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Detailed information for vg0200474832:

Variant ID: vg0200474832 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 474832
Reference Allele: CAlternative Allele: A
Primary Allele: CSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CCTCTATTGAAACCTATGGTGCTGAAGTTAATCTTTGCCAATCAGTACTATCTATCTATCTATTATATAATATATAATTAAATGAATAGAAAAAAGGAGC[C/A]
TCCACGTTCGCTCTCATGGCCTAGAAATTCTCACATTAATCGGAGAAAAAGAAGAAAAAGAAAAAGCAGAGTCCATATAGAAATACAATTTAAAAATAGA

Reverse complement sequence

TCTATTTTTAAATTGTATTTCTATATGGACTCTGCTTTTTCTTTTTCTTCTTTTTCTCCGATTAATGTGAGAATTTCTAGGCCATGAGAGCGAACGTGGA[G/T]
GCTCCTTTTTTCTATTCATTTAATTATATATTATATAATAGATAGATAGATAGTACTGATTGGCAAAGATTAACTTCAGCACCATAGGTTTCAATAGAGG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: