VCV001711111.2 - ClinVar

NC_000009.12:g.139481_407477del

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.

Pathogenic

no assertion criteria provided

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NC_000009.12:g.139481_407477del

Variation ID: 1711111 Accession: VCV001711111.2

Type and length

Deletion, 267,997 bp

Location

Cytogenetic: 9p24.3 9: 139481-407477 (GRCh38) [ 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 22, 2022	Jun 9, 2024	Oct 5, 2023

HGVS

Nucleotide	Protein	Molecular consequence
NC_000009.12:g.139481_407477del

Protein change

Other names

268-KB DEL, EX1-29DEL

Canonical SPDI

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

OMIM: 611432.0011 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.
DOCK8		-	-	GRCh38 GRCh37	2409	3010
DOCK8-AS1	-	-	-	GRCh38 GRCh37	-	410
LOC110120718	-	-	-	GRCh38	-	10
LOC126860552	-	-	-	GRCh38	-	220
LOC130001435	-	-	-	GRCh38	-	122
LOC130001436	-	-	-	GRCh38	-	116
LOC130001437	-	-	-	GRCh38	-	155
LOC130001438	-	-	-	GRCh38	-	130
LOC130001439	-	-	-	GRCh38	-	142
LOC130001440	-	-	-	GRCh38	-	142

There is 1 more gene affected by this variant. See the full set of genes in Variation Viewer (GRCh38).

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.
Combined immunodeficiency due to DOCK8 deficiency	Pathogenic (1)	no assertion criteria provided	Oct 5, 2023	RCV002292410.4

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 (Oct 05, 2023)	no assertion criteria provided Method: literature only	HYPER-IgE SYNDROME 2, AUTOSOMAL RECESSIVE, WITH RECURRENT INFECTIONS Affected status: not provided Allele origin: germline	OMIM Accession: SCV002584919.2 First in ClinVar: Oct 22, 2022 Last updated: Jun 09, 2024	Publications: PubMed (1) PubMed: 33290277 Comment on evidence: For discussion of the 268-kb deletion spanning exons 1 to 29 (chr9.139,481_407,477del, GRCh38) of the DOCK8 gene that was identified in compound heterozygous state in … (more) For discussion of the 268-kb deletion spanning exons 1 to 29 (chr9.139,481_407,477del, GRCh38) of the DOCK8 gene that was identified in compound heterozygous state in a patient with autosomal recessive hyper-IgE syndrome-2 (HIES2; 243700) by Pillay et al. (2021), see 611432.0010. (less)

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
Somatic reversion of pathogenic DOCK8 variants alters lymphocyte differentiation and function to effectively cure DOCK8 deficiency.	Pillay BA	The Journal of clinical investigation	2021	PMID: 33290277

Text-mined citations for this variant ...

Record last updated Jun 30, 2024

ClinVar Genomic variation as it relates to human health

NC_000009.12:g.139481_407477del

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...