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Detailed information for vg0222799001:

Variant ID: vg0222799001 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 22799001
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GCCCTGCTCAGAACCGTCTGTATTCGTCTTCACAATCCCGTCTTGTGATCCAATCTCAGATATTCAACAGCAAACCGCGTTCGCTATAATCCGATGTGAC[C/T]
AATCTTCCGCCCTCGATGTGCCTCTGCTCTGCACGATCTCGTCGGCCTGGCTTGGTCCACCCATACGCGCGCACTTTGTCACAAGCCTCTGCACAACAAG

Reverse complement sequence

CTTGTTGTGCAGAGGCTTGTGACAAAGTGCGCGCGTATGGGTGGACCAAGCCAGGCCGACGAGATCGTGCAGAGCAGAGGCACATCGAGGGCGGAAGATT[G/A]
GTCACATCGGATTATAGCGAACGCGGTTTGCTGTTGAATATCTGAGATTGGATCACAAGACGGGATTGTGAAGACGAATACAGACGGTTCTGAGCAGGGC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: