Search for Variation information by Variation ID:

Please input a variation ID (e.g., vg0722097923 , STR0500036000 ).

Detailed information for vg1114456299:

Variant ID: vg1114456299 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 14456299
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GAGCAAACTAGGGTTTTTTTGCGGGAGCGGAGAAGACGAGGGGCGCTTGAAGGCTAGAAAGTTTTGCGGCAAACGGACTTCAAAATGGATCCCCAAAACC[C/T]
CTTTAAATAAGCGCACTACCGACAGTGCGAATTCCAAGGAAAGGAGAGAGATGGCCGCCAGAAATTTCTGGGTCCGTTACGCGCAGCAGTTTTGGGACTT

Reverse complement sequence

AAGTCCCAAAACTGCTGCGCGTAACGGACCCAGAAATTTCTGGCGGCCATCTCTCTCCTTTCCTTGGAATTCGCACTGTCGGTAGTGCGCTTATTTAAAG[G/A]
GGTTTTGGGGATCCATTTTGAAGTCCGTTTGCCGCAAAACTTTCTAGCCTTCAAGCGCCCCTCGTCTTCTCCGCTCCCGCAAAAAAACCCTAGTTTGCTC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: