Total submissions: 3
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| International Society for Gastrointestinal Hereditary Tumours |
RCV000076338 | SCV000107363 | likely pathogenic | Lynch syndrome | 2019-06-21 | reviewed by expert panel | curation | Interrupts canonical donor splice site |
| Ambry Genetics | RCV003162495 | SCV003910171 | pathogenic | Hereditary cancer-predisposing syndrome | 2023-03-09 | criteria provided, single submitter | clinical testing | The c.2005+1G>C intronic pathogenic mutation results from a G to C substitution one nucleotide after coding exon 12 of the MSH2 gene. This variant was reported in a proband whose family history met Amsterdam criteria for Lynch syndrome; however, microsatellite instability (MSI) testing in her endometrial cancer was negative (Overbeek LI et al. Br J Cancer, 2007 May;96:1605-12). Another alteration impacting the same donor site (c.2005+1G>A) has been detected in Lynch syndrome families or in probands whose Lynch syndrome-associated tumors demonstrated high MSI and/or loss of MSH2/MSH6 expression by immunohistochemistry (Ambry internal data; Bécouarn Y et al. Gastroenterol. Clin. Biol. 2005;29:667-75; Bonadona V et al. JAMA 2011 Jun;305:2304-10). This variant is considered to be rare based on population cohorts in the Genome Aggregation Database (gnomAD). This nucleotide position is highly conserved in available vertebrate species. In silico splice site analysis predicts that this alteration will weaken the native splice donor site and will result in the creation or strengthening of a novel splice donor site; however, direct evidence is insufficient at this time (Ambry internal data). In addition to the clinical data presented in the literature, alterations that disrupt the canonical splice site are expected to cause aberrant splicing, resulting in an abnormal protein or a transcript that is subject to nonsense-mediated mRNA decay. As such, this alteration is classified as a disease-causing mutation. |
| Myriad Genetics, |
RCV003452872 | SCV004186623 | likely pathogenic | Lynch syndrome 1 | 2023-08-04 | criteria provided, single submitter | clinical testing | This variant is considered likely pathogenic. This variant occurs within a consensus splice junction and is predicted to result in abnormal mRNA splicing of either an out-of-frame exon or an in-frame exon necessary for protein stability and/or normal function. |