Total submissions: 1
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Institute for Genomic Statistics and Bioinformatics, |
RCV001268942 | SCV001448192 | pathogenic | Intellectual disability, autosomal dominant 8 | criteria provided, single submitter | clinical testing | Evaluation of c.1853G>T in GRIN1: The heterozygous transition from G>T to position 140056957 on chromosome 9 was replaced with 132 reads and has an alternative allele frequency (AAV) of 52% in the index, while both parents at this position the reference allele (cover at the nut 109 Reads, with the father 76 reads). The variant in the Exon 14 leads to the exchange of the highly conserved amino acid glycine to valine at position 618 in GRIN1. Bioinformatic prediction programs like MutationTaster, SIFT, PolyPhen, FATHMM, MetaSVM, REVEL and other levels this variant (CADD score 27.8) as pathogenic. To ACMG guidelines become c.1853G>T in GRIN1 also classified as pathogenic. Classification according to ACMG guidelines of c.1853G>T in GRIN1: pathogenic - PS2: Neumutation (another independent validation is pending). - PM2: The variant was identified in population genetic studies (such as GnomAD, Iranome, GME, 1kGP, etc.) not observed. - PM5: A variant at the same position (p.Gly618Arg) is observed in UniProt (VAR_079992) and ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/variation/981271) as probably pathogenic classified. - PP2: Variants that change their meaning have already been classified as disease-causing. The Zsciore for the gene GRIN1 is 6.22, indicating an intolerance to sense-changing variants. 83.8% of all sense-altering variants not classified as variants of uncertain clinical significance) in the GRIN1 gene are pathogenic, which is above the threshold of 51.0%; and 23.9% of clinically reported variants in the GRIN1 gene are pathogenic, which is above the threshold of 12.0%. - PP3: Bioinformatic prediction programs such as SIFT, Polyphen, REVEL, Mutation Scanner and others classify this variant as pathogenic. The gene GRIN1 encodes a subunit of the NMDA receptor complex, which is a heterotetrameric, ligand controlled ion channel with high calcium permeability and voltage dependent sensitivity acts against magnesium. Mutations in GRIN1 (MIM#138249) were detected in patients with the autosomal dominant inherited form of neuronal developmental disorder with or without hyperkinetic movements and seizures (MIM#614254).2,3 Both patients with mutations in the M2 domain (p.Gly618Arg and p.Gly620Arg) showed severe intelligence loss without seizures.3 In functional studies it was shown that, among others, the variants p.Gly618Arg and p.Gly620Arg lead to loss of function of the NMDA receptor. In the prioritization of the exome data using PEDIA the gene GRIN1 was placed at position 1. |