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Detailed information for vg1209049562:

Variant ID: vg1209049562 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 9049562
Reference Allele: AAlternative Allele: G
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele : A (evidence from allele frequency in Oryza rufipogon: A: 0.67, G: 0.33, others allele: 0.00, population size: 61. )

Flanking Sequence (100 bp) in Reference Genome:


GTTATCGACATCGGTTCTTCCGAACCGTTAGTCCTGCACCTACTTGAGGACTACGACTCCTCGTCGACAAGTACGCGACGTGAGGTATTGGCTATCGACG[A/G]
GACAGGCACATTGGCACGCGCTAACACCGGGGCGGAAAATATGACGTCTACACCGGCTCAGCACATCAGGACCCTCAACGCAATACTGAGGGAGACCCCT

Reverse complement sequence

AGGGGTCTCCCTCAGTATTGCGTTGAGGGTCCTGATGTGCTGAGCCGGTGTAGACGTCATATTTTCCGCCCCGGTGTTAGCGCGTGCCAATGTGCCTGTC[T/C]
CGTCGATAGCCAATACCTCACGTCGCGTACTTGTCGACGAGGAGTCGTAGTCCTCAAGTAGGTGCAGGACTAACGGTTCGGAAGAACCGATGTCGATAAC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: