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Detailed information for vg1125047295:

Variant ID: vg1125047295 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 25047295
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.99, T: 0.01, others allele: 0.00, population size: 69. )

Flanking Sequence (100 bp) in Reference Genome:


TTTCTATCATTTCGCCAAGCACTCTATTTCGAGTGATTCCACGATCTGGGCTTCAAGATGAGAAAATTGCATATCTACCGTCGCATAAAACTGGCTTCGC[C/T]
AGAATACCATTACTCAAATAGGTTTCACTAGAATACCATCCTCAACCGAGTACAATTTGATACAATGCCATTTTCATCATTTTCGGCTAATAGAAAAGGT

Reverse complement sequence

ACCTTTTCTATTAGCCGAAAATGATGAAAATGGCATTGTATCAAATTGTACTCGGTTGAGGATGGTATTCTAGTGAAACCTATTTGAGTAATGGTATTCT[G/A]
GCGAAGCCAGTTTTATGCGACGGTAGATATGCAATTTTCTCATCTTGAAGCCCAGATCGTGGAATCACTCGAAATAGAGTGCTTGGCGAAATGATAGAAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: