Search for Variation information by Variation ID:

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

Detailed information for vg0223953316:

Variant ID: vg0223953316 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 23953316
Reference Allele: AAlternative Allele: T
Primary Allele: ASecondary Allele: T

Inferred Ancestral Allele : A (evidence from allele frequency in Oryza rufipogon: A: 0.53, T: 0.47, others allele: 0.00, population size: 70. )

Flanking Sequence (100 bp) in Reference Genome:


TTACCTTCACCTGCTTGACCTTTCTGGTAATCGCTTCTCTGGGCAGATACCTCGCCTGAACAGTCTCCGAAAATTGCAAGTCCTCAACCTGAGTAACAAT[A/T]
TTTTGGACGGGATCATTCCGGACACGCTTACAAACTGTTCCAGTTTGACGCAGCTAGATTTGAGCATAAACTTATTTCAAGGCCAGATTCCCCTCGGCAT

Reverse complement sequence

ATGCCGAGGGGAATCTGGCCTTGAAATAAGTTTATGCTCAAATCTAGCTGCGTCAAACTGGAACAGTTTGTAAGCGTGTCCGGAATGATCCCGTCCAAAA[T/A]
ATTGTTACTCAGGTTGAGGACTTGCAATTTTCGGAGACTGTTCAGGCGAGGTATCTGCCCAGAGAAGCGATTACCAGAAAGGTCAAGCAGGTGAAGGTAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: