Search for Variation information by Variation ID:

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

Detailed information for vg0220796750:

Variant ID: vg0220796750 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 20796750
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.99, others allele: 0.00, population size: 313. )

Flanking Sequence (100 bp) in Reference Genome:


CCTAAATGTGTCCAAAATCCCACTCCTATGTGACAATGAGAGCGCCATTAAGATAGCTAATAACCCCGTCCAACATTCCCGAACCAAACACATAGATATT[C/T]
GCCATCATTTCTTGAGAGACCATTCCACAAGAGGCGACATAGATATCCAACATGTGAGAACCGACAAACAATTGGCGGATATGTTCACCAAGCCTCTAGA

Reverse complement sequence

TCTAGAGGCTTGGTGAACATATCCGCCAATTGTTTGTCGGTTCTCACATGTTGGATATCTATGTCGCCTCTTGTGGAATGGTCTCTCAAGAAATGATGGC[G/A]
AATATCTATGTGTTTGGTTCGGGAATGTTGGACGGGGTTATTAGCTATCTTAATGGCGCTCTCATTGTCACATAGGAGTGGGATTTTGGACACATTTAGG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: