NM_001191061.2(SLC25A22):c.784G>A (p.Glu262Lys) AND Inborn genetic diseases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Aug 28, 2017
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:: RCV002412197.2

Allele description [Variation Report for NM_001191061.2(SLC25A22):c.784G>A (p.Glu262Lys)]

NM_001191061.2(SLC25A22):c.784G>A (p.Glu262Lys)

Gene:

SLC25A22:solute carrier family 25 member 22 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11p15.5

Genomic location:

Preferred name:

NM_001191061.2(SLC25A22):c.784G>A (p.Glu262Lys)

HGVS:

NC_000011.10:g.792176C>T
NG_023407.1:g.11094G>A
NM_001191060.2:c.784G>A
NM_001191061.2:c.784G>AMANE SELECT
NM_024698.6:c.784G>A
NP_001177989.1:p.Glu262Lys
NP_001177989.1:p.Glu262Lys
NP_001177990.1:p.Glu262Lys
NP_078974.1:p.Glu262Lys
NC_000011.9:g.792176C>T
NM_001191060.1:c.784G>A
NM_024698.5:c.784G>A

Protein change:

E262K

Molecular consequence:

NM_001191060.2:c.784G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001191061.2:c.784G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_024698.6:c.784G>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
SCV002670921	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Aug 28, 2017)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002670921

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Aug 28, 2017)

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, SCV002670921.2

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

Description

The p.E262K variant (also known as c.784G>A), located in coding exon 8 of the SLC25A22 gene, results from a G to A substitution at nucleotide position 784. The glutamic acid at codon 262 is replaced by lysine, an amino acid with similar properties. This amino acid position is highly conserved in available vertebrate species. In addition, the in silico prediction for this alteration is inconclusive. 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: May 1, 2024

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