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Detailed information for vg1209921454:

Variant ID: vg1209921454 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 9921454
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.98, T: 0.01, others allele: 0.00, population size: 245. )

Flanking Sequence (100 bp) in Reference Genome:


TCGTGATTTTCGGCACTTTCCAGAAATTTTGAAAGATTTTGACTGGATTTGAAAAAACTTTGACCAAATTCCACAAAAAATTGAGAAAACCCGAAAATTT[C/T]
GGTCAGTATATTGATTGCCGGTGGGGTCCGAAATTTCGAACCGAATTGTAAACACTGGTATATCCATTTAGAGATATAGAGGCCAGATTTCTATCCATTA

Reverse complement sequence

TAATGGATAGAAATCTGGCCTCTATATCTCTAAATGGATATACCAGTGTTTACAATTCGGTTCGAAATTTCGGACCCCACCGGCAATCAATATACTGACC[G/A]
AAATTTTCGGGTTTTCTCAATTTTTTGTGGAATTTGGTCAAAGTTTTTTCAAATCCAGTCAAAATCTTTCAAAATTTCTGGAAAGTGCCGAAAATCACGA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: