VCV002999824.2 - ClinVar

NM_144997.7(FLCN):c.1595_1603del (p.Thr532_Leu535delinsMet)

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.

Uncertain significance

criteria provided, multiple submitters, no conflicts

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_144997.7(FLCN):c.1595_1603del (p.Thr532_Leu535delinsMet)

Variation ID: 2999824 Accession: VCV002999824.2

Type and length

Deletion, 9 bp

Location

Cytogenetic: 17p11.2 17: 17213792-17213800 (GRCh38) [ NCBI UCSC ] 17: 17117106-17117114 (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	Feb 29, 2024	Nov 3, 2024	Jan 9, 2024

HGVS

Nucleotide	Protein	Molecular consequence
NM_144997.7:c.1595_1603del MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_659434.2:p.Thr532_Leu535delinsMet	inframe indel
NM_001353229.2:c.1649_1657del	NP_001340158.1:p.Thr550_Leu553delinsMet	inframe indel
NM_001353230.2:c.1595_1603del	NP_001340159.1:p.Thr532_Leu535delinsMet	inframe indel
NM_001353231.2:c.1595_1603del	NP_001340160.1:p.Thr532_Leu535delinsMet	inframe indel
NM_144997.5:c.1595_1603del
NM_144997.5:c.1595_1603delCACAGAAGC	NP_659434.2:p.Thr532_Leu535delinsMet	inframe indel
NC_000017.11:g.17213792_17213800del
NC_000017.10:g.17117106_17117114del
NG_008001.2:g.28389_28397del
LRG_325:g.28389_28397del
LRG_325t1:c.1595_1603del	LRG_325p1:p.Thr532_Leu535delinsMet

... more HGVS ... less HGVS

Protein change

Other names

Canonical SPDI

NC_000017.11:17213791:GCTTCTGTG:

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.
FLCN		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	2404	2524

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.
Birt-Hogg-Dube syndrome	Uncertain significance (1)	criteria provided, single submitter	Mar 11, 2023	RCV003854935.2
not provided	Uncertain significance (1)	criteria provided, single submitter	Jan 9, 2024	RCV004775523.1

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.
Uncertain significance (Mar 11, 2023)	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015)) Method: clinical testing	Birt-Hogg-Dube syndrome Affected status: unknown Allele origin: germline	Labcorp Genetics (formerly Invitae), Labcorp Accession: SCV004661525.1 First in ClinVar: Feb 28, 2024 Last updated: Feb 28, 2024	Comment: In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant … (more) In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. This variant has not been reported in the literature in individuals affected with FLCN-related conditions. This variant is not present in population databases (gnomAD no frequency). This variant, c.1595_1603del, is a complex sequence change that results in the deletion of 4 and insertion of 1 amino acid(s) in the FLCN protein (p.Thr532_Leu535delinsMet). (less)
Uncertain significance (Jan 09, 2024)	criteria provided, single submitter (GeneDx Variant Classification Process June 2021) Method: clinical testing	Not Provided Affected status: yes Allele origin: germline	GeneDx Accession: SCV005385503.1 First in ClinVar: Nov 03, 2024 Last updated: Nov 03, 2024	Comment: In-frame deletion of 4 amino acids and insertion of 1 amino acid in a non-repeat region; Not observed at significant frequency in large population cohorts … (more) In-frame deletion of 4 amino acids and insertion of 1 amino acid in a non-repeat region; Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports a deleterious effect on protein structure/function; Has not been previously published as pathogenic or benign to our knowledge; This variant is associated with the following publications: (PMID: 17028174) (less)

Comment:

In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. This variant has not been reported in the literature in individuals affected with FLCN-related conditions. This variant is not present in population databases (gnomAD no frequency). This variant, c.1595_1603del, is a complex sequence change that results in the deletion of 4 and insertion of 1 amino acid(s) in the FLCN protein (p.Thr532_Leu535delinsMet).

Comment:

In-frame deletion of 4 amino acids and insertion of 1 amino acid in a non-repeat region; Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports a deleterious effect on protein structure/function; Has not been previously published as pathogenic or benign to our knowledge; This variant is associated with the following publications: (PMID: 17028174)

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 Nov 03, 2024

ClinVar Genomic variation as it relates to human health

NM_144997.7(FLCN):c.1595_1603del (p.Thr532_Leu535delinsMet)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...