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Detailed information for vg1018443385:

Variant ID: vg1018443385 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 18443385
Reference Allele: AAlternative Allele: G
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


ATTGGAGGTATTTTGGTTTTTTATCTATCCCCTTATATTCATCTTGGGAAGCTAGGGTTGGACATTTTGTGGGATAGAGGGAGTAGTCATAAATACGAGC[A/G]
GGTGCCAAGTGTAGAACTTGAACTTAGATGAACATGTATCACCAGAAGTAACATAATGAGCTATGATATTTAATATTATCACAAAACAATCTTTGTTAAC

Reverse complement sequence

GTTAACAAAGATTGTTTTGTGATAATATTAAATATCATAGCTCATTATGTTACTTCTGGTGATACATGTTCATCTAAGTTCAAGTTCTACACTTGGCACC[T/C]
GCTCGTATTTATGACTACTCCCTCTATCCCACAAAATGTCCAACCCTAGCTTCCCAAGATGAATATAAGGGGATAGATAAAAAACCAAAATACCTCCAAT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: