Search for Variation information by Variation ID:

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

Detailed information for vg0805548986:

Variant ID: vg0805548986 (JBrowse)Variation Type: SNP
Chromosome: chr08Position: 5548986
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.58, T: 0.42, others allele: 0.00, population size: 77. )

Flanking Sequence (100 bp) in Reference Genome:


TTAGTTTGTAGAATATAGTGGAATTGAAATAGAATAGAATCTTCAGTCCTCGGAGTCTTCGGAAGAATTCGGGTATGGCTCTAGTAGCTTTTCCTTCTTT[C/T]
GTAAGACTTGTACTTTTATTAGAATAATCTTCTTTATACTACTCTGATATTGTATTACTTTCCAAGTATATGAATACCAATTTTACTATATGTTCGAATT

Reverse complement sequence

AATTCGAACATATAGTAAAATTGGTATTCATATACTTGGAAAGTAATACAATATCAGAGTAGTATAAAGAAGATTATTCTAATAAAAGTACAAGTCTTAC[G/A]
AAAGAAGGAAAAGCTACTAGAGCCATACCCGAATTCTTCCGAAGACTCCGAGGACTGAAGATTCTATTCTATTTCAATTCCACTATATTCTACAAACTAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: