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Detailed information for vg1122446629:

Variant ID: vg1122446629 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 22446629
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GCTATCCATTGCTTCGCTTTCTTACCATCAATCTATCTATCTATTATCTACTCTATTATACCCTAAAAGAACATTAAATTTCCTACAAACGCTCTCATGC[C/T]
GCCATATGGTGCTCTAAAAAGCTCTCAAGCTGCCACAAGGCGCTATAATAAAATAGAAAAAAACTTAAAATTTCTGAGAAAAAAGAAAAAAAATATATCC

Reverse complement sequence

GGATATATTTTTTTTCTTTTTTCTCAGAAATTTTAAGTTTTTTTCTATTTTATTATAGCGCCTTGTGGCAGCTTGAGAGCTTTTTAGAGCACCATATGGC[G/A]
GCATGAGAGCGTTTGTAGGAAATTTAATGTTCTTTTAGGGTATAATAGAGTAGATAATAGATAGATAGATTGATGGTAAGAAAGCGAAGCAATGGATAGC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: