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Detailed information for vg1221691088:

Variant ID: vg1221691088 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 21691088
Reference Allele: AAlternative Allele: C
Primary Allele: ASecondary Allele: C

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GTACTCTGTTAATTCTAATTGTTATAAAATGTTACTCCCTCCGTATTTTAATGTATGACGCAGTTGACTTTGTGACAAACGTTTGACCTTTCGTCTTATT[A/C]
AAAAAAATTATATAATTATCATTTATTTTATTGTGACTTGATTTATCATCAAATGTTCTTTAAACATAACATAAGTATTTTTATATTTGCATAAAAAATT

Reverse complement sequence

AATTTTTTATGCAAATATAAAAATACTTATGTTATGTTTAAAGAACATTTGATGATAAATCAAGTCACAATAAAATAAATGATAATTATATAATTTTTTT[T/G]
AATAAGACGAAAGGTCAAACGTTTGTCACAAAGTCAACTGCGTCATACATTAAAATACGGAGGGAGTAACATTTTATAACAATTAGAATTAACAGAGTAC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: