NM_006516.4(SLC2A1):c.967G>A (p.Val323Met) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Sep 18, 2020
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:: RCV000439467.4

Allele description [Variation Report for NM_006516.4(SLC2A1):c.967G>A (p.Val323Met)]

NM_006516.4(SLC2A1):c.967G>A (p.Val323Met)

Gene:

SLC2A1:solute carrier family 2 member 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1p34.2

Genomic location:

Preferred name:

NM_006516.4(SLC2A1):c.967G>A (p.Val323Met)

HGVS:

NC_000001.11:g.42929215C>T
NG_008232.1:g.34962G>A
NM_006516.4:c.967G>AMANE SELECT
NP_006507.2:p.Val323Met
LRG_1132:g.34962G>A
NC_000001.10:g.43394886C>T
NM_006516.2:c.967G>A

Protein change:

V323M

Links:

dbSNP: rs749426767

NCBI 1000 Genomes Browser:

rs749426767

Molecular consequence:

NM_006516.4:c.967G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000515701	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Uncertain significance (Sep 18, 2020)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000515701

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Uncertain significance
(Sep 18, 2020)

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	yes	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From GeneDx, SCV000515701.4

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

Description

In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Identified in a patient with febrile seizures but did not segregate with the phenotype in the family; inherited from unaffected mother and absent in father and sister with febrile seizures (Hartmann et al., 2017)

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

Last Updated: Sep 29, 2024

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