Search for Variation information by Variation ID:

Please input a variation ID (e.g., vg0722097923 , STR0500036000 ).

Detailed information for vg0106722456:

Variant ID: vg0106722456 (JBrowse)Variation Type: SNP
Chromosome: chr01Position: 6722456
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CCCCGAAGAGCTACACCAATGACGTCGTGCTTCGGCAGAAGGCGGAGGATGACCACGGCATCGGTTTACTCGGCGACGACAATGATTGCCCCGCCTTCGA[C/T]
CGCCTTTGGAAGTACTGCCGCGGCTACGCCGGTGGGTCGCTTGCCGCGGCGCGCACGCTCGTCAACGGCGCCTCCGGATCTCACCGCCGCCGCATCGTGA

Reverse complement sequence

TCACGATGCGGCGGCGGTGAGATCCGGAGGCGCCGTTGACGAGCGTGCGCGCCGCGGCAAGCGACCCACCGGCGTAGCCGCGGCAGTACTTCCAAAGGCG[G/A]
TCGAAGGCGGGGCAATCATTGTCGTCGCCGAGTAAACCGATGCCGTGGTCATCCTCCGCCTTCTGCCGAAGCACGACGTCATTGGTGTAGCTCTTCGGGG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: