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Detailed information for vg0202346298:

Variant ID: vg0202346298 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 2346298
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CCGCCATCGCACACACTGACACACCTCTCCCTCTCCCTCCTCACCACCACCACCACCCCCCCGCGCCCCGTGTCCTCGCCGTCGCCGTCCTGTCCCATCC[C/T]
GTGCGTCCTTGTTAACAATGAAATTTGGTAAGCCCAAAGTTATCATCGGCTTAGAGTTAATATTGGCTTCAAAGTTCTAGAATCAGCCGATAAGAGTTAA

Reverse complement sequence

TTAACTCTTATCGGCTGATTCTAGAACTTTGAAGCCAATATTAACTCTAAGCCGATGATAACTTTGGGCTTACCAAATTTCATTGTTAACAAGGACGCAC[G/A]
GGATGGGACAGGACGGCGACGGCGAGGACACGGGGCGCGGGGGGGTGGTGGTGGTGGTGAGGAGGGAGAGGGAGAGGTGTGTCAGTGTGTGCGATGGCGG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: