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Detailed information for vg0222029032:

Variant ID: vg0222029032 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 22029032
Reference Allele: CAlternative Allele: T
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CAAGCCGGGAAGCAAGTTGGGAGTCCACATCCTATAAAAAACATCATGACTACAACAAGACCACTCGAGCTTCTTCATATGGATTTATTTGGGCCCGTGG[C/T]
CTACGTAAGCATTGGAGGTAATAAGTATGGTTTTGTTATTGTTGATGATTTTTCACGCTTCACTTGGGTGTACTTTCTCCATGACAAAAGCAAAGCTCAA

Reverse complement sequence

TTGAGCTTTGCTTTTGTCATGGAGAAAGTACACCCAAGTGAAGCGTGAAAAATCATCAACAATAACAAAACCATACTTATTACCTCCAATGCTTACGTAG[G/A]
CCACGGGCCCAAATAAATCCATATGAAGAAGCTCGAGTGGTCTTGTTGTAGTCATGATGTTTTTTATAGGATGTGGACTCCCAACTTGCTTCCCGGCTTG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: