VCV002685437.1 - ClinVar

GRCh37/hg19 12q14.1-15(chr12:61755618-70035424)x1

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

GRCh37/hg19 12q14.1-15(chr12:61755618-70035424)x1

Variation ID: 2685437 Accession: VCV002685437.1

Type and length

copy number loss, -

Location

Cytogenetic: 12q14.1-15 12: 61755618-70035424 (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	Jan 26, 2024	Jan 26, 2024	Nov 14, 2022

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.
LEMD3		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	549	638
HMGA2		Little evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	31	47
GRIP1		No evidence available	No evidence available	GRCh38 GRCh37	674	691
AVPR1A		-	-	GRCh38 GRCh37	30	38
C12orf56	-	-	-	GRCh38 GRCh37	7	17
CAND1		-	-	GRCh38 GRCh37	29	40
CCT2		-	-	GRCh38 GRCh37	320	340
CPM		-	-	GRCh38 GRCh37	27	37
CPSF6		-	-	GRCh38 GRCh37	20	31
DPY19L2		-	-	GRCh38 GRCh37	61	75

There are 32 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.

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	Nov 14, 2022	RCV003483154.1

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 (Nov 14, 2022)	criteria provided, single submitter (ACMG/ClinGen CNV Guidelines, 2019) Method: clinical testing	not provided Affected status: unknown Allele origin: unknown	Quest Diagnostics Nichols Institute San Juan Capistrano Accession: SCV004231671.1 First in ClinVar: Jan 26, 2024 Last updated: Jan 26, 2024	Comment: The copy number loss of 12q14.1q15 involves numerous protein-coding genes. This deletion overlaps the 12q14 microdeletion syndrome region (Heldt 2018, Fischetto 2017, Mc Cormack 2015, … (more) The copy number loss of 12q14.1q15 involves numerous protein-coding genes. This deletion overlaps the 12q14 microdeletion syndrome region (Heldt 2018, Fischetto 2017, Mc Cormack 2015, Nso-Roca 2014, Bibb 2012). Haploinsufficiency of LEMD3 is associated with autosomal dominant Buschke-Ollendorff syndrome and osteopoikilosis with or without melorheostosis (OMIM 166700). In addition, deletions of 12q14 affecting gene HMGA2 have been reported in patients with autosomal dominant Silver-Russell syndrome-5 (OMIM 618908, Hubner 2020, Mercadante 2020). Thus, based on current medical literature and gene content, this copy number variant (CNV) is interpreted as pathogenic. References Bibb et al., Am J Med Genet A. 2012 Feb;158A(2):417-22. PMID: 22140081 Deng et al., Front Genet. 2021 Sep 1;12:716874. PMID: 34539745 Fischetto et al., Am J Med Genet A. 2017 Jul;173(7):1922-1930. PMID: 28407409 Heldt et al., Eur J Med Genet. 2018 Aug;61(8):421-427. PMID: 29501611 Hubner et al., J Clin Endocrinol Metab. 2020 Jul 1;105(7):dgaa273. PMID: 32421827 Mc Cormack et al., Case Rep Genet. 2015;2015:192071. PMID: 26266063 Mercadante et al., Ital J Pediatr. 2020 Jul 28;46(1):108. PMID: 32723361 Nso-Roca et al., J Pediatr Endocrinol Metab. 2014 May;27(5-6):539-43. PMID: 24468604 (less)

Comment:

The copy number loss of 12q14.1q15 involves numerous protein-coding genes. This deletion overlaps the 12q14 microdeletion syndrome region (Heldt 2018, Fischetto 2017, Mc Cormack 2015, Nso-Roca 2014, Bibb 2012). Haploinsufficiency of LEMD3 is associated with autosomal dominant Buschke-Ollendorff syndrome and osteopoikilosis with or without melorheostosis (OMIM 166700). In addition, deletions of 12q14 affecting gene HMGA2 have been reported in patients with autosomal dominant Silver-Russell syndrome-5 (OMIM 618908, Hubner 2020, Mercadante 2020). Thus, based on current medical literature and gene content, this copy number variant (CNV) is interpreted as pathogenic. References Bibb et al., Am J Med Genet A. 2012 Feb;158A(2):417-22. PMID: 22140081 Deng et al., Front Genet. 2021 Sep 1;12:716874. PMID: 34539745 Fischetto et al., Am J Med Genet A. 2017 Jul;173(7):1922-1930. PMID: 28407409 Heldt et al., Eur J Med Genet. 2018 Aug;61(8):421-427. PMID: 29501611 Hubner et al., J Clin Endocrinol Metab. 2020 Jul 1;105(7):dgaa273. PMID: 32421827 Mc Cormack et al., Case Rep Genet. 2015;2015:192071. PMID: 26266063 Mercadante et al., Ital J Pediatr. 2020 Jul 28;46(1):108. PMID: 32723361 Nso-Roca et al., J Pediatr Endocrinol Metab. 2014 May;27(5-6):539-43. PMID: 24468604

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 Feb 04, 2024

ClinVar Genomic variation as it relates to human health

GRCh37/hg19 12q14.1-15(chr12:61755618-70035424)x1

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...