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Detailed information for vg1004990336:

Variant ID: vg1004990336 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 4990336
Reference Allele: AAlternative Allele: G
Primary Allele: ASecondary Allele: G

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CGAACAACGGTTTAAACGTTGAACTTTTCTGTGTTTGTTCCAATTTTCCTCGAAATATACTAATTTGAAACTCGGGACATTACAAGTATAGGGCTCCACC[A/G]
ACATGTGTTTAATTCCAAGTCAAAGTATGCAGGTGAGCATGCATTAAATTCTCCATTAATCATGTTATATATAATTAAGAGAATTTCCTAAATTAAAATA

Reverse complement sequence

TATTTTAATTTAGGAAATTCTCTTAATTATATATAACATGATTAATGGAGAATTTAATGCATGCTCACCTGCATACTTTGACTTGGAATTAAACACATGT[T/C]
GGTGGAGCCCTATACTTGTAATGTCCCGAGTTTCAAATTAGTATATTTCGAGGAAAATTGGAACAAACACAGAAAAGTTCAACGTTTAAACCGTTGTTCG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: