Search for Variation information by Variation ID:

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

Detailed information for vg1013103415:

Variant ID: vg1013103415 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 13103415
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: 0.06, others allele: 0.00, population size: 113. )

Flanking Sequence (100 bp) in Reference Genome:


ATAAACGGGGTAGCGCACGAGATTTAAAAGTGGATGGATGCGGAGACAATAAATTTTAGACAGTTCAGACCCTCTCAATGAGAGACAATACCCTAATCTT[G/A]
TTTGAGGATTTGAATCCGCCGGGTTGTGTATTGATCTAACGATCTGAGTTGTAATTCTATATGCTCATGCCCCTTAGAGGGGGCTCCCTGCCCACCTTAT

Reverse complement sequence

ATAAGGTGGGCAGGGAGCCCCCTCTAAGGGGCATGAGCATATAGAATTACAACTCAGATCGTTAGATCAATACACAACCCGGCGGATTCAAATCCTCAAA[C/T]
AAGATTAGGGTATTGTCTCTCATTGAGAGGGTCTGAACTGTCTAAAATTTATTGTCTCCGCATCCATCCACTTTTAAATCTCGTGCGCTACCCCGTTTAT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: