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Detailed information for vg1207827697:

Variant ID: vg1207827697 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 7827697
Reference Allele: GAlternative Allele: C
Primary Allele: CSecondary Allele: G

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.99, C: 0.01, others allele: 0.00, population size: 105. )

Flanking Sequence (100 bp) in Reference Genome:


AAGTAGTAGAATCACCATGCCAATCCACCGGTAATCCTGACTTGAGTGTTTTCCTTTTCACAGCTTCACCATGAGCCATCCAACGAGCCTACGCCAGACC[G/C]
GCCACCTTTAAGAGACTATGCTATCTCTGTAAATTCTTCTTCTGGACTCCACTTGCAATAGTGCTCCACTTTCTCTCCTATTATTACAGTCATCTTGCAA

Reverse complement sequence

TTGCAAGATGACTGTAATAATAGGAGAGAAAGTGGAGCACTATTGCAAGTGGAGTCCAGAAGAAGAATTTACAGAGATAGCATAGTCTCTTAAAGGTGGC[C/G]
GGTCTGGCGTAGGCTCGTTGGATGGCTCATGGTGAAGCTGTGAAAAGGAAAACACTCAAGTCAGGATTACCGGTGGATTGGCATGGTGATTCTACTACTT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: