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Detailed information for vg0202989092:

Variant ID: vg0202989092 (JBrowse)	Variation Type: SNP
Chromosome: chr02	Position: 2989092
Reference Allele: C	Alternative Allele: T
Primary Allele: C	Secondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:

CGCCTCCCAGCTGTGAGGGGCCGATGACGTCCTCTGCCGAGCCTGAAGCGAAGTCGAAGTCAGTGATGTCGAAGAGCACGGTGGAAGACAGCAAGCGGTC[C/T]
GACGAGGTCCTAGCATGGTCTAGTGGTGGACCTTGACTCGACGTGCCGGCTGCCTGTGACGAAGCCCCGGTGTACTGCTGGAACTGCGCTGAGTGCGAGG

Reverse complement sequence

CCTCGCACTCAGCGCAGTTCCAGCAGTACACCGGGGCTTCGTCACAGGCAGCCGGCACGTCGAGTCAAGGTCCACCACTAGACCATGCTAGGACCTCGTC[G/A]
GACCGCTTGCTGTCTTCCACCGTGCTCTTCGACATCACTGACTTCGACTTCGCTTCAGGCTCGGCAGAGGACGTCATCGGCCCCTCACAGCTGGGAGGCG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: