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Detailed information for vg1207672832:

Variant ID: vg1207672832 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 7672832
Reference Allele: GAlternative Allele: A
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 1.01, others allele: 0.00, population size: 268. )

Flanking Sequence (100 bp) in Reference Genome:


CAAATTTTAGAATTATTTTTTTGGACTTTGGAACCCAAGAATTTTCTTGCGCAAACTAGAATGAGAGAGAAAGTGAAGCAGGGAGAGAGTGAGTAGACCA[G/A]
TCTTAATGAGATAAGAATAATGCATCAATAGAGGATGATAGGAGTCGTATTGAGTCTAGCTAGACCTTGCTTTATTGTCGCCATAGGGCATATGGAGTAG

Reverse complement sequence

CTACTCCATATGCCCTATGGCGACAATAAAGCAAGGTCTAGCTAGACTCAATACGACTCCTATCATCCTCTATTGATGCATTATTCTTATCTCATTAAGA[C/T]
TGGTCTACTCACTCTCTCCCTGCTTCACTTTCTCTCTCATTCTAGTTTGCGCAAGAAAATTCTTGGGTTCCAAAGTCCAAAAAAATAATTCTAAAATTTG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: