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Detailed information for vg1218169236:

Variant ID: vg1218169236 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 18169236
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 0.70, C: 0.29, others allele: 0.00, population size: 76. )

Flanking Sequence (100 bp) in Reference Genome:


CAACTTGTAAGGTCGTGAGACCTAGATTTGTGAATTGGGCGTTATGTGACTCCTGTCGGTGAAGTGCGTTGAATCCCACACTCCTAGCAGGCGTAGAGTT[C/T]
AGCTTTCACGTGGAGTATCACCGGGCAATCCTCGAGAATATACTTGGATGTCAGCTTTTAGGTAGTATTCCTTGTCAGCTCTGGTTTTTGTACAAGGGAC

Reverse complement sequence

GTCCCTTGTACAAAAACCAGAGCTGACAAGGAATACTACCTAAAAGCTGACATCCAAGTATATTCTCGAGGATTGCCCGGTGATACTCCACGTGAAAGCT[G/A]
AACTCTACGCCTGCTAGGAGTGTGGGATTCAACGCACTTCACCGACAGGAGTCACATAACGCCCAATTCACAAATCTAGGTCTCACGACCTTACAAGTTG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: