VCV000236259.3 - ClinVar

NM_003491.4(NAA10):c.382T>A (p.Phe128Ile)

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.

(3)

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.

Pathogenic/Likely pathogenic

criteria provided, multiple submitters, no conflicts

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_003491.4(NAA10):c.382T>A (p.Phe128Ile)

Variation ID: 236259 Accession: VCV000236259.3

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: Xq28 X: 153932075 (GRCh38) [ NCBI UCSC ] X: 153197528 (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 24, 2016	Oct 26, 2024	Mar 31, 2016

HGVS

Nucleotide	Protein	Molecular consequence
NM_003491.4:c.382T>A MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_003482.1:p.Phe128Ile	missense
NM_001256119.2:c.341+241T>A		intron variant
NM_001256120.2:c.364T>A	NP_001243049.1:p.Phe122Ile	missense
NC_000023.11:g.153932075A>T
NC_000023.10:g.153197528A>T
NG_031987.1:g.8080T>A

... more HGVS ... less HGVS

Protein change

F128I, F122I

Other names

Canonical SPDI

NC_000023.11:153932074:A:T

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

ClinGen: CA10581583 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.
NAA10		Little evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	157	436

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.
Ogden syndrome	Pathogenic (2)	criteria provided, single submitter	Mar 31, 2016	RCV000225362.4
Intellectual disability	Likely pathogenic (1)	criteria provided, single submitter	Jan 1, 2014	RCV000824880.3

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.
Pathogenic (Mar 31, 2016)	criteria provided, single submitter (ACMG Guidelines, 2015) Method: clinical testing	Ogden syndrome Affected status: yes Allele origin: de novo	Institute of Human Genetics, FAU Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg Accession: SCV000267572.2 First in ClinVar: Jun 24, 2016 Last updated: Jun 24, 2016	Publications: PubMed (1) PubMed: 27094817 Other databases http://www.LOVD.nl/NAA10_000005 http://www.LOVD.nl/NAA10_000005 Age: 0-9 years Sex: female
Likely pathogenic (Jan 01, 2014)	criteria provided, single submitter (ACMG Guidelines, 2007) Method: clinical testing	Intellectual disability Affected status: yes Allele origin: de novo	Equipe Genetique des Anomalies du Developpement, Université de Bourgogne Accession: SCV000965789.1 First in ClinVar: Aug 26, 2019 Last updated: Aug 26, 2019
Likely pathogenic (Jun 01, 2022)	no assertion criteria provided Method: provider interpretation	Ogden syndrome Affected status: yes Allele origin: inherited	Solve-RD Consortium Accession: SCV005091285.1 First in ClinVar: Oct 26, 2024 Last updated: Oct 26, 2024 Comment: Variant identified during reanalysis of unsolved cases by the Solve-RD project. The Solve-RD project has received funding from the European Union’s Horizon 2020 research and … (more) Variant identified during reanalysis of unsolved cases by the Solve-RD project. The Solve-RD project has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 779257. (less)	Comment: Variant confirmed as disease-causing by referring clinical team

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.

Citations for germline classification of this variant

Title	Author	Journal	Year	Link
http://www.LOVD.nl/NAA10_000005	-	-	-	-

Text-mined citations for this variant ...

Record last updated Oct 27, 2024

ClinVar Genomic variation as it relates to human health

NM_003491.4(NAA10):c.382T>A (p.Phe128Ile)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...