Submissions for variant NM_000369.5(TSHR):c.202C>T (p.Pro68Ser)

gnomAD frequency: 0.00022  dbSNP: rs142063461

Total submissions: 11

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Genetic Services Laboratory, University of Chicago	RCV000504179	SCV000597612	likely pathogenic	Hypothyroidism due to TSH receptor mutations	2016-07-01	criteria provided, single submitter	clinical testing
Illumina Laboratory Services, Illumina	RCV000504179	SCV000915655	uncertain significance	Hypothyroidism due to TSH receptor mutations	2018-04-18	criteria provided, single submitter	clinical testing	The TSHR c.202C>T (p.Pro68Ser) variant has been reported in five studies in which it is found in at least 16 individuals affected with high TSH levels, including in five in a compound heterozygous state (two of whom were unrelated) and eleven in a heterozygous state (seven of whom were unrelated) (Tenenbaum-Rakover et al. 2009; Nicoletti et al. 2009; Calebiro et al. 2012; Deeb et al. 2016; Vignone et al. 2017). Only two of the above individuals had clinical symptoms of congenital hypothyroidism, and both individuals carried the p.Pro68Ser variant in a heterozygous state (Deeb et al. 2016; Vignone et al. 2017). The other individuals were classified as mildly affected with congenital hypothyroidism. The p.Pro68Ser variant was identified in a heterozygous state in three of 213 controls (Tenenbaum-Rakover et al. 2009; Nicoletti et al. 2009) and is reported at a frequency of 0.00332 in the Other population of the Exome Aggregation Consortium. One homozygote is reported in the South Asian population in the Genome Aggregation Database. Surface expression of the p.Pro68Ser variant was found to be reduced by 80% in HEK-293 cells and by 50% in COS-7 cells compared to wild type, but the biological activity as measured by cAMP production was not affected (Tenenbaum-Rakover et al. 2009; Nicoletti et al. 2009). Based on the collective evidence supporting a mild phenotype, the p.Pro68Ser variant is classified as a variant of unknown significance, but suspicious for pathogenicity for congenital hypothyroidism. This variant was observed by ICSL as part of a predisposition screen in an ostensibly healthy population.
Mendelics	RCV000989248	SCV001139491	uncertain significance	Familial hyperthyroidism due to mutations in TSH receptor	2023-04-21	criteria provided, single submitter	clinical testing
Illumina Laboratory Services, Illumina	RCV000989248	SCV001278112	benign	Familial hyperthyroidism due to mutations in TSH receptor	2017-04-27	criteria provided, single submitter	clinical testing	This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases was too high to be consistent with this variant causing disease. Therefore, this variant is classified as benign.
Invitae	RCV001223345	SCV001395489	pathogenic	not provided	2021-09-02	criteria provided, single submitter	clinical testing	This sequence change replaces proline with serine at codon 68 of the TSHR protein (p.Pro68Ser). The proline residue is moderately conserved and there is a moderate physicochemical difference between proline and serine. This variant is present in population databases (rs142063461, ExAC 0.1%). This missense change has been observed in individual(s) with clinical features of hypothyroidism (PMID: 19240155, 25557138). In at least one individual the data is consistent with the variant being in trans (on the opposite chromosome) from a pathogenic variant. It has also been observed to segregate with disease in related individuals. ClinVar contains an entry for this variant (Variation ID: 437071). Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Tolerated"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Class C0"). Experimental studies have shown that this missense change affects TSHR function (PMID: 19240155, 19820021). For these reasons, this variant has been classified as Pathogenic.
GeneDx	RCV001223345	SCV002097421	uncertain significance	not provided	2022-01-28	criteria provided, single submitter	clinical testing	Identified in the heterozygous state in a patient with congenital hypothyroidism in the published literature, although this variant was inherited from a parent with unknown clinical status (Oliver-Petit et al., 2021); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Published functional studies suggest this variant is associated with decreased TSH binding capacity and a reduction in cell-surface expression, but no overall effect on biological activity (Nicoletti et al., 2009; Tenenbaum-Rakover et al., 2009); Additional functional studies suggest this variant reduces TSH-stimulated downstream activity in cells transfected with P68S alone (simulating homozygosity) but no effect noted when cotransfecting P68S and wild-type TSHR (simulating heterozygosity) (Tenenbaum-Rakover et al., 2009); Observed in homozygous state in one clinically unaffected adult relative of an individual referred for genetic testing at GeneDx; This variant is associated with the following publications: (PMID: 27060741, 31589614, 25557138, 19820021, 19240155, 34248839, 34426522, 26556299, 33558524, 34200080, 26990548, 28444304)
Ambry Genetics	RCV002524319	SCV003709914	likely pathogenic	Inborn genetic diseases	2021-07-27	criteria provided, single submitter	clinical testing	The c.202C>T (p.P68S) alteration is located in exon 2 (coding exon 2) of the TSHR gene. This alteration results from a C to T substitution at nucleotide position 202, causing the proline (P) at amino acid position 68 to be replaced by a serine (S). Based on the available evidence, this alteration is likely pathogenic for autosomal recessive congenital nongoitrous hypothyroidism; however, the association of this alteration with autosomal dominant nonautoimmune hyperthyroidism is unlikely. Based on data from the Genome Aggregation Database (gnomAD), the TSHR c.202C>T alteration was observed in 0.05% (140/281886) of total alleles studied, with a frequency of 0.17% (18/10358) in the Ashkenazi Jewish subpopulation. This variant has been observed as compound heterozygous with other TSHR variants in several individuals with elevated TSH levels and it has been reported to segregate with elevated TSH in multiple families (Tennenbaum-Rakover, 2009; Tennenbaum-Rakover, 2015; Vigone, 2017). This amino acid position is highly conserved in available vertebrate species. In vitro functional studies show that in the homozygous and compound heterozygous states, this alteration leads to a significant reduction in TSHR activity compared to wild-type (Tennenbaum-Rakover, 2009). Based on the available evidence, this alteration is classified as likely pathogenic.
Revvity Omics, Revvity	RCV001223345	SCV004236983	uncertain significance	not provided	2023-05-01	criteria provided, single submitter	clinical testing
Center of Medical Genetics and Primary Health Care	RCV001005031	SCV000987284	uncertain significance	Malignant tumor of breast	2020-04-08	no assertion criteria provided	research	ACMG Guidelines 2015 criteria PP2 Pathogenic Supporting: 38 out of 52 non-VUS missense variants in gene TSHR are PATH = 73.1% > threshold of 51.0%, and 44 out of 118 clinically reported variants in gene TSHR are PATH = 37.3% > threshold of 12.0%. PP3 Pathogenic Supporting: 9 pathogenic predictions from DANN, DEOGEN2, EIGEN, FATHMM-MKL, M-CAP, MVP, MutationAssessor, MutationTaster and REVEL vs 2 benign predictions from PrimateAI and SIFT. PP4 Pathogenic Supporting: The variant was detected in a female patient diagnosed with breast cancer at the age of 28 y.o. However, the current data are insufficient to assess the role of the variant in the development of breast cancer. Therefore, this variant was classified as a Variant of Unknown Significance.
New York Genome Center	RCV001255029	SCV001431120	uncertain significance	Hypothyroidism	2019-11-06	no assertion criteria provided	clinical testing
Department of Pathology and Laboratory Medicine, Sinai Health System	RCV001223345	SCV001551832	uncertain significance	not provided		no assertion criteria provided	clinical testing	The TSHR p.P68S variant was identified in 2 of 382 proband chromosomes (frequency: 0.0052) from individuals with non-autoimmune subclinical hypothyroidism non-autoimmune hyperthyrotropinemia (Nicoletti_2009_PMID:19820021; Calebiro_2012_PMID:22049173). In a large consanguineous family with resistance to TSH, the p.P68S variant was found in 4 family members in the heterozygous state (1 mildly affected, 3 unaffected) and in 4 family members in the compound heterozygous state (2 affected, 2 mildly affected). Functional assays showed a decrease in TSHR activity when the p.P68S TSHR variant was transfected into HEK-293 cells alone, but not when transfected as wildtype-TSHR/p.P68S (mimicking heterozygosity) (Tenenbaum-Rakover_2009_PMID:19240155). The p.P68S variant was also identified in 4 of 111 pediatric patients; 3 patients had subclinical hypothyroidism (2 heterozygous, 1 compound heterozygous) and 1 patient had congenital hypothyroidism (heterozygous) (Vigone_2017_PMID:28561265). The variant was identified in dbSNP (ID: rs142063461), ClinVar (classified as uncertain significance by Illumina and as likely pathogenic by Genetic Services Laboratory, University of Chicago) and LOVD 3.0 (classified as likely pathogenic). The variant was identified in control databases in 140 of 281886 chromosomes (1 homozygous) at a frequency of 0.0004967 increasing the likelihood this could be a low frequency benign variant (Genome Aggregation Database March 6, 2019, v2.1.1). The variant was observed in the following populations: Ashkenazi Jewish in 18 of 10358 chromosomes (freq: 0.001738), South Asian in 37 of 30534 chromosomes (freq: 0.001212), Other in 5 of 7178 chromosomes (freq: 0.000697), Latino in 24 of 35272 chromosomes (freq: 0.00068), European (non-Finnish) in 55 of 128682 chromosomes (freq: 0.000427) and African in 1 of 24926 chromosomes (freq: 0.00004), but was not observed in the East Asian or European (Finnish) populations. The p.P68 residue is conserved across mammals and other organisms, and computational analyses (PolyPhen-2, SIFT, AlignGVGD, BLOSUM, MutationTaster) provide inconsistent predictions regarding the potential impact to the protein. The variant occurs outside of the splicing consensus sequence and in silico or computational prediction software programs (SpliceSiteFinder, MaxEntScan, NNSPLICE, GeneSplicer) do not predict a difference in splicing. Functional in vitro assays showed a decrease in cell surface expression of TSHR with the p.P68S compared to wildtype but no significant difference in biological activity (Nicoletti_2009_PMID:19820021). In summary, based on the above information the clinical significance of this variant cannot be determined with certainty at this time. This variant is classified as a variant of uncertain significance.