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Detailed information for vg1226987977:

Variant ID: vg1226987977 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 26987977
Reference Allele: GAlternative Allele: T
Primary Allele: GSecondary Allele: T

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.99, others allele: 0.00, population size: 295. )

Flanking Sequence (100 bp) in Reference Genome:


GGAATGATCTTGAGGTGCTTGTAGGATGGTGCTTTCAGTGAGAACTTTTCTTAGATGGATGTATATCTCTTCTTTATCAATGAAATGAGACAGAACTTCT[G/T]
CCTTTGTTTTTTTTTTAAAAAACTCTGGCTGTTAGGCTGGAGGGAATGAGGGAAAGACACAGGTAAGACAGTACAATCACCAAAAAAGTTAAAGGCACAA

Reverse complement sequence

TTGTGCCTTTAACTTTTTTGGTGATTGTACTGTCTTACCTGTGTCTTTCCCTCATTCCCTCCAGCCTAACAGCCAGAGTTTTTTAAAAAAAAAACAAAGG[C/A]
AGAAGTTCTGTCTCATTTCATTGATAAAGAAGAGATATACATCCATCTAAGAAAAGTTCTCACTGAAAGCACCATCCTACAAGCACCTCAAGATCATTCC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: