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Detailed information for vg1118143847:

Variant ID: vg1118143847 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 18143847
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.86, T: 0.14, others allele: 0.00, population size: 101. )

Flanking Sequence (100 bp) in Reference Genome:


CTTAAACCGTGCACTCAAGTGGTTTCGCTGAAGTGGCATCCTAGTCAGCAAAAAAAAAATTAAAAAAGTATTTGGGACATGGAGCTCAAGCTCACCTCCG[C/T]
AGCCGACTCGGCCTCCACCGGTCCTTTTCTCCCACTGCCGCCGTCGCGCCGGCCACCTCCTCTCCCGCCGCTGCCATCACGCCGGCCGCCTCCTCTCCTT

Reverse complement sequence

AAGGAGAGGAGGCGGCCGGCGTGATGGCAGCGGCGGGAGAGGAGGTGGCCGGCGCGACGGCGGCAGTGGGAGAAAAGGACCGGTGGAGGCCGAGTCGGCT[G/A]
CGGAGGTGAGCTTGAGCTCCATGTCCCAAATACTTTTTTAATTTTTTTTTTGCTGACTAGGATGCCACTTCAGCGAAACCACTTGAGTGCACGGTTTAAG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: