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Detailed information for vg1218129212:

Variant ID: vg1218129212 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 18129212
Reference Allele: TAlternative Allele: A
Primary Allele: ASecondary Allele: T

Inferred Ancestral Allele : A (evidence from allele frequency in Oryza rufipogon: A: 0.86, T: 0.14, others allele: 0.00, population size: 213. )

Flanking Sequence (100 bp) in Reference Genome:


TAGTGAAGGCTGTCTTGGAGATATCCTCTTCCCGAATCCTCAACTGGTGGTAGCCTGATCGCAGGTCTATTTTGGAAAACACCTTGGCTCCTTTCAGCTG[T/A]
TCGAACAGATCATCAATCCGCGGTAAAGGATATTTGTTCTTGATTGTGACCTCATTGAGTGCGCGATAATCGACACACATTCTCTTCGTCTTGTCCTTCT

Reverse complement sequence

AGAAGGACAAGACGAAGAGAATGTGTGTCGATTATCGCGCACTCAATGAGGTCACAATCAAGAACAAATATCCTTTACCGCGGATTGATGATCTGTTCGA[A/T]
CAGCTGAAAGGAGCCAAGGTGTTTTCCAAAATAGACCTGCGATCAGGCTACCACCAGTTGAGGATTCGGGAAGAGGATATCTCCAAGACAGCCTTCACTA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: