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Detailed information for vg1000453123:

Variant ID: vg1000453123 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 453123
Reference Allele: CAlternative Allele: T,A
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


AATCACTAGAAATAATGGCTGCGTTGTAACGGGTAAATATTATTTTAATCTTATTATTGTTATACAGTTTAATTAAGGTGAAATTCAATATGAGAATTCG[C/T,A]
TTGGATATATATATATATTTTTTGAAAATCATGAACTGCAATTAGAATTTCGATCATCTCAAGTTAGCATGCAAAATTTTTTAAAGAGATTTCTTATATG

Reverse complement sequence

CATATAAGAAATCTCTTTAAAAAATTTTGCATGCTAACTTGAGATGATCGAAATTCTAATTGCAGTTCATGATTTTCAAAAAATATATATATATATCCAA[G/A,T]
CGAATTCTCATATTGAATTTCACCTTAATTAAACTGTATAACAATAATAAGATTAAAATAATATTTACCCGTTACAACGCAGCCATTATTTCTAGTGATT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: