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Detailed information for vg1007941662:

Variant ID: vg1007941662 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 7941662
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.97, T: 0.02, others allele: 0.00, population size: 122. )

Flanking Sequence (100 bp) in Reference Genome:


TTAGGTATGTAATAATGAATTGTGAAATAAAGTTGAGTTTGAGTTGTTTTGTTGTTAGGTATATGTATGAATCAAATTCATATACCTAGGTATATACTCA[C/T]
AATTTGAAAATTTTTAAAAATTTGAGAGAATTTGTGTGTTTTATACCTTGGAGCCCAGGCACCATGGAGTCCCATATGGGTATCATATGCACCAACGATC

Reverse complement sequence

GATCGTTGGTGCATATGATACCCATATGGGACTCCATGGTGCCTGGGCTCCAAGGTATAAAACACACAAATTCTCTCAAATTTTTAAAAATTTTCAAATT[G/A]
TGAGTATATACCTAGGTATATGAATTTGATTCATACATATACCTAACAACAAAACAACTCAAACTCAACTTTATTTCACAATTCATTATTACATACCTAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: