Search for Variation information by Variation ID:

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

Detailed information for vg1214552269:

Variant ID: vg1214552269 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 14552269
Reference Allele: GAlternative Allele: A
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.95, A: 0.04, others allele: 0.00, population size: 107. )

Flanking Sequence (100 bp) in Reference Genome:


CGTGACTTATGCTTTTAAATTTTTTTAAAATTTTTCAAATAAGACAGACGATCAAAGTTAGGCACGGAAAATCATGACTGCATTTAAATTGGGACAGAGG[G/A]
AGTATTATATTTAAGTAATATTTATAAGAAATTATTTATAATCTTCTTCATCATTTGAAAAGAATGTATACTTATTTTTTTTAGAAAACATGTCAACGAA

Reverse complement sequence

TTCGTTGACATGTTTTCTAAAAAAAATAAGTATACATTCTTTTCAAATGATGAAGAAGATTATAAATAATTTCTTATAAATATTACTTAAATATAATACT[C/T]
CCTCTGTCCCAATTTAAATGCAGTCATGATTTTCCGTGCCTAACTTTGATCGTCTGTCTTATTTGAAAAATTTTAAAAAAATTTAAAAGCATAAGTCACG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: