Search for Variation information by Variation ID:

Please input a variation ID (e.g., vg0722097923 , STR0500036000 ).

Detailed information for vg0105166793:

Variant ID: vg0105166793 (JBrowse)Variation Type: SNP
Chromosome: chr01Position: 5166793
Reference Allele: CAlternative Allele: A
Primary Allele: ASecondary Allele: C

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


AAAGGCGAGACGGCGGCGGCGGAAGCCGGCGACGAGACGAAGCGAGAGGACCTAGTAGAGATCGAGGTGACGACGACGAGCGGCGGCAGCGGAGCGGCGG[C/A]
TGCGGCGGCGACAGGAGGAGATCAAGAGACTTGTTGCACGCTCAACGTGGACTTGCGCGGCGGCGGCGGCGGAGGCATGAGCACGACGGACGTTGTGCTC

Reverse complement sequence

GAGCACAACGTCCGTCGTGCTCATGCCTCCGCCGCCGCCGCCGCGCAAGTCCACGTTGAGCGTGCAACAAGTCTCTTGATCTCCTCCTGTCGCCGCCGCA[G/T]
CCGCCGCTCCGCTGCCGCCGCTCGTCGTCGTCACCTCGATCTCTACTAGGTCCTCTCGCTTCGTCTCGTCGCCGGCTTCCGCCGCCGCCGTCTCGCCTTT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: