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Detailed information for vg1116610872:

Variant ID: vg1116610872 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 16610872
Reference Allele: GAlternative Allele: A
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CAACATATGCCCCTAGAGGCACCCGGACCCCCCTTATATATGGGAAGGAGTCCGTGTTACAAAAGATAATCTATATCCCTAACGGAATATACAAATACAG[G/A]
TAAAATACAGTCGTAACCGACTAAGTCTCAAGGTGTTTCCTTGATGTACAAGTTAAGAAACAAACCCGAGATACAAATAAGATATTCTATATATATTCGG

Reverse complement sequence

CCGAATATATATAGAATATCTTATTTGTATCTCGGGTTTGTTTCTTAACTTGTACATCAAGGAAACACCTTGAGACTTAGTCGGTTACGACTGTATTTTA[C/T]
CTGTATTTGTATATTCCGTTAGGGATATAGATTATCTTTTGTAACACGGACTCCTTCCCATATATAAGGGGGGTCCGGGTGCCTCTAGGGGCATATGTTG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: