Search for Variation information by Variation ID:

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

Detailed information for vg0218086395:

Variant ID: vg0218086395 (JBrowse)	Variation Type: SNP
Chromosome: chr02	Position: 18086395
Reference Allele: C	Alternative Allele: T
Primary Allele: C	Secondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:

GGCACCTCCGATTTGTATATAATCACCAAAATAAATTCACTATAAATTTTGGCATGACCTCCCCTCTTTTTTGAAGAAATTTTGAAGCTTGCTCGGGCAG[C/T]
TGGAGGAGGAAGAAGACATATATATAGGGGTGGGACTTTAGTCCCGGTTGACTAAAGTTACGATCTTTAGTCCCGGTTGGTGTGATCCCGGGGGGCTTGA

Reverse complement sequence

TCAAGCCCCCCGGGATCACACCAACCGGGACTAAAGATCGTAACTTTAGTCAACCGGGACTAAAGTCCCACCCCTATATATATGTCTTCTTCCTCCTCCA[G/A]
CTGCCCGAGCAAGCTTCAAAATTTCTTCAAAAAAGAGGGGAGGTCATGCCAAAATTTATAGTGAATTTATTTTGGTGATTATATACAAATCGGAGGTGCC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: