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Detailed information for vg0220960199:

Variant ID: vg0220960199 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 20960199
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


ATGATATTTATCGATTCACCAGAAATTAAGTTTAAATTTGACATGCACCTTGAAAAAAAAAGATAAATTCGGGTATGGACACTACCACTACCCTATTATT[C/T]
ATATACCGAATTTATGTTTTTTATATATCAATGTGTAAGTTGAGTTTGGATCTTACATTTTTTTAGAGGTGGTATATGTATTTGTACGAACGCTGTCAAC

Reverse complement sequence

GTTGACAGCGTTCGTACAAATACATATACCACCTCTAAAAAAATGTAAGATCCAAACTCAACTTACACATTGATATATAAAAAACATAAATTCGGTATAT[G/A]
AATAATAGGGTAGTGGTAGTGTCCATACCCGAATTTATCTTTTTTTTTCAAGGTGCATGTCAAATTTAAACTTAATTTCTGGTGAATCGATAAATATCAT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: