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Detailed information for vg1117477788:

Variant ID: vg1117477788 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 17477788
Reference Allele: GAlternative Allele: C
Primary Allele: GSecondary Allele: C

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


ATAAATATTCTATTAAATATCATATAAATATTTTTAAAATATCTTCTACATATGTCCTATTTTAAATGCATTTTTAAATTTCCGTGTCCAATGCCTGTCT[G/C]
TCCGTCTTATTTAAAAAAATTATAATAAAATTAAAAAGAATTAGTCATACATAAAGTACTATTCATGTTTTATCATTTAATAACAACAAATATACTAATC

Reverse complement sequence

GATTAGTATATTTGTTGTTATTAAATGATAAAACATGAATAGTACTTTATGTATGACTAATTCTTTTTAATTTTATTATAATTTTTTTAAATAAGACGGA[C/G]
AGACAGGCATTGGACACGGAAATTTAAAAATGCATTTAAAATAGGACATATGTAGAAGATATTTTAAAAATATTTATATGATATTTAATAGAATATTTAT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: