NM_033409.4(SLC52A3):c.484G>A (p.Gly162Ser) AND Inborn genetic diseases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Sep 18, 2019
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:: RCV002334591.2

Allele description [Variation Report for NM_033409.4(SLC52A3):c.484G>A (p.Gly162Ser)]

NM_033409.4(SLC52A3):c.484G>A (p.Gly162Ser)

Gene:

SLC52A3:solute carrier family 52 member 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

20p13

Genomic location:

Preferred name:

NM_033409.4(SLC52A3):c.484G>A (p.Gly162Ser)

HGVS:

NC_000020.11:g.765291C>T
NG_027687.2:g.15695G>A
NM_001370085.1:c.484G>A
NM_001370086.1:c.484G>A
NM_033409.4:c.484G>AMANE SELECT
NP_001357014.1:p.Gly162Ser
NP_001357015.1:p.Gly162Ser
NP_212134.3:p.Gly162Ser
LRG_1394t1:c.484G>A
LRG_1394:g.15695G>A
LRG_1394p1:p.Gly162Ser
NC_000020.10:g.745935C>T
NM_033409.3:c.484G>A

Protein change:

G162S

Links:

dbSNP: rs896950205

NCBI 1000 Genomes Browser:

rs896950205

Molecular consequence:

NM_001370085.1:c.484G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001370086.1:c.484G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_033409.4:c.484G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

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

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002634864	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Sep 18, 2019)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002634864

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Sep 18, 2019)

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, SCV002634864.2

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

Description

The p.G162S variant (also known as c.484G>A), located in coding exon 1 of the SLC52A3 gene, results from a G to A substitution at nucleotide position 484. The glycine at codon 162 is replaced by serine, an amino acid with similar properties. This amino acid position is highly conserved in available vertebrate species. In addition, this alteration is predicted to be deleterious by in silico analysis. Since supporting evidence is limited at this time, 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: Sep 29, 2024

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