGTGGCAACATGAATATATACGCTTAATTTCCCCTTCTCTGTATGTAAAAGATACGAACAATCAATCAATCAATCGATCAATCTGCAGGACATTGCGAC[G/A]
CGGGTGATCGCGCGGGAGCTGAAGATCGAGGAGACGCCGGCGTGGAAGGTGATGACCCGGCACCCGGTGTTCGTGCCGTCGGAGACGCTGGCGGTGGAGG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: