NM_014251.3(SLC25A13):c.1910T>C (p.Val637Ala) AND not provided

Germline classification:: Uncertain significance (2 submissions)
Last evaluated:: Mar 1, 2021
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV000726730.10

Allele description [Variation Report for NM_014251.3(SLC25A13):c.1910T>C (p.Val637Ala)]

NM_014251.3(SLC25A13):c.1910T>C (p.Val637Ala)

Gene:

SLC25A13:solute carrier family 25 member 13 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

7q21.3

Genomic location:

Preferred name:

NM_014251.3(SLC25A13):c.1910T>C (p.Val637Ala)

Other names:

p.V637A:GTT>GCT

HGVS:

NC_000007.14:g.96121309A>G
NG_012247.2:g.205839T>C
NM_001160210.2:c.1913T>C
NM_014251.3:c.1910T>CMANE SELECT
NP_001153682.1:p.Val638Ala
NP_055066.1:p.Val637Ala
NC_000007.13:g.95750621A>G
NM_014251.2:c.1910T>C
NR_027662.2:n.1936T>C

Protein change:

V637A

Links:

dbSNP: rs148962110

NCBI 1000 Genomes Browser:

rs148962110

Molecular consequence:

NM_001160210.2:c.1913T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_014251.3:c.1910T>C - missense variant - [Sequence Ontology: SO:0001583]
NR_027662.2:n.1936T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Observations:

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
SCV000239187	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Uncertain significance (Mar 1, 2021)	germline	clinical testing	Citation Link,
SCV000702530	Eurofins Ntd Llc (ga)	criteria provided, single submitter (EGL ClinVar v180209 classification definitions)	Uncertain significance (Jul 27, 2018)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000239187

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Uncertain significance
(Mar 1, 2021)

germline

clinical testing

Citation Link,

SCV000702530

Eurofins Ntd Llc (ga)

criteria provided, single submitter

(EGL ClinVar v180209 classification definitions)

Uncertain significance
(Jul 27, 2018)

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	3	not provided	not provided	not provided	not provided	clinical testing
not provided	germline	yes	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From GeneDx, SCV000239187.12

#	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; Has not been previously published as pathogenic or benign to our knowledge

#	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

From Eurofins Ntd Llc (ga), SCV000702530.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	3	not provided	not provided	clinical testing	not provided

#	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		3	not provided	not provided	not provided

Last Updated: May 26, 2024

ClinVar

Relating variation to medicine