NM_144997.7(FLCN):c.95G>A (p.Gly32Glu) AND Birt-Hogg-Dube syndrome

This record was updated by the submitter. Please see the current version.

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jul 7, 2023
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV001062369.4

Allele description

NM_144997.7(FLCN):c.95G>A (p.Gly32Glu)

Gene:

FLCN:folliculin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

17p11.2

Genomic location:

Preferred name:

NM_144997.7(FLCN):c.95G>A (p.Gly32Glu)

HGVS:

NC_000017.11:g.17228043C>T
NG_008001.2:g.14146G>A
NM_001353229.2:c.95G>A
NM_001353230.2:c.95G>A
NM_001353231.2:c.95G>A
NM_144606.7:c.95G>A
NM_144997.7:c.95G>AMANE SELECT
NP_001340158.1:p.Gly32Glu
NP_001340159.1:p.Gly32Glu
NP_001340160.1:p.Gly32Glu
NP_653207.1:p.Gly32Glu
NP_659434.2:p.Gly32Glu
LRG_325t1:c.95G>A
LRG_325:g.14146G>A
NC_000017.10:g.17131357C>T
NM_144997.5:c.95G>A

Protein change:

G32E

Links:

dbSNP: rs587778366

NCBI 1000 Genomes Browser:

rs587778366

Molecular consequence:

NM_001353229.2:c.95G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001353230.2:c.95G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001353231.2:c.95G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_144606.7:c.95G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_144997.7:c.95G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Birt-Hogg-Dube syndrome
Synonyms:: BHD syndrome; Birt Hogg Dubé syndrome
Identifiers:: MONDO: MONDO:0800444; MedGen: C0346010; Orphanet: 122; OMIM: PS135150

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001227164	Invitae	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Jul 7, 2023)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001227164

Invitae

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Jul 7, 2023)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Invitae, SCV001227164.4

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

Description

Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt FLCN protein function. ClinVar contains an entry for this variant (Variation ID: 134424). This variant has not been reported in the literature in individuals affected with FLCN-related conditions. This variant is present in population databases (rs587778366, gnomAD 0.003%). This sequence change replaces glycine, which is neutral and non-polar, with glutamic acid, which is acidic and polar, at codon 32 of the FLCN protein (p.Gly32Glu). 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.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Jun 9, 2024

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