Gene entry
MAT1A
methionine adenosyltransferase 1A
- Chromosome
- 10
- Cytoband
- 10q22.3
- Variants (rsID)
- 22
MAT1A is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q22.3). Its official name is “methionine adenosyltransferase 1A”. The reference table lists 22 variants (rsID) for this gene.
Clinically classified variants
11 reference-table entries with clinical significance.
- rs10887711Benignsingle nucleotide variantHepatic methionine adenosyltransferase deficiency
- rs11595587Benignsingle nucleotide variantHepatic methionine adenosyltransferase deficiency
- rs17851642Benignsingle nucleotide variantHepatic methionine adenosyltransferase deficiency
- rs1832683Benignsingle nucleotide variantHepatic methionine adenosyltransferase deficiency
- rs1985908Benignsingle nucleotide variantHepatic methionine adenosyltransferase deficiency
- rs116528173Conflicting interpretationssingle nucleotide variantHepatic methionine adenosyltransferase deficiency
- rs118204001Likely pathogenicsingle nucleotide variantHepatic methionine adenosyltransferase deficiency
- rs118204003Pathogenicsingle nucleotide variantHepatic methionine adenosyltransferase deficiency
- rs118204006Pathogenicsingle nucleotide variantHepatic methionine adenosyltransferase deficiency
- rs1065766Uncertain significancesingle nucleotide variantHepatic methionine adenosyltransferase deficiency
- rs118204002Uncertain significancesingle nucleotide variantHepatic methionine adenosyltransferase deficiency
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.