Search for Variation information by Variation ID:

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

Detailed information for vg0139341179:

Variant ID: vg0139341179 (JBrowse)Variation Type: SNP
Chromosome: chr01Position: 39341179
Reference Allele: TAlternative Allele: C
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TCCCGAGTTTCTCTGAAACCGAGTGGCCTTGGAGGAGATTGGCGGCTGCCGTGCCTGAGGAAGACGACGACGACGCCATGTGGATGAAAGATGCGATCTA[T/C]
CGAGGTGGAAAAAGGATCTGATACCATGTGATAAAATGTGAAGCGTTGAACCCTTTGCCTCGGGCCGCATCTCTGTTAAATAGTGGTAGAAACAGCCTCT

Reverse complement sequence

AGAGGCTGTTTCTACCACTATTTAACAGAGATGCGGCCCGAGGCAAAGGGTTCAACGCTTCACATTTTATCACATGGTATCAGATCCTTTTTCCACCTCG[A/G]
TAGATCGCATCTTTCATCCACATGGCGTCGTCGTCGTCTTCCTCAGGCACGGCAGCCGCCAATCTCCTCCAAGGCCACTCGGTTTCAGAGAAACTCGGGA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: