Variants
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rs149496377

  • Likely benign

Your Genotype

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Description

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

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