VCV001691586.3 - ClinVar

NM_002576.5(PAK1):c.1016A>G (p.Glu339Gly)

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.

Uncertain significance

criteria provided, single submitter

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_002576.5(PAK1):c.1016A>G (p.Glu339Gly)

Variation ID: 1691586 Accession: VCV001691586.3

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 11q13.5 11: 77340746 (GRCh38) [ NCBI UCSC ] 11: 77051791 (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	Jun 18, 2022	Mar 4, 2023	Dec 9, 2021

HGVS

Nucleotide	Protein	Molecular consequence
NM_002576.5:c.1016A>G MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_002567.3:p.Glu339Gly	missense
NM_001128620.2:c.1016A>G	NP_001122092.1:p.Glu339Gly	missense
NM_001376268.1:c.1016A>G	NP_001363197.1:p.Glu339Gly	missense
NM_001376269.1:c.1016A>G	NP_001363198.1:p.Glu339Gly	missense
NM_001376270.1:c.1016A>G	NP_001363199.1:p.Glu339Gly	missense
NM_001376271.1:c.1016A>G	NP_001363200.1:p.Glu339Gly	missense
NM_001376272.1:c.1037A>G	NP_001363201.1:p.Glu346Gly	missense
NM_001376273.1:c.1016A>G	NP_001363202.1:p.Glu339Gly	missense
NM_001376274.1:c.1016A>G	NP_001363203.1:p.Glu339Gly	missense
NM_001376275.1:c.1016A>G	NP_001363204.1:p.Glu339Gly	missense
NM_001376276.1:c.1016A>G	NP_001363205.1:p.Glu339Gly	missense
NM_001376277.1:c.1016A>G	NP_001363206.1:p.Glu339Gly	missense
NM_001376278.1:c.1016A>G	NP_001363207.1:p.Glu339Gly	missense
NM_001376279.1:c.1016A>G	NP_001363208.1:p.Glu339Gly	missense
NM_001376280.1:c.1016A>G	NP_001363209.1:p.Glu339Gly	missense
NM_001376281.1:c.1016A>G	NP_001363210.1:p.Glu339Gly	missense
NM_001376282.1:c.1016A>G	NP_001363211.1:p.Glu339Gly	missense
NM_001376283.1:c.1016A>G	NP_001363212.1:p.Glu339Gly	missense
NM_001376284.1:c.1016A>G	NP_001363213.1:p.Glu339Gly	missense
NM_001376285.1:c.1016A>G	NP_001363214.1:p.Glu339Gly	missense
NM_001376286.1:c.1016A>G	NP_001363215.1:p.Glu339Gly	missense
NM_001376287.1:c.1016A>G	NP_001363216.1:p.Glu339Gly	missense
NM_001376288.1:c.1016A>G	NP_001363217.1:p.Glu339Gly	missense
NM_001376289.1:c.1016A>G	NP_001363218.1:p.Glu339Gly	missense
NM_001376290.1:c.1016A>G	NP_001363219.1:p.Glu339Gly	missense
NM_001376291.1:c.1016A>G	NP_001363220.1:p.Glu339Gly	missense
NM_001376292.1:c.1016A>G	NP_001363221.1:p.Glu339Gly	missense
NM_001376293.1:c.1016A>G	NP_001363222.1:p.Glu339Gly	missense
NM_001376294.1:c.1007A>G	NP_001363223.1:p.Glu336Gly	missense
NM_001376295.1:c.839A>G	NP_001363224.1:p.Glu280Gly	missense
NM_001376301.1:c.767A>G	NP_001363230.1:p.Glu256Gly	missense
NM_001376302.1:c.722A>G	NP_001363231.1:p.Glu241Gly	missense
NM_001376303.1:c.728A>G	NP_001363232.1:p.Glu243Gly	missense
NM_001376304.1:c.722A>G	NP_001363233.1:p.Glu241Gly	missense
NM_001376305.1:c.722A>G	NP_001363234.1:p.Glu241Gly	missense
NR_164797.1:n.1232A>G		non-coding transcript variant
NR_164798.1:n.1235A>G		non-coding transcript variant
NC_000011.10:g.77340746T>C
NC_000011.9:g.77051791T>C
NG_029900.2:g.138318A>G

... more HGVS ... less HGVS

Protein change

E336G, E339G, E346G, E241G, E243G, E256G, E280G

Other names

Canonical SPDI

NC_000011.10:77340745: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

dbSNP: rs2136238391 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.
PAK1		-	-	GRCh38 GRCh37	92	101

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.
not provided	Uncertain significance (1)	criteria provided, single submitter	Dec 9, 2021	RCV002254992.3

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.
Uncertain significance (Dec 09, 2021)	criteria provided, single submitter (GeneDx Variant Classification Process June 2021) Method: clinical testing	Not Provided Affected status: yes Allele origin: germline	GeneDx Accession: SCV002526172.2 First in ClinVar: Jun 18, 2022 Last updated: Mar 04, 2023	Comment: Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; … (more) Not observed at significant frequency in large population cohorts (gnomAD); 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 (less)

Comment:

Not observed at significant frequency in large population cohorts (gnomAD); 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

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 rs2136238391 ...

These citations are identified by LitVar using the rs number, so they may include citations for more than one variant at this location. Please review the LitVar results carefully for your variant of interest.

Record last updated Dec 25, 2023

ClinVar Genomic variation as it relates to human health

NM_002576.5(PAK1):c.1016A>G (p.Glu339Gly)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for rs2136238391 ...