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Detailed information for vg1007906158:

Variant ID: vg1007906158 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 7906158
Reference Allele: GAlternative Allele: A
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CGAGGATTAGGCTTCATCCGAGCCGTCGAGGATGCCTGTGGAGTGGTGTTCCCATTGCAGTCCAAGTCAAGGCTTAGCTCCAGTTATCTTTTAATTTTCC[G/A]
CTGCATTTGTGTAATGTCACGCCCAGAAATTCACTAGTAATTTCCGAACTTATTTGTGCATTAAATCCTCGTCCAGGAATCAGCCGAGGTACACAAACTG

Reverse complement sequence

CAGTTTGTGTACCTCGGCTGATTCCTGGACGAGGATTTAATGCACAAATAAGTTCGGAAATTACTAGTGAATTTCTGGGCGTGACATTACACAAATGCAG[C/T]
GGAAAATTAAAAGATAACTGGAGCTAAGCCTTGACTTGGACTGCAATGGGAACACCACTCCACAGGCATCCTCGACGGCTCGGATGAAGCCTAATCCTCG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: