Search for Variation information by Variation ID:

Please input a variation ID (e.g., vg0722097923 , STR0500036000 ).

Detailed information for vg0913746747:

Variant ID: vg0913746747 (JBrowse)	Variation Type: SNP
Chromosome: chr09	Position: 13746747
Reference Allele: T	Alternative Allele: A
Primary Allele: T	Secondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:

CCGAAGTTTCGCCCGATTGAGATATGGTCGCATAGCCATGATATATCGGCATAAAAATAAAGCCCGTCACGGATGACACTTACCTGTGACGGGCTATAGT[T/A]
GAGGCCCGATTGAGATGAGGGTTCCATATCTCAATCGGGCCCTAAAAGAAGCCCGTCACAGATGAGTGTCATCTGTGACGGGCTCCAACTAGAGGCCCGA

Reverse complement sequence

TCGGGCCTCTAGTTGGAGCCCGTCACAGATGACACTCATCTGTGACGGGCTTCTTTTAGGGCCCGATTGAGATATGGAACCCTCATCTCAATCGGGCCTC[A/T]
ACTATAGCCCGTCACAGGTAAGTGTCATCCGTGACGGGCTTTATTTTTATGCCGATATATCATGGCTATGCGACCATATCTCAATCGGGCGAAACTTCGG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: