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Detailed information for vg1220129699:

Variant ID: vg1220129699 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 20129699
Reference Allele: TAlternative Allele: G
Primary Allele: TSecondary Allele: G

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


AGGAAGAGGTGTTGGAAGCGGGACGACGGGATTCGCATCGGATTGATGGAGGTTTTTCTCATCGGACCGGACAACGCCCTGTGGGGAATGTTGCTTTTAC[T/G]
CCTGGGCGAGCTGGTGGGCGAGTTGATGACAGAACTCAGCCTCTGGAGGATCGAGTGGCAGCACTACGTGCTTATCGCAAGGCTAAGGGATTGTGTCACA

Reverse complement sequence

TGTGACACAATCCCTTAGCCTTGCGATAAGCACGTAGTGCTGCCACTCGATCCTCCAGAGGCTGAGTTCTGTCATCAACTCGCCCACCAGCTCGCCCAGG[A/C]
GTAAAAGCAACATTCCCCACAGGGCGTTGTCCGGTCCGATGAGAAAAACCTCCATCAATCCGATGCGAATCCCGTCGTCCCGCTTCCAACACCTCTTCCT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: