Search for Variation information by Variation ID:

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

Detailed information for vg0610556004:

Variant ID: vg0610556004 (JBrowse)Variation Type: SNP
Chromosome: chr06Position: 10556004
Reference Allele: TAlternative Allele: C
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 0.94, C: 0.06, others allele: 0.00, population size: 49. )

Flanking Sequence (100 bp) in Reference Genome:


AGAAATCCCACCAACCGTCGGCGGCTTTGCAACTATACTCCTATACACCCCGCTCGCTGCTTATCCTTTTTATTGTCATTGAGATTTTAAAAATTAAATA[T/C]
GATTATCAATGGGGTTTATTTTTTTACTTTATAGAAGTCTTGGCAACCGCCTTGCCCGTTTGCTTCACGGCCTACCTGTCGTCCATCTTTTTAATCGTCA

Reverse complement sequence

TGACGATTAAAAAGATGGACGACAGGTAGGCCGTGAAGCAAACGGGCAAGGCGGTTGCCAAGACTTCTATAAAGTAAAAAAATAAACCCCATTGATAATC[A/G]
TATTTAATTTTTAAAATCTCAATGACAATAAAAAGGATAAGCAGCGAGCGGGGTGTATAGGAGTATAGTTGCAAAGCCGCCGACGGTTGGTGGGATTTCT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: