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Detailed information for vg1000645768:

Variant ID: vg1000645768 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 645768
Reference Allele: AAlternative Allele: G
Primary Allele: ASecondary Allele: G

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.68, A: 0.32, others allele: 0.00, population size: 97. )

Flanking Sequence (100 bp) in Reference Genome:


TTTACAACAATTACGGCAATAGATCGGCGGTGACGGTTGTCCGCACGTACTTTCTCCTCACTATTGTTCCTTCCTTGTGATCGCTACGTGAGTAAGGGGT[A/G]
TCTTCGTTTGATAGGAGGATGCTAGGGTCAACCGTCACCGTGAAAGGGGGTTGCCCATCAAACTGATCGTAATCCTCGTCAGTCTTGTCGTCTACTCCAA

Reverse complement sequence

TTGGAGTAGACGACAAGACTGACGAGGATTACGATCAGTTTGATGGGCAACCCCCTTTCACGGTGACGGTTGACCCTAGCATCCTCCTATCAAACGAAGA[T/C]
ACCCCTTACTCACGTAGCGATCACAAGGAAGGAACAATAGTGAGGAGAAAGTACGTGCGGACAACCGTCACCGCCGATCTATTGCCGTAATTGTTGTAAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: