rs149496377
- Likely benign
Your Genotype
Sign InDescription
Ile2339Ile in Exon 23 of TRIOBP: This variant is not expected to have clinical s ignificance because it does not alter an amino acid residue, is not located with in the splice consensus sequence, and was identified in 0.5% (1/194) Chinese chr omosomes by the 1000 Genomes Project (http://www.1000genomes.org; dbSNP rs149496 377).
Reference Allele
C
Alternative Allele
T
Chromosome
22
Location
37772681
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001039141.3(TRIOBP):c.7017C>T (p.Ile2339=)
Allele
T
Clinical Significance
Likely benign