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Detailed information for vg0827595612:

Variant ID: vg0827595612 (JBrowse)	Variation Type: SNP
Chromosome: chr08	Position: 27595612
Reference Allele: C	Alternative Allele: T
Primary Allele: C	Secondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:

CGGAAACCGAATCGGCCAGTCGGAATTTTTTCGGAATTTCTCGGAATCGGAATCGAAAACGGAAATATTTTCTCGGAAACGGAATCGAATATGATAATAG[C/T]
AGTTTCCGTCGGAACCCGGAAACGATCGGAAACATTCCAGAAAAATTGTCGGAATTTCCGAAGTTAAAAAGCCCATAGATTCAATAGTCCATAATTCATC

Reverse complement sequence

GATGAATTATGGACTATTGAATCTATGGGCTTTTTAACTTCGGAAATTCCGACAATTTTTCTGGAATGTTTCCGATCGTTTCCGGGTTCCGACGGAAACT[G/A]
CTATTATCATATTCGATTCCGTTTCCGAGAAAATATTTCCGTTTTCGATTCCGATTCCGAGAAATTCCGAAAAAATTCCGACTGGCCGATTCGGTTTCCG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: