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Detailed information for vg0416712669:

Variant ID: vg0416712669 (JBrowse)Variation Type: INDEL
Chromosome: chr04Position: 16712669
Reference Allele: CAlternative Allele: A,CA,CGAACTATATAAATCCTTATTCCTTGCACCCCTTCTA,CAA
Primary Allele: CSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TCTTACCCCTGCATATTTTTCTCCATGAATCATTAATTCAACCCAAATGGCCATGAATTGTTTTCCGATCTATCTACCCTTATTCCTTGCACCCCTTCTA[C/A,CA,CGAACTATATAAATCCTTATTCCTTGCACCCCTTCTA,CAA]
AAAAAAAAGTCGAACTGTATAAATCTAGATATAGACATACTTTCTCCATCCTAAAAAGACGAATCTAAAACTGAATGTGACACATTCTAGTATAATGAAT

Reverse complement sequence

ATTCATTATACTAGAATGTGTCACATTCAGTTTTAGATTCGTCTTTTTAGGATGGAGAAAGTATGTCTATATCTAGATTTATACAGTTCGACTTTTTTTT[G/T,TG,TAGAAGGGGTGCAAGGAATAAGGATTTATATAGTTCG,TTG]
TAGAAGGGGTGCAAGGAATAAGGGTAGATAGATCGGAAAACAATTCATGGCCATTTGGGTTGAATTAATGATTCATGGAGAAAAATATGCAGGGGTAAGA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: