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Detailed information for vg1122614316:

Variant ID: vg1122614316 (JBrowse)Variation Type: INDEL
Chromosome: chr11Position: 22614316
Reference Allele: CAlternative Allele: T,CAA
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


AAGCTGTTTGTTCATCCTAGAGAGGTCTCGACATGGTTCGAATAACATGGCTATTGATGTGGCATACTGCAGGCATCATCATAGAACAAATAATCATGTA[C/T,CAA]
ATTTTTTTTCTTGAGAACCCATATGCATGCCTCTTCACATTTAAAATAAAGACAAAATTGGTTTTATAGCATCAAACGTTTGTGATTTTTGTATGTTAGC

Reverse complement sequence

GCTAACATACAAAAATCACAAACGTTTGATGCTATAAAACCAATTTTGTCTTTATTTTAAATGTGAAGAGGCATGCATATGGGTTCTCAAGAAAAAAAAT[G/A,TTG]
TACATGATTATTTGTTCTATGATGATGCCTGCAGTATGCCACATCAATAGCCATGTTATTCGAACCATGTCGAGACCTCTCTAGGATGAACAAACAGCTT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: