Search for Variation information by Variation ID:

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

Detailed information for vg1216757238:

Variant ID: vg1216757238 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 16757238
Reference Allele: AAlternative Allele: G
Primary Allele: ASecondary Allele: G

Inferred Ancestral Allele : A (evidence from allele frequency in Oryza rufipogon: A: 0.96, G: 0.04, others allele: 0.00, population size: 51. )

Flanking Sequence (100 bp) in Reference Genome:


AAGCCTCTTAATTTTGTTGACCAAGACATCGAATTGAGCCTGAGATTTGATCTTGCGATCTACATAAATAGATTTATATCAACGAGTGGGCATAAAGAAA[A/G]
GAATGGTTTTTAAAGTATTAGTTACCAGTACCTTCAACATCTTTCAGAGCCAAATCCCTTTGTCTTGCCAATTCGGCCTTGTCTTTCTCCAGAGCTTGGA

Reverse complement sequence

TCCAAGCTCTGGAGAAAGACAAGGCCGAATTGGCAAGACAAAGGGATTTGGCTCTGAAAGATGTTGAAGGTACTGGTAACTAATACTTTAAAAACCATTC[T/C]
TTTCTTTATGCCCACTCGTTGATATAAATCTATTTATGTAGATCGCAAGATCAAATCTCAGGCTCAATTCGATGTCTTGGTCAACAAAATTAAGAGGCTT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: