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Detailed information for vg1124221076:

Variant ID: vg1124221076 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 24221076
Reference Allele: TAlternative Allele: C
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TTATTTTGAATGAAAGAATTAATCTGAAGAAGTATCAAGGAGGGCAGAAAATCACCTAATTTGAAGACGGATAAGTTCAGTATTGCAATCATACACAAAG[T/C]
GAGTCCAGCAGCTCATCTTTTGATCCTTGATGGAATTCGGTGACAGAAAACTCTTAAGAGAGAAAGGTTCTGTCCTGATCATGCTAAGAACCTGCTGAGC

Reverse complement sequence

GCTCAGCAGGTTCTTAGCATGATCAGGACAGAACCTTTCTCTCTTAAGAGTTTTCTGTCACCGAATTCCATCAAGGATCAAAAGATGAGCTGCTGGACTC[A/G]
CTTTGTGTATGATTGCAATACTGAACTTATCCGTCTTCAAATTAGGTGATTTTCTGCCCTCCTTGATACTTCTTCAGATTAATTCTTTCATTCAAAATAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: