Search for Variation information by Variation ID:

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

Detailed information for vg1108715769:

Variant ID: vg1108715769 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 8715769
Reference Allele: CAlternative Allele: A
Primary Allele: CSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GATATCGTTTCATTGTTTATTCATGTGTAGGTGAGTCTTGATTCCTCCGAAGAGCAATGCCAGTGATGAATCGGGAGTCAACATAGGAGAAGATGGCATT[C/A]
AGAAGATCAGGATATCATGCAGGATGATTAGATTAAAGATTGTTGCACATGGTTGGTGAAGATTCCGTATGTCATACCTTGGAGATATTGTGTGTTTATG

Reverse complement sequence

CATAAACACACAATATCTCCAAGGTATGACATACGGAATCTTCACCAACCATGTGCAACAATCTTTAATCTAATCATCCTGCATGATATCCTGATCTTCT[G/T]
AATGCCATCTTCTCCTATGTTGACTCCCGATTCATCACTGGCATTGCTCTTCGGAGGAATCAAGACTCACCTACACATGAATAAACAATGAAACGATATC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: