VCV002580181.1 - ClinVar

NM_001005361.3(DNM2):c.37G>C (p.Val13Leu)

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_001005361.3(DNM2):c.37G>C (p.Val13Leu)

Variation ID: 2580181 Accession: VCV002580181.1

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 19p13.2 19: 10718279 (GRCh38) [ NCBI UCSC ] 19: 10828955 (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	Sep 23, 2023	Sep 23, 2023	Sep 19, 2023

HGVS

Nucleotide	Protein	Molecular consequence
NM_001005361.3:c.37G>C MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_001005361.1:p.Val13Leu	missense
NM_001005360.3:c.37G>C	NP_001005360.1:p.Val13Leu	missense
NM_001005362.3:c.37G>C	NP_001005362.1:p.Val13Leu	missense
NM_001190716.2:c.37G>C	NP_001177645.1:p.Val13Leu	missense
NM_004945.4:c.37G>C	NP_004936.2:p.Val13Leu	missense
NC_000019.10:g.10718279G>C
NC_000019.9:g.10828955G>C
NG_008792.1:g.5201G>C
NG_197946.1:g.442G>C
LRG_238:g.5201G>C
LRG_238t1:c.37G>C	LRG_238p1:p.Val13Leu
LRG_238t2:c.37G>C	LRG_238p2:p.Val13Leu

... more HGVS ... less HGVS

Protein change

V13L

Other names

Canonical SPDI

NC_000019.10:10718278:G: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.
DNM2		-	-	GRCh38 GRCh37	1137	1234
LOC130063529	-	-	-	GRCh38	-	71

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.
Autosomal dominant centronuclear myopathy	Uncertain significance (1)	criteria provided, single submitter	Sep 19, 2023	RCV003329146.3

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 (Sep 19, 2023)	criteria provided, single submitter (ACMG Guidelines, 2015) Method: clinical testing	Autosomal dominant centronuclear myopathy (Sporadic) Affected status: yes Allele origin: de novo	Department of Pathophysiology and Transplantation, University of Milan Accession: SCV004035232.1 First in ClinVar: Sep 23, 2023 Last updated: Sep 23, 2023	Comment: i) the variant is absent from population database (GnomAD MAF:0); ii) the variant was not present in patient’s parents, confirming de novo inheritance (previously observed … (more) i) the variant is absent from population database (GnomAD MAF:0); ii) the variant was not present in patient’s parents, confirming de novo inheritance (previously observed for several other pathogenic DNM2 variants) and excluding the chance of a rare (private) inherited polymorphism; iii) the affected position is highly conserved across species and among DNM2 homolog genes DNM1 and DNM3; iv) several pathogenicity prediction tools support (or does not exclude) the pathogenic role of this missense variant; v) the rate of benign missense DNM2 mutations is low; vi) histological analysis in patient's muscle detects the presence of centralized nuclei and fiber size variation / hypotrophy. (less) Clinical Features: Muscle weakness (present) , Fatigue (present) , Exercise intolerance (present) Age: 50-59 years Sex: female Ethnicity/Population group: Italian Geographic origin: Italy Method: Whole Exome Sequencing was performed on the affected proband starting with 100 ng of high-quality DNA. Agilent SureSelectXT Human All Exon V8 library preparation and target enrichment kit were used. The libraries underwent paired-end sequencing on a NextSeq2000 Illumina platform.

Comment:

i) the variant is absent from population database (GnomAD MAF:0); ii) the variant was not present in patient’s parents, confirming de novo inheritance (previously observed for several other pathogenic DNM2 variants) and excluding the chance of a rare (private) inherited polymorphism; iii) the affected position is highly conserved across species and among DNM2 homolog genes DNM1 and DNM3; iv) several pathogenicity prediction tools support (or does not exclude) the pathogenic role of this missense variant; v) the rate of benign missense DNM2 mutations is low; vi) histological analysis in patient's muscle detects the presence of centralized nuclei and fiber size variation / hypotrophy.

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 Jun 23, 2024

ClinVar Genomic variation as it relates to human health

NM_001005361.3(DNM2):c.37G>C (p.Val13Leu)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...