NM_152222.2(RELT):c.563G>A (p.Arg188Gln) AND Inborn genetic diseases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Feb 5, 2024
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:: RCV004443881.1

Allele description [Variation Report for NM_152222.2(RELT):c.563G>A (p.Arg188Gln)]

NM_152222.2(RELT):c.563G>A (p.Arg188Gln)

Gene:

RELT:RELT TNF receptor [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q13.4

Genomic location:

Preferred name:

NM_152222.2(RELT):c.563G>A (p.Arg188Gln)

HGVS:

NC_000011.10:g.73392406G>A
NM_001425248.1:c.563G>A
NM_001425249.1:c.563G>A
NM_001425250.1:c.563G>A
NM_001425251.1:c.515G>A
NM_001425252.1:c.563G>A
NM_032871.4:c.563G>A
NM_152222.2:c.563G>AMANE SELECT
NP_001412177.1:p.Arg188Gln
NP_001412178.1:p.Arg188Gln
NP_001412179.1:p.Arg188Gln
NP_001412180.1:p.Arg172Gln
NP_001412181.1:p.Arg188Gln
NP_116260.2:p.Arg188Gln
NP_689408.1:p.Arg188Gln
NC_000011.9:g.73103451G>A
NM_032871.3:c.563G>A
NR_189152.1:n.689G>A

Protein change:

R172Q

Molecular consequence:

NM_001425248.1:c.563G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001425249.1:c.563G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001425250.1:c.563G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001425251.1:c.515G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001425252.1:c.563G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_032871.4:c.563G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_152222.2:c.563G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Inborn genetic diseases
Identifiers:: MeSH: D030342; MedGen: C0950123

Recent activity

Clear Turn Off Turn On

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
SCV004939031	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Feb 5, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004939031

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Feb 5, 2024)

germline

clinical testing

Citation Link

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 Ambry Genetics, SCV004939031.1

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

Description

The c.563G>A (p.R188Q) alteration is located in exon 6 (coding exon 5) of the RELT gene. This alteration results from a G to A substitution at nucleotide position 563, causing the arginine (R) at amino acid position 188 to be replaced by a glutamine (Q). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#	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: May 7, 2024

ClinVar

Relating variation to medicine