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Detailed information for vg0216273226:

Variant ID: vg0216273226 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 16273226
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CCTTCTATTCATACTTCTCTCCAAAATCCTTACCCACATATCTCGTTGAGTAGTCAAACTCAAACTCCCAAGTTACACTCTCTTTCTCTAAATTATCCAT[C/T]
CCCTTTTGACTCGTCTCCGAATATTGTTCCCTTCCTTGACTCCTCCCCCTCATCCATATTCCTCTTCCAATTCAAGTCTCCAAATCAAAAACCCCAATTC

Reverse complement sequence

GAATTGGGGTTTTTGATTTGGAGACTTGAATTGGAAGAGGAATATGGATGAGGGGGAGGAGTCAAGGAAGGGAACAATATTCGGAGACGAGTCAAAAGGG[G/A]
ATGGATAATTTAGAGAAAGAGAGTGTAACTTGGGAGTTTGAGTTTGACTACTCAACGAGATATGTGGGTAAGGATTTTGGAGAGAAGTATGAATAGAAGG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: