NM_003038.5(SLC1A4):c.344G>A (p.Gly115Asp) AND Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome

Germline classification:: Likely pathogenic (1 submission)
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:: RCV003883284.1

Allele description [Variation Report for NM_003038.5(SLC1A4):c.344G>A (p.Gly115Asp)]

NM_003038.5(SLC1A4):c.344G>A (p.Gly115Asp)

Gene:

SLC1A4:solute carrier family 1 member 4 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2p14

Genomic location:

Preferred name:

NM_003038.5(SLC1A4):c.344G>A (p.Gly115Asp)

HGVS:

NC_000002.12:g.64989987G>A
NG_053002.1:g.6543G>A
NG_095373.1:g.687G>A
NM_001193493.2:c.-134+1367G>A
NM_001348406.2:c.-134+1367G>A
NM_001348407.2:c.-134+1433G>A
NM_003038.5:c.344G>AMANE SELECT
NP_003029.2:p.Gly115Asp
NC_000002.11:g.65217121G>A

Protein change:

G115D

Molecular consequence:

NM_001193493.2:c.-134+1367G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001348406.2:c.-134+1367G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001348407.2:c.-134+1433G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_003038.5:c.344G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome
Synonyms:: Spastic tetraplegia, thin corpus callosum, and progressive microcephaly
Identifiers:: MONDO: MONDO:0014725; MedGen: C4225254; Orphanet: 447997; OMIM: 616657

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004697630	Molecular Genetics Lab, CHRU Brest	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely pathogenic	biparental	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004697630

Molecular Genetics Lab, CHRU Brest

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely pathogenic

biparental

clinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	biparental	yes	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From Molecular Genetics Lab, CHRU Brest, SCV004697630.1

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

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

Last Updated: Mar 10, 2024

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