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Detailed information for vg0210593156:

Variant ID: vg0210593156 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 10593156
Reference Allele: TAlternative Allele: C
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GCAGCGACTCCATCCACGTCGTCGTCGTAGCGATCCGGTGAATGGTGGCGGGCGTAGCCTCATGCTGCACAGCGCTGGTTGATTGTATCACGGAGATCGA[T/C]
GGGGCGCCTACGAGGTGGGGAGCGAGGCCGTTCAACTTGACGCTCCCTGTGTCGTTCGGGAGGCGAGTGGACAGATCGCTCGTTGTGACCTCTGCTCCTG

Reverse complement sequence

CAGGAGCAGAGGTCACAACGAGCGATCTGTCCACTCGCCTCCCGAACGACACAGGGAGCGTCAAGTTGAACGGCCTCGCTCCCCACCTCGTAGGCGCCCC[A/G]
TCGATCTCCGTGATACAATCAACCAGCGCTGTGCAGCATGAGGCTACGCCCGCCACCATTCACCGGATCGCTACGACGACGACGTGGATGGAGTCGCTGC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: