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Detailed information for vg1123670478:

Variant ID: vg1123670478 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 23670478
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


AAAGACTCTGTAGTTTTCTCATTTCATTAATGAAATGGGAGAGGTTTATCCTCTCCTTCTAAAAAAAGGGGTGATAATGGGTGATAAAAAGAATTGATCG[C/T]
GCTGCAGGTGCCCAAATGGGTGATAAAAAGAATTGATCGCTTTTGGAGATCCTTCCTTTGGAAAGGAGAAGACCCTGACAAAACCAACCCGGGCAGCAGT

Reverse complement sequence

ACTGCTGCCCGGGTTGGTTTTGTCAGGGTCTTCTCCTTTCCAAAGGAAGGATCTCCAAAAGCGATCAATTCTTTTTATCACCCATTTGGGCACCTGCAGC[G/A]
CGATCAATTCTTTTTATCACCCATTATCACCCCTTTTTTTAGAAGGAGAGGATAAACCTCTCCCATTTCATTAATGAAATGAGAAAACTACAGAGTCTTT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: