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Detailed information for vg1214507607:

Variant ID: vg1214507607 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 14507607
Reference Allele: AAlternative Allele: G
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GTGTCCGCCCTCTCCTTCGCTCCAGCTTCAGCCTTTAGGGGTCCAGCCAGTGGCAATGGAGGTTGGTTGCCTGCTACTCCCAGTGGCAGCCGCGACCGCA[A/G]
CAGCAGTTCCAGCAGCTTAGAGCCGGGCAGTGGCGAGACGTACCTGCAGGACTCCAAGAGCCGCTCAGAGGGACCAGGAGACGAGCAGGAGGACGCCTTC

Reverse complement sequence

GAAGGCGTCCTCCTGCTCGTCTCCTGGTCCCTCTGAGCGGCTCTTGGAGTCCTGCAGGTACGTCTCGCCACTGCCCGGCTCTAAGCTGCTGGAACTGCTG[T/C]
TGCGGTCGCGGCTGCCACTGGGAGTAGCAGGCAACCAACCTCCATTGCCACTGGCTGGACCCCTAAAGGCTGAAGCTGGAGCGAAGGAGAGGGCGGACAC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: