VCV002499635.3 - ClinVar

GRCh38/hg38 19p13.12-13.11(chr19:15014099-16261691)

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

criteria provided, single submitter

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

GRCh38/hg38 19p13.12-13.11(chr19:15014099-16261691)

Variation ID: 2499635 Accession: VCV002499635.3

Type and length

copy number loss, -

Location

Cytogenetic: 19p13.12-13.11 19: 15014099-16261691 (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	Apr 30, 2023	Aug 18, 2023	Aug 14, 2023

HGVS

Protein change

Other names

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

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.
AKAP8		-	-	GRCh38 GRCh37	100	120
AKAP8L		-	-	GRCh38 GRCh37	38	67
AP1M1		-	-	GRCh38 GRCh37	15	32
BRD4		-	-	GRCh38 GRCh37	640	660
CASP14		-	-	GRCh38 GRCh37	60	76
CIB3		-	-	GRCh38 GRCh37	21	38
CYP4F11		-	-	GRCh38 GRCh37	57	73
CYP4F12		-	-	GRCh38 GRCh37	40	58
CYP4F2		-	-	GRCh38 GRCh37	53	79
CYP4F22		-	-	GRCh38 GRCh37	234	252

There are 97 more genes 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.
Chromosome 19p13.13 deletion syndrome	Pathogenic (1)	criteria provided, single submitter	Aug 14, 2023	RCV003223562.4

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 (Aug 14, 2023)	criteria provided, single submitter (ACMG/ClinGen CNV Guidelines, 2019) Method: curation	Chromosome 19p13.13 deletion syndrome Affected status: yes Allele origin: de novo	Daryl Scott Lab, Baylor College of Medicine Accession: SCV003919110.2 First in ClinVar: Apr 30, 2023 Last updated: Aug 18, 2023	Publications: PubMed (1) PubMed: 37673932 Comment: 1A, 2A, 3B (1.45) Clinical Features: Congenital total pulmonary venous return anomaly (present) , Necrotizing enterocolitis (present) , Conductive hearing impairment (present) , Atrial arrhythmia (present)

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
Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return.	Huth EA	European journal of human genetics : EJHG	2023	PMID: 37673932

Text-mined citations for this variant ...

Record last updated Jul 29, 2024

ClinVar Genomic variation as it relates to human health

GRCh38/hg38 19p13.12-13.11(chr19:15014099-16261691)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...