NM_000369.5(TSHR):c.1170T>G (p.Cys390Trp) AND multiple conditions

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: Jul 28, 2021
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV002490330.1

Allele description [Variation Report for NM_000369.5(TSHR):c.1170T>G (p.Cys390Trp)]

NM_000369.5(TSHR):c.1170T>G (p.Cys390Trp)

Gene:

TSHR:thyroid stimulating hormone receptor [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

14q31.1

Genomic location:

Preferred name:

NM_000369.5(TSHR):c.1170T>G (p.Cys390Trp)

HGVS:

NC_000014.9:g.81143228T>G
NG_009206.1:g.192704T>G
NM_000369.5:c.1170T>GMANE SELECT
NP_000360.2:p.Cys390Trp
LRG_523:g.192704T>G
NC_000014.8:g.81609572T>G

Protein change:

C390W; CYS390TRP

Links:

OMIM: 603372.0015; dbSNP: rs121908871

NCBI 1000 Genomes Browser:

rs121908871

Molecular consequence:

NM_000369.5:c.1170T>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Familial gestational hyperthyroidism
Identifiers:: MONDO: MONDO:0011309; MedGen: C1863959; OMIM: 603373

Name:: Familial hyperthyroidism due to mutations in TSH receptor
Synonyms:: HYPERTHYROIDISM, CONGENITAL NONAUTOIMMUNE; HYPERTHYROIDISM, NONAUTOIMMUNE, AUTOSOMAL DOMINANT; TOXIC THYROID HYPERPLASIA, AUTOSOMAL DOMINANT; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0012203; MedGen: C1836706; Orphanet: 424; OMIM: 609152

Name:: Hypothyroidism due to TSH receptor mutations
Synonyms:: HYPOTHYROIDISM DUE TO UNRESPONSIVENESS TO THYROTROPIN; HYPOTHYROIDISM, CONGENITAL, DUE TO TSH RESISTANCE; HYPOTHYROIDISM, NONAUTOIMMUNE; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0010142; MedGen: C3493776; Orphanet: 90673; OMIM: 275200

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002800578	Fulgent Genetics, Fulgent Genetics	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely pathogenic (Jul 28, 2021)	unknown	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002800578

Fulgent Genetics, Fulgent Genetics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely pathogenic
(Jul 28, 2021)

unknown

clinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	unknown	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From Fulgent Genetics, Fulgent Genetics, SCV002800578.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	unknown	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Jan 7, 2023

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