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Detailed information for vg1002445363:

Variant ID: vg1002445363 (JBrowse)	Variation Type: SNP
Chromosome: chr10	Position: 2445363
Reference Allele: C	Alternative Allele: T
Primary Allele: C	Secondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:

CATATCTAGTGACCTACTCCCTCCGTCCCAAAAAAAGGCAAACCCTGGGTTTCCGTGTCCAACTTTGACTGTCCATCTTATATGAATTTTTTTTATAATT[C/T]
GTATTTTCATTGTTGTTAGATAATAAAGCATGATTAATATTTTATGCGTGACTTGTCTTTTTAATTTTTTTCATAATTTTTTCAAATAAGACAGACGGTC

Reverse complement sequence

GACCGTCTGTCTTATTTGAAAAAATTATGAAAAAAATTAAAAAGACAAGTCACGCATAAAATATTAATCATGCTTTATTATCTAACAACAATGAAAATAC[G/A]
AATTATAAAAAAAATTCATATAAGATGGACAGTCAAAGTTGGACACGGAAACCCAGGGTTTGCCTTTTTTTGGGACGGAGGGAGTAGGTCACTAGATATG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: