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Detailed information for vg0216547473:

Variant ID: vg0216547473 (JBrowse)Variation Type: INDEL
Chromosome: chr02Position: 16547473
Reference Allele: TTGAlternative Allele: TGTGTGTG,TGTGTG,TGTGTGTGTG,TGTG,GTG,T
Primary Allele: TGTGTGTGSecondary Allele: TGTG

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GCGGAGTCTAGAGTGGAGTTGTTAATCGCTCTGAACCCCAGCCTCACCCCTCTAGTTCATTTTTTCATAATACTCTAGCCCACTCCACTCTTTATTTCTT[TTG/TGTGTGTG,TGTGTG,TGTGTGTGTG,TGTG,GTG,T]
TGTGTGTGTGTGTGTGTTGCTAGAGGAACTATACATCGCACTGACACCCCCCCCTCTAGTTCATTTTTTTCAAATCACTCCAATCGGGAATGGGAATCCC

Reverse complement sequence

GGGATTCCCATTCCCGATTGGAGTGATTTGAAAAAAATGAACTAGAGGGGGGGGTGTCAGTGCGATGTATAGTTCCTCTAGCAACACACACACACACACA[CAA/CACACACA,CACACA,CACACACACA,CACA,CAC,A]
AAGAAATAAAGAGTGGAGTGGGCTAGAGTATTATGAAAAAATGAACTAGAGGGGTGAGGCTGGGGTTCAGAGCGATTAACAACTCCACTCTAGACTCCGC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: