Search for Variation information by Variation ID:

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

Detailed information for vg1115925850:

Variant ID: vg1115925850 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 15925850
Reference Allele: AAlternative Allele: T
Primary Allele: ASecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GCAAAGCAAATCCAAAAGCAAAAGAAGACTCAACATTTTTGGTTGTTTCACTCACATATTCCAATGTCAAGCAATTAGCAAAATTGACGTCTTACAAAAC[A/T]
GTAATTTTAGAAAATAAAACTCCACAAGATTTACAATCATCATCATTAGGGTCCATAGATTTTAATCTATCAATTTCAGCTTTTAGAATTTCAATAGTGT

Reverse complement sequence

ACACTATTGAAATTCTAAAAGCTGAAATTGATAGATTAAAATCTATGGACCCTAATGATGATGATTGTAAATCTTGTGGAGTTTTATTTTCTAAAATTAC[T/A]
GTTTTGTAAGACGTCAATTTTGCTAATTGCTTGACATTGGAATATGTGAGTGAAACAACCAAAAATGTTGAGTCTTCTTTTGCTTTTGGATTTGCTTTGC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: