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Detailed information for vg1000442554:

Variant ID: vg1000442554 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 442554
Reference Allele: AAlternative Allele: G
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


ATACATCCCAACACATGGAGCCGACATGTTATATATAACTAGAAAAAATATCTGTGCGTTGCAATGGGTGAAGGCTATTTTGATTTTATTATTGTTATAT[A/G]
GTTTAGTTAAGGTGAAAATCATGAACTACGATTAGGAGTATGATCATCTCAAGTTAGCATGCGAGTTTTTTTTTTAAAAAATATTTCTTATATGACTCCT

Reverse complement sequence

AGGAGTCATATAAGAAATATTTTTTAAAAAAAAAACTCGCATGCTAACTTGAGATGATCATACTCCTAATCGTAGTTCATGATTTTCACCTTAACTAAAC[T/C]
ATATAACAATAATAAAATCAAAATAGCCTTCACCCATTGCAACGCACAGATATTTTTTCTAGTTATATATAACATGTCGGCTCCATGTGTTGGGATGTAT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: