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Detailed information for vg0912484636:

Variant ID: vg0912484636 (JBrowse)Variation Type: SNP
Chromosome: chr09Position: 12484636
Reference Allele: TAlternative Allele: C
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


AGTCAGAGACGTTCGCCGAGGTGCCCGGCTACCCGGACAACGTCCGCCGCGATGACAGCCGCGGCGGGTACTGGGTGGCGCTCAGCCGCGAGGCCGACAG[T/C]
GATGACATGGCGCCGACGGTGGCTGTGAGGGTGGTGGCGCCGGCCGCGAAGAATGGTAGCGCGGCGGTGGTGGCGGAGGCGCTCGCCGGATTCAGCTTCG

Reverse complement sequence

CGAAGCTGAATCCGGCGAGCGCCTCCGCCACCACCGCCGCGCTACCATTCTTCGCGGCCGGCGCCACCACCCTCACAGCCACCGTCGGCGCCATGTCATC[A/G]
CTGTCGGCCTCGCGGCTGAGCGCCACCCAGTACCCGCCGCGGCTGTCATCGCGGCGGACGTTGTCCGGGTAGCCGGGCACCTCGGCGAACGTCTCTGACT

Allele Frequencies:

Allele Effect: