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Detailed information for vg1203660130:

Variant ID: vg1203660130 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 3660130
Reference Allele: AAlternative Allele: G
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


AGTGATGTGTGTGCTCACAATCAATTTTTGGAAGCATTTTCTCCTTGGCCGTGTGTTCTGGAAATTTTCGGAAATTTCGAAAAGGATTTTCGGAAGTTCC[A/G]
AAAATTCACATAACTAAAATTTCACTTCTGGATATTTTTGGAAGTTTCCGAAAATAATTTTCGAAAGTTCCGAAAATTTGCAAAAGGTTGTTTTGGGTTC

Reverse complement sequence

GAACCCAAAACAACCTTTTGCAAATTTTCGGAACTTTCGAAAATTATTTTCGGAAACTTCCAAAAATATCCAGAAGTGAAATTTTAGTTATGTGAATTTT[T/C]
GGAACTTCCGAAAATCCTTTTCGAAATTTCCGAAAATTTCCAGAACACACGGCCAAGGAGAAAATGCTTCCAAAAATTGATTGTGAGCACACACATCACT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: