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Detailed information for vg0122207812:

Variant ID: vg0122207812 (JBrowse)Variation Type: SNP
Chromosome: chr01Position: 22207812
Reference Allele: AAlternative Allele: C
Primary Allele: CSecondary Allele: A

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.85, A: 0.15, others allele: 0.00, population size: 86. )

Flanking Sequence (100 bp) in Reference Genome:


GCTCATGTACGGTGGGACACGGGCTCACGGATGGAGTCTTGGACCTCGGGGACGGCGGGGAACAACGGTGCTGGTTGTGCTTAATTGGAGAAGCTCAAGG[A/C]
GGCGGCGCCGGTGAGGAGCTCACGGGCGGCAGCGACGGGCTCGCGAACGACGGCGAGGAGCTCGAGGACGGCGCCGGGATCGGGGGAGGTGTTCGATGCG

Reverse complement sequence

CGCATCGAACACCTCCCCCGATCCCGGCGCCGTCCTCGAGCTCCTCGCCGTCGTTCGCGAGCCCGTCGCTGCCGCCCGTGAGCTCCTCACCGGCGCCGCC[T/G]
CCTTGAGCTTCTCCAATTAAGCACAACCAGCACCGTTGTTCCCCGCCGTCCCCGAGGTCCAAGACTCCATCCGTGAGCCCGTGTCCCACCGTACATGAGC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: