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Detailed information for vg1202108506:

Variant ID: vg1202108506 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 2108506
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GCTTGCTGTTTAAAGTGTTTTAATTCAGATCAGAACAATTGCAGTTTAAATTTCTATATAATAAAGCTTAGTTCCTGAGCATCTGTTTTTCTCCGTTTCC[C/T]
CGTCTGCCCTTCCTCCAGATGGTCTACACCAGAACTGGCACCCGCACGACTGGCGAGGGCAGCAACGGCGAAGAACGCGCTGATGGTGTGCACCCCAACA

Reverse complement sequence

TGTTGGGGTGCACACCATCAGCGCGTTCTTCGCCGTTGCTGCCCTCGCCAGTCGTGCGGGTGCCAGTTCTGGTGTAGACCATCTGGAGGAAGGGCAGACG[G/A]
GGAAACGGAGAAAAACAGATGCTCAGGAACTAAGCTTTATTATATAGAAATTTAAACTGCAATTGTTCTGATCTGAATTAAAACACTTTAAACAGCAAGC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: