Search for Variation information by Variation ID:

Please input a variation ID (e.g., vg0722097923 , STR0500036000 ).

Detailed information for vg0221445039:

Variant ID: vg0221445039 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 21445039
Reference Allele: CAlternative Allele: T
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.91, T: 0.09, others allele: 0.00, population size: 263. )

Flanking Sequence (100 bp) in Reference Genome:


GTCCCCAGGTACACAACCCAATGGGTCAGCTTCAGCCTCCGCTCCACTACGACAGAAGCTGGCCTTTATTAAGTGCAAATGAATTTGGATCACAACTCAA[C/T]
AAACTCCACCTTGAGACAAATTCCTTCTTGTAGCATGAATCAATCCTTCACCCTGAACACAACAAAGACAAAAAAAAAACATTTTCGGCGCCAAACAGCC

Reverse complement sequence

GGCTGTTTGGCGCCGAAAATGTTTTTTTTTTGTCTTTGTTGTGTTCAGGGTGAAGGATTGATTCATGCTACAAGAAGGAATTTGTCTCAAGGTGGAGTTT[G/A]
TTGAGTTGTGATCCAAATTCATTTGCACTTAATAAAGGCCAGCTTCTGTCGTAGTGGAGCGGAGGCTGAAGCTGACCCATTGGGTTGTGTACCTGGGGAC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: