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Detailed information for vg1218287578:

Variant ID: vg1218287578 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 18287578
Reference Allele: GAlternative Allele: T
Primary Allele: GSecondary Allele: T

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.81, T: 0.18, others allele: 0.00, population size: 186. )

Flanking Sequence (100 bp) in Reference Genome:


AGCAAATGCTACTCATTATAAGGATTTCGACAAAGCAAATTTGTTCATCACTAAAGCCGAAGTCAATAGGAGTACTATTATGAATAAATTCAGACCTCAG[G/T]
CTCGAGGACGTAGTTCTCCCATAAATAAAACCATGTGTCATATAACAATTCTACTAAATATAGTAAGAGCATAGTTGAAAATGGTATTCGGTGCACTTTC

Reverse complement sequence

GAAAGTGCACCGAATACCATTTTCAACTATGCTCTTACTATATTTAGTAGAATTGTTATATGACACATGGTTTTATTTATGGGAGAACTACGTCCTCGAG[C/A]
CTGAGGTCTGAATTTATTCATAATAGTACTCCTATTGACTTCGGCTTTAGTGATGAACAAATTTGCTTTGTCGAAATCCTTATAATGAGTAGCATTTGCT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: