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Detailed information for vg1119869771:

Variant ID: vg1119869771 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 19869771
Reference Allele: AAlternative Allele: G
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GCATAAATCAATGGCTAGATATTTCTTATATTTTCTCTAATTTATTAGAGTGCCACATGGCATTATGAGAGCATTTGTAGAATGTCACGTGGCGGCTTGA[A/G]
AGCGTTTGTAGGAAGTTTAATAGATTTTTAGTATATAATAATAGAAGATAGATAGATAGATAGATAGATAGATGCTGGCTGTTGCGCATGTGTATCTGTG

Reverse complement sequence

CACAGATACACATGCGCAACAGCCAGCATCTATCTATCTATCTATCTATCTATCTTCTATTATTATATACTAAAAATCTATTAAACTTCCTACAAACGCT[T/C]
TCAAGCCGCCACGTGACATTCTACAAATGCTCTCATAATGCCATGTGGCACTCTAATAAATTAGAGAAAATATAAGAAATATCTAGCCATTGATTTATGC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: