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Detailed information for vg1002823994:

Variant ID: vg1002823994 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 2823994
Reference Allele: AAlternative Allele: C
Primary Allele: ASecondary Allele: C

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TTCGTATTGTAATTAAATTTGTAATGTTTTCATGTAAGATTGATCAAGCTTAAAAAGTCTAATTCTTTTTTAAAAAAAATTAAAATGTCTTGTGAAACGG[A/C]
GGGGTACAATTTTTTAAGACAAATGATCAAATATATTTTTTAAGTATACTCCCTCCGTCTCAAGAAGAACGTATTTTAATTTTTTGTTTTTATGTCCAAC

Reverse complement sequence

GTTGGACATAAAAACAAAAAATTAAAATACGTTCTTCTTGAGACGGAGGGAGTATACTTAAAAAATATATTTGATCATTTGTCTTAAAAAATTGTACCCC[T/G]
CCGTTTCACAAGACATTTTAATTTTTTTTAAAAAAGAATTAGACTTTTTAAGCTTGATCAATCTTACATGAAAACATTACAAATTTAATTACAATACGAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: