Variants
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rs1601672944

  • Likely benign

Your Genotype

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Description

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

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