VCV002683746.1 - ClinVar

NM_001083619.3(GRIA2):c.1883T>C (p.Phe628Ser)

Germline

Classification

The aggregate germline classification for this variant, typically for a monogenic or Mendelian disorder as in the ACMG/AMP guidelines, or for response to a drug. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the aggregate classification.

(1)

Stars represent the aggregate review status, or the level of review supporting the aggregate germline classification for this VCV record. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status. The number of submissions which contribute to this review status is shown in parentheses.

Likely pathogenic

no assertion criteria provided

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_001083619.3(GRIA2):c.1883T>C (p.Phe628Ser)

Variation ID: 2683746 Accession: VCV002683746.1

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 4q32.1 4: 157341302 (GRCh38) [ NCBI UCSC ] 4: 158262454 (GRCh37) [ NCBI UCSC ]

Timeline in ClinVar

	First in ClinVar Help The date this variant first appeared in ClinVar with each type of classification.	Last submission Help The date of the most recent submission for each type of classification for this variant.	Last evaluated Help The most recent date that a submitter evaluated this variant for each type of classification.
Germline	Jan 6, 2024	Jan 6, 2024	Jun 3, 2021

HGVS

Nucleotide	Protein	Molecular consequence
NM_001083619.3:c.1883T>C MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_001077088.2:p.Phe628Ser	missense
NM_000826.6:c.1883T>C	NP_000817.5:p.Phe628Ser	missense
NM_001083620.3:c.1742T>C	NP_001077089.2:p.Phe581Ser	missense
NM_001379000.3:c.1742T>C	NP_001365929.3:p.Phe581Ser	missense
NM_001379001.3:c.1742T>C	NP_001365930.3:p.Phe581Ser	missense
NC_000004.12:g.157341302T>C
NC_000004.11:g.158262454T>C

... more HGVS ... less HGVS

Protein change

F581S, F628S

Other names

p.Phe628Ser

Canonical SPDI

NC_000004.12:157341301:T:C

Functional consequence Help The effect of the variant on RNA or protein function, based on experimental evidence from submitters.

Global minor allele frequency (GMAF) Help The global minor allele frequency calculated by the 1000 Genomes Project. The minor allele at this location is indicated in parentheses and may be different from the allele represented by this VCV record.

Allele frequency Help The frequency of the allele represented by this VCV record.

Links

VarSome

Genes

Gene	OMIM	ClinGen Gene Dosage Sensitivity Curation		Variation Viewer Help Links to Variation Viewer, a genome browser to view variation data from NCBI databases.	Related variants
Gene	OMIM	HI score Help The haploinsufficiency score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team.	TS score Help The triplosensitivity score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team.		Within gene Help The number of variants in ClinVar that are contained within this gene, with a link to view the list of variants.	All Help The number of variants in ClinVar for this gene, including smaller variants within the gene and larger CNVs that overlap or fully contain the gene.
GRIA2		-	-	GRCh38 GRCh37	152	187

Conditions - Germline

Condition Help The condition for this variant-condition (RCV) record in ClinVar.	Classification Help The aggregate germline classification for this variant-condition (RCV) record in ClinVar. The number of submissions that contribute to this aggregate classification is shown in parentheses. (# of submissions)	Review status Help The aggregate review status for this variant-condition (RCV) record in ClinVar. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status.	Last evaluated Help The most recent date that a submitter evaluated this variant for the condition.	Variation/condition record Help The RCV accession number, with most recent version number, for the variant-condition record, with a link to the RCV web page.
Neurodevelopmental disorder with language impairment and behavioral abnormalities	Likely pathogenic (1)	no assertion criteria provided	Jun 3, 2021	RCV003482192.2

Submissions - Germline

Classification Help The submitted germline classification for each SCV record. (Last evaluated)	Review status Help Stars represent the review status, or the level of review supporting the submitted (SCV) record. This value is calculated by NCBI based on data from the submitter. Read our rules for calculating the review status. This column also includes a link to the submitter’s assertion criteria if provided, and the collection method. (Assertion criteria)	Condition Help The condition for the classification, provided by the submitter for this submitted (SCV) record. This column also includes the affected status and allele origin of individuals observed with this variant.	Submitter Help The submitting organization for this submitted (SCV) record. This column also includes the SCV accession and version number, the date this SCV first appeared in ClinVar, and the date that this SCV was last updated in ClinVar.	More information Help This column includes more information supporting the classification, including citations, the comment on classification, and detailed evidence provided as observations of the variant by the submitter.
Likely pathogenic (Jun 03, 2021)	no assertion criteria provided Method: clinical testing	Neurodevelopmental disorder with language impairment and behavioral abnormalities (Autosomal dominant inheritance) Affected status: yes Allele origin: germline	Clinical Genomics Laboratory, Stanford Medicine Accession: SCV004227896.1 First in ClinVar: Jan 06, 2024 Last updated: Jan 06, 2024	Comment: The p.Phe628Ser variant in the GRIA2 gene was identified de novo in this individual, but has not been previously reported in association with disease. This … (more) The p.Phe628Ser variant in the GRIA2 gene was identified de novo in this individual, but has not been previously reported in association with disease. This variant was absent from large population databases, including the Genome Aggregation Database (http://gnomad.broadinstitute.org/). Computational tools predict that this variant is deleterious; however, the accuracy of in silico algorithms is limited. The GRIA2 gene has fewer missense variants in the general population than expected. A low rate of missense variation may suggest that this gene is intolerant to missense variation. These data were assessed using the ACMG/AMP variant interpretation guidelines. In summary, there is sufficient evidence to classify the p.Phe628Ser variant as likely pathogenic for GRIA2- related disease in an autosomal dominant manner based on the information above. [ACMG evidence codes used: PS2_moderate, PM2, PP3, PP2] (less) Comment on evidence: Heterozygous (de novo)

Comment:

The p.Phe628Ser variant in the GRIA2 gene was identified de novo in this individual, but has not been previously reported in association with disease. This variant was absent from large population databases, including the Genome Aggregation Database (http://gnomad.broadinstitute.org/). Computational tools predict that this variant is deleterious; however, the accuracy of in silico algorithms is limited. The GRIA2 gene has fewer missense variants in the general population than expected. A low rate of missense variation may suggest that this gene is intolerant to missense variation. These data were assessed using the ACMG/AMP variant interpretation guidelines. In summary, there is sufficient evidence to classify the p.Phe628Ser variant as likely pathogenic for GRIA2- related disease in an autosomal dominant manner based on the information above. [ACMG evidence codes used: PS2_moderate, PM2, PP3, PP2]

Germline Functional Evidence

There is no functional evidence in ClinVar for this variation. If you have generated functional data for this variation, please consider submitting that data to ClinVar.

Comment:

Citations for germline classification of this variant

There are no citations for germline classification of this variant in ClinVar. If you know of citations for this variation, please consider submitting that information to ClinVar.

Text-mined citations for this variant ...

Record last updated Jul 07, 2024

ClinVar Genomic variation as it relates to human health

NM_001083619.3(GRIA2):c.1883T>C (p.Phe628Ser)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...