NM_001367916.1(MAGT1):c.-5C>T AND X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia

This record was updated by the submitter. Please see the current version.

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Apr 19, 2023
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:: RCV000797948.4

Allele description

NM_001367916.1(MAGT1):c.-5C>T

Genes:

LOC130068460:ATAC-STARR-seq lymphoblastoid active region 29781 [Gene]
MAGT1:magnesium transporter 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

Xq21.1

Genomic location:

Preferred name:

NM_001367916.1(MAGT1):c.-5C>T

HGVS:

NC_000023.11:g.77895415G>A
NG_016390.1:g.5154C>T
NG_033027.2:g.952G>A
NM_001367916.1:c.-5C>TMANE SELECT
NM_032121.5:c.92C>T
NP_115497.4:p.Ala31Val
LRG_353t1:c.92C>T
LRG_1250:g.952G>A
LRG_353:g.5154C>T
LRG_353p1:p.Ala31Val
NC_000023.10:g.77150912G>A
NG_033027.1:g.952G>A

Protein change:

A31V

Links:

dbSNP: rs199604767

NCBI 1000 Genomes Browser:

rs199604767

Molecular consequence:

NM_001367916.1:c.-5C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_032121.5:c.92C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia
Identifiers:: MONDO: MONDO:0010455; MedGen: C3275445; Orphanet: 317476; OMIM: 300853

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
SCV000937537	Invitae	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Apr 19, 2023)	germline	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

SCV000937537

Invitae

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Apr 19, 2023)

germline

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	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Invitae, SCV000937537.4

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

Description

Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Not Available"; PolyPhen-2: "Benign"; Align-GVGD: "Not Available". The valine amino acid residue is found in multiple mammalian species, which suggests that this missense change does not adversely affect protein function. ClinVar contains an entry for this variant (Variation ID: 644106). This variant has not been reported in the literature in individuals affected with MAGT1-related conditions. This variant is present in population databases (rs199604767, gnomAD 0.007%). This sequence change replaces alanine, which is neutral and non-polar, with valine, which is neutral and non-polar, at codon 31 of the MAGT1 protein (p.Ala31Val). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

#	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: Feb 20, 2024

ClinVar

Relating variation to medicine