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Detailed information for vg0815684621:

Variant ID: vg0815684621 (JBrowse)	Variation Type: SNP
Chromosome: chr08	Position: 15684621
Reference Allele: T	Alternative Allele: C
Primary Allele: C	Secondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:

AGACCGCTCTATTTTCCGTGCGGAGGGTCTCATCCAGGATCTCCGAACGCAGCTTAAGGCTGTGTTTGGAACCTTGGGATGGGAACTCATTCCCTCTGCA[T/C]
GGAAAACGGAGCGATCCATTAGAGCGCGATTAATTAAGTATTAGTTATTTTTTAAAAAAAATGGATTAATATAATTTTTTAAAGCAACTTTTGTATAAAA

Reverse complement sequence

TTTTATACAAAAGTTGCTTTAAAAAATTATATTAATCCATTTTTTTTAAAAAATAACTAATACTTAATTAATCGCGCTCTAATGGATCGCTCCGTTTTCC[A/G]
TGCAGAGGGAATGAGTTCCCATCCCAAGGTTCCAAACACAGCCTTAAGCTGCGTTCGGAGATCCTGGATGAGACCCTCCGCACGGAAAATAGAGCGGTCT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: