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Detailed information for vg1216893818:

Variant ID: vg1216893818 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 16893818
Reference Allele: TAlternative Allele: C
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 0.85, C: 0.16, others allele: 0.00, population size: 55. )

Flanking Sequence (100 bp) in Reference Genome:


ATTACATATTGGCACACATATTCTTAGAGAACATTCATGGCCTTGTAGTTGTATTACACACCTATGTGCTTCCATCGCTGGACTATTTGACATAGTTTGA[T/C]
GGCAAGCCTCAATTGCTTCTTCCATGAGAAAAGGGGAAACTTGATCGATTTCAAAGCAACCTAATGGTGGAAGTTTGATTCAGTGAGCCATTCATGAGAA

Reverse complement sequence

TTCTCATGAATGGCTCACTGAATCAAACTTCCACCATTAGGTTGCTTTGAAATCGATCAAGTTTCCCCTTTTCTCATGGAAGAAGCAATTGAGGCTTGCC[A/G]
TCAAACTATGTCAAATAGTCCAGCGATGGAAGCACATAGGTGTGTAATACAACTACAAGGCCATGAATGTTCTCTAAGAATATGTGTGCCAATATGTAAT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: