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Gene entry

ASS1

argininosuccinate synthase 1

Chromosome
9
Cytoband
9q34.11
Variants (rsID)
38

ASS1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q34.11). Its official name is “argininosuccinate synthase 1”. The reference table lists 38 variants (rsID) for this gene.

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Clinically classified variants

18 reference-table entries with clinical significance.

  • rs73541957Benignsingle nucleotide variantCitrullinemia type I|Citrullinemia
  • rs121908637Conflicting interpretationssingle nucleotide variantCitrullinemia type I|Citrullinemia
  • rs121908643Conflicting interpretationssingle nucleotide variantCitrullinemia type I
  • rs139031154Conflicting interpretationssingle nucleotide variantCitrullinemia type I|Citrullinemia
  • rs140715869Conflicting interpretationssingle nucleotide variantCitrullinemia type I|Citrullinemia
  • rs199751308Conflicting interpretationssingle nucleotide variantCitrullinemia type I|Citrullinemia
  • rs370595480Conflicting interpretationssingle nucleotide variantCitrullinemia type I|Citrullinemia
  • rs376371866Conflicting interpretationssingle nucleotide variantCitrullinemia type I|Citrullinemia
  • rs121908638Pathogenicsingle nucleotide variantCitrullinemia type I|Citrullinemia
  • rs121908639Pathogenicsingle nucleotide variantCitrullinemia type I|Citrullinemia
  • rs121908641Pathogenicsingle nucleotide variantCitrullinemia type I|Citrullinemia
  • rs121908646Pathogenicsingle nucleotide variantCitrullinemia, mild|Citrullinemia type I|Citrullinemia
  • rs121908647Pathogenicsingle nucleotide variantCitrullinemia, mild|Citrullinemia type I|Citrullinemia
  • rs148918985Pathogenicsingle nucleotide variantCitrullinemia|Citrullinemia type I
  • rs183276875Pathogenicsingle nucleotide variantCitrullinemia type I|Citrullinemia
  • rs192838388Pathogenicsingle nucleotide variantCitrullinemia type I|Citrullinemia
  • rs371265106Pathogenicsingle nucleotide variantCitrullinemia type I|Citrullinemia
  • rs121908648Uncertain significancesingle nucleotide variantCitrullinemia type I

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.