VCV000192273.1 - ClinVar

NM_199334.5(THRA):c.1193C>G (p.Pro398Arg)

Germline

Classification

no assertion criteria provided. Learn more about how ClinVar calculates review status.

Pathogenic

This classification is based on the single submission received

The aggregate germline classification for this variant, typically for a monogenic or Mendelian disorder as in the ACMG/AMP guidelines, or for response to a drug. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the aggregate classification.

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_199334.5(THRA):c.1193C>G (p.Pro398Arg)

Variation ID: 192273 Accession: VCV000192273.1

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 17q21.1 17: 40089416 (GRCh38) [ NCBI UCSC ] 17: 38245669 (GRCh37) [ NCBI UCSC ]

Timeline in ClinVar

	First in ClinVar Help The date this variant first appeared in ClinVar with each type of classification.	Last submission Help The date of the most recent submission for each type of classification for this variant.	Last evaluated Help The most recent date that a submitter evaluated this variant for each type of classification.
Germline	Sep 9, 2016	Sep 9, 2016	May 1, 2015

HGVS

Nucleotide	Protein	Molecular consequence
NM_199334.5:c.1193C>G MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_955366.1:p.Pro398Arg	missense
NM_001190918.2:c.1110+83C>G		intron variant
NM_001190919.2:c.1110+83C>G		intron variant
NM_003250.6:c.1110+83C>G		intron variant
NC_000017.11:g.40089416C>G
NC_000017.10:g.38245669C>G
NG_023345.1:g.32224C>G

... more HGVS ... less HGVS

Protein change

P398R

Other names

Canonical SPDI

NC_000017.11:40089415:C:G

Global minor allele frequency (GMAF) Help The global minor allele frequency calculated by the 1000 Genomes Project. The minor allele at this location is indicated in parentheses and may be different from the allele represented by this VCV record.

Allele frequency Help The frequency of the allele represented by this VCV record.

Links

ClinGen: CA10575716 OMIM: 190120.0005 dbSNP: rs876657396 VarSome

Genes

Gene	OMIM	ClinGen Gene Dosage Sensitivity Curation		Variation Viewer Help Links to Variation Viewer, a genome browser to view variation data from NCBI databases.	Related variants
Gene	OMIM	HI score Help The haploinsufficiency score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team.	TS score Help The triplosensitivity score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team.		Within gene Help The number of variants in ClinVar that are contained within this gene, with a link to view the list of variants.	All Help The number of variants in ClinVar for this gene, including smaller variants within the gene and larger CNVs that overlap or fully contain the gene.
THRA		No evidence available	No evidence available	GRCh38 GRCh37	95	119

Conditions - Germline

Condition Help The condition for this variant-condition (RCV) record in ClinVar.	Classification Help The aggregate germline classification for this variant-condition (RCV) record in ClinVar. The number of submissions that contribute to this aggregate classification is shown in parentheses. (# of submissions)	Review status Help The aggregate review status for this variant-condition (RCV) record in ClinVar. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status.	Last evaluated Help The most recent date that a submitter evaluated this variant for the condition.	Variation/condition record Help The RCV accession number, with most recent version number, for the variant-condition record, with a link to the RCV web page.
Congenital nongoitrous hypothyroidism 6	Pathogenic (1)	no assertion criteria provided	May 1, 2015	RCV000172855.3

Submissions - Germline

Classification Help The submitted germline classification for each SCV record. (Last evaluated)	Review status Help Stars represent the review status, or the level of review supporting the submitted (SCV) record. This value is calculated by NCBI based on data from the submitter. Read our rules for calculating the review status. This column also includes a link to the submitter’s assertion criteria if provided, and the collection method. (Assertion criteria)	Condition Help The condition for the classification, provided by the submitter for this submitted (SCV) record. This column also includes the affected status and allele origin of individuals observed with this variant.	Submitter Help The submitting organization for this submitted (SCV) record. This column also includes the SCV accession and version number, the date this SCV first appeared in ClinVar, and the date that this SCV was last updated in ClinVar.	Expand all rows Collapse all rows Help This column includes more information supporting the classification, including citations, the comment on classification, and detailed evidence provided as observations of the variant by the submitter.
Pathogenic (May 01, 2015) C Contributing to aggregate classification	no assertion criteria provided	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6	OMIM Accession: SCV000223830.2 First in ClinVar: Jun 08, 2015 Last updated: Sep 09, 2016	Publications: PubMed (1) PubMed: 25670821 Observation: 1 Collection method: literature only Allele origin: germline Affected status: not provided more Observation 1 Collection method: literature only Allele origin: germline Affected status: not provided Comment on evidence: In an 8-year-old Polish girl with congenital nongoitrous hypothyroidism (CHNG6; 614450), Tylki-Szymanska et al. (2015) identified heterozygosity for a c.1193C-G transversion (c.1193C-G, NM_199334) in the … (more) In an 8-year-old Polish girl with congenital nongoitrous hypothyroidism (CHNG6; 614450), Tylki-Szymanska et al. (2015) identified heterozygosity for a c.1193C-G transversion (c.1193C-G, NM_199334) in the THRA gene, resulting in a pro398-to-arg (P398R) substitution in the last exon of THRA isoform 1. The mutation occurred de novo in the proband. (less)

Citations for germline classification of this variant

Title	Author	Journal	Year	Link
Thyroid hormone resistance syndrome due to mutations in the thyroid hormone receptor α gene (THRA).	Tylki-Szymańska A	Journal of medical genetics	2015	PMID: 25670821

Text-mined citations for rs876657396 ...

These citations are identified by LitVar using the rs number, so they may include citations for more than one variant at this location. Please review the LitVar results carefully for your variant of interest.

Record last updated Jan 13, 2025