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Detailed information for vg1008204929:

Variant ID: vg1008204929 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 8204929
Reference Allele: GAlternative Allele: A
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CGTCTTTCGACGTATGCGGTTGTCATTTCGACAACAGCTAGCGCCGACCGTTGGGACCTCCGAGCGAAACCACTGAGAGCGAATGCCACCGAAGAGGGTC[G/A]
TGAAGGAGAAGGTTGCCAGGCGGAGGGAGAGCGACGCCGGACTGGACATGGCTGCCGAGGAAGGAGCAGAGCCTTCGGCGCCCGTGGCCGAAGATGGAGG

Reverse complement sequence

CCTCCATCTTCGGCCACGGGCGCCGAAGGCTCTGCTCCTTCCTCGGCAGCCATGTCCAGTCCGGCGTCGCTCTCCCTCCGCCTGGCAACCTTCTCCTTCA[C/T]
GACCCTCTTCGGTGGCATTCGCTCTCAGTGGTTTCGCTCGGAGGTCCCAACGGTCGGCGCTAGCTGTTGTCGAAATGACAACCGCATACGTCGAAAGACG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: