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Detailed information for vg0142134296:

Variant ID: vg0142134296 (JBrowse)Variation Type: SNP
Chromosome: chr01Position: 42134296
Reference Allele: CAlternative Allele: A,T
Primary Allele: CSecondary Allele: A

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.85, A: 0.13, T: 0.03, others allele: 0.00, population size: 78. )

Flanking Sequence (100 bp) in Reference Genome:


CGTGACTGTAAGTACTGAACTACTCACATCCATTGCGTTTTGACAAATTGACCCTTTTCAAAAACTTATTTCGAAACTAACCTCTGCCAAAAACTTCAAC[C/A,T]
AAAAATAAGCCGTCGGCTCAGCGCCAAGGGTCTTGGCGCTGATGTTGTGCATGAAAGCGCCAACATGCTTGGCGCTGACATTGTGCCACCGTGGCGGCCG

Reverse complement sequence

CGGCCGCCACGGTGGCACAATGTCAGCGCCAAGCATGTTGGCGCTTTCATGCACAACATCAGCGCCAAGACCCTTGGCGCTGAGCCGACGGCTTATTTTT[G/T,A]
GTTGAAGTTTTTGGCAGAGGTTAGTTTCGAAATAAGTTTTTGAAAAGGGTCAATTTGTCAAAACGCAATGGATGTGAGTAGTTCAGTACTTACAGTCACG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: