Search for Variation information by Variation ID:

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

Detailed information for vg1220880817:

Variant ID: vg1220880817 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 20880817
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.98, T: 0.02, others allele: 0.00, population size: 88. )

Flanking Sequence (100 bp) in Reference Genome:


CATTCCAAACATTCACACTTAACATATACAAGATTGATCCTTGGATGGTGCAAAATCCCTCTTAAACTTATGCTCAATTAGCTAATTTTTCCTATATTCA[C/T]
GAAAAATATAGCTTTATGATCAAATCCATATGCGACAAATCCTAGAAGATGAGTGTGCTAAATACTATTTAGAGAAGATGGAGGACAGACACATAACAAA

Reverse complement sequence

TTTGTTATGTGTCTGTCCTCCATCTTCTCTAAATAGTATTTAGCACACTCATCTTCTAGGATTTGTCGCATATGGATTTGATCATAAAGCTATATTTTTC[G/A]
TGAATATAGGAAAAATTAGCTAATTGAGCATAAGTTTAAGAGGGATTTTGCACCATCCAAGGATCAATCTTGTATATGTTAAGTGTGAATGTTTGGAATG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: