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Detailed information for vg1016565386:

Variant ID: vg1016565386 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 16565386
Reference Allele: CAlternative Allele: A
Primary Allele: ASecondary Allele: C

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.73, A: 0.28, others allele: 0.00, population size: 204. )

Flanking Sequence (100 bp) in Reference Genome:


AGAGTCCCTTTTCGATCAATAGATACTCTGAAGGTGTTGATTGCTACATATCACTGTGAGCTACCATTCATGAAGGGCAAAATTTGCTACAGGACACGCA[C/A]
AAATCGTGTAATTAGCTGTAAGACACCAAAAAACGCGTCGCTGCCCACGGACACTACGAAAGTTGTGCAATTGGCTGTAGAACACTGGAGTTAATATTTT

Reverse complement sequence

AAAATATTAACTCCAGTGTTCTACAGCCAATTGCACAACTTTCGTAGTGTCCGTGGGCAGCGACGCGTTTTTTGGTGTCTTACAGCTAATTACACGATTT[G/T]
TGCGTGTCCTGTAGCAAATTTTGCCCTTCATGAATGGTAGCTCACAGTGATATGTAGCAATCAACACCTTCAGAGTATCTATTGATCGAAAAGGGACTCT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: