Search for Variation information by Variation ID:

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

Detailed information for vg0325133506:

Variant ID: vg0325133506 (JBrowse)	Variation Type: SNP
Chromosome: chr03	Position: 25133506
Reference Allele: T	Alternative Allele: C
Primary Allele: T	Secondary Allele: C

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:

TAATATGATTTTTTAAAGCAACTTTTCTATAGAAATTGTTTGCAAAAAACACACCGTTTAGTAGTTCGGGAAGCGTGCGCGCAGAAAACAAAACTATCTT[T/C]
CTCTCTTTCTCCTGCGCTCGAACACAGGCTTAGGGTGTGTTTGAGAAGAAGGGGATTGAGGAGATTTGGAGATACGCAAAACGAGGTGAGCCATTAACTC

Reverse complement sequence

GAGTTAATGGCTCACCTCGTTTTGCGTATCTCCAAATCTCCTCAATCCCCTTCTTCTCAAACACACCCTAAGCCTGTGTTCGAGCGCAGGAGAAAGAGAG[A/G]
AAGATAGTTTTGTTTTCTGCGCGCACGCTTCCCGAACTACTAAACGGTGTGTTTTTTGCAAACAATTTCTATAGAAAAGTTGCTTTAAAAAATCATATTA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: