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Detailed information for vg1114869858:

Variant ID: vg1114869858 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 14869858
Reference Allele: TAlternative Allele: G,C
Primary Allele: TSecondary Allele: G

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 1.00, others allele: 0.00, population size: 117. )

Flanking Sequence (100 bp) in Reference Genome:


AGTCGTTGCTCCACAGAAAACTCTACCGACAAAGAAACCAGCCGTACCAACGCCACTGACCTTCAAGACAATGGCCAGCAAGACTCTTCGCGAGTTCGCT[T/G,C]
TTCCCTCTGCTGACAATGTGGCCGTCGAGCCACAAGTCAACATAGGAGATGTGGATTTCGATTTGAAGTCCAGCCTCATCATGATGGCGCAGGCTAGCCT

Reverse complement sequence

AGGCTAGCCTGCGCCATCATGATGAGGCTGGACTTCAAATCGAAATCCACATCTCCTATGTTGACTTGTGGCTCGACGGCCACATTGTCAGCAGAGGGAA[A/C,G]
AGCGAACTCGCGAAGAGTCTTGCTGGCCATTGTCTTGAAGGTCAGTGGCGTTGGTACGGCTGGTTTCTTTGTCGGTAGAGTTTTCTGTGGAGCAACGACT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: