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Detailed information for vg0103252222:

Variant ID: vg0103252222 (JBrowse)Variation Type: SNP
Chromosome: chr01Position: 3252222
Reference Allele: CAlternative Allele: T
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GAAACACTAGGTCTAGCAGCAACCAATTTATCTTATCACATACCGTCCTCATTTGCCAATCTCAAGTCCTTGAAGCGTTTGGGTATGAGCACGGCACGAA[C/T]
TTCCAAGGAGCTGCCCTCTTTATTAGATAAGCTTCCTTCATTGACAGAACTGGAATTGCAAGGATCGGAATCAGGCTTGGAGAAGGCGGTATTATCTTGG

Reverse complement sequence

CCAAGATAATACCGCCTTCTCCAAGCCTGATTCCGATCCTTGCAATTCCAGTTCTGTCAATGAAGGAAGCTTATCTAATAAAGAGGGCAGCTCCTTGGAA[G/A]
TTCGTGCCGTGCTCATACCCAAACGCTTCAAGGACTTGAGATTGGCAAATGAGGACGGTATGTGATAAGATAAATTGGTTGCTGCTAGACCTAGTGTTTC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: