Submissions for variant NM_000251.3(MSH2):c.211G>C (p.Gly71Arg)

dbSNP: rs587782659

Total submissions: 9

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Ambry Genetics	RCV000132075	SCV000187139	pathogenic	Hereditary cancer-predisposing syndrome	2023-09-07	criteria provided, single submitter	clinical testing	The c.211G>C pathogenic mutation (also known as p.G71R), located in coding exon 1 of the MSH2 gene, results from a G to C substitution at nucleotide position 211. The amino acid change results in glycine to arginine at codon 71, an amino acid with dissimilar properties. However, this change occurs in the last base pair of coding exon 1, which makes it likely to have some effect on normal mRNA splicing. In one study, this variant was detected in two unrelated individuals diagnosed with early-onset colon cancer, whose tumors showed loss of MSH2/MSH6 protein expression by immunohistochemistry (IHC). Both families met Bethesda criteria and this variant was not detected in 188 controls. Further RNA studies indicated that this variant led to a partial deletion of exon 1, resulting in a premature truncation of MSH2 (Vargas-Parra GM et al. Int J Cancer, 2017 Oct;141:1365-1380). This variant has been identified in a proband who met Amsterdam II criteria for Lynch syndrome and tumor demonstrated loss of MSH2/MSH6 expression by IHC (Ambry internal data). This variant has also been identified in multiple probands whose Lynch syndrome-associated tumor demonstrated high microsatellite instability and/or loss of MSH2 or MSH2/MSH6 expression by IHC (Ambry internal data). This nucleotide position is highly conserved in available vertebrate species. In silico splice site analysis predicts that this alteration may 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). This variant is considered to be rare based on population cohorts in the Genome Aggregation Database (gnomAD). Based on the supporting evidence, this alteration is interpreted as a disease-causing mutation.
Invitae	RCV000535324	SCV000625353	likely pathogenic	Hereditary nonpolyposis colorectal neoplasms	2024-01-14	criteria provided, single submitter	clinical testing	This sequence change replaces glycine, which is neutral and non-polar, with arginine, which is basic and polar, at codon 71 of the MSH2 protein (p.Gly71Arg). RNA analysis indicates that this missense change induces altered splicing and may result in an absent or disrupted protein product. This variant is not present in population databases (gnomAD no frequency). This missense change has been observed in individual(s) with clinical features of Lynch syndrome and/or breast cancer (PMID: 28577310, 32522261; Invitae). It has also been observed to segregate with disease in related individuals. ClinVar contains an entry for this variant (Variation ID: 142708). An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant is likely to be tolerated. Variants that disrupt the consensus splice site are a relatively common cause of aberrant splicing (PMID: 17576681, 9536098). Studies have shown that this missense change results in activation of a cryptic splice site and introduces a premature termination codon (PMID: 35676339). The resulting mRNA is expected to undergo nonsense-mediated decay. In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic.
Quest Diagnostics Nichols Institute San Juan Capistrano	RCV000985801	SCV001134350	likely pathogenic	not provided	2019-05-15	criteria provided, single submitter	clinical testing	Not found in the total gnomAD dataset, and the data is high quality (0/221594 chr). Found in at least one symptomatic patient in literature. Predicted to negatively affect a known splice site. Assessment of experimental evidence suggests this variant results in abnormal protein function.
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	RCV000503476	SCV001337820	likely pathogenic	Lynch syndrome	2020-01-14	criteria provided, single submitter	clinical testing	Variant summary: MSH2 c.211G>C (p.Gly71Arg) results in a non-conservative amino acid change located in the DNA mismatch repair protein MutS-like, N-terminal domain (IPR007695) of the encoded protein sequence. Four of four in-silico tools predict a damaging effect of the variant on protein function and weakens a 5' donor site. At least one publication reports experimental evidence that this variant affects mRNA splicing and results in aberrant transcript which is predicted to generate a truncated protein (p.Tyr66Serfs*10) (Vargas-Parra_2017). The variant was absent in 218268 control chromosomes (gnomAD). c.211G>C has been reported in the literature in individuals affected with Lynch Syndrome, including one family suggesting co-segregation of the variant and the disease (Vargas-Parra_2017). Three ClinVar submitters (evaluation after 2014) cite the variant as likely pathogenic. Based on the evidence outlined above, the variant was classified as likely pathogenic.
Color Diagnostics, LLC DBA Color Health	RCV000132075	SCV001342611	likely pathogenic	Hereditary cancer-predisposing syndrome	2022-03-11	criteria provided, single submitter	clinical testing	This missense variant replaces glycine with arginine at codon 71 of the MSH2 protein. Computational prediction suggests that this variant may have deleterious impact on protein structure and function (internally defined REVEL score threshold >= 0.7, PMID: 27666373). An RNA assay detect two aberrant splice products but the splicing defect was incomplete (PMID: 28577310). This variant has been reported in individuals affected with suspected Lynch syndrome (PMID: 28577310, ClinVar: SCV000187139, SCV000625353), or breast cancer (PMID: 32522261). It has been shown that this variant segregates with disease (PMID: 28577310). This variant has not been identified in the general population by the Genome Aggregation Database (gnomAD). Based on the available evidence, this variant is classified as Likely Pathogenic.
Clinical Genomics Laboratory, Washington University in St. Louis	RCV003453090	SCV004177083	pathogenic	Lynch syndrome 1	2023-10-14	criteria provided, single submitter	clinical testing	The MSH2 c.211G>C (p.Gly71Arg) variant has been reported in two individuals affected with Lynch syndrome (Vargas-Parra GM et al., PMID: 28577310). This variant is absent from the general population (gnomAD v.2.1.1), indicating it is not a common variant. This variant falls on the last nucleotide of exon 1, which is part of the consensus splice site for this exon. Functional studies show that the variant results in a partial deletion of exon 1, which is predicted to generate a truncated protein (p.Tyr66Serfs*10), and impacts protein function (Vargas-Parra GM et al., PMID: 28577310). Computational predictors indicate that this variant would alter splicing, evidence that correlates to an impact of this variant on MSH2 function. This variant has been reported in the ClinVar database as a likely pathogenic variant by five submitters and pathogenic by one submitter. Based on available information and the ACMG/AMP guidelines for variant interpretation (Richards S et al., PMID: 25741868), this variant is classified as pathogenic.
Myriad Genetics, Inc.	RCV003453090	SCV004186737	likely pathogenic	Lynch syndrome 1	2023-07-26	criteria provided, single submitter	clinical testing	This variant is considered likely pathogenic. mRNA analysis has demonstrated abnormal mRNA splicing occurs [Myriad internal data].
Baylor Genetics	RCV003453090	SCV004194549	likely pathogenic	Lynch syndrome 1	2023-06-13	criteria provided, single submitter	clinical testing
Department of Pathology and Laboratory Medicine, Sinai Health System	RCV001353465	SCV000592455	likely pathogenic	Carcinoma of colon		no assertion criteria provided	clinical testing	The p.Gly71Arg variant has not been reported in the literature nor previously identified by our laboratory. The variant occurs in the last base of exon 1. This position has been shown to be part of the splicing consensus sequence and variants involving this position sometimes affect splicing. In-silico or computational prediction software (SpliceSiteFinder, MaxEntScan, NNSPLICE, GeneSplicer, HumanSpliceFinder) predicts a greater than 10% difference in splicing in 4 out of 5 different programs. This residue is conserved in mammals but not in lower organisms, and computational analyses (SIFT, AlignGVGD) do not suggest a high likelihood of impact to the protein. However, the information from these software analyses is not predictive enough to rule out pathogenicity. In summary, based on the above information, the clinical significance of this variant cannot be determined with certainty at this time, although we would lean towards a more pathogenic role for this variant. This variant is classified as Predicted Pathogenic.