NM_130849.4(SLC39A4):c.1202G>A (p.Trp401Ter) AND not provided

Germline classification:: Pathogenic (1 submission)
Last evaluated:: Dec 12, 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:: RCV001881535.3

Allele description [Variation Report for NM_130849.4(SLC39A4):c.1202G>A (p.Trp401Ter)]

NM_130849.4(SLC39A4):c.1202G>A (p.Trp401Ter)

Gene:

SLC39A4:solute carrier family 39 member 4 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

8q24.3

Genomic location:

Preferred name:

NM_130849.4(SLC39A4):c.1202G>A (p.Trp401Ter)

HGVS:

NC_000008.11:g.144414043C>T
NG_012234.2:g.7848G>A
NM_001374839.1:c.920G>A
NM_017767.3:c.1127G>A
NM_130849.4:c.1202G>AMANE SELECT
NP_001361768.1:p.Trp307Ter
NP_060237.3:p.Trp376Ter
NP_570901.3:p.Trp401Ter
NC_000008.10:g.145639427C>T

Protein change:

W307*

Links:

dbSNP: rs2130796764

NCBI 1000 Genomes Browser:

rs2130796764

Molecular consequence:

NM_001374839.1:c.920G>A - nonsense - [Sequence Ontology: SO:0001587]
NM_017767.3:c.1127G>A - nonsense - [Sequence Ontology: SO:0001587]
NM_130849.4:c.1202G>A - nonsense - [Sequence Ontology: SO:0001587]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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
SCV002151569	Invitae	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Pathogenic (Dec 12, 2021)	germline	clinical testing	PubMed (2) [See all records that cite these PMIDs] 12955721, 28492532

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002151569

Invitae

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Pathogenic
(Dec 12, 2021)

germline

clinical testing

PubMed (2)
[See all records that cite these PMIDs]

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

Mutation spectrum of human SLC39A4 in a panel of patients with acrodermatitis enteropathica.

Küry S, Kharfi M, Kamoun R, Taïeb A, Mallet E, Baudon JJ, Glastre C, Michel B, Sebag F, Brooks D, Schuster V, Scoul C, Dréno B, Bézieau S, Moisan JP.

Hum Mutat. 2003 Oct;22(4):337-8.

PubMed [citation]

PMID:: 12955721

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, SCV002151569.3

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (2)

Description

This variant has not been reported in the literature in individuals affected with SLC39A4-related conditions. For these reasons, this variant has been classified as Pathogenic. This sequence change creates a premature translational stop signal (p.Trp401*) in the SLC39A4 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in SLC39A4 are known to be pathogenic (PMID: 12955721). This variant is not present in population databases (gnomAD no frequency).

#	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