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Detailed information for vg1110064581:

Variant ID: vg1110064581 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 10064581
Reference Allele: CAlternative Allele: A
Primary Allele: CSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TTGTTATGCATCTTTAGTCTGGTTATTTCAACCGGGACTAAAGATGAGATTATGCGTCCCAGTTGCACAACCGAGACTAAAAACGGTTGCGAACCCTTCT[C/A]
CAGCAATGGTGGTGGATCCGCCGGTAGTTTCGAGTTATGACAACGACAAATTCTAGTGTTTTTGGATTCTTTTTGTTCTTTTTCAAAATTATGTTTTCAG

Reverse complement sequence

CTGAAAACATAATTTTGAAAAAGAACAAAAAGAATCCAAAAACACTAGAATTTGTCGTTGTCATAACTCGAAACTACCGGCGGATCCACCACCATTGCTG[G/T]
AGAAGGGTTCGCAACCGTTTTTAGTCTCGGTTGTGCAACTGGGACGCATAATCTCATCTTTAGTCCCGGTTGAAATAACCAGACTAAAGATGCATAACAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: