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Detailed information for vg1220336226:

Variant ID: vg1220336226 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 20336226
Reference Allele: TAlternative Allele: C
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 0.98, others allele: 0.00, population size: 68. )

Flanking Sequence (100 bp) in Reference Genome:


TTTGAGCATGCATTGATTCCTATCCCTTGTCTACCTTAGAAGTCAGACCTGTTCTTCGATCGCAAGCGCTGCTCCGAGCTTTAGAGTCGCCACCCTTAGC[T/C]
TTATCGTCTTCTTAGTCTGTTTGCTTGCTAGTTTTTGTATTTAGGTTTGTTGCTTGTGGGTTAGTCGGCGGTCGATTTCATGTGTGAGTGGTATGACAGC

Reverse complement sequence

GCTGTCATACCACTCACACATGAAATCGACCGCCGACTAACCCACAAGCAACAAACCTAAATACAAAAACTAGCAAGCAAACAGACTAAGAAGACGATAA[A/G]
GCTAAGGGTGGCGACTCTAAAGCTCGGAGCAGCGCTTGCGATCGAAGAACAGGTCTGACTTCTAAGGTAGACAAGGGATAGGAATCAATGCATGCTCAAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: