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Detailed information for vg0209217731:

Variant ID: vg0209217731 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 9217731
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


ATTAATTATTCTGTACAATAATTAATAGAAACATAGTGAAAAAACCAAACCTAGATCTTCATCTTGCTGAACTCTTTTTGTCCATTGTGCAAGTTTCTTC[C/T]
GGTTCATTCGCATTTTCCTTGGTTGGCTACCCCTAGGATCCACAAAATCAAGGCCGGAAATCTGTCTCACAAATTTCGTGACCAAACCTGAAAACCCTTC

Reverse complement sequence

GAAGGGTTTTCAGGTTTGGTCACGAAATTTGTGAGACAGATTTCCGGCCTTGATTTTGTGGATCCTAGGGGTAGCCAACCAAGGAAAATGCGAATGAACC[G/A]
GAAGAAACTTGCACAATGGACAAAAAGAGTTCAGCAAGATGAAGATCTAGGTTTGGTTTTTTCACTATGTTTCTATTAATTATTGTACAGAATAATTAAT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: