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Gene entry

TRAPPC9

trafficking protein particle complex subunit 9

Chromosome
8
Cytoband
8q24.3
Variants (rsID)
220

TRAPPC9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 8 (region 8q24.3). Its official name is “trafficking protein particle complex subunit 9”. The reference table lists 220 variants (rsID) for this gene.

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Clinically classified variants

18 reference-table entries with clinical significance.

  • rs117206975Benignsingle nucleotide variantIntellectual disability, autosomal recessive 13
  • rs3735802Benignsingle nucleotide variantIntellectual Disability, Recessive|History of neurodevelopmental disorder|Intellectual disability, autosomal recessive 13
  • rs112551069Conflicting interpretationssingle nucleotide variantIntellectual Disability, Recessive|History of neurodevelopmental disorder
  • rs114949291Conflicting interpretationssingle nucleotide variantIntellectual Disability, Recessive|History of neurodevelopmental disorder
  • rs117632905Conflicting interpretationssingle nucleotide variantIntellectual Disability, Recessive
  • rs117685875Conflicting interpretationssingle nucleotide variantIntellectual Disability, Recessive|History of neurodevelopmental disorder
  • rs139631202Conflicting interpretationssingle nucleotide variantIntellectual Disability, Recessive|Intellectual disability, autosomal recessive 13|History of neurodevelopmental disorder|Intellectual disability
  • rs147127279Conflicting interpretationssingle nucleotide variantIntellectual Disability, Recessive|History of neurodevelopmental disorder|Intellectual disability
  • rs148976893Conflicting interpretationssingle nucleotide variantIntellectual Disability, Recessive|History of neurodevelopmental disorder
  • rs34179337Conflicting interpretationssingle nucleotide variantIntellectual Disability, Recessive|History of neurodevelopmental disorder
  • rs35578974Conflicting interpretationssingle nucleotide variantIntellectual Disability, Recessive|History of neurodevelopmental disorder|Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome
  • rs267607137Pathogenicsingle nucleotide variantIntellectual disability, autosomal recessive 13
  • rs587780486Pathogenicsingle nucleotide variantIntellectual disability, autosomal recessive 13
  • rs143778652Uncertain significancesingle nucleotide variantIntellectual Disability, Recessive|History of neurodevelopmental disorder|Intellectual disability, autosomal recessive 13|Intellectual disability
  • rs144046998Uncertain significancesingle nucleotide variantIntellectual Disability, Recessive
  • rs199948844Uncertain significancesingle nucleotide variant
  • rs200963473Uncertain significancesingle nucleotide variantHistory of neurodevelopmental disorder|Intellectual disability, autosomal recessive 13
  • rs35318201Uncertain significancesingle nucleotide variant

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.