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Detailed information for vg1202046442:

Variant ID: vg1202046442 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 2046442
Reference Allele: GAlternative Allele: A
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


AGTAAAGTGTATTAGATTGAGAATTTTTCTTGGGATCCCCTTTACATGGCCCTAGGGGTCTATTTATATCCTTGTTACAGGCCCCCCTATTAGGGTTTAG[G/A]
TTTTACAGGGGAATTTACATGGTTGCCCTTGTGAAAGGGACATTTACATGGGTATACAGTGTCATTGGCATACATGGGCCTCTAATGGGCCTGGTTGGCG

Reverse complement sequence

CGCCAACCAGGCCCATTAGAGGCCCATGTATGCCAATGACACTGTATACCCATGTAAATGTCCCTTTCACAAGGGCAACCATGTAAATTCCCCTGTAAAA[C/T]
CTAAACCCTAATAGGGGGGCCTGTAACAAGGATATAAATAGACCCCTAGGGCCATGTAAAGGGGATCCCAAGAAAAATTCTCAATCTAATACACTTTACT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: