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Detailed information for vg0108957658:

Variant ID: vg0108957658 (JBrowse)Variation Type: SNP
Chromosome: chr01Position: 8957658
Reference Allele: AAlternative Allele: T
Primary Allele: ASecondary Allele: T

Inferred Ancestral Allele : A (evidence from allele frequency in Oryza rufipogon: A: 1.01, others allele: 0.00, population size: 245. )

Flanking Sequence (100 bp) in Reference Genome:


GCATTTCAAATGGGGCCTTAATCTCTAACTCTTGCTCAATGGATTGGGCCTGGTTGTAGTTTTACAAATTTACAATACAATAATGTAGAAGGGAAAGTCT[A/T]
TTTTTTTCTCCCTTGATTATAAGTCGAGTCTGATTGGCATCCACTAATCGCACAACCAGATATAGAGAGTCCTTAAACTATCAAACCGGCTTGTTTTGAC

Reverse complement sequence

GTCAAAACAAGCCGGTTTGATAGTTTAAGGACTCTCTATATCTGGTTGTGCGATTAGTGGATGCCAATCAGACTCGACTTATAATCAAGGGAGAAAAAAA[T/A]
AGACTTTCCCTTCTACATTATTGTATTGTAAATTTGTAAAACTACAACCAGGCCCAATCCATTGAGCAAGAGTTAGAGATTAAGGCCCCATTTGAAATGC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: