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Detailed information for vg1003133816:

Variant ID: vg1003133816 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 3133816
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 0.73, C: 0.28, others allele: 0.00, population size: 82. )

Flanking Sequence (100 bp) in Reference Genome:


TACTCTCCCTCCTCTCTATCCATGCATGGATGCATGAATTCAAAATGAATTTTCTCCTAAACTACTTATCTAATATACTATCCGATAACACTCTTATATT[C/T]
GTTGTAATTAAATCTTCACGACAAGATATGGCGTGATTATGTTCTGATGTAAAAAAACATATGTTTTAGTCCGTTAATACTTAATGTTTCATAGCAACAT

Reverse complement sequence

ATGTTGCTATGAAACATTAAGTATTAACGGACTAAAACATATGTTTTTTTACATCAGAACATAATCACGCCATATCTTGTCGTGAAGATTTAATTACAAC[G/A]
AATATAAGAGTGTTATCGGATAGTATATTAGATAAGTAGTTTAGGAGAAAATTCATTTTGAATTCATGCATCCATGCATGGATAGAGAGGAGGGAGAGTA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: