Search for Variation information by Variation ID:

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

Detailed information for vg0221025908:

Variant ID: vg0221025908 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 21025908
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CGTTTAATATTTCAAATATGTGTCAGTATATACGATGTAACACGCCAAAATTTTACACCTATGAATCTAAACACCCCCTTAGTGTGCGTGAAGATTCTGA[C/T]
GCCAAAGTTGTTCGGCGACCCCATCAATTGTGGTACTTAATATTGTGGTTAATATTGTGGTTTATACGAAGTTCTCGGTTTCAAAGCAGTAAGAAAATTT

Reverse complement sequence

AAATTTTCTTACTGCTTTGAAACCGAGAACTTCGTATAAACCACAATATTAACCACAATATTAAGTACCACAATTGATGGGGTCGCCGAACAACTTTGGC[G/A]
TCAGAATCTTCACGCACACTAAGGGGGTGTTTAGATTCATAGGTGTAAAATTTTGGCGTGTTACATCGTATATACTGACACATATTTGAAATATTAAACG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: