Search for Variation information by Variation ID:

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

Detailed information for vg0810860589:

Variant ID: vg0810860589 (JBrowse)Variation Type: SNP
Chromosome: chr08Position: 10860589
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 1.00, others allele: 0.00, population size: 281. )

Flanking Sequence (100 bp) in Reference Genome:


ATGTTGAACCATTAAAACACCTTGTCAATGTATGTACTCTGGCTTAATCCAATTAGCCTCTTTGATGTATCTCTATAGATCCTTATGCCCAGAATATATG[C/T]
TGTTTCCCCTAAGTCCTTCATTGAAAAACTATTTTTCAACGATGTCTTAACGGATTCAAGCATAGGAATATCGTTCCCAATCAATAATATGTCATCTACA

Reverse complement sequence

TGTAGATGACATATTATTGATTGGGAACGATATTCCTATGCTTGAATCCGTTAAGACATCGTTGAAAAATAGTTTTTCAATGAAGGACTTAGGGGAAACA[G/A]
CATATATTCTGGGCATAAGGATCTATAGAGATACATCAAAGAGGCTAATTGGATTAAGCCAGAGTACATACATTGACAAGGTGTTTTAATGGTTCAACAT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: