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Detailed information for vg1128647951:

Variant ID: vg1128647951 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 28647951
Reference Allele: TAlternative Allele: A
Primary Allele: TSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CCCCCCAAATATTTCTGCATTCCTCCAAATTTTACCAACCAATTTGTATTCATCCAAAATTCATCTCAACCATTTGCAACAACCAACCCTAAATCATCTA[T/A]
ACATTCATGTTTTTAAATCACATTTGCAACTATTGCAGTGCCATCTGCCACATTGCAAAACCCCTGCAAACCCCCCAACCACATTGCATTCACCCAAATT

Reverse complement sequence

AATTTGGGTGAATGCAATGTGGTTGGGGGGTTTGCAGGGGTTTTGCAATGTGGCAGATGGCACTGCAATAGTTGCAAATGTGATTTAAAAACATGAATGT[A/T]
TAGATGATTTAGGGTTGGTTGTTGCAAATGGTTGAGATGAATTTTGGATGAATACAAATTGGTTGGTAAAATTTGGAGGAATGCAGAAATATTTGGGGGG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: