Search for Variation information by Variation ID:

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

Detailed information for vg0910031361:

Variant ID: vg0910031361 (JBrowse)Variation Type: SNP
Chromosome: chr09Position: 10031361
Reference Allele: AAlternative Allele: C,T
Primary Allele: ASecondary Allele: C

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.66, A: 0.34, others allele: 0.00, population size: 74. )

Flanking Sequence (100 bp) in Reference Genome:


GAAGAACTATATTTTTTGGGAGTTACCATATTGGGAATTTTTGGACGTCCGCCACGCAATCGACGTGATGCACCTCACTAAGAACCTTTGCGTAAATCTG[A/C,T]
TGGGCTTTTAAGGTGTATATGGGAAGTCGAAAGATACACTGGAAGCACGTAATGATATGAAGCATATGGAACAACGCGGCGACCTTCACCTAGAACCAAA

Reverse complement sequence

TTTGGTTCTAGGTGAAGGTCGCCGCGTTGTTCCATATGCTTCATATCATTACGTGCTTCCAGTGTATCTTTCGACTTCCCATATACACCTTAAAAGCCCA[T/G,A]
CAGATTTACGCAAAGGTTCTTAGTGAGGTGCATCACGTCGATTGCGTGGCGGACGTCCAAAAATTCCCAATATGGTAACTCCCAAAAAATATAGTTCTTC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: