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Detailed information for vg0901033665:

Variant ID: vg0901033665 (JBrowse)Variation Type: SNP
Chromosome: chr09Position: 1033665
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TGACATGTCATTCACAGTTAGCATAGGGCAGCGCGATGGAGTACTCACCTGAGGACGGTCGGTAGGGCTCGGTGGCGGCGGCGCTGGGCTCGGTGGAGGG[C/T]
GTCGCTGGTCGGTGGAGGTGGCGTTGGGCTCGGTGGAGGCAGCGGTCTCGGTGGCGGCGGTGGCGGGCTCGGCAACGGAGGAGTTTGCGGCGGCAGCGCC

Reverse complement sequence

GGCGCTGCCGCCGCAAACTCCTCCGTTGCCGAGCCCGCCACCGCCGCCACCGAGACCGCTGCCTCCACCGAGCCCAACGCCACCTCCACCGACCAGCGAC[G/A]
CCCTCCACCGAGCCCAGCGCCGCCGCCACCGAGCCCTACCGACCGTCCTCAGGTGAGTACTCCATCGCGCTGCCCTATGCTAACTGTGAATGACATGTCA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: