Search for Variation information by Variation ID:

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

Detailed information for vg1001361549:

Variant ID: vg1001361549 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 1361549
Reference Allele: GAlternative Allele: A
Primary Allele: ASecondary Allele: G

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GGAGAGATCTGTTTTTCTACTTTCTATTTTTAGTTTAGGAAACCTAAAAACAAATTTTGGGGGAGATTATATGTTAGAGCATCACCGATAGATTACGTAC[G/A]
ATCTCTCTCCAAAAATTTGTTTTTTGTTTTTCTAAACTAAAAATAGGAAGTAAATAAACTGATCTCCCAAAGAGGAAGTCTAAATTTTTATGTAAAAAAA

Reverse complement sequence

TTTTTTTACATAAAAATTTAGACTTCCTCTTTGGGAGATCAGTTTATTTACTTCCTATTTTTAGTTTAGAAAAACAAAAAACAAATTTTTGGAGAGAGAT[C/T]
GTACGTAATCTATCGGTGATGCTCTAACATATAATCTCCCCCAAAATTTGTTTTTAGGTTTCCTAAACTAAAAATAGAAAGTAGAAAAACAGATCTCTCC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: