VCV001712487.2 - ClinVar

NM_001242896.3(DEPDC5):c.413+1G>A

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.

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_001242896.3(DEPDC5):c.413+1G>A

Variation ID: 1712487 Accession: VCV001712487.2

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 22q12.2 22: 31768864 (GRCh38) [ NCBI UCSC ] 22: 32164850 (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	Oct 30, 2022	Mar 11, 2023	Sep 20, 2022

HGVS

Nucleotide	Protein	Molecular consequence
NM_001242896.3:c.413+1G>A MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.		splice donor
NM_001007188.4:c.413+1G>A		splice donor
NM_001136029.4:c.413+1G>A		splice donor
NM_001242897.2:c.413+1G>A		splice donor
NM_001363852.2:c.413+1G>A		splice donor
NM_001363854.2:c.413+1G>A		splice donor
NM_001364318.2:c.413+1G>A		splice donor
NM_001364319.2:c.413+1G>A		splice donor
NM_001364320.2:c.413+1G>A		splice donor
NM_001369901.1:c.329+1G>A		splice donor
NM_001369902.1:c.329+1G>A		splice donor
NM_001369903.1:c.413+1G>A		splice donor
NM_014662.6:c.413+1G>A		splice donor
NC_000022.11:g.31768864G>A
NC_000022.10:g.32164850G>A
NG_034067.1:g.19914G>A

... more HGVS ... less HGVS

Protein change

Other names

Canonical SPDI

NC_000022.11:31768863:G:A

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.
DEPDC5		-	-	GRCh38 GRCh37	2337	2368

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.
Epilepsy, familial focal, with variable foci 1	Likely pathogenic (2)	criteria provided, multiple submitters, no conflicts	Sep 20, 2022	RCV002294742.2

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 (-)	criteria provided, single submitter (ACMG Guidelines, 2015) Method: clinical testing	Epilepsy, familial focal, with variable foci 1 (Autosomal dominant inheritance) Affected status: yes Allele origin: paternal	Wangler Lab, Baylor College of Medicine Accession: SCV002587797.1 First in ClinVar: Oct 29, 2022 Last updated: Oct 29, 2022	Comment: This splice donor DEPDC5 variant at c.413+1G>A was seen on exome through the Texome project (R01HG011795).This variant has been observed in gnomAD with a frequency … (more) This splice donor DEPDC5 variant at c.413+1G>A was seen on exome through the Texome project (R01HG011795).This variant has been observed in gnomAD with a frequency of <0.001%.This variant is predicted to disrupt the splicing donor site which may cause exon skipping, intron retention, or other splicing defects (SpliceAI: 0.900). We believe this variant is likely pathogenic. (less) Age: 0-9 years Sex: male
Likely pathogenic (Sep 20, 2022)	criteria provided, single submitter (ACMG Guidelines, 2015) Method: clinical testing	Epilepsy, familial focal, with variable foci 1 Affected status: unknown Allele origin: unknown	Baylor Genetics Accession: SCV003835625.1 First in ClinVar: Mar 11, 2023 Last updated: Mar 11, 2023

Comment:

This splice donor DEPDC5 variant at c.413+1G>A was seen on exome through the Texome project (R01HG011795).This variant has been observed in gnomAD with a frequency of <0.001%.This variant is predicted to disrupt the splicing donor site which may cause exon skipping, intron retention, or other splicing defects (SpliceAI: 0.900). We believe this variant is likely pathogenic.

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 Apr 06, 2024

ClinVar Genomic variation as it relates to human health

NM_001242896.3(DEPDC5):c.413+1G>A

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...