Search for Variation information by Variation ID:

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

Detailed information for vg0223848979:

Variant ID: vg0223848979 (JBrowse)	Variation Type: SNP
Chromosome: chr02	Position: 23848979
Reference Allele: A	Alternative Allele: T
Primary Allele: A	Secondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:

CCCCTACCCCTTTGTACCCGCCCCCTAAACCTAATACCTAATTGGTCAAGGGCATCGTCGTTGTCAAGCTCGCAAGAGTGGAAGGAGAAGGTCACGGTGC[A/T]
CGAATCTCAGAGCCGATCAGAGCATCCAAATTTTGAAAGATGGGGTTTCGATTATGTCCAATGGAGGTTAGAAATTCTGATACTAGTTTTCATGCCATTG

Reverse complement sequence

CAATGGCATGAAAACTAGTATCAGAATTTCTAACCTCCATTGGACATAATCGAAACCCCATCTTTCAAAATTTGGATGCTCTGATCGGCTCTGAGATTCG[T/A]
GCACCGTGACCTTCTCCTTCCACTCTTGCGAGCTTGACAACGACGATGCCCTTGACCAATTAGGTATTAGGTTTAGGGGGCGGGTACAAAGGGGTAGGGG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: