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Detailed information for vg1217404715:

Variant ID: vg1217404715 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 17404715
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TACTCCACACAAAATAAATTAAATTTCGATTACTATATGAATTTAGAGAATAGATTTATTTGTTATTTTAAAGTAACTTAATATATATAATTTTTGTAAA[C/T]
AAAATGCATTGTTTGACAGTTCTATTATATTTTTTAAACAAAATGCATCGTTTAACAATTCTATTATAAATCAAGTTAAAATTTGTATGTTAATCAGAAA

Reverse complement sequence

TTTCTGATTAACATACAAATTTTAACTTGATTTATAATAGAATTGTTAAACGATGCATTTTGTTTAAAAAATATAATAGAACTGTCAAACAATGCATTTT[G/A]
TTTACAAAAATTATATATATTAAGTTACTTTAAAATAACAAATAAATCTATTCTCTAAATTCATATAGTAATCGAAATTTAATTTATTTTGTGTGGAGTA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: