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Detailed information for vg0507818456:

Variant ID: vg0507818456 (JBrowse)	Variation Type: SNP
Chromosome: chr05	Position: 7818456
Reference Allele: C	Alternative Allele: T,G
Primary Allele: C	Secondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:

TGGTGTTCTCTCTCGAAGGTGAAGCTGAAGTTTCGATATAGAAAACATGAAACCCCATAACTTGAAAAATAGATCTAACTGATATGTTAAAACAACTTCT[C/T,G]
TAAAAAAGATTTTATATGAAATTATCATATAGTATTTGAAAAAAACGTGTTAACGAAAACATAGATAAAATATACTACCTTCGTCCGAAAATATAAGAGA

Reverse complement sequence

TCTCTTATATTTTCGGACGAAGGTAGTATATTTTATCTATGTTTTCGTTAACACGTTTTTTTCAAATACTATATGATAATTTCATATAAAATCTTTTTTA[G/A,C]
AGAAGTTGTTTTAACATATCAGTTAGATCTATTTTTCAAGTTATGGGGTTTCATGTTTTCTATATCGAAACTTCAGCTTCACCTTCGAGAGAGAACACCA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: