Search for Variation information by Variation ID:

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

Detailed information for vg1000740409:

Variant ID: vg1000740409 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 740409
Reference Allele: TAlternative Allele: C
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.84, T: 0.16, others allele: 0.00, population size: 93. )

Flanking Sequence (100 bp) in Reference Genome:


TCAGACCACTTCATCTTGGGTGCAGCCCCCTGCCATGTCGAACAAACCTCACGTTCCACTTTTTTGTATTCTCGCTTTGAAGAGTACACTATGGAGCCTC[T/C]
GAAGATGTGCGAGACATGAAGATCGGAATCTGGGTATGTGAAGTCCGAATCCTGAGTGGTTGCCTCAGTGGCCTTCTCGACTACACGTACTTGCTTGCCC

Reverse complement sequence

GGGCAAGCAAGTACGTGTAGTCGAGAAGGCCACTGAGGCAACCACTCAGGATTCGGACTTCACATACCCAGATTCCGATCTTCATGTCTCGCACATCTTC[A/G]
GAGGCTCCATAGTGTACTCTTCAAAGCGAGAATACAAAAAAGTGGAACGTGAGGTTTGTTCGACATGGCAGGGGGCTGCACCCAAGATGAAGTGGTCTGA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: