Search for Variation information by Variation ID:

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

Detailed information for vg0203127408:

Variant ID: vg0203127408 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 3127408
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: 345. )

Flanking Sequence (100 bp) in Reference Genome:


GAGTTGTCAAATGTATCAAACTGGCCTCCAGTTGGAATAGGTCCTTCCAGGTCATTGTTAGAAACATTGAAGGCAGAAAGGAAGTGCAGCTTGTTCAGTT[C/T]
CAAAGGGATTGCACCCATTAGATTGTTGCTAGACAAGTCTAGCATCTCCAGGTTGGTGAGGTTGCAAATTGCTTGTGGGATCTCTCCAGAGAAGCTATTG

Reverse complement sequence

CAATAGCTTCTCTGGAGAGATCCCACAAGCAATTTGCAACCTCACCAACCTGGAGATGCTAGACTTGTCTAGCAACAATCTAATGGGTGCAATCCCTTTG[G/A]
AACTGAACAAGCTGCACTTCCTTTCTGCCTTCAATGTTTCTAACAATGACCTGGAAGGACCTATTCCAACTGGAGGCCAGTTTGATACATTTGACAACTC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: