VCV000596803.5 - ClinVar

NM_004006.3(DMD):c.10087-2A>G

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.

(2)

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_004006.3(DMD):c.10087-2A>G

Variation ID: 596803 Accession: VCV000596803.5

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: Xp21.2 X: 31178807 (GRCh38) [ NCBI UCSC ] X: 31196924 (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	Dec 16, 2018	Dec 24, 2022	Dec 16, 2022

HGVS

Nucleotide	Protein	Molecular consequence
NM_004006.3:c.10087-2A>G MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.		splice acceptor
NM_000109.4:c.10063-2A>G		splice acceptor
NM_004009.3:c.10075-2A>G		splice acceptor
NM_004010.3:c.9718-2A>G		splice acceptor
NM_004011.4:c.6064-2A>G		splice acceptor
NM_004012.4:c.6055-2A>G		splice acceptor
NM_004013.3:c.2707-2A>G		splice acceptor
NM_004014.3:c.1900-2A>G		splice acceptor
NM_004015.3:c.883-2A>G		splice acceptor
NM_004016.3:c.883-2A>G		splice acceptor
NM_004017.3:c.883-2A>G		splice acceptor
NM_004018.3:c.883-2A>G		splice acceptor
NM_004019.3:c.883-2A>G		splice acceptor
NM_004020.4:c.2707-2A>G		splice acceptor
NM_004021.3:c.2707-2A>G		splice acceptor
NM_004022.3:c.2707-2A>G		splice acceptor
NM_004023.3:c.2707-2A>G		splice acceptor
NC_000023.11:g.31178807T>C
NC_000023.10:g.31196924T>C
NG_012232.1:g.2165803A>G
LRG_199:g.2165803A>G

... more HGVS ... less HGVS

Protein change

Other names

Canonical SPDI

NC_000023.11:31178806: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: rs1569420861 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.
DMD		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	9338	9631

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	Pathogenic (1)	criteria provided, single submitter	Apr 27, 2018	RCV000732750.4
Duchenne muscular dystrophy	Likely pathogenic (1)	criteria provided, single submitter	Dec 16, 2022	RCV002470964.1

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 (Apr 27, 2018)	criteria provided, single submitter (EGL ClinVar v180209 classification definitions) Method: clinical testing	not provided Affected status: unknown Allele origin: germline	Eurofins Ntd Llc (ga) Accession: SCV000860734.1 First in ClinVar: Dec 16, 2018 Last updated: Dec 16, 2018	Other databases http://www.egl-eurofins.com/emvc… http://www.egl-eurofins.com/emvclass/emvclass.php?approved_symbol=DMD Number of individuals with the variant: 1 Sex: mixed
Likely pathogenic (Dec 16, 2022)	criteria provided, single submitter (ACMG Guidelines, 2015) Method: clinical testing	Duchenne muscular dystrophy Affected status: yes Allele origin: germline	Laboratory of Medical Genetics, National & Kapodistrian University of Athens Accession: SCV002769646.1 First in ClinVar: Dec 24, 2022 Last updated: Dec 24, 2022	Publications: PubMed (1) PubMed: 25741868 Comment: PVS1, PM2

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
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	Genetics in medicine : official journal of the American College of Medical Genetics	2015	PMID: 25741868
http://www.egl-eurofins.com/emvclass/emvclass.php?approved_symbol=DMD	-	-	-	-

Text-mined citations for rs1569420861 ...

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 Jun 10, 2023

ClinVar Genomic variation as it relates to human health

NM_004006.3(DMD):c.10087-2A>G

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for rs1569420861 ...