Search for Variation information by Variation ID:

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

Detailed information for vg0317440491:

Variant ID: vg0317440491 (JBrowse)	Variation Type: SNP
Chromosome: chr03	Position: 17440491
Reference Allele: C	Alternative Allele: T
Primary Allele: C	Secondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:

TATAAAAGTAATTTATACTCTCTCCATCTACTTTTGATAAGCATATTTTTAAATCTGAAAAATTTATTTTTGATAGGCATATTTCAATTCAACAACTTAT[C/T]
ATCTTAATGACTTTCTTGGATTTAATGCGTGACTCTCCATTCTTCCACACAAGATTGGCTACATGGGCATCGAGAAATGTAAATATTAATAAATCACTTG

Reverse complement sequence

CAAGTGATTTATTAATATTTACATTTCTCGATGCCCATGTAGCCAATCTTGTGTGGAAGAATGGAGAGTCACGCATTAAATCCAAGAAAGTCATTAAGAT[G/A]
ATAAGTTGTTGAATTGAAATATGCCTATCAAAAATAAATTTTTCAGATTTAAAAATATGCTTATCAAAAGTAGATGGAGAGAGTATAAATTACTTTTATA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: