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Detailed information for vg0216956622:

Variant ID: vg0216956622 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 16956622
Reference Allele: AAlternative Allele: G
Primary Allele: ASecondary Allele: G

Inferred Ancestral Allele : A (evidence from allele frequency in Oryza rufipogon: A: 0.94, G: 0.06, others allele: 0.00, population size: 68. )

Flanking Sequence (100 bp) in Reference Genome:


GGTTTTATAAACTATAACACATATATGTACAATTTGTGAACAATGTTACTAATATTTTGTCAGATGAAGAAATAACAAAAAAAAGTTTTAGATCTTGATG[A/G]
GTTATACTATTTTGTTGTTGATGACTTTTTCAATTGAAATCATTTAGTATTTGAAAATATTGTTTGAAGTTGTCATATTTTCAAATTCAAATTCAAAATG

Reverse complement sequence

CATTTTGAATTTGAATTTGAAAATATGACAACTTCAAACAATATTTTCAAATACTAAATGATTTCAATTGAAAAAGTCATCAACAACAAAATAGTATAAC[T/C]
CATCAAGATCTAAAACTTTTTTTTGTTATTTCTTCATCTGACAAAATATTAGTAACATTGTTCACAAATTGTACATATATGTGTTATAGTTTATAAAACC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: