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Detailed information for vg0109515272:

Variant ID: vg0109515272 (JBrowse)Variation Type: SNP
Chromosome: chr01Position: 9515272
Reference Allele: TAlternative Allele: C
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TCCAGTTATTAAAATTTGGCAGCAAATTAAATGTAGTCACTTTTTTTATAACTTTACTAAAATTTGGTAAGGTTGAAAATGGCTTCAAAGTGAATAGGCC[T/C]
ATAGAGACACATAGATCGTTATTAGAGAGAGAGAGAGGGGGGGATTATATACGTAGATAATAAGCGAATGCAACAAGCTGATGTGTGGTGCTATCCTAGA

Reverse complement sequence

TCTAGGATAGCACCACACATCAGCTTGTTGCATTCGCTTATTATCTACGTATATAATCCCCCCCTCTCTCTCTCTCTAATAACGATCTATGTGTCTCTAT[A/G]
GGCCTATTCACTTTGAAGCCATTTTCAACCTTACCAAATTTTAGTAAAGTTATAAAAAAAGTGACTACATTTAATTTGCTGCCAAATTTTAATAACTGGA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: