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Detailed information for vg1218108461:

Variant ID: vg1218108461 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 18108461
Reference Allele: GAlternative Allele: A
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TTACGTTTTGTTTCTTTGTCCGGCCCACAGTATAGATGCGAAAGTATTCTTTTTTTTTAAAAAAAAATAACACATCTAATCTAATAGTCTAAAGTATTGG[G/A]
TCCACCAATTTAAATGAAAATCGACGGTGAGATTTAACAGTGCCATGTGGCGGTCTAGGAGTATTTATAGGAACGTCACGTGGCGGTTTGAGAGCGTTTC

Reverse complement sequence

GAAACGCTCTCAAACCGCCACGTGACGTTCCTATAAATACTCCTAGACCGCCACATGGCACTGTTAAATCTCACCGTCGATTTTCATTTAAATTGGTGGA[C/T]
CCAATACTTTAGACTATTAGATTAGATGTGTTATTTTTTTTTAAAAAAAAAGAATACTTTCGCATCTATACTGTGGGCCGGACAAAGAAACAAAACGTAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: