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Detailed information for vg0234907967:

Variant ID: vg0234907967 (JBrowse)Variation Type: INDEL
Chromosome: chr02Position: 34907967
Reference Allele: AATAlternative Allele: A
Primary Allele: AATSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CATGGCTACTGCCACTACTGAATTGTCAGTTGAGTTCTTTGAACATGGAATGTGTAGAGACATTGAATCCTTTCAGAAATCTCACCTAGAATGAAAAAAA[AAT/A]
AAGCATGCTTGGAAACATACGAGCAATTTGAAGTTTGAGAAAGAGGGTAGTTTTAAGTTATGGCTATCAAATAACTTACAGTTCTTTCATTAAAAAAAAC

Reverse complement sequence

GTTTTTTTTAATGAAAGAACTGTAAGTTATTTGATAGCCATAACTTAAAACTACCCTCTTTCTCAAACTTCAAATTGCTCGTATGTTTCCAAGCATGCTT[ATT/T]
TTTTTTTCATTCTAGGTGAGATTTCTGAAAGGATTCAATGTCTCTACACATTCCATGTTCAAAGAACTCAACTGACAATTCAGTAGTGGCAGTAGCCATG

Allele Frequencies:

Allele Effect: