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Detailed information for vg1100922069:

Variant ID: vg1100922069 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 922069
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CGGTCTGACACAATCTTTTTGGGGCAGCCAAATCTACATACGACATGGGTCATGTAGAGTTCTGCTAGCTTCTTTCCATCAAAGGTGGTTTTCACTGGCA[C/T]
GAAATGAGCTGATTTCGTGAGTCGATCCACGATTACCTAGATGGAGTCGTACCCGCTAGGGGTTGTTGGCAAGCCGGTGATGAAATCCATTCCGATCTCT

Reverse complement sequence

AGAGATCGGAATGGATTTCATCACCGGCTTGCCAACAACCCCTAGCGGGTACGACTCCATCTAGGTAATCGTGGATCGACTCACGAAATCAGCTCATTTC[G/A]
TGCCAGTGAAAACCACCTTTGATGGAAAGAAGCTAGCAGAACTCTACATGACCCATGTCGTATGTAGATTTGGCTGCCCCAAAAAGATTGTGTCAGACCG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: