Description
The p.G750D pathogenic mutation (also known as c.2249G>A), located in exon 13 of the PMS2 gene, results from a G to A substitution at nucleotide position 2249. The glycine at codon 750 is replaced by aspartate, an amino acid with similar properties. In one study, this alteration was detected in trans with a full gene PMS2 deletion and the severe phenotype in this family was consistent with biallelic PMS2 mutations. The proband was diagnosed with rectal cancer at age 22 and a brain tumor at age 23, while a brother was diagnosed with colorectal cancer (CRC) at age 21. The proband's tumor as well as adjacent normal tissue demonstrated loss of PMS2 expression on IHC (Senter et al. Gastroenterology. 2008 August; 135(2): 419–428). In another family, the p.G750D alteration was reported in conjunction with the PMS2 frameshift mutation c.2019delT in a proband with café-au-lait macules, a glioblastoma at age 31, and CRC at age 32. Tumor testing showed MSI-H and absence of PMS2 staining on IHC. This patient's family history included hematologic cancers, renal cancer, and CRC (van Galen et al. Hereditary Cancer in Clinical Practice. 2011, 9(Suppl 1):P38). This alteration was also reported in a suspected Lynch syndrome family and the proband had co-occurrence with PMS2 p.E330_E381del. The clinical features of the proband included: CRC diagnosed twice at ages 22 and 32, polyps at age 38, a glioblastoma at age 40, and café-au-lait macules (Lavoine N et al. J. Med. Genet. 2015 Nov;52:770-8). In another study, this alteration was reported in conjunction with PMS2 p.S46I in a male with colon cancer diagnosed at ages 41 and 50 and tumor results demonstrated MSI-H as well as loss of PMS2 expression on IHC (Goodenberger ML et al. Genet. Med. 2016 Jan;18:13-9). Based on an internal structural analysis, this variant is anticipated to result in a significant decrease in protein structural stability (Gueneau E et al. Nat. Struct. Mol. Biol. 2013 Apr; 20(4):461-8). This missense alteration is located in a region that has a low rate of benign missense variation (Lek M et al. Nature. 2016 Aug 18;536(7616):285-91; DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans using Ensembl Resources. Firth H.V. et al. 2009. Am.J.Hum.Genet. 84, 524-533 (DOI: dx.doi.org/10/1016/j.ajhg.2009.03.010)). This variant is considered to be rare based on population cohorts in the Genome Aggregation Database (gnomAD). This amino acid position is highly conserved in available vertebrate species. In addition, this alteration is predicted to be deleterious by in silico analysis. Based on the supporting evidence, this alteration is interpreted as a disease-causing mutation.
| # | Sample | Method | Observation |
|---|
| Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences |
|---|
| 1 | germline | unknown | not provided | not provided | not provided | | not provided | not provided | not provided | not provided |
