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Detailed information for vg1016820034:

Variant ID: vg1016820034 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 16820034
Reference Allele: GAlternative Allele: A
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CGTGGTGTTCCCCATCCCGGAGACGTCGCACCGGCAAGTGCACCACGTGACGAGCAAGGCGATCAGGCTGGGATCGGGCGGAGACGGCACGGTAGGGTGG[G/A]
TGGACATCTGGCGCGGCATCCTCCTCTGCGACGTGCTCCACGAGAGCCCCAAGCTCCGCGACGTGCCGCTGCCGCCGCCGGCGAAGGGGAACAGCCACAG

Reverse complement sequence

CTGTGGCTGTTCCCCTTCGCCGGCGGCGGCAGCGGCACGTCGCGGAGCTTGGGGCTCTCGTGGAGCACGTCGCAGAGGAGGATGCCGCGCCAGATGTCCA[C/T]
CCACCCTACCGTGCCGTCTCCGCCCGATCCCAGCCTGATCGCCTTGCTCGTCACGTGGTGCACTTGCCGGTGCGACGTCTCCGGGATGGGGAACACCACG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: