NM_000369.5(TSHR):c.929G>A (p.Arg310His) AND TSHR-related disorder

Germline classification:: Likely benign (1 submission)
Last evaluated:: Jan 5, 2024
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

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:: RCV004530043.2

Allele description [Variation Report for NM_000369.5(TSHR):c.929G>A (p.Arg310His)]

NM_000369.5(TSHR):c.929G>A (p.Arg310His)

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.929G>A (p.Arg310His)

HGVS:

NC_000014.9:g.81142987G>A
NG_009206.1:g.192463G>A
NM_000369.5:c.929G>AMANE SELECT
NP_000360.2:p.Arg310His
NP_000360.2:p.Arg310His
LRG_523t1:c.929G>A
LRG_523:g.192463G>A
LRG_523p1:p.Arg310His
NC_000014.8:g.81609331G>A
NM_000369.2:c.929G>A

Protein change:

R310H

Links:

dbSNP: rs139286618

NCBI 1000 Genomes Browser:

rs139286618

Molecular consequence:

NM_000369.5:c.929G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: TSHR-related disorder
Synonyms:: TSHR-Related Disorders; TSHR-related condition
Identifiers:

Recent activity

Clear Turn Off Turn On

Gm9291 predicted pseudogene 9291 [Mus musculus]
Gm9291 predicted pseudogene 9291 [Mus musculus]
Gene ID:668660

Gene
Gm9291 AND (alive[prop]) (1)
Gene
B3GNT4 [Pteropus giganteus]
B3GNT4 [Pteropus giganteus]
Gene ID:120616054

Gene
Homo sapiens GLI2 transcription factor (Gli2) mRNA, partial cds, alternatively s...
Homo sapiens GLI2 transcription factor (Gli2) mRNA, partial cds, alternatively spliced
gi|66933083|gb|DQ004396.1|

Nucleotide
multidrug resistance protein A [Acinetobacter pittii PHEA-2]
multidrug resistance protein A [Acinetobacter pittii PHEA-2]
gi|375134880|ref|YP_004995530.1|

Protein

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004728339	PreventionGenetics, part of Exact Sciences	no assertion criteria provided	Likely benign (Jan 5, 2024)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004728339

PreventionGenetics, part of Exact Sciences

no assertion criteria provided

Likely benign
(Jan 5, 2024)

germline

clinical testing

Help

Summary from all submissions

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

Details of each submission

From PreventionGenetics, part of Exact Sciences, SCV004728339.2

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

Description

This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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

Last Updated: Nov 10, 2024

ClinVar

Relating variation to medicine