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Detailed information for vg1004777607:

Variant ID: vg1004777607 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 4777607
Reference Allele: GAlternative Allele: A
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 1.00, others allele: 0.00, population size: 250. )

Flanking Sequence (100 bp) in Reference Genome:


ATCATAAAAGTAATTTGTGATTTTTCATCAAAATATAATCATGTGAGATCTTGTTGTAAAGATTTAATTGTTACGAACACAATGGTATAATCGGATCGTA[G/A]
ATCAGATGAGTAGTTTAAGAGAAAATTTCATAAGAAGAAAAAAAATATGCACAACCTAATAGCAAAAACTACTTGCATGCATGTCTGTCACGCTACTAGT

Reverse complement sequence

ACTAGTAGCGTGACAGACATGCATGCAAGTAGTTTTTGCTATTAGGTTGTGCATATTTTTTTTCTTCTTATGAAATTTTCTCTTAAACTACTCATCTGAT[C/T]
TACGATCCGATTATACCATTGTGTTCGTAACAATTAAATCTTTACAACAAGATCTCACATGATTATATTTTGATGAAAAATCACAAATTACTTTTATGAT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: