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Detailed information for vg0137169061:

Variant ID: vg0137169061 (JBrowse)Variation Type: SNP
Chromosome: chr01Position: 37169061
Reference Allele: AAlternative Allele: G
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


ACTGAGAAAATTTTTCCATGAATTATTTTGGTCTGAAGGAGTACTGGGCTTATATCAGTTAGTCATACATTGACAAGAAGAAATAATTTGAGAGAATTCA[A/G]
TTAAAGTTAATCAAGCTGAAATTAAGTTATAAAGATAATCATTTATGATTCAGCTGACAGAAGCTTGAGATTGGCTCAAATCTGGATGCATATAGATTTG

Reverse complement sequence

CAAATCTATATGCATCCAGATTTGAGCCAATCTCAAGCTTCTGTCAGCTGAATCATAAATGATTATCTTTATAACTTAATTTCAGCTTGATTAACTTTAA[T/C]
TGAATTCTCTCAAATTATTTCTTCTTGTCAATGTATGACTAACTGATATAAGCCCAGTACTCCTTCAGACCAAAATAATTCATGGAAAAATTTTCTCAGT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: