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Detailed information for vg1217896822:

Variant ID: vg1217896822 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 17896822
Reference Allele: GAlternative Allele: A,T
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.92, A: 0.08, others allele: 0.00, population size: 89. )

Flanking Sequence (100 bp) in Reference Genome:


TTAGTTCACACTAAAATTAAAAGTTTGGTTGAAATTGGAACGATGTGACGAAAAAGTTGGAAGATTGTGTGTAAGAAAGTTTTGATGTGATGAAAAAGTT[G/A,T]
GAAGTTTGAATAATTATTTTGAAACTAAACACGGCCCTATATATGGTGTCCTTTTTTCTAGACTATCTATTTATGTTGAATTCTTAACCATAAGTCCATT

Reverse complement sequence

AATGGACTTATGGTTAAGAATTCAACATAAATAGATAGTCTAGAAAAAAGGACACCATATATAGGGCCGTGTTTAGTTTCAAAATAATTATTCAAACTTC[C/T,A]
AACTTTTTCATCACATCAAAACTTTCTTACACACAATCTTCCAACTTTTTCGTCACATCGTTCCAATTTCAACCAAACTTTTAATTTTAGTGTGAACTAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: