rs1601672944
- Likely benign
Your Genotype
Sign InDescription
The p.Tyr2325Tyr variant in TRIOBP is classified as likely benign because it doe s not alter an amino acid residue, it is not located within the splice consensus sequence, and splice prediction algorithms do not predict a newly created splic e site. ACMG/AMP Criteria applied: BP4, BP7.
Reference Allele
T
Alternative Allele
C
Chromosome
22
Location
37772639
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001039141.3(TRIOBP):c.6975T>C (p.Tyr2325=)
Allele
C
Clinical Significance
Likely benign